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Monday, May 25, 2009

Renal Artery Stenosis: bedside rapid Diagnosis even in its initial stage with Quantum-Biophysical-Semeiotics

Overlooked Quantum-Biophysical-Semeiotics does really exists(1-12). See also www.semeioticabiofisica.it Interestingly, due to the presence of no local realm in all biological systems, in one second doctors may recognize that in urinary tract there is something wrong (10). Soon thereafter physicians can localize the precise site of disorder, ascertaining the real nature. As regards early diagnosis of renal artery stenosis, Quantum Biophysical Semeiotics allows doctor to bedside recognize kidney disorders, since initial stages of INHERITED Real Risk. Perhaps, for instance, available evidence does not clearly support one treatment approach over another for atherosclerotic renal artery stenosis. However, we must admit that patients with such as disorder are properly diagnosed exclusively a long time after initial disease onset, as in our case. Unfortunately, all around the world, General Practitioners know only the traditional physical semeiotics, that isn't so efficacious to allow doctor to recognize, since its first stage, Renal Artery Stenosis. Nowadays, physicians can bedside recognize SINCE BIRTH real risk of kidney diseases, both oncological and degenerative in nature (1-10). In order to recognize Renal Artery Stenosis, the following easy and quick manoeuvre proved to be really efficacious in my long year clinical experience: in health, doctor first of all delimits kidney area, as I described, e.g., in above-cited website, Technical Page N° 5 (14, 15). Subsequently, doctor increases the pressure of sthetoscope bell- piece, localized on kidney cutaneous projection, causing kidney dilation (due its congestion) immediately , than kidney size reduces (due to de- congestion)to its minimal value. At this point, in health pressure prompt interruption is "rapidly" - in 2 sec or less - followed by the return of kidney to its normal size, indicating a physiological blood flow in renal artery (15). On the contrary, in case of renal artery stenosis such as latency time results more than 2 sec., in relation to the severity of underlying disease (16). Interesting information about renal inherited real risk are illustrated in my previous paper (16).

References:

1. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica Quantistica. 15 Dicembre 2007 http://www.ilpungolo.com/leggi- tutto.asp?IDS=13&NWS=NWS5243

2. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica Endocrinologica: Meccanica Quantistica e Meccanismi d’Azione Ormonali. Dicembre 2007, www.fce.it, http://www.fcenews.it/index.php?option=com_content&task=view&id=816&Itemid=45

3. Stagnaro Sergio e Paolo Manzelli. Natura Quantistica di una Originale Manovra Semeiotico-Biofisica di Epatopatia . Dicembre 2007, http://www.fcenews.it/index.php?option=com_content&task=view&id=862&Itemid=45

4. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica: Realtà non- locale in Biologia. Dicembre 2007, www.ilpungolo.com, http://www.ilpungolo.com/leggi-tutto.asp?IDS=13&NWS=NWS5217

5. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica Quantistica: la manovra di attivazione surrenalica jatrogenetica, 09-1-2008, http://www.fcenews.it/index.php?option=com_content&task=view&id=161&Itemid=63

6. Stagnaro Sergio. Bedside Biophysical-Semeiotic Osteocalcin Test in Diagnosing and Monitoring Diabetes. The Lancet, January 28, 2008. http://www.thelancet.com/journals/lancet/article/PIIS0140673608601014/comments?action=view&totalComments=2

7. Stagnaro Sergio. Il test Semeiotico-Biofisico della Osteocalcina nella prevenzione primaria del diabete mellito. Febbraio 2008. http://www.fcenews.it/index.php?option=com_content&task=view&id=909&Itemid=47

8. Stagnaro Sergio. Esperimento di Lory e Crisi dei Fondamenti della Medicina Occidentale. www.ilpungolo.com. 17 Febbraio 2008 http://www.ilpungolo.com/leggi-tutto.asp?NWS=NWS5387&IDS=13

9. Stagnaro Sergio e Paolo Manzelli. L’Esperimento di Lory. Scienza e Conoscenza, N° 23, 13 Marzo 2008. http://www.scienzaeconoscenza.it//articolo.php?id=17775

10. Stagnaro Sergio. Reale Rischio Congenito di Cancro Renale Diagnosticato con la Semeiotica Biofisica: il Segno di Pollio. www.ilpungolo.com, 25 Marzo 2008, http://www.ilpungolo.com/leggi- tutto.asp?NWS=NWS5480&IDS=13

11. Stagnaro Sergio. Biological System Functional Modification parallels Gene Mutation. www.Nature.com,March 13, 2008, http://blogs.nature.com/nm/spoonful/2008/03/gout_gene.html 12. Stagnaro Sergio. Melanoma? Escluso in 1 Secondo con La Semeiotica Biofisica Quantistica. Il Reale Rischio Congenito di Melanoma. www.ilpungolo.com, 9 Aprile 2008, http://www.ilpungolo.com/leggi- tutto.asp?IDS=13&NWS=NWS5524

13. Stagnaro Sergio. Diagnosi clinica di cuore sano in un secondo! 7 Aprile 2008, http://www.fcenews.it/index.php?option=com_content&task=view&id=1218&Itemid=47

14. Stagnaro Sergio . Also Family Physicians are able of greatest clinical Discoveries! Annals Family Medicine,(16 April 2008), http://www.annfammed.org/cgi/eletters/6/2/175

15. Stagnaro-Neri M., Stagnaro S. Introduzione alla Semeiotica Biofisica. Il Terreno Oncologico. Ed. Travel Factory, Roma, 2004. http://www.travelfactory.it

16) Stagnaro Sergio. Renin-angiotensin blockade and kidney disease inherited real risk. The Lancet.com, September 23, 2008. http://www.thelancet.com/journals/lancet/article/PIIS014067360861212X/comments?action=view&totalComments=2#1841

Friday, May 22, 2009

Quantum-Biophysical-Semeiotic bedside Detecting Atherosclerosis from initial, asymptomatic Stage. Inherited real Risk.

Endoarteriolar Blocking Devices (EBD), derived from arteriolar medial layer, and ubiquitous in a single point of vascular wall with two (= arterioles) or more (= small arteries) layers of smooth muscle cells, according to Hammersen [1], protruding to the lumen, show very different structure and form, under physiological and pathological conditions: small cushions with wide base, polypoid formations, generally pedunculated [2-5], sphincteric formations, intimal contractile architectures. More precisely speaking, only type II, normal, physiological, EBD, localized in arterioles, are ubiquitous.

EBD are playing a primary role in local microcirculatory flow-motion regulation, as the following clinical evidence demonstrates: when they are abnormal, from both functional and structural quantum-biophysical-semeiotic viewpoint, EBD bring about Functional Microcirculatory Reserve (FMR) impairment, contributing to cause inherited real risk of disorders, like CAD, whose onset will possibly occur after years or decades, as allows me to state a 53-year-long clinical experience with the original physical semeiotics [6-19]. Under such as condition, we observe tissue acidosis, assessed as lowering of gastric aspecific reflex latency time, indicating lowered tissue oxygenation.

Interestingly, the initial stage of whatever disorder, i.e., the inherited real risk, is characterised exclusively by a reflex duration lasting 4 sec. (NN < nn =" 8" style=""> utilizing apnoea test.

In health, the duration of apnoea is inversely correlated with latency time lowering, and directly related to gastric aspecific reflex lasting time (7-9).

Quantum-biophysical Semeiotics allows doctor to find physiological, both type I and type II, EBD, the later exclusively in those biological systems which need temporarily high blood supply, as skeletal muscle, right cerebral hemisphere of individuals CAEMH-positive, and conjunctival mucosa, emphasizing their central role in microcirculatory flow-motion regulation, under physiological as well as pathological conditions,

Beside normal or physiological, either inherited or newborn, type I (= small arteries), and type II (= arterioles), EBD, according to S.B. Curri [4,5], do really exist type I, newborn-pathological EBD, until now unknown by physicians. They are sub-divided in two subtypes: a) subtype, characteristic of oncological real risk, and b) subtype, aspecific, in all other disorder inherited real risks and present in different biological systems, I discovered and described in earlier papers, (See: Physiology, and Pathology,

http://www.semeioticabiofisica.it/microangiology,) [6,7].

These microcirculatory structures play a pivotal role in the patho-physiology of most common and serious human diseases, including diabetes, hypertension, ATS, CVD, cancer, permitting to define the link existing between genetic factor and phenotype, according to Angiobiopathy theory [6-18].

In fact, decade-long clinical study of Endoarteriolar Blocking Devices has allowed me to discover and assess “quantitatively” the genetic abnormalities of all biological systems, preconditioning outcome is based on.

As a consequence of above remarks, EBD clinical evaluation proved to be a paramount tool to bedside recognize individuals at inherited real risk of the more frequent and dangerous human disorders, as well as to comprehend fully the underlying different quantum-biophysical-semeiotic constitutions, I have formerly described, since the birth [9-20].

Due to these reasons, I emphasize the essential value of knowing both anatomy and physiology of such microcirculatory structures, i.e., EBD, both physiological and pathological, at the present time unfortunately either ignored or overlooked by clinicians around the world. EBD are useful to understand the importance of Clinical Microangiology, and particularly its branch, I suggested to term Clinical Microangiology of Endoarteriolar Blocking Devices [6-21].

Furthermore, Quantum-biophysical Semeiotics allows doctor to bed-side detect the persistent opening (technically speaking, hyperstomy) of all artero-venous anastomoses (AVA), ethimologically understood, as clinical and experimental evidence suggests.

In healthy and young inividual, this reflex, that shows an intensity smaller than 2 cm, disappears rapidly if digital pressure becomes “highly intense”. In addition, if the subject hand is raised to 10-15 cm. above the heart level, “mean-intense” digital pressure applied on the finger-pulp does not cause upper ureteral reflex.

On the contrary, in arteriosclerotic patients, from initial stage of its inherited risk, “mean-intense” digital pressure, applied upon the microcirculatory bed, e.g. on the microvessels of a finger pulp, scars, great or little joints, of individuals lying down in the supine position, psycho-physically relaxed with open eyes (= melatonin secretion inhibition) brings about upper ureteral reflex (= upper ureteral tracts dilate about 2,5 cm.), lasting characteristically “stiff” also during “extreme-intense” pressure [6-21].

In other words, in health, under the later condition, AVA are closed, and simultaneously type I and II EBD contract, when evaluated as middle ureteral reflex (See later on), facilitating the blood-flow through nutritional capillaries (= type I, associated, Microcirculatory Functional Reserve activation). Furthermore, since the very early stage of arteriosclerosis, such as reflex persists “stiff” also under the latter conditions, hindering blood supply to local parenchyma.

Interestingly, this quantum-biophysical-semeiotic sign increases suddenly when the patient moves the other, vertically raised hand as waving good-bye – "slightest effort test" – because of the increasing of blood viscosity, bedside detected. Analogously, during the "simulated cold test" (= patient is thinking to dip his hands or a single finger in ice-cold water), arterio-venous anastomoses result slightly opened in healthy subjects.

On the contrary, under identical conditions, AVA opening appears to be particularly increased in patients involved by arteriosclerosis, even initial or asymtomatic: 1,5 cm. vs 2,8 cm., respectively: p<0,001,>

Finally, middle ureteral reflex, different in type, size, duration, nature, induced by digital pressure of different intensity, applied, e.g., on tissue-micro-vascular-units of finger tip, gives useful information about the diverse EBD, type I AVA as well as type II, group I, group II AVA, where present as in the foot-sole (16)

As a consequence, doctor can now-a-days assess the diverse EBDs at the bedside in easiest way, calculating the duration of heart-aspecific gastric and/or -caecal reflex duration: in presence of “normal” EBD alteration and type I newborn-pathological, type I, subtype b), EBD, reflex lasts 4 sec. or more (NN = less than 4 sec.), correlated with the seriousness of underlying disorder. Moreover, the final tonic Gastric Contraction (= intense tissue acidosis) indicates the presence of newborn-pathological, type I, subtype a), “oncological”, EBD, characterized by a large amount of smooth muscle cells.

Certainly, who knows the “direct” evaluation of middle ureteral reflexes can utilize a very refined, exhaustive, and reliable method [6-21].

Finally, knowing the precise location of physiological, type I, EBD (i.e., skeletal muscle, conjunctival mucosa, and right emisphere of individuals CAEMH-positive), doctor recognizes more quickly the type I, subtype a) and b), newborn-pathological EBD.

At this point, reader has to take into account that pathological EBD can transform in physiological type, reducing contemporaneously their number, under efficacious therapy (diet, ethimologically speaking (= BMI about 25, physical exercise, avoiding tobacco smoking, a.s.o.), Melatonin, personalized applications of NIR-LED, a.s.o.), thus ameliorating local microcirculatory blood-flow (= pH), evaluated as duration of latency time and reflex lasting.

It is well known for many years that patients with coronary heart disease may have no symptoms [20, 22], and that the electocardiographic feature of ischaemia may be induced by exercise without accompanying angina [22]. Nevertheless, such "silent ischaemia" has only recently been recognized to be an important feature of ischaemic heart disease [7, 18]. The silent ischaemia prevalence is unknown, although over a quarter of myocardial infarctions are unrecognized and half of them cause no symptoms at all [14]. According to Cohn, there are three categories of people with silent ischaemia, who may be at such risk [5]. People of type 1° have no symptoms and no history of myocardial infarction or angina; those of type 2° are symptomless survivors of myocardial infarction; fìnally, patients of type 3° have angina together with episodes of silent ischaemia, whose mechanisms in most cases are obscure.

My data suggest that quantum-biophysical-semeiotic methods, illustrated above, are reliable, helpful, and then advisable in bed-side detecting individuals, even asymptomatic, who have to undergo, promptly and rationally, whatever stress testing, such as electrocardiographic exercise test, atrial pacing, thallium stress redistribution scintigraphy, exercise radionuclide ventriculography, and spiral CT, a.s.o., during which silent ischaemia usually may be elicited, corroborating bedside diagnosis [1, 2, 21]. Furthermore, the clinical, quantum-biophysical-semeiotic selection of asymptomatic patients is interesting, because it can be applied on very large scale, helping doctors in actively searching for ischemic heart disease, particularly serious when silent, from the clinical viewpoint. As a matter of facts, a lot of data suggest that episodic, silent ischemia carries a poor prognosis in stable coronary artery disease [3, 23].

Given the accumulating evidence that ischemia, whether silent or not, carries a poor prognosis in patients with known coronary artery disease, it is justifìed to follow an active policy even in patients who are totally free of symptoms [4, 22]. Essentially, the rationale for the use of histangioprotective drugs (like L-Carnitine, Co Q10, Coniugated-Melatonin, a.s.o.), associated with personalized applications of NIR-LED, in patients with ischemic heart disease clinically silent.

Three necessary premises:

Firstly, the favourable effects of these products on lipid and glucose metabolism, ameliorating mitochondrial respiratory chain, I illustrated previously [14, 20-24].

Secondly, the positive influence of these drugs on angina pectoris as well as on myocardial ischaemic preconditioning, because they improve blood flow in cardiac tissue microcirculatory units [8, 9, 20, 23].

Thirdly, when utilized in early stage, histangio-protective drugs can ameliorate coronary microcirculatory remodelling, e.g., lowering the number of newborn-pathological type I, subtype b) EBD: the intensity of specific middle ureteral reflex significantly decreases under such treatment [23].

Practically, in order to ascertain clinically silent ischaemia it is advisable to assess shape and intensity of low ureteral reflex oscillations, i.e. vasomotion, as illustrated above, which permits doctor to calculate the fractal dimension of myocardial microvessels deterministic chaos (NN > 3 < oscillation =" 3/1">

As far as myocardial ischaemic preconditioning is concerned, it is suffìcient and hence advisable in day-to-day practice to assess the latency time of the second heart-gastric aspecific reflex, i.e., in the second evaluation, performed exactly after 5 sec. interruption, namely soon after 5 sec. from the end of basal evaluation: in health, latency time raises in a significant manner from 8 sec. (basal value) to 16 sec., i. e., to doubly value.

Another difficult, but also refined, elegant method proved to be reliable: the assessment of shortening of left ventricle enlargement duration during the above-described test (NN = from 7 sec. to 5 sec.) and/or conversely the prolonged latency time from 3 sec. to 5 sec. or more, preceding another ventricle dilation, paralleling Ejection Fraction of left ventricle. This latter evaluation, however, is a little more difficult to ascertain by doctors not experienced and skilled in the field of the original semeiotics.

From the practical view-point, both duration (NN <> 3 sec. < class="referencia">[7-10].

Actually, relevant data are easily obtained also by means of the latency time of heart-caecum and/or-aspecific gastric reflex, which informs about myocardial oxygen supply: in health, during “mean” digital pressure upon the skin projection area of heart, basal latency time value is 8 sec. However, doctor must remember that in case of CAD inherited real risk and CAD initial stage, such as parameter value is still normal (NN = 8 sec.), but reflex lasts 4 sec. or more (NN <>

In addition, in health, during "intense" digital pressure upon cutaneous projection area of the heart, as above described, and immediately after about 7 sec. apnea test or Valsalva's manoeuvre, the basal latency time of cardiac-gastric aspecific reflex (basal value = 8 sec.) raises significantly to 16 sec., as well as after preconditioning (i.e., doubly value) (p<0,02),>

In conclusion, in a long, well-established, clinical experience, the above-described quantum-biophysical-semeiotic methods proved to be reliable, easy to perform on very large scale, useful, and suitable for detecting ischemic coronary disease, even clinically silent or really initial, i.e. since CAD “real risk” [23].

Finally, Quantum-biophysical Semeiotics allows doctor to bedside recognize, in only one second, normal heart, as well as arteries [23,24-27]: in health, “intense” digital pressure, applied upon skin projection area of the heart and respectively of a large artery, does not bring about “simultaneously” gastric aspecific reflex.

References

1. Hammersen F (1968). Zur ultrastruktur der arterio-veno¨sen anastomosen. In: Hammersen F, Gross D (eds). Die Arterio-venoesen Anastomosen Anatomie, Physiologie, Pathologie, Klinik. Verlag Hans Hubert: Bern und Stuttgart. pp 24–37.

2. Bailey I.K.,Griffìth L.S.C., Rouleau J,Strauss H.W., Pitt B., ThalUum201 myocardial perfusion imaging at rest and during exercise. Comparative sensitivity to electrocardiography in coronary artery disease, Circulation, 1977, 55, 79.

3. Bonow R.O., Bacharach S.L., Gren M.V., La Fremere R.L., Ehstein S.E., Prognostic implicaiions of symptomatic versus asymtomatic (silent) myocardial ischemia induced by exercise in mild symptomatic and in asymptomatic patients with angiographically dociimented coronary artery diseas, Am. J. Cardio!., 1987, 60, 77.

4. Curri S.B. Le Microangiopatie. Inverni della Beffa, Milano, 1986.

5. Curri S.B. Pannicolopatia Mammaria da Stasi, Parte seconda. Inverni della Beffa, Milano, 1984

6. Stagnaro Sergio. Newborn-pathological Endoarteriolar Blocking Devices in Diabetic and Dislipidaemic Constitution and Diabetes Primary Prevention. The Lancet. March 06 2007. http://www.thelancet.com/journals/lancet/article/PIIS0140673607603316/comments?totalcomments=1 and especially: www.fce.it, http://www.fceonline.it/docs/stagnaro.pdf

7. Stagnaro-Neri M., Stagnaro S. Introduzione alla Semeiotica Biofisica. Il Terreno Oncologico. Travel Factory, Roma, 2004. http://www.travelfactory.it

8. Stagnaro Sergio. Teoria Patogenetica Unificata, 2006, Ed. Travel Factory, Roma.

9. Stagnaro Sergio. Role of Coronary Endoarterial Blocking Devices in Myocardial Preconditioning -c007i. Lecture, V Virtual International Congress of Cardiology. http://www.fac.org.ar/qcvc/llave/c007i/stagnaros.php
10.
Stagnaro S., Stagnaro-Neri M., Single Patient Based Medicine.La Medicina Basata sul Singolo Paziente: Nuove Indicazioni della Melatonina. Ed. Travel Factory, Roma, 2005. http://www.travelfactory.it
11. Stagnaro Sergio. New bedside way in Reducing mortality in diabetic men and women. Ann. Int. Med. http://www.annals.org/cgi/eletters/0000605-200708070-00167v1
12. Stagnaro Sergio. Newborn-pathological Endoarteriolar Blocking Devices in Diabetic and Dislipidaemic Constitution and Diabetes Primary Prevention. The Lancet. March 06 2007. http://www.thelancet.com/journals/lancet/article/PIIS0140673607603316/comments?totalcomments=1

13. Stagnaro Sergio. Epidemiological evidence for the non-random clustering of the components of the metabolic syndrome: multicentre study of the Mediterranean Group for the Study of Diabetes. Eur J Clin Nutr. 2007 Sep;61(9):1143-4. Epub 2007 Feb 7. [MEDLINE]

14. Stagnaro-Neri M, Stagnaro S., Deterministic chaotic biological system: the microcirculatory bed, Gazz. Med. It.-Arch. Sci. Med., 1994, 153, 99.

15. Stagnaro S., Moscatelli G., Biophysical Semeiotics, Deterministic Chaos and Biological System, Gazz. Med. It. Arch. Sci . Med. 1996, 155, 125.

16. Stagnaro-Neri M., Stagnaro S., Auscultatory percussion evaluation of arteriovenous anastomoses dysfunction in early arteriosclerosis, Acta Medica Mediterranea, 1989, 5, 141.

17. Stagnaro-Neri M., Stagnaro S., Deterministic Chaos, Preconditioning and Myocardial Oxygenation evaluated clinically with the aid of Biophysical Semeiotics in the Diagnosis of ischaemic Heart Disease even silent. Acta Med. Medit. 13, 109, 1997.

18. Stagnaro-Neri M., Stagnare S., La manovra di Ferrero-Marigo nella diagnosi clinica di Iperinsulinemia - Insulinoresistenza, Acta Med. Medit., 1997, 13, 15.

19. Stagnaro Sergio. Role of Coronary Endoarterial Blocking Devices in Myocardial Preconditioning - c007i. Lecture, V Virtual International Congress of Cardiology, 2007. http://www.fac.org.ar/qcvc/llave/c007i/stagnaros.php

20. Stagnaro S., Stagnaro-Neri M., La Melatonina nella Terapia del Terreno Oncologico e del “Reale Rischio” Oncologico. Ed. Travel Factory, Roma, 2004.

21. Stagnaro S., Stagnaro-Neri M., Le Costituzioni Semeiotico-Biofisiche.Strumento clinico fondamentale per la prevenzione primaria e la definizione della Single Patient Based Medicine. Ed. Travel Factory, Roma, 2004.

22. Wood P., Me Gregor M., Magidson O., Writteker W. The effort test in angina pectoris, Br. Heart J., 1950, 12, 363.

23. Stagnaro Sergio. Il “Reale Rischio” Semeiotico-Biofisico. Ruolo diagnostico e fisiopatologico dei Dispositivi Endoarteriolari di Blocco, neoformati patologici tipo I, sottotipo a) e b). Ed. Travelfactory, Roma, in press.

24. Stagnaro S., Stagnaro-Neri M., La Melatonina nella Terapia del Terreno Oncologico e del “Reale Rischio” Oncologico. Ed. Travel Factory, Roma, 2004.

25. Stagnaro Sergio. Diagnosi clinica di cuore sano in un secondo! 7 Aprile 2008. www.fce.it http://www.fcenews.it/index.php?option=com_content&task=view&id=1218&Itemid=47

26. Stagnaro Sergio. Bedside Biophysical-Semeiotic Osteocalcin Test in Diagnosing and Monitoring Diabetes. The Lancet, January 28, 2008.
http://www.thelancet.com/journals/lancet/article/PIIS0140673608601014/comments?action=view&totalComments=2; See especially, http://www.fceonline.it/docs/stagnaro.pdf

27. Stagnaro Sergio. Semeiotica Biofisica Quantistica: Diagnosi Clinica di Melanoma a partire dal suo Reale Rischio Congenito. www.fcenews.it, 23 luglio 2008, http://www.fcenews.it/index.php?option=comcontent&task=view&id=1599&Itemid=45

Thursday, May 21, 2009

Quantum-Biophysical-Semeiotic Bed-Side Evaluation of Endothelial Function

Introduction.

It is generally admitted that endothelial dysfunction is an important factor in both the onset and the development of atherosclerosis, as I demonstrated in earlier papers two decades ago, from the clinical view-point (1-6).

In fact, endothelium plays a pivotal role in the maintenance of vascular tone, taking part to the blood flow regulation in response to changes in tissue and organ perfusion requirements (5,6). When blood flow increases through a vessel, such as vessel dilates: from quantum-biophysical-semeiotic view-point, under such as condition, suddenly the enhancement occurs of both arterial-“in toto” ureteral reflex and arterial-gastric aspecific reflex (Fig.1), the latter easier to be assessed, (See http://www.semeioticabiofisica.it).

Fig.1

Gastric aspecific reflex ( in the stomach both fundus and body are dilated, while antral-pyloric region contracts) caused by digital pressure, applied on brachial artery of a patients in supine position, at rest.

One speaks of the phenomenon called flow-mediated dilatation (FMD). Over the past decade, a clinical quantum-biophysical-semeiotic technique has evolved to evaluate both flow-mediated vasodilation (FMD) and acethylcholine-mediated vasodilation (= Valsalva’s Manoeuvre), an important endothelium-dependent function, assessed, for instance, in the brachial artery (See website http://www.semeioticabiofisica.it/microangiologia).

In health, these stimuli provoke the endothelium to release free radical nitric oxide (NO), probably also by means of PPARS action (22), with subsequent vasodilation that can be assessed and quantified at the bed-side in different ways, as an index of vasomotor function. This technique is attractive because it is non-invasive and allows repeated measurements on very large scale. An increase in flow through the brachial artery can be induced by causing post-ischemic dilation in the downstream vascular bed of the distal forearm, that can be achieved by inflating a cuff placed around the forearm to supra-systolic pressure producing an ischemia in the distal vascular bed.

Really more simple, easier, faster to be performed, and, therefore, preferable in day-to-day practice, is the following bed-side manoeuvre: doctor applies an “intense”, obstructive digital pressure upon brachial artery, and immediately assesses the intensity of gastric aspecific reflex (or “in toto” ureteral reflex): NN = no aspecific gastric reflex happens.

On the contrary, in Arterioscleotic Constitution as well as in overt arteriopathy, of whatever nature the reflex intensity is 0,5 cm. or more, in relation ti the severity of underlying disorder (Fig.1)

After the rapid with-drawl of digital pressure (or of the cuff pressure), a sudden increase of blood flow through the dilated vascular bed occurs, due to flow-mediated vaso-dilation. Firstly, physiologically the reflex disappears rapidly, and soon thereafter, a further reflex occurs spontaneously, showing a three times higher intensity.

In health, the significant increase in shear stress in the down-stream artery causes a NO-dependent dilation of the brachial artery, that can be evaluated clinically also in a different way, i.e., paralleling the basal value of finger pulp-gastric aspecific reflex, evaluated as latency time (in health, 8 sec., if digital pressure upon finger-pulp is “mean intense”) with the second value, which increases to 16 sec., i.e., doubled value.

The arterial dilator response to shear-stress can be almost completely blocked by pre-treatment with nitric oxide synthase inhibitors (7, 8) and therefore it has been suggested that the phenomenon is predominantly due to endothelial release of radical nitric oxide. In fact, the endothelium can no longer be viewed as a static physical barrier that simply separates blood from tissue. It is evident that disturbed endothelial function may be an early marker of an ongoing atherosclerotic process. Thus, inherited endothelial dysfunction has increasingly been recognized to play an important role in a number of conditions associated with a high prevalence of atherosclerotic CVDs (1-6), according to my Microvascular Arteriosclerosis Theory (partly illustrated in above-cited website, URL

http://www.semeioticabiofisica.it/microangiologia/Documenti/Eng/A%20Stadio%20preipertensiv%.

A 53-year-long “clinical” experience allows me to state that endothelial function assessed by this method correlates significantly with invasive testing of coronary endothelial function (7, 9) and with the severity and extent of coronary atherosclerosis (10).

Interestingly, at this point, coronary artery endothelial function can analogously be easily evaluated by means of Quantum-Biophysical Semeiotics (1, 2, 11). The precise mechanisms for the acute detection of shear forces and subsequent signal transduction to modulate vasomotor tone are not fully understood. The endothelial cell membrane contains specialized ion channels, such as calcium-activated potassium channels, that open in response to shear stress (5). The effect of potassium channel opening is to hyperpolarize the endothelial cell, increasing the driving force for calcium entry (there are no voltage-gated calcium channels in endothelial cells). Calcium activates an enzyme, endothelial nitric oxide synthase (eNOS), and the subsequent generation of NO appears to account for FMD (6).

In humans, the measurement of FMD has been widely adopted to explore endothelial function. However, a number of variations of the method have been described. Cuff placement above or below the scanned part of the artery has been described, and varying duration and pressures for cuff inflation have been used. The brachial artery has been the target artery in most studied, but radial and femoral arteries have also been measured (7). Due to these technical modifications, the normal ranges established in some laboratories differ from normal ranges observed in others (7-8).

In my long clinical experience, Valsalva’s manoeuvre proved to be quiet practical, easy, reliable, and useful, lasting only 5 sec.: in health, manoeuvre-dependent acetylcholine secretion brings about notoriously smooth muscle cells relexation, in the identical way, illustrated above.

In my opinion, based on a large number of clinical quantum-biophysical-semeiotic observations, underlying patho-physiological action mechanism of acetylcholine are more complex, acting favourably also on healthy microcirculation, increasing both vasomotility and vasomotion.

On the contrary, in case of DM, dyslipidaemia, arterial hypertension, a.s.o., doctor mainly either does not observe any change or worsening condition, in relation to the severity of underlying disorder. Diet, ethimologically speaking, and physical exercise (walkig 45 minutes/day, 120 steeps/min), Coniugated Melatonin, improve in general endothelial function rapidly, according to other authors (12).

In addition, melatonin-adenosine, a potent histangioprotective substance (21, 23), in my experience proved to increase vasomotility and vasomotion in the microcirculatory bed of both tissue, and arterial wall.

On contrast, FMD is inversely correlated with age, type 2 diabetes mellitus, dyslipidaemia, hypertension, and tobacco smoking: smokers have decreased FMD (1-6).

In addition, inactivation of endothelium-derived nitric oxide due to increased production of oxygen free radicals in the vessel wall is thought to be an important mechanism for endothelial dysfunction (13, 14-23).

As a result, much interest has focused on antioxidants, such as vitamin E, vitamin C, and other free radical scavengers, like melatonin, as I demonstrated previously, for the first time “clinically” (14-27), since they remove successfully free radicals and, therefore, improve endothelial function.

* Sergio Stagnaro MD

Via Erasmo Piaggio 23/8, CP. 42

16039 Riva Trigoso (Genoa) Europe

Founder of Quantum Biophysical Semeiotics

Who's Who in the World (and America)

since 1996 to 2009

Ph 0039-0185-42315

Cell. 3338631439

www.semeioticabiofisica.it

dottsergio@semeioticabiofisica.it

References

1) Stagnaro S., Stagnaro-Neri M., Basi microcircolatorie della semeiotica biofisica. Atti del XVII Cong. Naz. Soc. Ital. Studio Microcircolazione, Firenze ott. 1995, Biblioteca Scient. Scuola Sanità Militare, 1995, 2, 94.

2) Stagnaro-Neri M., Stagnaro S., Semeiotica Biofisica: valutazione della compliance arteriosa e delle resistenze arteriose periferiche. Atti del XVII Cong. Naz. Soc. Ital. Studio Microcircolazione, Firenze Ott. 1995, Biblioteca Scient. Scuola Sanità Militare, 2, 93.

3) Stagnaro-Neri M., Stagnaro S., Auscultatory Percussion Evaluation of Arterio-venous Anastomoses Dysfunction in early Arteriosclerosis. Acta Med. Medit. 5, 141, 1989

4) Stagnaro-Neri M., Stagnaro S. Indagine clinica percusso-ascoltatoria delle unità microvascolotessutali della plica ungueale. Acta Med. Medit. 4, 91, 1988.

5) Il test della Apnea nella Valutazione della Microcircolazione cerebrale Stagnaro S., Stagnaro-Neri M., in Cefalalgici. Atti, Congr. Naz. Soc. Ita. Microangiologia e Microcircolazione. A cura di C. Allegra. Pg. 457, Roma 10-13 Settembre 1987. Monduzzi Ed. Bologna

6) Stagnaro S., Valutazione percusso-ascoltatoria della microcircolazione cerebrale globale e regionale. Atti, XII Congr. Naz. Soc. It. di Microangiologia e Microcircolazione. 13-15 Ottobre, Salerno, e Acta Medit. 145, 163, 1986.

7) Joannides R, Haefeli WE, Linder L, et al. Nitric oxide is responsible for flow-dependent dilatation of human peripheral conduit arteries in vivo. Circulation 1995;91:1314-19.
8) Agewall S, Hulthe J, Fagerberg B, et al. Post-occlusion brachial artery vasodilatation after ischaemic handgrip exercise is nitric oxide mediated. Clin Physiol Funct Imaging 2002;22:18-23.

9) Takase B, Uehata A, Akima T, et al. Endothelium-dependent flow-mediated vasodilation in coronary and brachial arteries in suspected coronary artery disease. Am J Cardiol 1998;82:1535-39.

10) Neunteufl T, Katzenschlager R, Hassan A, et al. Systemic endothelial dysfunction is related to the extent and severity of coronary artery disease. Atherosclerosis 1997;129:111-18.
11)
Stagnaro S. A clinical efficacious maneouvre, reliable in bed-side diagnosing coronary artery disease, even initial or silent, as well as "heart coronary risk". 3rd Virtual International Congress of Cardiology, FAC, 2003, http://www.fac.org.ar/tcvc/marcoesp/marcos.htm

12) Sowers JR, Lester MA. Diabetes and cardiovascular disease. Diabetes Care. 1999;22(suppl 3):C14-C20.

13) Ohara Y, Peterson TE, Zheng B, Kuo JF, Harrison DG. Lysophosphatidylcholine increases vascular superoxide anion production via protein kinase C activation. Arterioscler Thromb 1994;14:1007-13.
14)
Stagnaro-Neri M., Stagnaro S., Amlodipina: Calcio-Antagonista e Scavenger dei Radicali Liberi. Tec. 4, 43, 1993.

15) Stagnaro-Neri M., Stagnaro S., Ketanserina: antagonista dei recettori 5Ht2-serotoninergici e scavenger dei radicali liberi. Clin. Ter. 141, 465, 1992 [MEDLINE]

16) Stagnaro-Neri M., Stagnaro S., Radicali liberi e alterazioni del microcircolo nelle flebopatie ipotoniche costituzionali. Min. Angiol. 18, Suppl. 2 al N. 4, 105, 1993.

17) Stagnaro Stagnaro-Neri M., Stagnaro S., Silimarina: un potente scavenger dei radicali liberi. Studio clinico percusso-ascoltatorio. Epat. 38, 3, 1992.

18) Stagnaro S., Stagnaro-Neri M. Il danno da radicali liberi sul microcircolo. Congr. Naz. SISM., Milano,10 giugno,1991, Comun. Atti, Min. Angiologica, Suppl. 1, N°1 16,398,1991

19) Stagnaro-Neri M., Stagnaro S., Acidi grassi w-3, scavengers dei radicali liberi e attivatori del ciclo Q e della sintesi del Co Q10. Gazz. Med. It. – Arch. Sc. Med. 151, 341, 1992 (Infotrieve)

20) Stagnaro Sergio, Stagnaro-Neri Marina. Introduzione alla Semeiotica Biofisica. Il Terreno oncologico”. Travel Factory SRL., Roma, 2004. http://www.travelfactory.it/semeiotica_biofisica.htm

21) Stagnaro S., Stagnaro-Neri M., La Melatonina nella Terapia del Terreno Oncologico e del “Reale Rischio” Oncologico. Ediz. Travel Factory, Roma, 2004.

22) John A. Polikandriotis; Louis J. Mazzella; Heidi L. Rupnow; C. Michael Hart

Arteriosclerosis, Thrombosis, and Vascular Biology. 2005;25: 1810.

23) Stagnaro Sergio Endothelial cell function can ameliorate under safer drugs, such as Melatonin-Adenosine. BMC Cardiovascular disorders. 2004. http://www.biomedcentral.com/1471-2261/4/4/comments

24) Stagnaro Sergio. Role of Coronary Endoarterial Blocking Devices in Myocardial Preconditioning - c007i. Lecture, V Virtual International Congress of Cardiology, 2007. http://www.fac.org.ar/qcvc/llave/c007i/stagnaros.php

25) Stagnaro Sergio. Pre-Metabolic Syndrome and Metabolic Syndrome: Biophysical-Semeiotic Viewpoint. www.athero.org, 29 April, 2009. http://www.athero.org/commentaries/comm904.asp

26) Stagnaro Sergio. CAD Inherited Real Risk, Based on Newborn-Pathological, Type I, Subtype B, Aspecific, Coronary Endoarteriolar Blocking Devices. Diagnostic Role of Myocardial Oxygenation and Biophysical-Semeiotic Preconditioning. www.athero.org, 29 April, 2009 http://www.athero.org/commentaries/comm907.asp

27) Stagnaro Sergio. Epidemiological evidence for the non-random clustering of the components of the metabolic syndrome: multicentre study of the Mediterranean Group for the Study of Diabetes. Eur J Clin Nutr. 2007 Feb 7; [MEDLINE]


Tuesday, May 19, 2009

Quantum-Biophysical-Semeiotic Hypertensive Constitution.


Abstract

It's evident that neither all people become hypertensive nor all hypertensive patients are suffering from left ventricular impairment as well as from other well-known hypertension-dependent complications, regardless of environmental conditions. Indeed, the existence of biophysical-semeiotic hypertensive constitution accounts for the reason that only some individuals are hypertensive, and among them, only those with real risk in well defined biological system, are involve by myocardial failure or by other known hypertension complications. In the article, bedside diagnosis of both biophysical-semeiotic hypertensive constitution and hypertension complication real risk is fully described.

Key Words.

Biophysical-Semeiotics. Hypertensive Constitution. Hypertension. Clinical Microcirculation.

Introduction.

In the primary prevention of arterial hypertension, based on the pre-morbid, pre-metabolic stage (See: Arteriosclerotic Constitution in the website http://www.semeioticabiofisica.it, and particularly the URL

http://www.semeioticabiofisica.it/semeioticabiofisica/Documenti/Eng/Costituzione%20ipertensiv%), we have to devote a particular discussion to pre-hypertensive state of arterial hypertension (AH), component of pre-metabolic, and obviously, metabolic syndrome, classic and “variant”, often associated to other human Congenital Acidosic Enzyme-Metabolic Histangiopathy-a (CAEMH-a) -dependent diseases. CAEMH-a is a singular, functional mitochondrial cytopathy, inherited almost always by mother (1-3). For further information See above-cited website and Bibliography.

Really, the pre-hypertensive state allowed me to define clinically the hypertensive constitution, discussed in this article.

In order to understand such as topic usefully, we must remember that the primary function of blood circulation as well as of complex mechanisms, which rule pressure values (i.e., cardiac out-put, peripheral arteriolar resistance, blood volume, arterial compliance), is represented by physiological tissue supply of material-information-energy (O2, various metabolites, enzymes, hormones, a.s.o.), and by catabolites removal, in particular CO2 and produkts of tissue secretion.

Possible pH tissue variations bring about necessarily haemodinamic-haemorheological modificatioms, aiming to maintain metabolic “homeostasis” or, more exactly speaking, to keep in the normal ranges the physiological condition of deterministic chaos, both microvascular and parechymal, according to my Angiobiopathy theory (4).

Notoriously, blood circulation influences cellular metabolism, which, in turn, interferes on the regulation of blood pressure complex mechanisms, as prostaglandyns synthesis, thromboxane, radical NO, vasoactive amines, neurotransmitters, a.s.o., beside pH oscillations, axones reflexes and baro-receptorial mechanisms.

Our research data have, published in 1990, we demonstrated that Congenital Acidosic Enzyme-Metabolic Hystangiopaty-a (CAEMH-a) represents the conditio sine qua non “also” of essential arterial hypertension, as we suggested for a lot of years, on the base od clinical evidence (1-4).

On the other hand, all authors agree on the fundamental role played by “genetic factor” on the onset of arterial hypertension (4, 20-24).

Analogously to diabetes mellitus, arteriosclerosis, malignancies, and all other severe human diseases, also in arterial hypertension it is possible to observe an early, first stage, clinically silent, although initial tissue hypoxic disorder, particularly in skeletric muscle, which we suggested to term pre-hypertensive stage (4), on the analogy of what we wrote in the introductory article on Quantum-Biophysical-Semeiotic Constitutions (5, 9).

All individuals, which have suffered over the last years from an episode of the so-called “white-cloth” arterial hypertension (or have had arterial hypertension in the past, but now are normotensive) are under this condition, that takes a part of the so-called Grey Zone, namely the site of primary prevention.

However, nowadays, doctors belittle real significance of such hypertensive episodes, considered mainly as trivial and transitory consequence of commonplace neuro-hormonal reaction to stress situations, while they really represent the peak of an ice-berg, to which we have to pay all our attention and devote an accurate biophysical-semeiotic evaluation.

In fact, in individuals CAEMH-a positive of great intensity, particularly if localized in microvascular, e.g., muscular tissue, the reaction of smooth muscle cells of resistance vessels (i.e., small arteries and arterioles, according to Hammersen) to vasomotor physiological stimuli appears clearly exceeding, as we will say later (4, 15, 32).

In “initial” stage, however, such abnormal reaction can be still counterbalanced by vasodilation upward, i.e. in the vasa publica, according to Ratschow, and by blood re-distribution in various destricts, especially in the splancnic territory.

In other words, in pre-clinical, initial, pre-hypertensive stage, as well as in hypertensive constitution, blood pressure does not result increased at all – a part from episode of sympathetic hypertonus and/or Renine-Angiotensin-Aldosterone System (RAAS) – but peripheral blood supply is slightly “reduced”, causing tissue disorder, due to acidosis, as consequence of increased peripheral arteriolar resistances (PAR), which bring about elastic vessels dilation and opening of Arterio-Venous Anastomoses, functionally speaking, in always CAEM-a-positive individuals (5, 9, 10).

Methods.

With the aid of Biophysical Semeiotics doctor can quickly recognize bedside such as special microcirculatory situation, e.g., in skeletric muscles by the method of the preconditioning.
In healthy, at basal line, latency time of biceps muscle-gastric aspecific reflex (= in the stomach, both fundus and body dilate, while antral-pyloric junction contracts), when digital pressure stimulation is “mean-intense, results 8 sec., and it lasts for <> (= parameter value of paramount importance, duew to the fact that it is inversely correlated with Microcirculatory Functional Reserve), while at second evaluation, performed after 5 sec. exactly, latency time increases to ³ 12 sec.

On the contrary, in a subject with hypertensive constitution under identical experimental condition, basal latency time appears normal (NN = 8 sec.), but the duration results 4 sec. or more, and it does not ameliorate or sometimes lowers in the second evaluation, pathogical preconditioning, in relation to the severity of hypertensive “real risk” itself, as a consequence of impaired Microcirculatory Functional Reserve (9) (For further technical information, See

http://www.semeioticabiofisica.it/microangiologia).

In the pre-hypertensive state, which can last clinically silent years or decades, and, then, very difficult to recognize by physical orthodox semeiotics (21, 26, in 4), doctor observes the typical microcirculatory metabolic abnormalities in post-absorptive state, i.e. at least 4 hours after meels, characterized by AL + PL duration (= duration of microcirculatory wave oscillation, which parallel ureteral reflexes) of pancreatic vasomotion (for instance, more easy to detect, duration of pancreatic body inferior margin lowering: see Technical Page 5, in above-cited website) lasting more than those of muscular, hepatic and adipose tissues, evaluated by means of upper (vasomotility) and lower (vasomotion) reflex oscillations, during “light” stimulation of related trigger-points (Fig 1).

Fig.1

The figure shows physiological vasomotion of all biological systems, assessed directly (e.g., as values of pancreas periodic, deterministic chaotic oscillations: lowering of inferior pancreatic margin) or indirectly as ureteral reflexes fluctuations, upper – vasomotility – and lower – vasomotion – brought about by “light” stimulation of related trigger-points, e.g., muscular and central, adipose tissue.

In other words, there is dissociation between insulin secretive-metabolic activity and that of “peripheral” tissues, indicating, in a refined biophysical-semeiotic manner, hyperinsulinaemia-insulinresistance: “classic” metabolic syndrome (5, 6, 10, 11, 12).

On the contrary, in the “variant” metabolic syndrome, the AL + PL Phase of liver vaso-dynamics, under identical condition, i. e., in the post-absorptive state, results lower than those of adipose tissue, musculare tissue, and above all of pancreas, which is the most instense (AL + PL) of all .

In other words, in case of “variant” metabolic syndrome, exclusively hepatic insulin receptors are normally sensitive to the hormone, and, under the above-mentioned circumstance, i.e., after at least 4 hours after meels, insulin normally controls hepatic glucose secretion, but not the lipidic secretion from “central” adipose tissue (13, 14).

At this point, it is necessary to underline that insulin secretion activity, if not properly ameliorated by diet, etymologically speaking, and/or histangioprotective drugs, such as coniugated melatonine can go on slowly towards progressive its insufficiency (6), characterized by gradual, before limited, and after widespread, changing of pancreatic beta-cell insulin activity from type I, associated, (in which both vasomotility and vasomotion are intense: active hyperaemia), to type II, intermediate (origin of IGT) and, finally, to type III, dyssociated (first stage of microcirculatory insufficiency), when pancreatic tissue acidosis is highest (real begin of DM). (See also Diabetic Constitution and Diabetes Mellitus in Practical Applications, in above-cited website and in the website www.indmedica.org, 2 Cyber Lectures: Diabetic and Dyslipidaemic constitutions).

Starting from this stage, pancreatic interstitium becomes more large than the normally, mainly due to amyloid deposit, as formerly demostrated: pancreatic-“in toto” ureteral reflex results ³ 1 cm. (NN < 1 cm.) (See Diabetes mellitus, in http://www.semeioticabiofisica.it, Practical Applications, URL

http://www.semeioticabiofisica.it/semeioticabiofisica/Documenti/Eng/Diagnosis%20DM,%20amyloid.doc).

At this point, we can finally understand more clearly the really frequent association between arterial hypertension and DM, which appears “always” on the common base of a congenital inherite factor, i.e. CAEMH-a., particularly intense in both Langherans’s pancreatic isles and skeletric muscle arteriols, i.e, resitance vessel wall-

For the first time it is possible to speak of real beginning of diabetes mellitus, a term until now used without scientific support, namely in acritical manner, despite the progress of sophysticated instrumental semeiotics.

At a large number of congresses I have showed the misuse of such termin in front of well-known diabetologists, who appeared without exception surprised, annoyed and totally unable to falsify our statement (7).

DM type II, so-called NIDDM, – more than 94% of all cases – from biophysical-semeiotic viewpoint shows a precise, clear-cut beginning, which corresponds to the first onset of pancreatic isles microcirculatory activation type II, intermediate, in individuals involved by dyslipidaemic “and” diabetic constitutions, causing histangic acidosis anf further, pancreatic amyloyd deposit, and reduction of local insulin receptors sensitivity, essential factor in the self-regulation of hormone secretion.

In a few words, such characteristic microcirculatory condition parallels the activation of “only” vasomotility, evaluated at the bed-side as fluctuations of upper ureteral reflex, during “light” stimulation of pancreatic trigger-points: AL + PL, i.e. duration of oscillation wave (Fig.1), is 7-8 sec. (NN = 6 sec.), whereas vasomotion, i.e. the fluctuations of lower ureteral reflex, shows a AL + PL duration unchanged (6 sec.), due to impairment of loca AVA and especially of Endoarteriolar Blocking Devices (EBD).

From the haemoreological-microcirculatory view-point, that indicates an impairment of Microcirculatory Functional Reserve, and consequently initial abnormality of insulin secretion, according to Angiobiopathy theory.

In addition, it has to be considered that elastic artery dilation, evaluated clinically by means of Biophysical Semeiotics, as it will be once more illustrated in following, aims to counterbalance the dangers of increased peripheral artery resistance. However, repeated and acute dilation, e.g. during stresses, brings about initial alterations of endothels (denuding) and smooth muscle cells endo-reduplication, with subsequent arterial wall structural abnormalities, as intimal thikening (4, 25, 26).

At this point, we briefly remember the contemporaneous alterations of local vasa-vasorum, caused mainly by wall dilation, which brings about, in turn, further impairment of related microcirculation and consequently arterial wall damage.

In biophysical semeiotic detecting pre-hypertensive state, i.e. hypertensive constitution and hyrtension real risk, beside muscular preconditioning, illustrated above, to which we will return later, a primary role is played by the diagram of finger-pulp tissue microvascular unit, in which Phase A is reduced (gastric aspecific reflex < 1 cm.) and disappearing time of tGC results prolonged, after rapid interruption of digital pressure: Oxygen Recovery Time < 1 cm. (O2RT) (15-17).

Interestingly, O2RT (NN £ 2 sec.) is in relation to the recovery of normal tissue oxygenation, after interruption of jatrogenetically induced histangic acidosis, “aerobic” glycolisis restoration, H+ washing, and, then, post-ischaemic reactive hyperaemia, strictly related to Microcirculatory Functional Reserve, always altered also in the pre-hypertensive state, as clinical and experimental evidence shows: O2RT (NN = 2 sec.) > 2 sec., directly related to the seriousness of hypertensive constitution.

Unavoidable to evaluate pre-hypertensive state, it proved to be ausculatory percussory outlining of common femoral artery, which can be performed with the bell-piece of stethoscope, properly localized on this arterial vessel at the groin, or, in a practical way, immediately under umbelicus, at right or at left.

At this point, auscultatory percussion has to be applied, directly and “gently” from right to left and viceverse, right below umbelicus as far as hypophonetic and intense sound is perceived, indicating the cutaneous projection area of common femoral artery: if the individual, which is examined, performes boxer’s test or, apnea test or Restano’s manoeuvre (contemporaneously, he performes the two tests), in healthy, the artery dilates clearly; on the contrary, in hypertensive state as well as in hypertensive patients, of course, the vessel dilate just a little or does not dilate at all (70).


Quantum-Biophysical-Semeiotic evaluation of hypertensive constitution and hypertension real risk.

By recognizing the pre-clinical condition, pre-hypertensive stage or hypertensive constitution, as well as hypertension real risk, which may evolve to arterial hypertension, doctor has to consider accurately a lot of parameters, really different in bed-side evaluation difficulty.

1) Systolic arterial pressure (SAP).

2) Diastolic arterial pressure (DAP)

3) Mean arterial pressure (MAP = SAP – DAP/3 + DAP)

4) Heart rate (HR).

5) Systo-diastolic oscillations of left ventricle at rest and during boxer’s test (NN = 1 and, respectively, 2 cm.): this paramter may be overlooked, although it is really interesting.

6) Tissue pH, evaluated as latency time of Critical Point (CP) of 5 cm. in tissue-microvascular-unit diagram. In healthy young, CP is generally absent (Fig. 2).

7) O2 Recovery Time (O2 RT), assessed as latency time of tGC disappearing (NN = 2 ± 0,5 sec.) .

8) Arterial peripheral resistance (APR = MAP/10 x O2 RT); normal value £ 20.

9) Basal arterial diameter (BAD), evaluated, e.g., as diameter of cutaneous projection of common iliac artery in a relaxed patient (NN £ 2 cm.).

10) Dilation index (DI = Max AD/BAD; NN ³ 2 cm.); artery diameter is assessed at basal line and, then, during boxer’s test, for instance.

11) Arterial compliance (Co = DI x 10 / O2RT; NN = 8-17).

12) Skeletal muscle preconditioning.

In practice, the preconditioning can be performed at the level of biceps muscle (or other muscle, of course). It is a simple, and reliable manoeuvre, which permits rapidly by itself to diagnose hypertensive constitution: in healthy, in supine position and psycho-physically relaxed with open eyes to avoid melatonin secretion, doctor evaluates basal lt of biceps muscle-gastric aspecific reflex and/or caecal reflex by mean of “mean-intense” pressure (NN = 8 sec.).

After 5 sec. “exactly” – preconditioning the same parameter is evaluated for the second time: in healthy, latency time appears prolonged significantly, while in the individual with hypertensive constitution, and, of course, in hypertensive patient, latency time is either unchanged or lowered, in inverse relation to the seriousness of arterial hypertension.

Without going on in the pathophysiology discussion, in which we are not concern at this moment, this method allows doctor to “quantify” peripheral arterial resistance. In a 50-year-long well established experience, the method proved to be reliable in 100% of cases.

It is easy to understnd that DI is related directly to distension ability of arterial wall, i.e., to arterial wall elasticity, impoortant factor of arterial compliance, evaluated by a different, more refined method (12-14).

In individuals under 60 years of age, DI is ³ 2 cm., when evaluated as cutaneous projection area of vessel, while over 60 years DI appears reduced to less than 2 cm.

Clinical and experimental evidence suggests that O2RT is related to PAR, as we demonstrated in an our research: r = + 0,84; tr = 4,378; p <>

Generally, Co is assessed by Bramwell and Hill’s formula, which consider the speed of wave puls and vascular elasticity, observed with sophysticated methods.

However, at the bed-side it proved reliable the datum obtained by this formula, opportunely modified, using DI, which gives information about common iliac artery elasticity ( or, of course, of other artery) and O2RT inversely related to blood-flow in tisssue-microvascular unit, during the phase of post-ischaemic hyperaemia (exclusively because of calculation reasons, DI is multiplied for 10). In aging, over 60 years, Co results <>

At this point, it is possible clinically to face the aethiopathogenetic problems of AI in a new way, i.e., trying to define pre-hypertensive state, which shows a particular hypertensive constitution, analogously at what we described as regards the diabetic, migraine constitution rheumatic arteriosclerotic constitution, and other constitution, such the oncological terrain.

Exclusively in this way it is possible to bed-side recognize pre-clinic stage of arterial hypertension, whose knowledge is essential for the primary prevention of hypertension.

Among young individuals, CAEH-a positive, with blood pressure in normal ranges, it is relatively easy to regognize those with increased PAR (> 20), even during stress test, DI < 2 cm., O2RT > 2 sec. and Co < style=""> physiological conditions.


Biophysical-Semeiotic Evaluation of Natriuretic Peptides.

From practical view-point, I advice such as “easy” evaluation of NP, offering a lot of usefull and interesting information on NP biological activity, particularly as hypertensive constitution is concerned.

In fact, individuals with hypertensive consitution (pre-hypertensive state) as well as overt hypertension, show a significantly decreased renal biological activity of natriuretic peptides, as patients involved by CAD, when down-regulation of renal specific receptors is caused by high levels of NP.

As a consequence, the impaired biological renal activity of natriuretic peptides plays a paramount role in bedside detecting hypertensive biophysical-semeiotic constitution. (For further technical information, See in above-mentioned website, the URL

http://www.semeioticabiofisica.it/semeioticabiofisica/Documenti/Eng/BNP%20engl.doc .

In following, an easy way reliable in such evaluation is described: in healthy, lying down in supine position, “intense”, sub-occlusive digital pressure is applied upon phemoral artery at the groin (or on another great muscular artery); the subsequent artery dilation upstrem brings about left cardiac atrial and left ventrical dilation, and then NPs secretion. After about 15 sec., kidney does not fluctuates as usually, showing congestion for 30 sec. exactly.

On the contrary, in individuals with hypertesive constitution and obviously overt hypertension, kidney congestion lasts for a time varying between 20 sec. and less than 30 sec., in relation to the severity of underlying disorder.

Hypertensive Constitution

PAR > 20

DI < 2 cm.

O2RT > 2 sec.

Co <>

Muscolar Preconditioning pathologic

Evaluation of Natriuretic Peptides

Getting rid of abnormalities of pre-clinical, pre-metabolic stage, we can hpefully prevent the serious diseases, which otherwise can onset, and, mainly the well-known complications in different biological systems.

On the contrary, we must rely only on treatments of high arterial pressure, often apparently efficacious, due to the fact that complication are already present and therapeutic monitoring is based exclusively upon lowered pressure values, gathered by the aid of a sphygmomanometer, which nothing are able to say about what really happen in target organs and tissue.

Actually, at the beginning of third millennium, doctors, for the fist time, agree with those few colleagues, who over years state that arterial hypertension, evaluated untill now at the level of vasa publica in a large variety of ways, is not significant as regards what really happens in tissue-microvascular-units under the same conditions.

In other words, the urgency of assessing organs damage begins to play the deserving role, also in the mind of those with scarse ability of criticism and creative imagination.

Really, since the descovery of CAEMH I stated without success that our colleagues would pay a great deal of attention to this mitochondrial cytopathology, overlooked for too long time, since I have realized that the war against the most serious human diseases, including arterial hypertension, can obtain the best results only in case of a prompt selection of individuals at “real risk” for them, so that they undergo “clincal” tests, reliable in “quantifying” such as risk, initiating rapidly the correct diet, etymologically speaking, that normalizes the muscular reactions, pathological at the beginning during boxer’s test, simulated stress test, “sucking simulation test, in which rythmic mamma palpation physiologically brings about – by nervous reflex, inhibiting dopamine neurons of TIDA – increase of PRL secretion, which enhances peripheral arteriolar resistance as well as insulin secretion, and negative consequences, we previously described (4, 10).

It is worth for saying that primary prevention of AH allows doctors to prevent contemporaneously also disorders and syndromes (ATS, DM, gout, malignancies, in indivuals, of course, with “oncological terrain”, a.s.o.) with favorable influences, both individual and social (20-22).

In fact, clinical evidence demonstrates that, beside AH, in the same patient there are frequently other serious disorders, cause of morbidity and mortality, based upon the commom genetic factor, i.e. CAEMH

The authors agree generally on both exsistence and importance of “genetic factor” of arterial hypertension, which has to explain following facts:

1) sympatethic hypertonus;

2) “intense and rapid “ response of a-adrenergic receptors, present in fifferent way in arterial and venous districts;

3) “rapid and intense” response of the vessels, which dilate;

4) “rapid and intense” congestion and subsequent similar decongestion of splancin organs, a part from intestine.


Clinical evidence in favour of pre-hypertensive state.

In hypertensive state, in fact, in a previous research performed on 249 individuals CAEMH-a, negative for AH, in the age between 15-80 years, the duration of kidney congestion during boxer’s test, resulted 4-5 sec., while in 467 individuals, comparable to age, CAEMH-a positive, among them 175 hypertensive (37,5%), and the other normotensive, but with family history positive for AH (292; 62,5%), kidney congestion duration was <>

CAEMH-a – as we demonstrated previously (2-4, 9, 10, 11, 14, 18, 19) – represents the conditio sine qua non of ATS, migraine, DM, autimmune disorders, incuding Acute Benigne Variant Polymyalgya Rheumatica (18, 19), tumours (10), solid and liquid, : “all” hypertensive individuals, we observed over the last 50 years, are or were involved by the mitochondrial cytopathology, I described, as allows us to state also the clinical evidence: digital pressure, applied on a nail-fold, e.g. of the big toe, of a young CAEMH-a negative, causes temporary dilation of homolateral common iliac artery (0,5 cm.), while both aorta and controlateral common iliac artery “practically” show unchanged diameters.

On the contrary, in the young CAEMH-a positive homolateral iliac artery shows a dilation ³ 1 cm. and, simultaneously, both aorta and controlateral common iliac artery dilate clearly and significantly, permitting thus pressure values to be normal.

Really, CAEMH-a is the genetic factor, clinically “quantifiable”, at the base of various formes of neuro-vegetative dystonia (8), of particular a2-receptors overactivity, as in case of alexytimia, frequently associated to AH (4, 28). The incapacity for speaking correctly and describe emotions by Autonomous Nervous System, due to internal tensions, plays a primary role in the pathogenesis of AH associated with this nervous disorder.

From the above remarks, in order to prevent efficaciously AH we have to be considered, in “healthy subjects, i.e. without AH or other clinical phenomenology, but CAEMH-a positive, the possibility of assessing hemoreological-haemodynamic as well as metabolic-biochemical modifications (post-absorptive state with abnormalities in central and peripheral vessels dynamics), even caused by numerous tests: boxer’s test, simulated stress, apnea test, sucking simulated test, Restano’s manoeuvre, a.s.o.

We must consider interesting the data collected, as usually, by tissue-microvascular-unit of finger-pulp or nail-foild, in which A Phase is characteristically of small intensity and O2RT is > 2 sec.

Beside the family history, the results of this evaluation allow to recognize promptly individuals at “real” risk for arterial hypertension, starting from the initial stage, we suggested to term pre-hypertensive state of AH, in which tissue pH appears to be lowered, O2RT prolonged, PAR increased, DI abnormal, arterial Co pathological, according to the values, illustrated above in the scheme.

These individuals show metabolic-biochemical conditions, characteristic of pre-morbid state, in which is present hyperinsulinaemia-insulinresistance,observable, the first, by specific renal test (brief kidney congestion and prolonged decongestion; NN 4-5 sec. and, respectively, 10 sec.) and by suprarenal glands evaluation (reduced microvascular activity since the third fluctuation), during insulinaemic acute pick secretion, due to the phenomenon of down-regulation of kidneys insulin receptors as well as insulin “vasocostriction” action caused by functional dysendotelization, as we observe as regards acethyl-choline

In conclusion, by a large number of biophysical semeiotic methods, of different difficulty and refinement (we illustrated above some among the less difficult methods, although reliable and practically easy to perform) nowadays is possible to recognize individual at risk for AH, since the first two decades of life, in a “quantitative” manner, due to the severity of their hypertensive constitution.

Consequently, now we can perform fortunately the primary prevention of this widespread and dangerous disease, notoriously complicated, if diagnosed to late, by morbidity and mortality, which can nowadays be prevented, because we can detect the disease in its pre-morbid stage, before complications onset, clinically, and, therefore, on very large scale.


* Sergio Stagnaro MD

Via Erasmo Piaggio 23/8, CP. 42

16039 Riva Trigoso (Genoa) Europe

Founder of Quantum Biophysical Semeiotics

Who's Who in the World (and America)

since 1996 to 2009

Ph 0039-0185-42315

Cell. 3338631439

www.semeioticabiofisica.it

dottsergio@semeioticabiofisica.it

Referencees

1) Stagnaro S., Istangiopatia Congenita Acidosica Enzimo-Metabolica condizione necessaria non sufficiente della oncogenesi. XI Congr. Naz. Soc. It. di Microangiologia e Microcircolaz. Abstracts, pg 38, 28 Settembre-1 Ottobre, Bellagio, 1983.

2) Stagnaro S., Istangiopatia Congenita Acidosica Enzimo-Metabolica. X Congr. Naz. Soc. It. di Microangiologia e Microcircolazione. Atti, 61. 6-7 Novembre, Siena, 1981.

3) Stagnaro S., Istangiopatia Congenita Acidosica Enzimo-Metabolica. Gazz Med. It. – Asch. Sci, Med. 144, 423, 1985.

4) Stagnaro-Neri M., Stagnaro S., Stadio pre-ipertensivo e monitoraggio terapeutico della ipertensione arteriosa. Omnia Medica Therapeudica. Archivio, 1-13, 1989-90.

5) Stagnaro-Neri M., Stagnaro S. Introduzione alla Semeiotica Biofisica. Il Terreno Oncologico. Travel Factory, Roma, 2004. http://www.travelfactory.it/semeiotica_biofisica.htm

6) Stagnaro-Neri M., Stagnaro S., Sindrome di Reaven, classica e variante, in evoluzione diabetica. Il ruolo della Carnitina nella prevenzione del diabete mellito. Il Cuore. 6, 617, 1993.

7) Stagnaro S., Risk of Type 2 Diabetes. N Engl J Med. 2002 Jan 24;346(4):297-298. letter [MEDLINE].

8) Stagnaro-Neri M, Stagnaro S., Valutazione clinica percusso-ascoltatoria del sistema nervoso vegetativo e del sistema renina-angiotensina, circolatorio e tessutale. Arch. Med. Int. XLIV, 17378, 1992.

9) Stagnaro S., Stagnaro-Neri M., Le Costituzioni Semeiotico-Biofisiche.Strumento clinico fondamentale per la prevenzione primaria e la definizione della Single Patient Based Medicine. Travel Factory, Roma, 2004. http://www.travelfactory.it/libro_costituzionisemeiotiche.htm

10) Stagnaro-Neri M., Stagnaro S. Introduzione alla Semeiotica Biofisica. Il Terreno Oncologico. Travel Factory, Roma, 2004. http://www.travelfactory.it/semeiotica_biofisica.htm

11) Stagnaro Sergio. Bedside Assessing ANS, RAAS, and IIR: a complex Relation to type 2 Diabetes. Cardiovascular Diabetology,15 November 2005. http://www.cardiab.com/content/4/1/15/comments#215501

12) Stagnaro Sergio. Microalbuminuria and Diabetes Mellitus: a primary predictor. CMAJ. 22 August, 2002. http://www.cmaj.ca/cgi/eletters/163/5/561.

13) Stagnaro Sergio. Single Patient Based Medicine: its paramount role in Future Medicine. Public Library of Science. 2005.http://medicine.plosjournals.org/perlserv/?request=read-response.

14) Stagnaro S., Stagnaro-Neri M. Single Patient Based Medicine.La Medicina Basata sul Singolo Paziente: Nuove Indicazioni della Melatonina. Travel Factory, Roma, 2005. http://www.travelfactory.it/libro_singlepatientbased.htm

15) Stagnaro-Neri M., Stagnaro S. Indagine clinica percusso-ascoltatoria delle unità microvascolotessutali della plica ungueale. Acta Med. Medit. 4, 91, 1988.

16) Stagnaro-Neri M., Stagnaro S., Semeiotica Biofisica: valutazione della compliance arteriosa e delle resistenze arteriose periferiche. Atti del XVII Cong. Naz. Soc. Ital. Studio Microcircolazione, Firenze Ott. 1995, Biblioteca Scient. Scuola Sanità Militare, 2, 93, 1995.

17) Stagnaro-Neri M., Stagnaro S., Auscultatory Percussion Evaluation of Arterio-venous Anastomoses Dysfunction in early Arteriosclerosis. Acta Med. Medit. 5, 141, 1989.

18) Stagnaro S., Auscultatory Percussion of Rheumatic Diseases. X European Congress of Rheumatology. Moscow. 26 June-July, Proceedings, pg 175, 1983.

19) Stagnaro S., Polimialgia Reumatica Acuta Benigna Variante. Clin. Ter. 118, 193,1986 [Medline]

20) Kannel W.B., Schatzkin A. — Analisi dei Fattori di Rischio. Progressi in Patologia Vascolare,Vol. XXVII, 5.-9, 1984

21) Malamani V. — L'evoluzione del pensiero medico in tema di ipertensione. Fed. Med. XXXVIII, 5, 511-516,1985.

22) Patzscheke U. Milde Hypertonie: Behandein Oder Nicht Behandein? Med. Klin. 21, 80, 574-578, 1985.

23) Ratschow M. Angiologia. Patologia, Clinica E Terapia Dei Disturbi Circolatori Periferici. I Ed. Italiana Pag. 115 Casa Editrice Ambrosiana. Milano, 1962.

24) Zanchetti A. Ipertensione Arteriosa: Filosofia Attuale Di Un Trattamento Flessibile E Personalizzato. Il Polso, Ottobre 1987, Pag. 41-47.

25) Pickering G. High Blood Pressure. Ii Ed. London. J. &A. Chruchill, 1986, Pg. 35.

26) Schirosa G. Le Malattie Del Cuore. I Ed. Vol. Ipag. 61 Società Editrice Universo. Roma 1970.

27) Schwartz S.M., Ross R. La Proliferazione Cellulare Nell'arteriosclerosi E Nell'ipertensione. Progressi In Patologia Vascolare, Voi. XXVII, N° 4, 63-81, 1984.

28) Ciraolo O., Quartarone M., Barbera N. E Coli. Alexitimia E Ipertensione. Atti Ix Congr. Naz. Soc. It. Patologia Vascolare. Copanello 6-9 Giungo 1987. Pg. 639-644 Monduzzi Editore Bologna 1987.


Monday, May 11, 2009

Quantum Biophysical Semeiotics: The Theory of Angiobiopathy



Introduction.

Microvessels and microcirculation play a paramount role in Quantum Biophysical Semeiotics.

In reality, chaotic-determinist dynamics of the biological systems, present in the three zones, Zone White (health), Grey Zone (pre-pathology) and Black Zone (disease) (1-5), are caused by the analogous oscillations of the single structures of relative tissue microvascular units, i.e., microcirculatory bed, according to Anglo-Saxon Authors (6-10). From the conceptual point of view, problematics regarding micro-circle and the microcirculation, are comprised, as well as analyzed, in the best way, when we are thinking, for analogy, to the street map of a city or country: from the large peripheral street begin wide roads, to only sense, different for number, directed towards the centre. The main roads, in double sense, progressively go shrinking itself till to become small street. In the vascular structure, the wider roads correspond to the Ratschow’s "vasa publica", while smallest, under 100 micron, represents for analogy the "vasa privata" , that participate to the formation of tissue microvascular unit (11). Naturally, blood “return” is realized by micro and the venous macro-vessel and the lymphatic ones.

The Theory of Angiobiopathy

For the first time in clinical way (V. http://www.semeioticabiofisica.it), thanks to Quantum Biophysical Semeiotics, has been realized biological-molecular study of parenchimal activity by studying the related micro-vessels and microcirculation in the biological systems, both at rest and under utilization of numerous substances, completing the assessment during dynamic tests, much rich of information. This theory, Angiobiopathy Theory, completes usefully Angiobiotopy theory, according to F. Tischendorf, brilliant student of microvessel anatomy, friend and collaborator of my Master of Microangiology-Microcirculation, S.B. Curri.

According to Angiobiopathy Theory a determined parenchyma is supplied of a specific microvascular system, really complex from the structural point of view, result of an co-organization happened in the course of evolution. In reality, such anatomy of tissue-micro-vascular unit can modify within the same apparatus, due to physiological reasons, correlated constantly with particular situations of the local tissue, as it happens in the skin microcirculation of lower limb. Tischendorf’s definition of Angiobiotopy as reagards the Zone White (Health), emphasises the anatomical aspect, and it has been completed from the Angiobiopathy Theory, that emphasizes parenchimal-microvessel correlations also in the pre-pathological conditions, Grey Zone ("locus" of the primary prevention), and in the several diseases, Black Zone, as I have illustrated in previous papers (1-6). In other words, between parenchyma and relative micro-vascular system is present constantly an anatomical and functional correlation, bedside assessed not only in physiological but also in pre-pathological and pathological conditions, as clinical evidence demonstrates.

To this point, I call for attention to above-mentioned analogy, in order to comprise in details these Medicine advances, really fundamental for Clinical Microangiology. We think next to the existing relationship between the houses of a country or a quarter and the local roads, ways, alleys, but also the water, gas, etc. In fact, as the vessels of every tissue, they supply material-energy-information for the life of the inhabitants and provide to remove the harmful debris, catabolites, events of essential importance for the survival of residents (7-21).

We still continue with the aid of the same analogy in order to explain a fundamental concept in the Quantum Biophysical Semeiotics: from the movement of the several feeding goods, materials, newspapers, books, a.s.o., and flowing drinkable water, as well as black water, sewer, or drainage white water, in a limited city area, can obtain precise information on the culture, understanding broadly speaking, of a community and on the way people face the several existential problems. Therefore, the reader can easily comprise that the way “to be and to work” of the microvessels, included the vase vasorum (12), studied now also with Clinical Microangiology, using a stethoscope (the 6-10) (www.semeioticabiofisica.it/microangiologia), gives information, anatomo-functional in origin, about correspondent biological system, aim of doctor’s evaluation.

In health, the micro-vascular oscillations as well as macro-oscillations, are chaotic-determinist, unforeseeable, apparently stocastic, showing an intensity (0,5 - 1,5 cm., conventional measure) and duration of the cycles (oscillating between 9 and 12 sec., i.e., 6 circle /sec.), but regulated, in reality, from a more refined order, than binds them inside of a strange attractor in the space phase (1-11).

From the above microcirculatory remarks, derives that Clinical investigation allows doctor to gather, for the first time clinical, precious information on the biological system function and structure, through the data observed on the structure and activity of the relative microcirculatory system, both at rest and during stress tests. The evaluation of biological activity is based above all on bedside analysing micro-vascular system of several parenchymas under different situations, normal or not, according to Angiobiopaty theory.

In reader’s interest, to comprise the real significance of Angiobiopaty, whose role is fundamental in the Quantum Biophysical Semeiotics, is firstly unavoidable to examine in details the concept of Angiobiotopy , according to Tischendorf.

First of all, it is not surprising the fact that the biological systems adapt, so to speak, the relative tissue-micro-vascular units to the single request of their various regions. For example, the system of the so-called “preferential channels” represents, for still unknown reasons, a structural particularitity of intestine and eye conjunctive, while the formation of meshes of the arterioles and the venules characterises the skeletal musculature. Naturally, a structural disposition of both above-mentioned vessel types can be observed - in less or more intense way - also in other organs and tissue, for instance, to mesentery and pia mater. In mesentery the formation of ring-like anastomoses of the arteries and the veins is limited generally to the branches of greater bore, while the smallest arteries and the arteriole are subdivided dycotomically of new, like branches of a tree, in order to end in the capillaries. Moreover, during their transformation in smaller vessels its diameter constantly becomes conical: for this their form is not still cylindrical, but conical and is fine. According to S.B. Curri, we may admit the hypothesis that these structural differences regarding microvessel modifications are not connected exclusively to the various function of the supplied tissues, but also to their various disposition it spaces, and therefore, to topographical factors. Thus as an example the micro-structure of the human skin constitutes one of the more meaningful aspects of the combination between the "structural principle to net" and the dycotomic subdivision of the capillaries. While in derma deeper regions micro-vessels form the artero-arterioses and veno-venose anastomoses in the subpapillare plex, cutaneous arterial and venous, the capillaries in epidermis from small arteries end in smallest vessels: these are found horizontal under epidermis, circulating itself in a capillary after other that heads vertically towards high; or they go directly towards the epidermis layer bases, circulating in many capillaries to form of small bush. An other example of micro-vessel structure is represented from the capillary beds of the liver and of the spleen, that show how much clearly the anatomical structure of an organ and its specific functions are in a position to modifying distribution model space of the little vessels, radically different from the two above-mentioned fundamental models.

It can be said therefore that the rules of the architectonic plan of the capillary nets are subordinated to the organ-specific architectonic peculiarities. From above shortly reported information, one comprehends that the structure of the capillary beds cannot be identical, always the same, and that differences are present, so that various structural principles can coexist. On the other hand, there are body regions, e.g., eye conjunctive, whose circle ends much irregular and it seems un-forseable: thus, it’s possible one or another type of microcirculatory bed. As states my Master, main goal of the future researches is to determine for every important region of an organ or tissue - from patho-physiological view-point – what is the constructive plan of the capillary bed. The intuition, before, and the demonstration, then, of the correlation tightened between structure and function of every parenchyma and that one of the relative micro-vascular system represents the central aspect of the Angiobiopathy theory, that has opened revolutionary new way to diagnosis, differential-diagnosis, therapeutic monitoring and clinical research.

Krogh was right!

As Krogh had previewed in its Lecture in occasion of the Nobel Prize ceremony in 1920 (1), the study of the micro-vessels shows today fortunately its original, essential and reliable utilization in bedside examination of all biological systems, beside obviously macro- and micro-circulatory system, in physiological and pathological conditions, emphasising a paramount value in diagnosing and researching, thanks to Quantum Biophysical Semeiotics.

In fact, the clinical study of the micro-circle and the microcirculation of every apparatus and tissue, allows to doctor bedside gathering reliable information on structure and functions of all biological system, as well as to recognize and analyze biological and biological-molecular events of the relative parenchyma, under different conditions. Moreover, in every biological systems there is no-local realm, I have demonstrated for the first time, wherein information is simultaneous, beside the well-known local realm. At this point, I have to thank my friend Paolo Manzelli, discoverer of the triadic nature of information (12-24), for his precious advices on Quantum Physics.

Interestingly, the "intense" digital pressure, applied, e.g., upon trigger-points of the neuronal centres for release hormone, provokes the simultaneous associated microcirculatory activation of type I, physiological, in all nervous system, including the above-mentioned centres.

In health, “simultaneously” with the beginning of the stimulation, the stomach does not show any modification of its form and volume, which occurs only after the physiological latency time, as aspecific gastric reflex. In other words, under this experimental condition, is absent the simultaneous non-specific gastric reflex at the beginning of the test.

On the contrary, in presence of whatever cerebral lesion, both structural and functional in nature, like CAEMH (1-7), we simultaneously observe aspecific gastric reflex, whose intensity in cm. parallels th seriousness of underlying disorder (12-24. Therefore, on the base of the no-local realm in Biology, it is possible to bedside recognize, with a stethoscope, in a second, in reliable, elegant, and quick way, brain disorders, and analogously those of different parenchyma, by means of the evaluation of the relative tissue-microvascular units, “simultaneously” activated in the correspondent biological system by such “intense” stimulation of the relative trigger-points (10-25). The data, quickly gathered, direct subsequently the physical examination towards the really suffering biological system or tissue, allowing to utilise it at the best loosing less time.

References

  1. Stagnaro-Neri M., Stagnaro S. Introduzione alla Semeiotica Biofisica. Il Terreno Oncologico. Travel Factory, Roma, 2004. http://www.travelfactory.it
  2. Stagnaro S., Stagnaro-Neri M., La Melatonina nella Terapia del Terreno Oncologico e del “Reale Rischio” Oncologico. Travel Factory, Roma, 2004.
  3. Stagnaro S., Stagnaro-Neri M., Le Costituzioni Semeiotico-Biofisiche.Strumento clinico fondamentale per la prevenzione primaria e la definizione della Single Patient Based Medicine. Travel Factory, Roma, 2004.
  4. Stagnaro S., Stagnaro-Neri M., Single Patient Based Medicine.La Medicina Basata sul Singolo Paziente: Nuove Indicazioni della Melatonina. Travel Factory, Roma, 2005.
  5. Stagnaro Sergio. Teoria Patogenetica Unificata, 2006, Ed. Travel Factory, Roma.
  6. Stagnaro Sergio. Semeiotica Biofisica Quantistica: La Teoria dell’Angiobiopatia. www.fce.it, http://www.fcenews.it/index.php?option=com_content&task=view&id=1451&Itemid=47
  7. Stagnaro S., Istangiopatia Congenita Acidosica Enzimo-Metabolica. Gazz Med. It. – Asch. Sci, Med. 144, 423, 1985.
  8. Stagnaro-Neri M., Stagnaro S., Auscultatory Percussion Evaluation of Arterio-venous Anastomoses Dysfunction in early Arteriosclerosis. Acta Med. Medit. 5, 141, 1989.
  9. Stagnaro-Neri M., Moscatelli G., Biophysical Semeiotics: deterministic Chaos and biological Systems. Gazz. Med. It. – Arch. Sc. Med. 155, 125, 1996.
  10. Stagnaro-Neri M., Stagnaro S., Deterministic Chaos, Preconditioning and Myocardial Oxygenation evaluated clinically with the aid of Biophysical Semeiotics in the Diagnosis of ischaemic Heart Disease even silent. Acta Med. Medit. 13, 109, 1997.
  11. Stagnaro Sergio. Diagnosi clinica di cuore sano in un secondo! 7 Aprile 2008. www.fce.it http://www.fcenews.it/index.php?option=com_content&task=view&id=1218&Itemid=47
  12. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica Endocrinologica: Meccanica Quantistica e Meccanismi d’Azione Ormonali. Dicembre 2007, www.fce.it, http://www.fcenews.it/index.php?option=com_content&task=view&id=816&Itemid=45
  13. Stagnaro Sergio e Paolo Manzelli. Natura Quantistica di una Originale Manovra Semeiotico-Biofisica di Epatopatia. Dicembre 2007, www.fce.it, http://www.fcenews.it/index.php?option=com_content&task=view&id=862&Itemid=45
  14. Stagnaro Sergio e Paolo Manzelli. Semeiotica Biofisica Quantistica. http://www.ilpungolo.com/leggi-tutto.asp?IDS=13&NWS=NWS5243 2007
  15. Stagnaro Sergio e Paolo Manzelli, Semeiotica Biofisica Quantistica: la manovra di attivazione surrenalica jatrogenetica. 09-1-2008, http://www.fcenews.it/index.php?option=com_content&task=view&id=161&Itemid=63
  16. Stagnaro Sergio e Paolo Manzelli. L’Esperimento di Lory. Scienza e Conoscenza, N° 23, 13 Marzo 2008. http://www.scienzaeconoscenza.it//articolo.php?id=17775
  17. Stagnaro Sergio. Non Local Realm. Response to Selection for Social Signalling Drives the Evolution of Chameleon Colour Change. (01 February 2008). www.plos.com, http://biology.plosjournals.org/perlserv/?request=read-response&doi=10.1371/journal.pbio.0060025
  18. Stagnaro Sergio. La Diagnosi Clinica nella Semeiotica Biofisica Quantistica. www.fce.it 02-05-2008, http://www.fcenews.it/index.php?option=com_content&task=view&id=1285&Itemid=47
  19. Stagnaro Sergio. Semiotica Biofisica Quantistica: Diagnosi di Cuore sano in un Secondo in paziente distante 200 KM! www.fce.it, 07-05-2008 http://www.fcenews.it/index.php?option=com_content&task=view&id=1316&Itemid=47
  20. Stagnaro Sergio. Role of NON-LOCAL Realm in Primary Prevention with Quantum Biophysical Semeiotics. www.nature.com, 01 Feb, 2008-05-17 http://www.nature.com/news/2008/080130/full/451511a.html
  21. Stagnaro Sergio e Manzelli Paolo. Semeiotica Biofisica Quantistica: Livello di Energia libera tessutale e Realtà non locale nei Sistemi biologici. www.fce.it , 29 maggio 2008, http://www.fcenews.it/index.php?option=com_content&task=view&id=1421&Itemid=47
  22. Stagnaro Sergio. SEMIOTICA BIOFISICA Quantistica. Scienza&Conoscenza, 8-10-2008 http://www.scienzaeconoscenza.it/articolo.php?id=21568
  23. Stagnaro Sergio. Benjamin Libet’s experiments: Quantum Biophysical Semeiotics view-point! The General Science Journal. 31 Dec. 2008. http://www.wbabin.net/comments/stagnaro.htm
  24. Stagnaro Sergio. Quantum Biophysical Semeiotics Enlightens Benjamin Libet’s Experiments. www.fce.it, 14 gennaio 2009. http://www.fceonline.it/index.php?option=com_content&task=view&id=2194&Itemid=45
  25. Stagnaro Sergio. Ruolo dell’Angiobiopatia nella Semeiotica Biofisica Quantistica, www.ilpungolo.com, 29 Maggio 2008, http://www.ilpungolo.com/leggi-tutto.asp?IDS=13&NWS=NWS5609

* Sergio Stagnaro MD

Via Erasmo Piaggio 23/8, CP. 42

16039 Riva Trigoso (Genoa) Europe

Founder of Quantum Biophysical Semeiotics

Who's Who in the World (and America)

since 1996 to 2009

Ph 0039-0185-42315

Cell. 3338631439

www.semeioticabiofisica.it

dottsergio@semeioticabiofisica.it

Thursday, May 7, 2009

Quantum Biophysical Semeiotics Evaluation of pancreatic beta-Cell Function by means of acute pick stimulation of GH-RH secretion.




Introduction.

Among other well-known biological activities, Growth Hormone (GH) plays an important role in metabolism, as well as in regulating insulin secretion from the b-pancreatic cells, additionally controlling GH-RH secretion (analogously, e.g., thyroid hormone) (1-8).

Interestingly, the emerging age of Quantum Biophysical Semeiotics allows doctors, especially General Practitioners, to assess pancreas chaotic-determinist oscillations (fluctuations – 6 x sec. – of pancreatic body vertical diameter) (1-8), correlated with functional endocrine activity of the gland, according to Angiobiopathy theory (6-12).

(For technical information,See http://www.semeioticabiofisica.it, Technical Page 4).

The acute stimulation of GH-RH secretion, is brought about by “mean-intense” digital pressure applied on the related trigger-points (Fig.1 and 2).

Consequently, with the aid of Quantum Biophysical Semeiotics, physicians can evaluate bedside endocrine pancreas efficiency during the acute stimulation of the GH-RH and, thereby, obtaining useful and reliable GH information regarding current insulin secretion activity and efficiency (1, 2, 4, 7, 8).

Moreover, quantum-biophysical-semeiotic preconditioning (9), (also http://www.semeioticabiofisica.it ), enables the the practitioner can assimilate information (using the variables of Auscultatory Percussion and so-called Auscultatory Percussion-Reflex-Diagnostic, which studies non-linear dynamics of all biological systems) regarding the patient’s condition, as well as the possible insulin secretion evolution: physiological insulin secretion, hypersecretion of insulin (IIR) with or without initial failure of the pancreatic b-cells (prediabetes), overt type 1 and type 2 diabetes mellitus, even in early phase.

Finally, bedside evaluation can also reveal pancreatic endocrine activity, employing analogously other “endogenous” hormones of insulin counter-regulation (i.e., thyroid hormone, glucagone, adrenalin) (6, 7).

Method.

With the subject in supine position, psycho-physically relaxed (eyes open to avoid the melatonin secretion), the practitioner performs repetitive auscultatory percussion of a short tract of the lower pancreatic margin, assessing accurately its fluctuations, chaotic-determinist under physiological condition (Fig. 1).

For comprehensible reasons, the gathered data are meal-dependent, showing different parametric values in relation to the meals, i.e., in the absorptive or in the post-absorptive state.

However, in the practice, such as fact results neither important nor significant.

Notoriously, in overt type 2 diabetes, that is to say in manifest disorder, the dimensionality (i.e., value of deterministic chaos in a determined biological system, in our case the pancreas) fluctuations appear significantly and gradually reduced, all equal, and minimal, showing the fractal dimension of 1, i.e., topological dimension (6).

At this point, General Practitioner applies “mean-intense” digital pressure on the trigger-points of GH-RH neuronal centre, that is located 2 cm. over external auditory meatus (Fig. 2), evaluating accurately the pancreatic size behaviour.

In health, after approximately 6 seconds, the pancreas decongests suspending temporarily its secretive activity: the lower margin of the pancreatic body rises and remains in this higher position for 10 sec. exactly. In the absorptive state, the duration is approximately 11-12 seconds (in a non significant manner).

Under this experimental condition, pancreatic microcirculation shows the phenomenon of “microcirculatory disactivation”, characterized from minimal microvessel activity, resulting from the lesser flow-motion: in both vasomotility and vasomotion, according to Hammersen (7) fluctuation intensity is hardly 0,5 cm., and the durartion of AL + PL phase appears to be 5 sec., (6, 8, 10,11, 12) (See the above cited web site http://www.semeioticabiofisica.it/microangiologia).

On the contrary, in the subject with insulin hypersecretion (IIR), the pancreas decongestion (i.e., pancreatic functional rest) appears prolonged (12-14 sec. significantly) in direct relationship with the intensity of insulin secretion (i.e., hyperinsulinaemia).

The behavior of the pancreas during the biophysical-semeiotic preconditioning is briefly illustrated, allowing the practioner to immediately recognize insulin hypersecretion (IIR), with or without slow tendency to the b-pancreatic cell failure, and, lastly, overt type 2 diabetes.

In diabetes mellitus, even in its initial phases, the duration of pancreatic decongestion appears significantly reduced (£ 9 sec.), in obvious relation the severity of the underlying disorder.

Beside evaluation can result in important data regarding insulin secretion using quantum-biophysical-semeiotic preconditioning. (After accurately assessing the duration of pancreatic decongestion brought about by the acute peak of the GHRH secretion, withdraw the digital pressure, consequently removing the hormonal hypersecretion of GH, for 5 seconds exactly. Immediately repeat the evaluation a second time, as described above.)

In a healthy patient, the duration of the pancreatic decongestion rises from exactly 10 sec. (i.e., normal basal value) to 14 sec., in a statistically significant way, a result of the physiological activation of local Microcirculatory Functional Reserve (9, 10).

Interestingly, in hyperinsulinsecretion (IIR), one observes a large number of parameter (i.e., duration) behaviours, which parallel the present functional efficacy of the endocrine pancreas activity, in individuals with or without diabetic constitution (11):

a) in preconditioning, the duration of pancreatic decongestion can arise either to more than 14 sec. or hardly to 11-12 sec. in not meaningful way, in relation to the efficiency condition of insulin secretion;

b) the duration does not show modification, so that it persists unchanged in the comparison of the initial, basal value;

c) this parametric value (= duration length) results reduced, e.g., 9 sec., indicating the “quantitative” alteration of b-cell secretion.

Identical are the data collected also, for example, using the stimulation of the TSH-RH (Fig.2), that provokes the acute peak of thyroid hormone secretion, as demonstrates the contemporaneous associated microcirculatory activation, type 1, in the thyroid (8, 9): “variant” biophysical semeiotics test.

Discussion and conclusions.

Today, literature worldwide reflects an increased urgency for early recognition of the Metabolic Syndrome, and its risk factors (CAD, CVD, type 2 DM, etc.) as well as its pathophysiological and clinical definition (13-15).

From quantum-biophysical-semeiotic view-point (6, 12, 14, 15), Pre-Metabolic Syndrome, always precedes Metabolic Syndrome for years and even decades, (V. also http://www.semeioticabiofisica.it/microangiologia), and involves both sexes, with or without diabetes, but “all” experiencing dyslipidaemic complication..

For this reason, we can finally understand why glucose metabolism alterations and type 2 diabetes are present only in well-defined patient population with metabolic syndrome, as well as why doctors can now fortunately recognize numerous early clinical stages of the metabolic syndrome resulting in positive and favorable benefits in primary prevention..

Because of the numerous and dangerous complications of Metabolic Syndrome in individuals with both dyslipidaemia and diabetes, large scale optimal primary prevention of metabolic syndrome, is needed to allow doctors the diagnostic “clinical” tool, to determine pancreatic endocrine complications and enabling future monitoring.

As recent as four years ago, Biophysical Semeiotic testing became a reliable and useful means for clinicians, to assess insulin-secretion conditions, physiological and pathological, including functional failure of pancreatic b-cells, even in the initial stage.

In conclusion, Quantum-Biophysical Semeiotic testing, above briefly described, is a useful tool for diagnosis, therapeutic monitoring, and clinical research.

References.

1) Stagnaro S., Stagnaro-Neri M. Valutazione percusso-ascoltatoria del Diabete Mellito. Aspetti teorici e pratici. Epat. 32, 131, 1986.

2) Stagnaro-Neri M., Stagnaro S., Il Segno di Bilancini-Lucchi nella diagnosi clinica del diabete mellito. The Pract. Ed. It. 176, 30,1993.

3) Stagnaro-Neri M., Stagnaro S., Sindrome di Reaven, classica e variante, in evoluzione diabetica. Il ruolo della Carnitina nella prevenzione del diabete mellito. Il Cuore. 6, 617, 1993 [Medline]

4) Stagnaro S., Diet and Risk of Type 2 Diabetes. N Engl J Med. 2002 Jan 24;346(4):297-298. letter [Medline]

5) Stagnaro S. Pre-metabolic syndrome: the real initial stage of metabolic-syndrome, type 2 diabetes and arteroscleropathy. Cardiovascular Diabetology 2004, 3:1

http://www.cardiab.com/content/3/1/1/comments.

6) Stagnaro Sergio, Stagnaro-Neri Marina. Introduzione alla Semeiotica Biofisica. Il Terreno oncologico”. Travel Factory SRL., Roma, 2004.

http://www.travelfactory.it/semeiotica_biofisica.htm.

7) Cited in: S.B. Curri. Le Microangiopatie. Inverni della Beffa, Verona, 1986.

8) Stagnaro-Neri M., Stagnaro S., Semeiotica Biofisica: valutazione clinica del picco precoce della secrezione insulinica di base e dopo stimolazione tiroidea, surrenalica, con glucagone endogeno e dopo attivazione del sistema renina-angiotesina circolante e tessutale. Acta Med. Medit. 13, 99, 1997.

9) Stagnaro-Neri M., Stagnaro S., Semeiotica Biofisica: la manovra di Ferrero-Marigo nella diagnosi clinica della iperinsulinemia-insulino resistenza. Acta Med. Medit. 13, 125,1997.

10) Stagnaro-Neri M., Stagnaro S., Deterministic Chaos, Preconditioning and Myocardial Oxygenation evaluated clinically with the aid of Biophysical Semeiotics in the Diagnosis of ischaemic Heart Disease even silent. Acta Med. Medit. 13, 109,1997.

11) Stagnaro S., Stagnaro-Neri M., Le Costituzioni Semeiotico-Biofisiche. Strumento clinico fondamentale per la prevenzione primaria e la definizione della Single Patient Based Medicine. Ediz. Travel Factory, Roma, 2004. http://www.travelfactory.it/semeiotica_biofisica.htm

12) Stagnaro S., Stagnaro-Neri M., Single Patient Based Medicine.La Medicina Basata sul Singolo Paziente: Nuove Indicazioni della Melatonina. Travel Factory SRL., Roma, 2005. http://www.travelfactory.it/semeiotica_biofisica.htm

13) Kahn R., Buse J., Ferrannini E. and Stern M. The Metabolic Syndrome: Time for a Critical Appraisal.Joint statement from the American Diabetes Association and the European Association for the Study of Diabetes . Diabetes Care 28:2289-2304, 2005.

14) Stagnaro Sergio. Pre-Metabolic Syndrome and Metabolic Syndrome: Biophysical-Semeiotic Viewpoint. www.athero.org, 29 April, 2009. http://www.athero.org/commentaries/comm904.asp
15) Stagnaro Sergio. CAD Inherited Real Risk, Based on Newborn-Pathological, Type I, Subtype B, Aspecific, Coronary Endoarteriolar Blocking Devices. Diagnostic Role of Myocardial Oxigenation and Biophysical-Semeiotic Preconditioning. www.athero.org, 29 April, 2009 http://www.athero.org/commentaries/comm907.asp

Tuesday, May 5, 2009

Cerebral Tumour detected by Quantum-Biophysical Semeiotics since its Inherited Real Risk.



Introduction

From its initial stage, brain oncological process, occupying space, provokes local circulatory modifications of both hyperemic and ischemic type, secondary to biochemical and/or compressive events. Quantum Biophysical Semeiotics (BS) permits doctor to observe microcirculatory phenomena as well as variations of the tissue pH at the bed-side (See: my website www.semeioticabiofisica.it) (1-8).

Furthermore, the cerebral potentials (1, 5), whether spontaneous or evoked, clearly altered or totally absent in case of tumour, may be evaluated “quantitatively” with the aid of BS, even in early stage.

In following, it is referred both the usefulness and reliability of such as semeiotics in diagnosing cerebral tumour, even in the initial phase of Inherited Real Risk (6, 9-14).

Method

As regards QBS of cerebral tumour, it is enough to know, from the technological point of view, the auscultatory percussion of the stomach (in above-cited website, Technical Page N° 1), which is performed with digital percussion, directly and “gently”, applied on abdominal skin, from outer areas towards the bell-piece of stethoscope along radial and centripetal lines, as indicated in Fig.1

When percussion is applied on organ or viscera skin projection areas, percussory sound is perceived as altered, modified, dull or hyperfonetic, in relation to the density of investigated structure, in any case “as originating from a site close to the doctor’s ears”.

Obviously, a complete knowledge of QBS permits doctor to gather further information.

There are a large number of other Quantum Biophysical Semeiotics data referring to cerebral tumour; however, as follows, are referred only some unavoidable signs, easy to evaluate and reliable in bed-side detecting cerebral tumour.

Quantum Biophysical Semeiotic Signs of Cerebral Tumour

At first doctor has to ascertain the so-called oncological terrain (6), conditio sine qua non of malignancy , and is composed particularly of:

1) Congenital Acidosic Enzyme-Metabolic Histangiopaty (CAEMH). Briefly, digital pressure of “middle” intensity upon skin projection area, e.g., of temporal convolutions (temporal lobe), brings about a gastric aspecific reflex more intense when right cerebral lobe is stimulated, due to the right cerebral dominance, typical for CAEMH: dominance of the right Planum temporale. (2,10).

2) Psycho-neuro-endocrine-immunological system dysfunction (6): in a easy manner doctor ascertains this pathological condition inviting the patient to close intensively his (her) eyes (= dark increases melatonin secretion, which in turns stimulates the secretion of endogenous oppioids, the so-called orchestra directors of immunological system): after 15 sec.

In health, digital pressure of small intensity, directly applied ,e.g., on a breast gland, causes gastric aspecific reflex with latency time of 3 sec.( i.e. acute antibody synthesis syndrome).

On the contrary, when eyes are open, latency time is 6 sec.(i.e. chronic antibody synthesis syndrome).

3) Suck simulated test to provoke Prolactin Secretion: repeated palpation of mammary gland provokes, in healthy individuals of both sexes and of middle age, gastric aspecific reflex of exact 6 sec. duration. In case of inflammatory process, as flu, however, duration results prolonged (7 sec. exactly). Finally, in subject with oncological terrain duration appears ³ 7 sec., in a direct relation to the degree of the psycho-neuro-endocrine-immunological system dysfunction.

The duration is very prolonged, of course, in case of tumour. Physiologically, the test presents the most elevated duration in pregnacy, due to the particular endocrine situation, since initial stage.

In a patient, who presents with a symptomatology suggestive of cerebral tumour (or in asymptomatic patient, of course) other QBS signs are properly investigated.

An interesting sign, particularly useful and reliable in bed-side detecting the presence of “something wrong” in the head is the following:

4) Aspecific gastric-oculo reflex. In health, the appearance of gastric aspecific reflex, physiologically symmetric, during digital pressure on the eye-ball (when patient’s eyes are closed, naturally) after a latency time 6 sec. and 1-2 cm. in intensity.

On the contrary, in case of cerebral neoplasia as well as other cerebral disorder, when pressure is exerted on the homolateral eye-ball, doctor observes initially a gastric aspecific reflex (lt 3 sec.; intensity > 2 cm.; duration 3 sec.), and, soon thereafter, the “autoimmune syndrome”: gall-bladder and stomach contract (gastric tonic contraction = GTC) and spleen become empty of blood: in practice, it is sufficient for the diagnosis ascertaining GTC.

In diagnosing clinically the cerebral tumour, a major role is played by the:

5) Cerebral-gastric aspecific reflex: finger-pulp as well as finger-nail pressure (type I and type II, respectively) on skin projection area of the tumour provokes the “autoimmune syndrome”, as described above. Finally, in the presence of cerebral malignancy, there is always the:

6) Reticulo-Endothelial System Hyperfunction Syndrome (RESHS) of “complete” type, that corresponds to BSR, but it is more sensitive and sensible.

In health, finger-pulp pressure on the middle line of sternal-body, iliac crests and skin projection area of the spleen causes aspecific gastric reflex after a latency time = 10 sec.exactly.

On the contrary, in case of cerebral cancer latency time results lowered, in relation to disorder seriousness.

Finally, one must remember that acute phase proteins are augmented and both the acute autoantibody secretion syndrome and circulating immuncomplex syndrome (boxer’s test, i.e. patient is clenching his or her fists, brings about gastric tonic contraction -GTC-, after appearing gastric aspecific reflex lasting 3 sec.) are present (2-9).

Due to the lack of reader’s Quantum Biophysical Semeiotic knowledge, at this moment I do not illustrate numerous other signs of cerebral tumour.

To summarize, QBS diagnosis of cerebral tumour is based (at least) on the following signs:

1) Congenital Acidosic Enzymo-Metabolic Histangiopathy (CAEMH), which plays a primary role in the psycho-neuro-endocrine-immunological system dysfunction, I termed as Oncological Terrain.

2) Oncological terrain (1-6);

3) Reticulo Endothelial System Hyperfunction Syndrome (RESHS) type “complete” (4);

4) Oculo-gastric aspecific reflex and then gastric tonic contraction (GTC) (1-6, 9,14);

5) Cerebro-gastric aspecific reflex (type I and II) followed by GTC(1-6, 9,14);

5) Acute phase proteins augmentation (3, 6);

6) Acute autoantibody secretion syndrome ((1-6, 9,14);

7) Circulating Immunocomplex Syndrome, above-described .

In addition, a lot of clinical microangiological signs, gathered at the bed-side by evaluating both vasomotility and vasomotion of cerebral microvessels, are actually interesting and precious in recognizing also cerebral malignancy since its first stage: due to reader’s inadequate Quantum Biophysical semeiotic knowledge: I will illustrate these signs next, in the future.

As far as Cerebral Evoked Potentials is concerned, it is well-known that visive, auditory and somato-sensorial stimuli, through nervous in-puts, provoke physiologically the activation of corresponding nervous centres by mean of depolarization. Consequently, local cerebral microcirculation results more or less activated, allowing doctor to evaluate these events by means of Quantum Biophysical Semeiotics.

If a subject looks at a light source, e.g., due to the stimulation of optic channels, impulses reache the bilateral cortical-occipital region and activate it, that is, they evoke electrical potentials, demonstrating the anatomo-functional integrity of such nervous structures. Analogously, auditive and somato-sensorial stimuli (the later really more practical and therefore advisable) provoke electrical potentials, obviously in corresponding cortical centres.

Experimental (an individual is invited, e.g., to move or to “think of moving “ a hand) and clinical (epileptic focus, e.g.) evidence suggests that the cerebral evoked potentials can be evaluated by means of Quantum Biophysical Semeiotics, because of the hemoreological and microcirculatory phenomenology of the active hyperemic areas (In termes of Cinical Microangiology: activation type I, associated, of both vasomotility and vasomotion). In fact, the finger-pulp pressure of “middle” intensity on the cutaneous projection of an activated cerebral zone causes gastric aspecific reflex. Consequently, in case of cerebral malignancy, the absence of the cerebral evoked potentials shows the suffering of precise nervous channels, due to a disorder, easily ascertained at the bed side.

References

1) Stagnaro S., Stagnaro-Neri M. Auscultatory Percussion in Detection Focal Liver Lesions even Clinically Silent. Acta Med. Medit. 8, 89-94, 1992.

2) Stagnaro S., Auscultatory percussion of the cerebral tumour: Diagnostic importance of the evoked potentials, Biol. Med., 7, 171-175, 1985.

3) Stagnaro-Neri M., Stagnaro S., Cancro della mammella: prevenzione primaria e diagnosi precoce con la percussione ascoltata. Gazz. Med. It. – Arch. Sc. Med. 152, 447, 1993.

4) Stagnaro S., Sindrome percusso-ascoltatoria di Iperfunzione del Sistema Reticolo-IstiocitarioMin. Med. 74, 479, 1983 [MEDLINE].

5) Stagnaro S., Percussione Ascoltata degli Attacchi Ischemici Transitori. Ruolo dei Potenziali Cerebrali Evocati. Min. Med. 1985, 76, 1211 [MEDLINE].

6) Stagnaro Sergio, Stagnaro-Neri Marina. Introduzione alla Semeiotica Biofisica. Il Terreno oncologico”. Travel Factory SRL., Roma, 2004.

7) Stagnaro S., Stagnaro-Neri M., Le Costituzioni Semeiotico-Biofisiche.Strumento clinico fondamentale per la prevenzione primaria e la definizione della Single Patient Based Medicine. Ediz. Travel Factory, Roma, 2004.

8) Stagnaro Sergio. Bed-Side Prostate Cancer Detecting, even in early stages (“Real Risk” of Cancer): BMC Family Practice, 6:24 doi:10.1186/1471-2296-6-24 http://www.biomedcentral.com/1471-2296/6/24/comments#202466

9) Sergio Stagnaro Mitochondrial Bed-Side Evaluation: a new Way in the War against Cancer (21 December 2005). Cancer Cell International http://www.cancerci.com/content/5/1/34/comments#218502

10) Stagnaro S. Genes and Cancer: a clinical view-point. The Oncological Terrain. BioMed Central Informatics, 2004. http://www.biomedcentral.com/1471-2105/5/21/comments#10454

11) Stagnaro S., Stagnaro-Neri M., Oncological Terrain, conditio sine qua non of Oncogenesis, GUT, 2004. http://www.gutjnl.com/cgi/eletters?lookup=by_date&days=60

12) Stagnaro Sergio. "Genes, Oncological Terrain, and Breast Cancer", World Journal of Surgical Oncology. 2005, http://www.wjso.com/content/3/1/45/comments#205475

13)Stagnaro Sergio. GPs , Quantum Biophysical Semeiotics, and bedside cancer diagnosis. 08 July 2007, International Seminar of Surgical Oncology, http://www.issoonline.com/content/4/1/11/comments#281539

14) Stagnaro Sergio. Overloking Oncological Terrain and oncological Real Risk, no paper is up-dated! 18 January 2008 Ann. Intern Med. http://www.annals.org/cgi/eletters/147/11/775