2006, Number 1
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Gac Med Mex 2006; 142 (1)
Implicaciones clínicas y pronósticas del estudio circadiano de la modulación simpático-vagal de la variabilidad de la frecuencia cardiaca en pacientes con hipertensión arterial pulmonar grave
Rosas-Peralta M, Sandoval-Zárate J, Attie F, Pulido T, Santos E, Granados MZ, Miranda T, Escobar V
Language: Spanish
References: 44
Page: 19-28
PDF size: 293.09 Kb.
ABSTRACT
Background: A reduction of heart rate variability (HRV) is currently considered an independent risk factor for morbidity, mortality and severity of several cardiac disease, however, the dynamic sympathovagal modulation on HRV during 24 hr in primary pulmonary hypertension (PPH) had not been described.
Methods: 24 hr Holter monitoring (HM) were recorded in 32 patients (mean age 34, +/-12, 90% female) with severe primary pulmonary hypertension (mean pulmonary pressure, 9O:t:12mm Hg), and in 34 patients (mean age 36 +/-14, 60% female) with Eisenmenger syndrome (ES) secondary to septal ventricular defect or atent ductus arteriosus. A control group (n=44) paired for age, gender and arterial pulmonary pressure was included. HRV time and spectral parameters (mean, SDNN, SDANN, rMSSD, PNN50, LF, HF and LF/HF ratio) were analyzed during three periods: 24 hr; day (8-22:00), night (23-07:00) and also every hour of recording at 5 min-intervals). After detection of sympatho-vagal balance 15 patients were randomized, Treprostinil (prostaglandin) was administered to 6 patients and subcutaneous placebo to 9.
Results: HRV frequency parameters during 24 hr HM were significantly different among groups. LF/HF (day) 5.9:1:12.5:1:1P.001and LF/HF night)2.8:t1vs.1.5:1:.8.034. Sympathovagal modulation on 24hr HRV showed that heart rate circadian rhythm is clearly altered in both PPH and ES, but the sympathetic tone in PPH is higher at l 24hr. (p<.05), after administering treprostinil a recovery of sympathovagal balance was observed.
Conclusions: Autonomic cardiac disturbance is clearly present in PPH and ES. The circadian rhythm of HRV is first lost due to an increase of sympathetic tone. These changes may be markers of autonomic disbalance that favor the development of arrhythmias and sudden death. The sympathovagal balance in PPH could be considered an important risk marker.
REFERENCES
Cohen MC, Rohtla KM, Lavery CE, Muller JE, Mittleman MA. Metaanalysis of the morning excess of acute myocardial infarction and sudden cardiac death. Am J Cardiol 1997;79:1512–6.
Lee KL, Woodlief LH, Topol EJ, et al. Predictors of 30-day mortality in the era of reperfusion for acute myocardial infarction: results from international trial of 41021 patients. Circulation. 1995;91:1659-1668.
D’Alonzo GE, Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension. Results from national prospective registry. Ann Intern Med 1991;115:343–9.
Rich S. Executive summary from the world symposium primary pulmonary hypertension 1998. 1998.
Miyamoto S, Nagaya N, Satoh T, et al. Clinical correlates and prognostic significance of six-minute walk test patients with primary pulmonary hypertension. Comparison with cardiopulmonary exercise testing. Am J Respir Crit Care Med 2000;161:487–92.
Singh SJ, Morgan MD, Scott S, et al. Development of shuttle walking test of disability in patients with chronic airways obstruction. Thorax 1992;47:1019–24.
Yock P, Popp R. Noninvasive estimation of right ventricular systolic presure by Doppler ultrasound in patients with tricuspid regurgitation. Circulation 1994;70:657.
Gurtner HP. Aminorex and pulmonary hypertension. Review. Cor Vasa 1985;27:160–71.
Langleben D. Familial primary pulmonary hypertension. Chest 1994;105:13S–16S.
Loyd JE, Primm RK, Newman JH. Familial primary pulmonary hypertension: clinical patterns. Am Rev Respir Dis 1984;129:194-197.
Rubin LJ. Primary pulmonary hypertension. N Engl J Med 1997;336:111–7.
Fuster V, Steele PM, Edwards WD, et al. Primary pulmonary hypertension: natural history and the importance of thrombosis. Circulation 1984;70:580–7.
Kanemoto N. Natural history of pulmonary hemodynamics in primary pulmonary hypertension. Am Heart J 1987;114:407–13.
Rector TS, Cohn JN. Prognosis in congestive heart failure. Ann Rev Med. 1994;45:341-350.
The primary pulmonary hypertension study group. N Engl J Med 1996;334:296–302.
Ravy O, Azarian R, Brenot F, et al. Clinical significance the pulmonary vasodilator response during short-term infusion of prostacyclin in primary pulmonary hypertension. Circulation 1996;93:484–8.
Altman R, Scazziota A, Rouvier J, et al. Coagulation and fibrinolytic parameters in patients with pulmonary hypertension. Clin Cardiol 1996;19:549–54.
Welsh CH, Hassell KL, Badesch DB, et al. Coagulation and fibrinolytic profiles in patients with severe pulmonary hypertension. Chest 1996;110:710–7.
D’Alonzo GE, Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension. Results from national prospective registry. Ann Intern Med 1991;115:343–9.
Miyamoto S, Nagaya N, Satoh T, et al. Clinical correlates and prognostic significance of six-minute walk test patients with primary pulmonary hypertension. Comparison with cardiopulmonary exercise testing. Am J Respir Crit Care Med 2000;161:487–92.
Singh RB, Cronélisen G, Weydhal A, et al. Circadian heart rate and blood pressure variability considered for research and patient care. Int J Cardiol 2003;87:9-28.
Vaidya AB, Bhatt MA. Chronobiology of ischemic heart disease events: relevance of ancient insights in human lifestyle. J Assoc Phys India 1999;47:629–30.
Mehta SR, Das S, Karloopia SD, Mathur P, Dham SK, Raghunathan D. The circadian pattern of ischemic heart disease in Indian population. J Assoc Phys India 1998;46:767–77.
Pell S, D’Allonzo CA. Acute myocardial infarction in a large industrial population. J Am Med Assoc 1963; 185:831–8.
Smolensky M, Halberg F, Sargent F. II: Chronobiology of the life sequence. In: Itoh S, Ogata K, Yoshimura H, editors, Advances in climatic physiology, Tokyo: Igaku Shoin, 1972, pp. 281–318.
Reinberg A, Gervais P, Halberg F et al. Mortalite des adultes: rythmes circadiens et circannuels dans un hôpital parisien et en ´ France. Nouv Presse Med 1973;2:289–94.
Wennerblom B, Lurje L, Karsson T, Tygesen H, Vahisalo R, Hjamarson A. Circadian variation of heart rate variability and the rate of autonomic change in the morning hours in healthy subjects and angina patients. Int J Cardiol 2001;79:61–9.
Churisna SK, Ganelina IE. On the distribution of incidence of acute myocardial infarction within a 24-hour period. Kardiologia 1975;15:115–8.
Christ M, Seyffart K, Wehling M. Attenuation of heart rate variability in postmenopausal women on progestin containing hormone replacement therapy. Lancet 1999;353:1939–40.
La Rovere MT, Bigger Jr. JT, Marcus FI et al. Baroreflex sensitivity and heart-rate variability in prediction of total cardiac mortality after myocardial infarction. ATRAMI (Autonomic Tone and Reflexes After Myocardial Infarction) Investigators. Lancet 1998;351:478–84.
Bigger Jr. JT, Fleish JL, Steinman RC, Rolnitzsky LM, Kleiger RE, Rottman JN. Frequency domain measures of heart period variability and mortality after myocardial infarction. Circulation 1992;85:164–71.
Rich S, McLaughlin V. The effects of chronic prostacyclin therapy cardiac output and symptoms in primary pulmonary hypertension. J AmColl Cardiol. 1999;34:1184–1187.
Barst R, Rubin L, Long W, et al. A comparison of continuous intravenous epoprostenol (prostacyclin) with conventional therapy for primary pulmonary hypertension. N Engl J Med. 1996;334:296–301.
McLaughlin V, Genthner D, Panella M, et al. Reduction in pulmonary vascular resistance with long-term epoprostenol (prostacyclin) therapy primary pulmonary hypertension. N Engl J Med. 1998;338:273–277.
Sandoval J, Bauerle O, Palomar A, et al. Survival in primary pulmonary hypertension: validation of a prognostic equation. Circulation. 1994;89:1733– 1744.
Uretsky BF, Jesup M, Konstam MA, et al. Multicenter trial of oral enoximone in patients with moderate to moderately severe congestive heart failure: lack of benefit compared to placebo. Enoximone Multicenter Trial Group. Circulation. 1990;82:774–780.
Packer M, Carver JR, Rodenheffer RJ, et al for the PROMISE Study Research Group. Effect of oral milrinone on mortality in severe chronic heart failure. N Engl J Med. 1991;325:468–475.
Feldman AM, Bristow MR, Parmley WW, et al. Effects of vesnarinone morbidity and mortality in patients with heart failure. N Engl J Med 1993;329:149–155.
Cohn JN, Goldstein SO, Greenberg BH, et al. A dose-dependent increase in mortality with vesnarinone among patients with severe heart failure. N Engl J Med. 1998;339:1810–1816.
Clapp LH, Finney P, Turcato S, et al. Differential effects of stable prostacyclin analogs on smooth muscle proliferation and cyclic AMP generation in human artery. Am J Respir Cell Mol Biol. 2002;26:194–201.
Badesch D, Tapson V, McGoon, et al. Continuous intravenous epoprostenol for pulmonary hypertension due to the scleroderma spectrum disease. Ann Intern Med. 2000;132:425–434.
Rosenzweig E, Kerstin D, Barst R. Long-term prostacyclin for pulmonary hypertension with associated congenital heart defects. Circulation. 1999;99:1858–1865.
Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability, standards of measurement, physiological interpretation and clinical use. Circulation 1996;93:1043–65.
Bailar JC III, Mosteller F, eds. Medical uses of statistics. 2nd ed. Waltham, Mass.: NEJM Books, 1992;261-9:281-291.