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October 17, 2003American Journal of Hypertension501 citationsOpen Access

Efficacy of low-dose spironolactone in subjects with resistant hypertension

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MNMari Nishizaka

Key Result

Adding low-dose spironolactone to multidrug regimens in subjects with resistant hypertension reduced blood pressure by a mean of 25/12 mm Hg at 6 months, regardless of primary aldosteronism status.

Study Design

Type

Observational (n=76)

Structured PICO

Does low-dose spironolactone reduce blood pressure in subjects with resistant hypertension?

P
Population
76 African American and white subjects with resistant hypertension (34 with biochemical primary aldosteronism) on multidrug regimens including a diuretic and an angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB).
I
Intervention
Low-dose spironolactone (12.5 to 25 mg/d, titrated up to 50 mg/d if blood pressure remained uncontrolled) added to baseline antihypertensive regimen.
O
Outcome
Blood pressure reduction at 6 weeks, 3 months, and 6 months.surrogate

Low-dose spironolactone provides significant additive blood pressure reduction in patients with resistant hypertension, regardless of the presence of primary aldosteronism.

Abstract

BACKGROUND: Previous reports have demonstrated the antihypertensive efficacy of high doses of spironolactone in subjects with primary aldosteronism and, to a lesser degree, subjects with resistant hypertension. METHODS: In current analysis, we examined the antihypertensive benefit of adding low-dose spironolactone to multidrug regimens that included a diuretic and an angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) in subjects with resistant hypertension with and without primary aldosteronism. Subjects referred for resistant hypertension were evaluated with an early morning plasma renin activity, 24-h urinary aldosterone and sodium during a high dietary salt ingestion. The diagnosis of primary aldosteronism was confirmed with a renin activity 12 mug/24 h and urinary sodium >200 mEq/24 h. After biochemical evaluation, spironolactone (12.5 to 25 mg/d) was added to each subject's antihypertensive regimen. If blood pressure (BP) remained uncontrolled, the dose of spironolactone was titrated up to 50 mg/d. Follow-up BP was determined at 6 weeks, 3 months, and 6 months. RESULTS: A total number of 76 subjects were included in the analysis, 34 of whom had biochemical primary aldosteronism. Low-dose spironolactone was associated with an additional mean decrease in BP of 21 +/- 21/10 +/- 14 mm Hg at 6 weeks and 25 +/- 20/12 +/- 12 mm Hg at 6-month follow-up. The BP reduction was similar in subjects with and without primary aldosteronism and was additive to the use of ACE inhibitors, ARBs, and diuretics. CONCLUSIONS: We conclude that low-dose spironolactone provides significant additive BP reduction in African American and white subjects with resistant hypertension with and without primary aldosteronism.

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Cite This Study

Mari Nishizaka (2003) conducted an observational in Resistant hypertension (n=76). Spironolactone was evaluated on Decrease in blood pressure. Adding low-dose spironolactone to multidrug regimens in subjects with resistant hypertension reduced blood pressure by a mean of 25/12 mm Hg at 6 months, regardless of primary aldosteronism status.

synapsesocial.com/papers/6a0ec4ae2eca052da647c434https://doi.org/10.1016/s0895-7061(03)01032-x
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