Imanova N. I.

Prognostic Opportunities of Heart Rhythm Variability Investigation in Patients with Cardio-Vascular Disease


About the author:

Imanova N. I.

Heading:

LECTURES

Type of article:

Scentific article

Annotation:

Heart rate variability is one of the indicators of the functional state of the autonomic nervous system. Reduction of this indicator’s levels in some ways is a marker of autonomic deregulation and takes place in the case of diseases associated with an imbalance of the autonomic nervous system. The study of heart rate variability provides an opportunity to improve understanding of the physiological conditions, the impact of treatment and disease mechanisms. Changes in heart rhythm can be assessed using a variety of methods: measures the area of time, statistical, geometrical and frequency methods. Each of these methods has its advantages and disadvantages in certain types of applications. Although cardiac automaticity inherent pacemaker’s different tissues, heart rate and rhythm to a large extent under the control of the autonomic nervous system. HRV is defined as the severity of fluctuations in heart rate (HR) in relation to its average. The clinical significance of HRV was assessed in 1965 when Hon and Lee noted that fetal distress syndrome preceded by changes in the RR- intervals even before there were changes of heart rate directly. Twenty years ago, V. M. Sayers focused on the existence of physiological rhythms, which obeyed the difference between individual blows of heart rate. During the 1970s , invented many simple techniques to identify interval R-R differences to assess autonomic neuropathy in patients with diabetes. Association of higher- risk after myocardial infarction mortality with a decrease in HRV was first defined by M. M. Wolf and his colleagues in 1977. In 1981 – S. Akselrod et al. presented a powerful spectral analysis of heart rate rhythm to quantify the change in control heartbeat. These studies have HR contribution to understanding the background of autonomous oscillations R-R interval heart rate. Parasympathetic division of nervous system, whose influence on heart rate through neurotransmitter acetylcholine and sympathetic division, whose influence is via epinephrine and norepinephrine, interact. At rest predominant parasympathetic activity and changes in heart rhythm are significantly dependent of parasympathetic modulation. Decreased HRV may be associated with different pathologies: heart and diseases of other body systems. Decreased HRV after myocardial infarction may reflect a decrease in parasympathetic influence on the heart, which leads to increased sympathetic influences and electrical instability of the myocardium. One of the hypotheses suggests the inclusion of cardio-cardiac, sympathetic and parasympathetic reflexes, and consists in the fact that changes in the geometry of the heart, which is reduced in the case of areas of necrosis and disturbance of hemodynamics lead to “wrong” excite sympathetic impulses in fibers by mechanical damage of sensory nerve endings. Sympathetic arousal, in turn, reduces the tone of the parasympathetic fibers directed to the sinus node. Another explanation – a decrease of vitality sinus node response to changes in the neural regulation. Diabetes mellitus is one of the causes of autonomic neuropathy. Clinical symptoms consist of signs of damage of sympathetic and parasympathetic nerve fibers and frequently associated with distal sensorimotor polyneuropathy. The course of cardiovascular autonomic neuropathy is asymptomatic nature in 1/5 of patients and appears only in the study of HRV. Cardiac autonomic neuropathy in patients with type 1 diabetes is associated with the activity of the sympathoadrenal system. Moreover, increased activity of sympathoadrenal system is a factor of atherosclerosis in adult patients regardless of the presence of diabetes. Increased blood pressure combined with adverse electrophysiological phenomena in the myocardium of the left ventricle, associated with its hypertrophy and dysfunction of the autonomic nervous system. The risk of cardiac autonomic neuropathy is depend on the duration of diabetes and degree of glycemic control and increases in parallel with the development and progression of complications of other diseases such as retinopathy, nephropathy, vasculopathy and others. Therefore, the holding of periodic 24-hour Holter measurement can detect minor violations of autonomic balance in a timely manner and appropriately adjust the development of pathology. Individual prediction value based on the HRV is small. However, the combination with other methods significantly improves the positive predictive accuracy of the HRV (by clinical sensitivity range of 25% to 75%) for cardiac death and arrhythmias. HRV has significant potential for impact assessment of the role of vegetative nervous system in healthy subjects and in patients with various cardiovascular and non-cardiovascular disorders. The study of HRV provides an opportunity to improve our understanding of the physiological conditions, the impact of treatment and disease mechanisms. Heart rate variability research needed to determine the sensitivity, specificity and predictive value of the method in the distribution of individuals in relation to the threat of disease and death in the future.

Tags:

heart rate variability, cardio-vascular diseases, vegetative nervous system

Bibliography:

  • 1. Алиева А. Н. Оценка вариабельности сердечного ритма при артериальной гипертензии / А. Н. Алиева, А. М. Кошелев, Т. Б. Касатова // Лечебное дело. – 2004. – №1. – С. 53-59.
  • 2. Бобров В. А. Фармакодинамические эффекты комбинированной формы эналаприла в сочетании с гидрохлоро-тиазидом при эссенциальной гипертензии / В. А. Бобров, В. И. Зайцева, И. В. Давыдова [и др.] // Укр. кардиол. журн. – 1998. – №6. – С. 40-43.
  • 3. Бойчак М. П. Состояние вегетативной нервной системы у больных ишемической болезнью сердца с начальной сер-дечной недостаточностью / М. П. Бойчак // Проблеми мед. науки та освіти. – 2002. – №2. – С. 28-32.
  • 4. Воронин И. М. Вариабельность и спектральный анализ сердечного ритма в диагностике дисфункции синусового узла / И. М. Воронин, ю. А. Говша, Т. А. Истомина [и др.] // Кардиология. – 1999. – №10. – С. 32-34.
  • 5. Дабровски А. Суточное мониторирование ЕКГ: Пер. с польск. / А. Дабровски, Б. Дабровски, Р. Пиотрович. – М.: Мед-практика, 2000. – 208 с.
  • 6. Иманова Н. И. Прогностические возможности вариабельности сердечного ритма у больных гипертонической болез-нью / Н. И. Иманова // Проблеми медичної науки та освіти. – 2002. – №2. – С. 86-88.
  • 7. Исаева А. С. Влияние пропранолола на вариабельность сердечного ритма и фазовую структуру сердечного цикла у здоровых добровольцев / А. С. Исаева, Е. П. Мележик, А. В. Бильченко [и др.] // Лікарська справа. – 2002. – №2. – С. 99-103.
  • 8. Перуцкий Д. И. Оценка вариабельности сердечного ритма в практической кардиологии: современное состояние про-блемы / Д. И. Перуцкий, ю. И. Афанасьев // Вестник современной клинической медицины. – 2008. – Т. 1(1). – С. 73-81.
  • 9. Попов В. В. Вариабельность сердечного ритма: возможности применения в клинической медицине и физиологии / В. В. Попов, Л. Н. Фрицше // Укр. мед. часопис. – 2006. – №2 (52). – С. 50-62.
  • 10. Селивоненко С. В. Спектральный анализ сердечного ритма как показатель вегетативной регуляции сердечно-сосу-дистой системы / С. В. Селивоненко // Тер. архив. – 2002. – №1. – С. 59-61.
  • 11. Стрюк Р. И. Вариабельность сердечного ритма / Р. И. Стрюк, Е. Я. Парнес, Д. Г. Иоселиани [и др.] // Кардиология. – 2005. – №12. – С. 53-57.
  • 12. Цибадзе А. Д. Вариабельность сердечного ритма при непролиферативной диабетической ретинопатии / А. Д. Цибад-зе, Л. Р. Цуцкиридзе, Р. Б. Курашвили [и др.] // Медицина неотложных состояний. – 2009. – №3-4. – С. 22-23.
  • 13. Яблучанский Н. И. Вариабельность сердечного ритма в современной клинике / Н. И. Яблучанский, Б. Я. Кантор, А. В. Мартыненко [и др.]. – Донецк: ЧНИПФ Будень, 1997. – 108 с.
  • 14. Cerati D. Single cardiac vagal fiber activity, acute myocardial ischaemia, and risk for sudden death / D. Cerati, P. J. Schwartz// Circ. Res. – 1991. – Vol. 69. – P. 1389-1401.
  • 15. Bella J. N. Relations of left ventricular mass to fat-free body mass: the strong heart study / J. N. Bella, R. B. Devreux, N. Roman // Circulation. – 1998. – Vol. 98. – P. 2538–2544.
  • 16. Bigger J. T. Frequency domain measures of heart period variability and mortality after myocardial infarction / J. T. Bigger, J. L. Fleiss, R. C. Steinman // Circulation. – 1992. – Vol. 85. – P. 164-171.
  • 17. Bigger J. T. Predicting mortality after myocardial infarction from the response of RR variability to antiarrhythmic drug therapy / J. T. Bigger, L. M. Rolnitzky, R. C. Steinman // J. Am. Coll. Cardiol. – 1994. – Vol. 23. – P. 733-740.
  • 18. Borghi C. Effects of different dosages of hydrochlorothiazide on blood pressure and the renin-angiotensin-aldosterone system in mild to moderate essential hypertension / C. Borghi, S. Borghi, F. V. Costa // Curr. Ther. Res. – 1992. – Vol. 51. – P. 859-869.
  • 19. Carlsen J. E. Relation between dose of bendrofluazide, antihypertensive effect, and adverse biochemical effects / J. E. Carlsen, L. Kober, C. Torp-Pedersen // Br. Med. J. – 1990. – Vol. 300. – P. 974-978.
  • 20. De Ferrari G. M. Scopolamine increases vagal tone and vagal reflexes in patients after myocardial infarction / G. M. De Ferrari, M. Mantica, E. Vanoli // J. Am. Coll. Cardiol. – 1993. – Vol. 22. – P. 1327-1334.
  • 21. Freeman R. Spectral analysis of heart rate in diabetic neuropathy / R. Freeman, J. P. Saul, M. S. Roberts // Arch. Neurol. – 1991. – Vol. 48. – P. 185-190.
  • 22. Heart Rate Variability. Standards of Measurement, Physiological Interpretation, and Clinical Use. Task Force of the European Society of Cardiology the North American Society of Pacing Electrophysiology // Circulation. – 1996. – Vol. 93. – P. 1043-1065.
  • 23. Kamath M. V. Power spectral analysis of heart rate variability: a noninvasive signature of cardiac autonomic function / M. V. Kamath, E. L. Fallen // Crit. Rev. Biomed. Eng. – 1993. – Vol. 21. – P. 245-311.
  • 24. Kienzle M. G. Clinical haemodynamic and sympathetic neural correlates of heart rate variability in congestive heart failure / M. G. Kienzle, D. W. Ferguson, C. L. Birkett // Am. J. Cardiol. – 1992. – Vol. 69. – P. 482-485.
  • 25. Malik M. Components of heart rate variability: what they really mean and what we really measure / M. Malik, A. J. Camm // Am. J. Cardiol. – 1993. – Vol. 72. – P. 821-822.
  • 26. Malik M. Heart rate variability and clinical cardiology / M. Malik, A. J. Camm // Br. Heart. J. – 1994. – Vol. 71. – P. 3-6.
  • 27. Malliani A. Cardiovascular neural regulation explored in the frequency domain / A. Malliani, M. Pagani, F. Lombardi // Circulation. – 1991. – Vol. 84. – P. 1482-1492.
  • 28. Malliani A. Power spectral analysis of heart rate variability: a tool to explore neural regulatory mechanisms / A. Malliani, F. Lombardi, M. Pagani // Br. Heart. J. – 1994. – Vol. 71. – P. 1-2.
  • 29. Neutel J. M. Low-dose antihypertensive combination therapy; its rationale and role in cardiovascular risk management / J. M. Neutel // Am. J. Hypertens. – 1999. – Vol. 12. – S. 73-79.
  • 30. Port S. Systolic blood pressure and mortality / S. Port, L. Demar, R. Jennrich // Lancet. – 2000. – Vol. 355. – P. 175-180.
  • 31. Rimoldi O. Analysis of short-term oscillations of R-R and arterial pressure in conscious dogs / O. Rimoldi, S. Pierini, A. Ferrari// Am. J. Physiol. – 1990. – Vol. 258. – P. 967-976.
  • 32. Pittrow D. B. Impact of a law-dose reserpine/thiazide combination on left ventricular hypertrophy / D. B. Pittrow, H. J. Horn, K. Detmar // Am. J. Hypetension. – 1997. – Vol. 10 (Part 2). – A. 50.
  • 33. Schwartz P. J. Interventions changing heart rate variability after acute myocardial infarction / P. J. Schwartz, G. M. De Ferrari// Heart rate variability. – Armonk, Ny: Futura, 1995. – P. 407-420.
  • 34. Tsuji H. Reduced heart rate variability and mortality risk in an elderly cohort: the Framingham Heart Study / H. Tsuji, F. J. Venditti, E. S. Manders // Circulation. – 1994. – Vol. 90. – P. 878-883.

Publication of the article:

«Bulletin of problems biology and medicine» Issue 2 part 3 (109), 2014 year, 76-81 pages, index UDK 616. 12/. 14