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March 1, 2009Clinical Journal of the American Society of NephrologyOpen Access

Aldosterone Antagonists for Preventing the Progression of Chronic Kidney Disease

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Why the study?

Does the addition of aldosterone antagonists reduce proteinuria in adult CKD patients already on RAS blockers?

Population

11 randomized clinical trials pooling 991 adult patients with proteinuric chronic kidney disease already on…

Comparison

Addition of selective and nonselective… vs ACEi and/or ARB plus placebo.

Design

Meta-analysis, randomized clinical trials included, placebo-controlled

Key result

Adding nonselective aldosterone antagonists to ACEi/ARB therapy significantly reduced 24 h proteinuria (WMD -0.80 g; 95% CI -1.27, -0.33) but increased the risk of hyperkalemia (RR 3.06).

Authors

SNSankar D. NavaneethanSNSagar U. NigwekarASAshwini R. Sehgal

Discussion

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Overview

Reduces proteinuria in CKD on RAS blockers but raises hyperkalemia risk; leaves open long-term outcome effects.

Study Design

Type

Meta-Analysis (n=991)

Structured PICO

Does the addition of aldosterone antagonists reduce proteinuria in adult CKD patients already on RAS blockers?

P
Population
11 randomized clinical trials pooling 991 adult patients with proteinuric chronic kidney disease (CKD) already on renin-angiotensin system (RAS) blockers.
I
Intervention
Addition of selective and nonselective aldosterone antagonists (AA) to angiotensin-converting enzyme inhibitors (ACEi) and/or angiotensin receptor blockers (ARB).
C
Comparator
ACEi and/or ARB plus placebo.
O
Outcome
24 h proteinuriasurrogate

Main Result

Effect estimate: WMD -0.80 g (95% CI -1.27, -0.33)

Adding aldosterone antagonists to RAS blockers in CKD patients reduces proteinuria but significantly increases the risk of hyperkalemia, with unknown effects on long-term clinical outcomes.

Limitations

  • Data on cardiovascular outcomes, long-term renal outcomes and mortality were not available in any of the trials.

Cite This Study

Navaneethan et al. (2009) conducted a meta-analysis in Chronic kidney disease with proteinuria (n=991). Aldosterone antagonists (selective and nonselective) vs. ACEi and/or ARB plus placebo was evaluated on 24 h proteinuria (WMD -0.80 g, 95% CI -1.27, -0.33). Adding nonselective aldosterone antagonists to ACEi/ARB therapy significantly reduced 24 h proteinuria (WMD -0.80 g; 95% CI -1.27, -0.33) but increased the risk of hyperkalemia (RR 3.06).

synapsesocial.com/papers/6a0ba8f84f6759c6fca25464https://doi.org/10.2215/cjn.04750908
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