Hypertension, Vol 11, 452-456, Copyright © 1988 by American Heart Association
GP Reams, A Hamory, A Lau and JH Bauer
Twenty-six essential hypertensive patients were entered into a protocol to
assess the blood pressure and renal effects of the dihydropyridine calcium
antagonist nifedipine (30-120 mg/day given in divided doses) administered
for 4 weeks. Nifedipine monotherapy effectively lowered blood pressure in
73% of the patients. Glomerular filtration rate and effective renal plasma
flow were increased 13.3 and 19.6%, respectively. The filtration fraction
and urinary albumin excretion remained unchanged. Renal vascular resistance
was markedly reduced (25.2%). Changes observed in renal function were
independent of the patients' initial glomerular filtration rate.
Furthermore, there was no correlation between the systemic and renal
effects of nifedipine monotherapy. Patients with a poor systemic blood
pressure response exhibited increases in both glomerular filtration rate
(+13%) and effective renal plasma flow (+20%), changes comparable with
increases in glomerular filtration rate (+13%) and effective renal plasma
flow (+19%) observed in patients achieving a goal blood pressure response
(diastolic blood pressure less than or equal to 90 mm Hg, or a greater than
or equal to 10 mm Hg decrease in diastolic blood pressure, or both). These
results suggest that nifedipine monotherapy has the potential to improve
renal function abnormalities encountered in the essential hypertensive
state independently of its effect on systemic blood pressure.
ARTICLES
Effect of nifedipine on renal function in patients with essential hypertension
Department of Medicine, University of Missouri School of Medicine, Columbia 65212.
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