Key result
Adding spironolactone to ramipril significantly reduced proteinuria at 3 months compared to ramipril alone (42.0% vs 1.4% reduction; P<0.001), with no advantage of triple over dual blockade.
Why the study?
Does spironolactone reduce proteinuria in patients with persistent proteinuria on long-term ACE inhibitor therapy?
RCT (n=41)
double-blind
randomized
Does spironolactone reduce proteinuria in patients with persistent proteinuria on long-term ACE inhibitor therapy?
Spironolactone is an effective adjuvant therapy to ACE inhibitors for reducing persistent proteinuria, whereas triple RAAS blockade offers no significant advantage over dual blockade.
Supports adding spironolactone to ACEI for proteinuria reduction; extends evidence for dual but not triple RAAS blockade.
Studies have shown that dual therapy with angiotensin-converting enzyme inhibitors (ACEI) and either angiotensin II receptor blockers or aldosterone receptor antagonists is more effective in reducing proteinuria than either agent used alone. The questions that remain are as follows: (1) Which of these agents should be used as dual therapy with the ACEI? (2) Does a higher level of blockade of the renin-angiotensin-aldosterone system with triple therapy offer an advantage over dual blockade? A 3-mo randomized, double-blind, placebo-controlled study was performed in 41 patients with proteinuria >1.5 g/d. Four treatment groups were compared: (1) Ramipril + spironolactone placebo + irbesartan placebo, (2) ramipril + irbesartan + spironolactone placebo, (3) ramipril + irbesartan placebo + spironolactone, and (4) ramipril + irbesartan + spironolactone. The percentage change in protein excretion differed according to treatment arm (ANOVA: F(3,35) = 8.6, P < 0.001). Pair-wise comparison showed that greater reduction in protein excretion occurred in treatment regimens that incorporated spironolactone. The reduction in proteinuria at 3 mo was as follows: Group 1, 1.4%; group 2, 15.7%; group 3, 42.0%; and group 4, 48.2%. The reduction in proteinuria among patients who were taking spironolactone-containing regimens was sustained at 6 and 12 mo. This study suggests that aldosterone receptor blockade offers a valuable adjuvant treatment when used with ACEI therapy for the reduction of proteinuria. Results suggest no advantage of triple blockade over dual blockade of the renin-angiotensin-aldosterone system to reduce proteinuria.
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Chrysostomou et al. (2006) conducted an RCT in persistent proteinuria (n=41). Spironolactone vs. Placebo (added to ramipril) was evaluated on percentage change in protein excretion (p=< 0.001). Adding spironolactone to ramipril significantly reduced proteinuria at 3 months compared to ramipril alone (42.0% vs 1.4% reduction; P<0.001), with no advantage of triple over dual blockade.
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