ISSN: 1885-5857 Impact factor 2023 7.2
Vol. 55. Num. 11.
Pages 1137-1142 (November 2002)

Effect of Angiotensin Blockade on the Orthostatic Response in Patients with Systemic Arterial Hypertension

Efecto de la inhibición de la acción de la angiotensina sobre la respuesta al ortostatismo en pacientes con hipertensión arterial sistémica

Liliana GalvánaKathrine Jáuregui-RenaudbManlio F MárquezaAntonio G HermosilloaManuel Cárdenasa

Options

Introduction and objectives. The effect of the treatment of arterial hypertension with angiotensin inhibitors on the autonomic response to orthostatism was studied. Patients and method. In 20 hypertensive patients, enalapril (10 to 20 mg) was administered daily for four weeks. Then, irbesartan (150 to 300 mg) was given for four weeks. Finally, 10 mg of enalapril combined with 150 mg of irbesartan was prescribed for another four weeks. Heart rate variability at rest and during the head-up tilt test with controlled respiration was assessed at the beginning and end of each period. Results. Mean arterial pressure showed a similar reduction in the three treatment periods. There were no changes in heart rate. Heart rate variability at rest showed differences in the spectral high-frequency component between the control and the treatment periods (p = 0.10). There was an increase in the high-frequency component between the control and the third (p = 0.047) and the fourth periods (p = 0.03). In the head-up tilt test there was a decrease in total spectral high-frequency power. Conclusions. There was no increase in orthostatic intolerance with these drugs in hypertensive patients. The absence of changes in heart rate in spite of a decrease in blood pressure suggests resetting of the baroreflex function. The long-term control of hypertension with these drugs may have a favorable effect on heart rate variability, with an increase in parasympathetic activity.

Keywords

Orthostatic response
Systemic arterial hypertension
Angiotensin inhibition

INTRODUCTION

In spite of the benefits of hypertensive treatment for cardiovascular and renal complications, the majority of clinical trials have not shown a significant reduction in morbidity and mortality of cardiac origin in patients with systemic arterial hypertension.1 Various studies that have used the cardiac frequency variability2-4 and measurement of baroreflex activity5,6 to evaluate autonomous modulation of the heart have shown diminished vagal cardiac activity in patients with arterial hypertension.

Vasodilator antihypertensive medications, by reducing arterial pressure, activate a series of mechanisms mediated by the autonomous nervous system (ANS). There are few published studies on the effects of hypertensive medications on autonomous nervous system function in the hypertensive heart. Adrenergic beta-blockers increase tonic and reflexive vagal cardiac activity.7 The effects of calcium antagonists are heterogeneous, and depend on the class of pharmacological agent used and the way it is administered. Nifedipine increases sympathetic activity and reduces vagal activity.8 Verapamil, diltiazem, and amlodipine decrease sympathetic activity without modifying vagal activity.9

Recently, Guastí et al,10 in a study carried out on hypertensive patients at rest, did not find a modulating effect of the rennin-angiotensin system on the autonomous control of arterial pressure. Our study was designed to ascertain whether treatment of arterial hypertension via inhibition of angiotensin influences the response of the ANS on orthostasis. To inhibit angiotensin action we used an angiotensin-converting enzyme inhibitor (ACEI), an angiotensin II AT1 receptor blocker, and a combination of both. The study was not designed to compare the different pharmaceutical agents, as was the study by Guastí et al,10 but to study the effect of the inhibition of angiotensin on the autonomous control of the cardiovascular apparatus.

PATIENTS AND METHOD

The study protocol was approved by our bioethics committee and the patients signed an informed consent form. The study was performed on 20 patients (13 women, 7 men) with system arterial hypertension between the ages of 30 and 70 years (mean age 57.3 years±9.55 years) recruited from outpatient clinics of the Instituto Nacional de Cardiología Ignacio Chávez (Ignacio Chavez National Institute of Cardiology). The diagnosis of systemic arterial hypertension was established in accordance with the 6th report of the Joint National Committee for the prevention, detection, evaluation, and treatment of elevated arterial pressure in the United States of America.11

We excluded from the study patients with lesions in the target organs with functional changes (the brain, heart, or kidney), as well as those patients who presented with secondary hypertension, diabetes mellitus, thyroid dysfunction, or who were taking medications acting on the ANS, digitalis, diuretics, anti-arrhythmia agents, steroids, or cimetidine. On the patients recruited, we obtained a complete clinical history, ECG and chest X-ray in the AP and oblique positions, blood cytology, general urine analysis and glucose, urea and blood creatinine testing; all studies were normal or negative. All patients were in sinus rhythm.

Arterial pressure was obtained by the sphygmomanometer method 3 times, with the patient seated and the humeral artery in the thoracic location of the heart. We used as the final arterial pressure the average of the 3 pressure readings taken. All the readings, in all patients, were performed by the same observer.

After a one-week drug washout the patients were given 10 mg of enalapril. One week later the patients were reevaluated: if the average arterial pressure had decreased 10 mm Hg or more the same drug dose was maintained, and if the reduction was less than 10 mmHg the dose was increased to 20 mg for 4 weeks. After another one-week washout we administered 150 mg of irbesartan per day, and the same dose was continued if at the end of one week the average arterial pressure decreased by 10 mm Hg; if the reduction was less than 10 mm Hg, we increased the dose to 300 mg for 4 weeks. In the final phase, after another week of washout, the patient received 10 mg of enalapril and 150 mg of irbesartan for 4 weeks. The exact amount of drugs per the dosage regimen were given to the patient at each visit, with instructions to return any medication not taken in order to assure that the medication regimen was adequately followed. A washout period of one week was occurred between each treatment regimen, taking into account that the effective half-life of enalapril is 11 hours and of irbesartan is 11 to 15 hours.

The final office consult in each time period was scheduled to occur between the hours of 9:00 and 10:00 a.m., after a 12-hour fast; the patients abstained from imbibing alcoholic beverages 48 hours prior to the consult and caffeine 12 hours prior to the consult.

At the beginning of the study and at the end of each stage of treatment we measured the cardiac frequency variability in repose and in passive orthostasis. In an environment with a stable temperature (24 to 25°C) and dim light, after 20 minutes of repose in the supine decubitus position, we instructed the patient to breathe at a frequency of 12 respirations per minute, guided by a metronome audiocassette recording. The patient remained in repose with controlled respiration another 5 minutes, and then while continuing controlled respiration, undergoing passive inclination on a tilt-table inclined to 70° for 30 minutes or until a positive response was elicited. The patients were instructed not to talk and to keep their eyes closed during the tests. We measured arterial pressure with a sphygmomanometer at one-minute intervals. The tilt test was considered positive when the decrease in systolic arterial pressure (SAP) was greater than 30 mm Hg, the absolute systolic number was less than 90 mm Hg, bradycardia was less than 50 beats/minute, or we observed a decrease to numbers lower than baseline, or both.12,13

The electrocardiographic signal was measured continuously via a commercial 2-channel Holter system (Medilog Oxford V7, London, UK). The signal was digitized. After visual review of the ECG, the R-R intervals were calculated during 5-minute periods. R-R interval variability was analyzed in the frequency domain via Fourier rapid transform with 2 Hz resampling. The spectral potency was calculated for frequency bands: total 0.04 to 0.4 Hz, low frequencies of 0.04 to 0.15 Hz, and high frequencies of 0.15 to 0.4 Hz. We calculated the ratio of low frequencies to high frequencies (LF to HF).

The high frequency band reflects vagal cardiac activity related to respiration14 and the low frequency band is considered an indication of sympathetic and vagal modulation.15 The values obtained were converted to their natural algorithms by not having a normal distribution pattern.

Statistical analysis of the measurements of arterial pressure and cardiac frequency were performed using variance analysis. The analysis of the measurements of cardiac frequency variability were performed after logarithmic transform, with the Friedman test and the Wilcoxon test, with a significant value being P=.05.

RESULTS

Measurement at rest

The decubitus arterial pressure before beginning the study was 162 mm Hg±15.8 mm Hg systolic arterial pressure (SAP) and 101 Hg±9.2 mm Hg diastolic arterial pressure (DAP), with a mean pressure of 121 mm Hg±9.8 mm Hg.

The effect of the pharmaceutical agents, on both SAP and DAP, in decubitus was similar at the end of the three treatment periods (Figure 1). The decrease in mean arterial pressure with the administration of enalapril was 10 mm Hg±9.5 mm Hg and 11 mm Hg±12 mm Hg with irbesartan. When combined treatment was administered, the average decrease in arterial pressure was 14 mm Hg±11.5 mm Hg. In all patients we obtained a hypotensive response of a similar magnitude. Although the arterial pressure decreased, we did not observe significant changes in cardiac frequency (Figure 2).

Fig. 1. Mean and confidence interval of the average arterial pressure of patients studied in the decubitus position and at the end of each treatment period.

Fig. 2. Mean and standard deviation of cardiac frequency at rest during the four stages of the study.

Analysis of cardiac frequency variability at rest showed a tendency toward an increase in the density of the spectral power of high frequencies in the three stages of treatment (Table 1); (P=.10, Friedman). On comparison of each of the treatment stages with respect to the stage without treatment, we identified a significant increase in the high frequency component both in the third stage with irbesartan treatment alone (P=.047, Wilcoxon) and in the fourth stage with combined treatment (P=.03, Wilcoxon) (Table 1).

Tilt test

We did not observe a positive response to the tilt test at any treatment stage, and there were no significant changes in arterial pressure or cardiac frequency during the first minute of the test (Figures 3 and 4).

Fig. 3. Mean and standard deviation of the systolic and diastolic arterial pressure at rest, in the dorsal decubitus position (e), and during the first minute of total body passive tilt (e) in the four stages of the study.

Fig. 4. Mean and standard deviation of cardiac frequency at rest, in the dorsal decubitus position (e), and during the first minute of total body passive tilt (e) in the four stages of the study.

Nevertheless, there was an additional finding that did not alter the final result of the test upon comparison of the results of the tilt test without treatment with the tests performed at the end of each stage of the study. During the three last measurements, the density of total spectral power had a tendency to diminish, principally due to the decrease in the low frequency component with an increase in the LF to HF ratio (Table 2).

DISCUSSION

Angiotensin II activates both the central nervous system and the peripheral sympathetic nervous system, and is an important regulator of noradrenalin liberation in the sympathetic nerve endings. Therefore, it modulates cardiac and sympathetic vascular activity.16

Angiotensin converting enzyme inhibitors (ACEI) and angiotensin II receptor blockers are the medications that are considered to be effective antihypertensive agents.17-19 It has been demonstrated that despite long-term use of ACEI, plasma concentrations of active angiotensin persist, and when an angiotensin receptor blocker is added, the hemodynamic effects of the ACEI blocker are increased.20

In patients of advanced age, the prevalence of orthostatic hypotension varies from 13% to 30%. The diagnosis most frequently associated with this is systemic arterial hypertension, which can contribute to an increase in the mortality rate for high-risk patients.21 In the group of patients we studied we did not find an increase in orthostatic intolerance despite the vasodilator effect of the pharmaceutical agents used.

The 70° tilt table test was negative for all patients in all the stages of the study. This test is based on the fact that upon adopting the bipedal stance there is an accumulation of venous blood in the legs due to the gravitational effect, with a consequent decrease in the venous return, triggering a Bezold-Jarisch effect. Myocardial contraction in a small volume cavity stimulates the C-receptor fibers of the myocardium which, in turn, produces an intense vagal reflex with arterial hypotension and a decrease in cerebral blood flow.12,13

The fact that the cardiac frequency is not altered despite the decrease in arterial pressure during the observation period suggests that during inhibition of angiotensin effects a readjustment of the baroreflex function is produced. These findings are similar to those described by Guastí et al10 in a comparative study of the effects of enalapril and losartan. In the same study, the investigators did not identify differences in the effects of these drugs on cardiac frequency variability at rest.

Our study was not designed to compare drugs, as was the study by Guastí et al,10 but to identify whether or not the vasodilator effect of the drugs could interfere with cardiovascular control of orthostasis.

In the patients studied we found that sustained long-term control of arterial pressure numbers in the hypertensive patient could have a favorable effect on cardiac frequency variability. After two months of treatment, spectral power in the high frequency band began to increase; this increase continued throughout the rest of the study.

This observation shows that, apart from the long-term control of arterial hypertension, use of these drugs also increases parasympathetic activity.

The variability of R-R intervals is the result of many different factors that are individual as well as environmental in nature. Their study is useful for evaluating the autonomous modulation of the heart, both in the frequency domain as well as in the time domain.22,23 When spectral techniques are used for the analysis of recorded short stable periods, the relative power of the different variation frequencies of the R-R intervals can be identified. The high frequency component, approximately 0.25 Hz, has been related to respiration and efferent vagal activity.24-26 The low frequency component, approximately 0.1 Hz, has been related to neurohumoral factors, the baroreceptor reflex, parasympathetic influence, and to central control mechanisms.21,27 As far as very low frequency oscillations are concerned, the evidence suggests that they principally depend on parasympathetic activity.28 Nevertheless, for the interpretation of R-R interval variability is necessary to consider the study conditions and the respiration characteristics. The appropriate reproducibility of measurements is only achieved when the recording is performed with controlled respiration,26 as was the case in our study.

The results obtained show that the inhibition of angiotensin action, despite its hypotensive effect via vasodilatation, does not change the neurohumoral and cardiac responses to orthostasis,29 and can be used with increasing the risk of orthostatic hypertension in high-risk patients.

We did not find an increase in orthostatic intolerance in our patients with the use of the pharmaceutical agents we administered. The fact that the cardiac frequency was unchanged despite the decrease in arterial pressure suggests a readjustment of the baroreflex function.

The sustained control of arterial pressure numbers in hypertensive patients with these drugs may have a favorable effect on cardiac frequency variabi lity, with an increase in parasympathetic activity.


Correspondence: Dr. M. Cárdenas.
Subdirección de Investigación Clínica.
Instituto Nacional de Cardiología Ignacio Chávez.
Juan Badiano, 1. Tlalpan 14080. México, D.F.
E-mail: yog.14080@yahoo.com

Bibliography
[1]
MacMahon S, Peto R, Cutler J, Collins R, Sorlie P, Neaton J, et al..
Blood pressure, stroke, and coronary artery disease. Part 1. Prolonged differences in blood pressure: prospective observational studies corrected for the regression dilution bias..
Lancet, (1990), 335 pp. 765-74
[2]
Guzzetti S, Piccaluga E, Casati R, Ceruti S, Lombardi F, Pagani M..
Sympathetic predominance in essential hypertension: a study employing spectral analysis of heart rate variability..
J Hypertens, (1988), 6 pp. 711-7
[3]
Chakko S, Mulingtapang RF, Huikuri H, Kessler KM, Materson BJ, Myerburg RJ..
Alterations in heart rate variability and its circadian rhythm in hypertensive patients with left ventricular hypertrophy free of coronary artery disease..
Am Heart J, (1993), 126 pp. 1364-72
[4]
Huikuri HV, Ylitalo A, Pikkujämsä MJ, Airaksinen K, Rantala AO, Lilja M, et al..
Heart rate variability in systemic hypertension..
Am J Cardiol, (1996), 77 pp. 1073-7
[5]
Bristow JD, Honour AJ, Pickering GW, Sleight P, Smyth HS..
Diminished baroreflex sensitivity in high blood pressure..
Circulation, (1979), 39 pp. 48-54
[6]
Ylitalo A, Airaksinen J, Tahvanainen KU.O, Kuusela TA, Ikäheimo MJ, Rantala A, et al..
Baroreflex sensitivity in drug-treated systemic hypertension..
Am J Cardiol, (1997), 80 pp. 1369-72
[7]
Vesalainen RK, Kantola I M, Airaksinen J, Tahvanainen KU.O, Kaila TJ..
Vagal cardiac activity in essential hypertension. The effects of metoprolol and ramipril..
Am J Hypertens, (1998), 11 pp. 649-58
[8]
Okabayashi J, Matsubayashi K, Doi Y, Sato T, Ozawa T..
Effects of nifedipine and enalapril on cardiac autonomic nervous function during tilt test in elderly patients with hypertension..
Hypertens Res, (1997), 20 pp. 1-6
[9]
Leenen FH, Fourney A..
Comparison of the effects of amlodipine and diltiazem on 24 hour blood pressure, plasma cathecholamines, and left ventricular mass..
Am J Cardiol, (1996), 78 pp. 203-7
[10]
Guastí L, Petrozzino MR, Mainardi LT, Grimoldi P, Zanotta D, Garganico D, et al..
Autonomic function and baroreflex sensitivity during angiotension-converting enzime inhibition or angiotensin II AT-1 receptor blockade in essential hypertensive patients..
Acta Cardiol, (2001), 56 pp. 289-95
[11]
The sixth report of the Joint National Committee on preventio.n, detectio.n, evaluatio.n, and treatment of high blood pressure..
Arch Intern Med, (1997), 157 pp. 2413-46
[12]
Hermosillo AG, Márquez MF, Jáuregui-Renaud K, Cárdenas M..
. México D.F.: Intersistemas.
. México D.F.: Intersistemas, (1982), pp. 596-7
[13]
García Civera R, Sanjuan Maneza R, Ruiz Granell R, Morell Cabedo S, Porres Azpiroz J, Ruiz Ros V, et al..
Rendimiento diagnóstico de un protocolo de estudio de síncope de causa no aparente..
Rev Esp Cardiol, (2001), 54 pp. 425-30
[14]
Pomerantz M, Macaulay RJ.B, Caudill MA, Kutz I, Adam D, Gordon D, et al..
Assement of autonomic function in humans by heart rate spectral analysis..
Am J Physiol, (1985), 248 pp. H151-3
[15]
Pagani M, Lombardi F, Guzzetti S, Rimaldi O, Furlan R, Pizzinelli P..
Power spectral analysis of heart rate variability as a marker of sympatho-vagal interaction in man and conscions dog..
Cir Res, (1986), 59 pp. 178-93
[16]
Lonn EV, Yusuf S, Jha P, Montague TJ, Teo K, Benedict CR, et al..
Emerging role of angiotensin-converting enzime inhibitors in cardiac and vascular protection..
Circulation, (1994), 90 pp. 2056-69
[17]
Veterans Administration Cooperative Study Group on Antihypertensive Agents..
Low-dose captopril for the treatment of mild to moderate hypertension..
Arch Intern Med, (1984), 144 pp. 1947-53
[18]
Zusman RM..
Renin-and non-renin-mediated antihypertensive actions of converting-enzyme inhibitors..
Kidney Int, (1984), 25 pp. 969-83
[19]
Tewksbury DA..
Angiotensinogen. Biochemistry and molecular biology. En: Laragh JH, Brenner BM, editors. Hypertension: pathophysiology, diagnosis and management. New York: Raven Press.
Angiotensinogen. Biochemistry and molecular biology. En: Laragh JH, Brenner BM, editors. Hypertension: pathophysiology, diagnosis and management. New York: Raven Press, (1990), pp. 1197-216
[20]
Baruch L, Anand I, Cohen IS, Ziesche S, Judd D, Cohn JN..
Augmented short-and long-term hemodynamic and hormonal effects of an angiotensin receptor blocker added to angiotensin converting enzime inhibitor therapy in patients with heart failure..
Vasodilatador Heart Failure Trial (V-HeFT) Study Group Circulation, (1999), 99 pp. 2658-64
[21]
Hale WA, Chambliss ML..
Should primary care patients be screened for orthostatic hypotension?.
J Fam Pract, (1999), 48 pp. 547-52
[22]
Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology..
Heart rate variability. Standards of measurements, physiological interpretation, and clinical use..
Circulation, (1996), 93 pp. 1043-65
[23]
Palma Gamiz JL, Arribas Jiménez A, González Juanatrey JR, Marín Huerta E, Martín Ambrosio ES..
Guías de práctica clínica de la Sociedad Española de Cardiología en la monitorización ambulatoria del electrocardiograma y presión arterial..
Rev Esp Cardiol, (2000), 53 pp. 91-109
[24]
Grossman P, Karemaker J, Wieling W..
Prediction of tonic parasympathetic cardiac control using respiratory sinus arrhytmia. The need for respiratory control..
Psychophysiology, (1991), 28 pp. 201-16
[25]
Hayano J, Mukai S, Sakakibara M, Okada A, Takata K, Fujinami T..
Effects of respiratory interval on vagal modulation of heart rate..
Am J Physiol, (1994), 267 pp. H33-40
[26]
Piepoli M, Sleight P, Leuzzi S, Valle F, Spadacini G, Passino C, et al..
Origin of respiratory sinus arrythmia in conscious humans: a important role for arterial carotid baroreceptors..
Circulation, (1997), 95 pp. 1813-21
[27]
Pitzalis MV, Mastropasqua F, Massari F, Forleo C, Di Maggio M, Passantino A..
Short and long-term reproducibility of time and frequency domain heart rate variability measurements in normal subjects..
Cardiovasc Res, (1996), 32 pp. 226-33
[28]
Taylor JA, Carr DL, Myers CM, Eckberg DL..
Mechanisms underlying very-low-frequency RR interval oscillations in humans..
Circulation, (1998), 98 pp. 547-55
[29]
Parati G, Di Rienzo M, Mancia G..
Dynamic modulation of baro-reflex sensitivity in health and disease..
Ann NY Acad Sci, (2001), 940 pp. 469-87
Are you a healthcare professional authorized to prescribe or dispense medications?