Arterial blood flow waveform shapes – their original quantification and importance in chosen aspects of physiology and psychology: A review

• Autorzy: Gólczewski Tomasz

Identyfikatory

DOI

10.1016/j.bbe.2021.04.007

• Języki publikacji: EN

Abstrakty

EN

Arterial blood flow waveform shape (ABFWS) analysis is usually employed in vessels diagnosis. This review presents links between ABFWS and some other physiological and psychological aspects. ABFWS for brachial and common carotid arteries is quantified with a Waveform Age (WA) index. WA well correlates with calendar age (CA): r = 0.79 and 0.88 for carotid and brachial arteries, respectively. The mean (expected) WA for a particular CA is equal to it. WA depends on blood flow wave reflections: WA is older for lower reflections (smaller flow pulsatility). An upper death limit of WA seems to exist; hypertension in the elderly may be a defense mechanism protecting against exceeding this limit. Relationships between WA and heart rate, fatigue and cognitive functions are most interesting. Regardless of breathing pattern, respiratory induced changes of heart rate are strongly correlated with WAs that were 1.7 s earlier (r = 0.87). Fatigue is associated with WA increase (p < 0.002); in a way, fatigue accompanies aging or temporary mimics it. WA is significantly lower than CA in persons with high intelligence quotient and significantly higher in patients with intellectual disability of unknown etiology (p < 0.000001). WA relatively well correlates with Matrices Tests scores (r = 0.65 for a linear combination of WAs for all the four arteries; 42 students, 16 yrs, the same social and educational levels). ABFW-Sdependent production of vasoactive substances (including nitric oxide being also a neurotransmitter) by endothelium, might be responsible for those surprising relationships. ABFWS can be treated, though only to some extent, as a kind of Damasio’s somatic markers.

Słowa kluczowe

EN

aging; cognitive functions; fatigue; hypertension; nitric oxide; respiratory sinus arrhythmia

PL

starzenie się; funkcje poznawcze; zmęczenie; nadciśnienie; tlenek azotu

• Wydawca: Nałęcz Institute of Biocybernetics and Biomedical Engineering of the Polish Academy of Sciences ; Elsevier
• Czasopismo: Biocybernetics and Biomedical Engineering
• Rocznik: 2021
• Tom: Vol. 41, no. 4
• Strony: 1418--1435
• Opis fizyczny: Bibliogr. 78 poz., rys., tab., wykr.

Twórcy

autor

Gólczewski Tomasz

• Nalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Ksiecia Trojdena 4, 02-109 Warsaw, Poland

Bibliografia

• [1] Onohara T, Okadome K, Yamamura S, Mii S, Sugimachi K. Simulated blood flow and the effects on prostacyclin production in the dog femoral artery. Circ Res 1991;68:1095–9.
• [2] Sanders KM, Ward SM. Nitric oxide as a mediator of nonadrenergic noncholinergic Neurotransmission. Am J Physiol 1992;262:G379–92.
• [3] Vincent SV. Nitric oxide neurons and neurotransmission. Prog Neurobiol 2010;90:246–55.
• [4] Sanders KM, Ward SM. Nitric Oxide and its role as a nonadrenergic, non-cholinergic inhibitory neurotransmitter in the gastrointestinal tract. Br J Pharmacol 2019;176(2):212–27.
• [5] Sang Y, Wu X, Miao J, Cao M, Ruan L, Zhang C. Determinants of brachial-ankle pulse wave velocity and vascular aging in healthy older subjects. Med Sci Monit 2020; 26: e923112-1–e923112-7.
• [6] Reshetnik A, Tölle M, Eckardt K-U, van der Giet M. Would oscillometry be able to solve the dilemma of blood pressure independent pulse wave velocity – A novel approach based on long-term pulse wave analysis? Front Physiol 2020;11 579852.
• [7] Pahlevan NM, Mazandarani SP. Estimation of wave condition number from pressure waveform alone and its changes with advancing age in healthy women and men. Front Physiol 2020;11:313.
• [8] Gólczewski T. A method of presentation of chosen hemodynamic values as vectors in the L2(T) space for biological states differentiation. Warsaw: IBBE PAS Works 1994;38 (PhD Thesis) [in Polish].
• [9] Gólczewski T, Krajewski A. A vector based approach to agerelated changes of Doppler velocity waveforms in the brachial artery. Ultrasound Med Biol 1987;13:15–8.
• [10] Merillon JP, Fontenier GJ, Lerallut JF, Jaffrin MY, Motte GA, Genain CP, et al. Aortic input impedance in normal man and arterial hypertension: its modification during changes in aortic pressure. Cardiovasc Res 1982;16:646–56.
• [11] O’Rourke MF. Arterial function in health and disease. Churchill Livingstone; 1982.
• [12] Bender AD. The effect of increasing age on the distribution of peripheral blood flow in man. J Am Geriatr Soc 1965;13:192–8.
• [13] Gólczewski T. Physiological death of old men without any disease. Materials of the VI Prerovske Geriatricke Dny 1986.
• [14] Ogliari G, Westendorp R, Muller M, Mari D, Torresani E, Felicetta I. Blood pressure and 10-year mortality risk in the Milan geriatrics 75+ cohort study: role of functional and cognitive status. Age Ageing 2015;44:932–7.
• [15] Gólczewski T. Influence of sleep on functional state of cardiovascular system estimated with ‘‘Tomed” system. In: 1st International Congress of the Polish Sleep Research Society. p. sup.13.
• [16] Akerstedt T, Froberg JE. Psychophysiological circadian rhythms in women during 72h of sleep deprivation. Waking Sleep 1977;1:387–94.
• [17] Gólczewski T. Does the shape of arterial blood flow waveform impact the central nervous system. In: Proc. The XI Domestic Conference ‘‘Biocybernetics and Biomedical Engineering” 1999; t1:26-30 [in Polish].
• [18] Goriounova NA, Heyer DB, Wilbers R, et al. Large and fast human pyramidal neurons associate with intelligence. Elife 2018;18(7) e41714.
• [19] Davis HE, Assaf GS, McCorkell L, Wei H, Low RJ, Re’em Y, Redfield S, Austin JP, Akrami A. Characterizing long COVID in an international cohort: 7 months of symptoms and their impact. medRxiv 2020.12.24.20248802; doi: https://doi.org/10.1101/2020.12.24.20248802.
• [20] Ratchford SM, Stickford JL, Province VM, Stute N, Augenreich MA, Koontz LK, et al. Vascular alterations among young adults with SARS-CoV-2. Am J Physiol Heart Circ Physiol 2021;320(1):H404–10.
• [21] Checa P, Fernández-Berrocal P. The role of intelligence quotient and emotional intelligence in cognitive control processes. Front Psychol 2015;6:1853.
• [22] Dalise AM, Prestano R, Fasano R, Gambardella A, Barbieri M, Rizzo MR. Autonomic nervous system and cognitive impairment in older patients: evidence from long-term heart rate variability in real-life setting. Front Aging Neurosci 2020;12:40.
• [23] Gólczewski T. Dynamics of flow alteration is the feature of pulsatile blood flow that influences the autonomic nervous system. BAMS 2005;1:81–6 [in Polish].
• [24] De Burgh Daly M. Interactions between respiration and circulation. Compr Physiol 2011, Supplement 11: Handbook of Physiology, The Respiratory System, Control of Breathing: 529–594.
• [25] Elstad M, O’Callaghan EL, Smith AJ, Ben-Tal A, Ramchandra R. Cardiorespiratory interactions in humans and animals: rhythms for life. Am J Physiol Heart Circ Physiol 2018;315(1): H6–H17.
• [26] Billman GE. The LF/HF ratio does not accurately measure cardiac sympatho-vagal balance. Front Physiol 2013;4:26.
• [27] Hoskins PR, Johnstone FD, Chambers SE, Hadded NG, Whit G, McDicken WN. Heart rate variation of umbilical artery Doppler waveforms. Ultrasound Med Biol 1989;15:101–5.
• [28] Khoo MCK, Chalacheva P. Respiratory modulation of peripheral vasoconstriction: a modeling perspective. J Appl Physiol (1985). 2019 Nov 1;127(5):1177–86.
• [29] O’Leary DS, Woodbury DJ. Role of cardiac output in mediating arterial blood pressure oscillations. Am J Physiol 1996;271: R641–6.
• [30] Aletti F, Hammond RL, Sala-Mercado JA, Chen X, O’Leary DS, Baselli G, et al. Cardiac output is not a significant source of low frequency mean arterial pressure variability. Physiol Meas 2013;34(9):1207–16.
• [31] Hogan N, Casadei B, Paterson DJ. Nitric oxide donors can increase heart rate independent of autonomic activation. J Appl Physiol 1999;87:97–103.
• [32] Trzebski A, Raczkowska M, Kubin L. Carotid baroreceptor reflex in man, its modulation over the respiratory cycle. Acta Neurobiol Exp (Wars) 1980;40(5):807–20.
• [33] Mohrman DE, Heller LJ, editors. Cardiovascular Physiology. New York: McGrawHill; 2006.
• [34] Bolton B, Carmichael EA, Stürup G. Vaso-constriction following deep inspiration. J Physiol 1936;86(1):83–94.
• [35] Cevese A, Grasso R, Poltronieri R, Schena F. Vascular resistance and arterial pressure low-frequency oscillations in the anesthetized dog. Am J Physiol. 1995;268(Heart Circ Physiol 37):H7-16.
• [36] Cerutti C, Barres C, Paultre C. Baroreflex modulation of blood pressure and heart rate variabilities in rats: assessment by spectral analysis. Am J Physiol 1994;266 (Heart Circ Physiol 35):H1993–H2000.
• [37] Babaeizadeh S, Zhou SH, Liu X, et al. A novel heart rate variability index for evaluation of left ventricular function using five-minute electrocardiogram. Comput Cardiol 2007;34:473–6.
• [38] Gólczewski T. A new approach to the genesis of primary arterial hypertension - a biocybernetic hypothesis. BAMS 2005;1:73–80.
• [39] Johnson PC. Autoregulation of blood flow. Circ Res 1986;59:483–95.
• [40] Avolio A. Ageing and wave reflection. J Hypertens 1992;10 (Suppl):S83–6.
• [41] Merillon JP, Fontenier GJ, Lerallut JF, et al. Aortic input impedance in normal man and arterial hypertension: its modification during changes in aortic pressure. Cardiovasc Res 1982;16:646–56.
• [42] Dobrin PB. Mechanical properties of arteries. Physiol Rev 1978;58:397–460.
• [43] Dobrin PB. Vascular mechanics. Compr Physiol 2011:65–102.
• [44] Runge TM, Grover FL, Cohen DJ, Bohls FO, Ottmers SE, Saadatmanesh V. Comparison of a steady flow pump to a preload responsive pulsatile pump in left atrial-to-aorta bypass in canines. Artif Organs 1991;15:35–41.
• [45] O’Neil MP, Alie R, Guo LR, Myers ML, Murkin JM, Ellis CG. Microvascular responsiveness to pulsatile and nonpulsatile flow during cardiopulmonary bypass. Ann Thorac Surg 2018;105:1745–53.
• [46] Nakano T, Tominaga R, Nagano I, Okabe H, Yasui H. Pulsatile flow enhances endothelium-derived nitric oxide release in the peripheral vasculature. Am J Physiol Heart Circ Physiol 2000;278:H1098–104.
• [47] Noris M, Morigi M, Donadelli R, Aiello S, Foppolo M, Todeschini M, et al. Nitric oxide synthesis by cultured endothelial cells is modulated by flow conditions. Circ Res 1995;76:536–43.
• [48] Vedrinne C, Tronc F, Martinot S, et al. Better preservation of endothelial function and decreased activation of the fetal renin-angiotensin pathway with the use of pulsatile flow during experimental fetal bypass. J Thorax Cardiovasc Surg 2000;120:770–7.
• [49] Ziegler T, Bouzourene K, Harrison VJ, Brunner HR, Hayoz D. Influence of oscillatory and unidirectional flow environments on the expression of endothelin and nitric oxide synthase in cultured endothelial cells. Arterioscler Throm Vasc Biol 1998;18:686–92.
• [50] Donato AJ, Gano LB, Eskurza I, et al. Vascular endothelial dysfunction with aging: endothelin-1 and endothelial nitric oxide synthase. Am J Physiol Heart Circ Physiol 2009;297(1): H425–32.
• [51] Raignault A, Bolduc V, Lesage F, Thorin E. Pulse pressuredependent cerebrovascular eNOS regulation in mice. J Cereb Blood Flow Metab 2017;37(2):413–24.
• [52] Sezai A, Shiono M, Nakata K, et al. Effects of pulsatile CPB on interleukin-8 and endothelin-1 levels. Artif Organs 2005;29 (9):708–13.
• [53] Cheng JL, Au JS, MacDonald MJ. Peripheral artery endothelial function responses to altered shear stress patterns in humans. Exp Physiol 2019;104:1126–35.
• [54] Ündar A. Universal and precise quantification of pulsatile and non-pulsatile pressure-flow waveforms is necessary for direct and adequate comparisons among the results of different investigators. Perfusion 2003;18:135–6.
• [55] Thayer JF, Lane RD. A model of neurovisceral integration in emotion regulation and dysregulation. J Affect Disord 2000;61 (3):201–16.
• [56] Dernellis J, Panaretou M. Aortic stiffness is an independent predictor of progression to hypertension in nonhypertensive subjects. Hypertension 2005;45:426–41.
• [57] Humphrey JD, Harrison DG, Figueroa CA, Lacolley P, Laurent S. Central artery stiffness in hypertension and aging: a problem with cause and consequence. Circ Res 2016;118 (3):379–81.
• [58] Cameron J, Dart A. Exercise training increases total systemic arterial compliance in humans. Am J Physiol Heart Circ Physiol 1994;266:H693–701.
• [59] Bhuva AN, D’Silva A, Torlasco C, et al. Training for a first-time marathon reverses age-related aortic stiffening. J Am Coll Cardiol 2020;75(1):60–71.
• [60] Thijssen DH, Dawson EA, Tinken TM, Cable NT, Green DJ. Retrograde flow and shear rate acutely impair endothelial function in humans. Hypertension 2009;53(6):986–92.
• [61] Avlund K. Fatigue in older adults: an early indicator of the aging process? Aging Clin Exp Res 2010;22(2):100–15.
• [62] Fukae K, Tominaga R, Tokunaga S, Kawachi Y, Imaizumi T, Yasui H. The effects of pulsatile and nonpulsatile systemic perfusion on renal sympathetic nerve activity in anesthetized dogs. J Thorac Cardiovasc Surg 1996;111 (2):478–84.
• [63] Singer J, Trollor JN, Baune BT, Sachdev PS, Smith E. Arterial stiffness, the brain and cognition: a systematic review. Ageing Res Rev 2014;15:16–27.
• [64] Edlavitch S, Gurland BJ, Golden R, Greenlick M, Perry HM, Schoenberger J. Rates of depression in elderly volunteers with isolated systolic hypertension. Int J Geriatric Psychiat 1987;2:111–7.
• [65] Ravindrarajah R, Hazra NC, Hamada S, et al. Systolic blood pressure trajectory, frailty, and all-cause mortality >80 years of age: Cohort study using electronic health records. Circulation 2017;135(24):2357–68.
• [66] Alipour H, Goldust M. The association between blood pressure components and cognitive functions and cognitive reserve. Clin Exp Hypertens 2016;38:95–9.
• [67] Guo Z, Fratiglioni L, Winblad B, Viitanen M. Blood pressure and performance on the Mini-Mental State Examination in the very old. Cross-sectional and longitudinal data from the Kungsholmen Project. Am J Epidem 1997;145:1106–13.
• [68] Peralta CA, Katz R, Newman AB, Psaty BM, Odden MC. Systolic and diastolic blood pressure, incident cardiovascular events, and death in elderly persons: the role of functional limitation in the Cardiovascular Health Study. Hypertension 2014;64:472–80.
• [69] Post Hospers G, Smulders YM, Maier AB, Deeg DJ, Muller M. Relation between blood pressure and mortality risk in an older population: role of chronological and biological age. J Intern Med 2015;277(4):488–97.
• [70] Tadic M, Cuspidi C, Hering D. Hypertension and cognitive dysfunction in elderly: blood pressure management for this global burden. BMC Cardiovasc Disord 2016;16(1):208.
• [71] Rivasi G, Lucenteforte E, Turrin G, Balzi D, Bulgaresi M, Nesti N, et al. Blood pressure and long-term mortality in older patients: results of the Fiesole Misurata Follow-up Study. Aging Clin Exp Res 2020;32(10):2057–64.
• [72] Conroy SP, Westendorp RGJ, Witham MD. Hypertension treatment for older people—navigating between Scylla and Charybdis. Age Ageing 2018;47:505–8.
• [73] Damasio AR. Descartes error: emotion, reason and the human brain. New York: Avon; 1994.
• [74] Güemes A, Georgiou P. Review of the role of the nervous system in glucose homoeostasis and future perspectives towards the management of diabetes. Bioelectron Med 2018;4:9.
• [75] Sher LD, Geddie H, Olivier L, Cairns M, Truter N, Beselaar L, et al. Chronic stress and endothelial dysfunction: mechanisms, experimental challenges, and the way ahead. Am J Physiol Heart Circ Physiol 2020;319:H488–506.
• [76] Cherubini JM, Cheng JL, Williams JS, MacDonald MJ. Sleep deprivation and endothelial function: reconciling seminal evidence with recent perspectives. Am J Physiol Heart Circ Physiol 2021;320:H29–35.
• [77] Chciałowski A, Gólczewski T. Spirometry: a need for periodic updates of national reference values. In: Pokorski M, editor. Pulmonology advances in experimental medicine and biology, vol. 1222. Cham: Springer; 2019. https://doi.org/10.1007/5584_2019_432.
• [78] Gólczewski T, Lubiński W. Spirometry: quantification of the shape of the maximal expiratory flow-volume curve. Biocybern Biomed Eng 2008;28(3):19–30.