(Hypertension. 1997;30:422.)
© 1997 American Heart Association, Inc.
Articles |
From the Division of Nephrology and the Clinical Research Unit, Department of Medicine, University of Maryland School of Medicine (Baltimore) (M.R.W., P.S.H., M.T.B.); and the Hypertension Center, Departments of Surgery, Medicine, and Public Health Sciences, Bowman-Gray School of Medicine, Winston-Salem, NC (J.M.F.).
Correspondence to Matthew R. Weir, MD, University of Maryland School of Medicine, Department of Medicine, Nephrology Division, 22 S Greene St, Baltimore, MD 21201-1595. E-mail mweir{at}ummpa.ab.umd.edu
Abstract Since salt intake may affect blood pressure response
to antihypertensive drugs, an individuals salt-sensitivity status may
be an important consideration in the selection of a medication. The
purpose of this single-blind study was to assess the impact of salt
sensitivity on the antihypertensive effects of isradipine. A total of
21 evaluable hypertensive patients (10 white, 11 black) 35 to 73 years
of age (mean 55.9 years) were randomized to a low-salt diet (mean
24-hour urine sodium 100±14 mmol) or a high-salt diet (mean
24-hour urine sodium 210±22 mmol) for 7 weeks, followed by
crossover to the other diet after a 2-week washout period. On each diet
regimen, patients received placebo for 2 weeks, followed by optimal
titration of isradipine (2.5 to 10 mg BID) for blood pressure control
during the last 5 weeks. On the high-salt diet, salt-sensitive
hypertensives (mean arterial blood pressure increase
5 mm Hg, n=5) exhibited a
systolic/diastolic blood pressure change of
-18.7/-19.6 mm Hg from 157.2/102.9 mm Hg after 5 weeks of
isradipine treatment, whereas on a low-salt diet, blood pressure change
was -6.9/-12.0 mm Hg from 148.7/97.3 mm Hg.
Nonsalt-sensitive patients (n=16) exhibited a
systolic/diastolic blood pressure change of
-12.6/-7.6 mm Hg from 155.3/98.6 mm Hg on the high-salt
diet and -19.2/-10.9 mm Hg from 161.0/102.6 mm Hg on the
low-salt diet after treatment with isradipine. The absolute blood
pressure attained in both salt-sensitive and nonsalt-sensitive
patients was almost identical with isradipine therapy despite variation
in dietary salt, although slightly higher doses of isradipine were
required in the salt-sensitive group. Consequently, isradipine, and
perhaps calcium antagonists in general, manifests a more
robust blood pressurelowering effect in the setting of high sodium
intake. This effect does, however, appear to be largely confined to
individuals who are salt sensitive.
Key Words: hypertension dietary salt salt sensitivity
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