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Aldosterone Antagonists Reduce the Risk of Cardiovascular Mortality in Dialysis Patients: A Meta-Analysis
1Division of Nephrology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Insights
Aldosterone antagonists significantly reduce cardiocerebrovascular (CCV) and all-cause mortality in dialysis patients. This treatment improves cardiac function and reduces left ventricular mass, despite increased risks of hyperkalemia and gynecomastia.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Cardiovascular disease is the leading cause of mortality in patients undergoing maintenance dialysis.
- Aldosterone antagonists are established treatments for heart failure, but their role in dialysis patients is unclear.
Purpose of the Study:
- To systematically assess the efficacy and tolerability of aldosterone antagonists in patients undergoing maintenance dialysis.
- To evaluate the impact of aldosterone antagonists on cardiocerebrovascular (CCV) mortality and cardiac function.
Main Methods:
- A meta-analysis of 10 randomized controlled trials (RCTs) involving 1172 chronic dialysis patients.
- Searched major biomedical databases including PubMed, EMBASE, and Cochrane Library.
- Primary endpoint: CCV mortality. Secondary endpoints: all-cause mortality, left ventricular mass index (LVMI), and left ventricular ejection fraction (LVEF).
Main Results:
- Aldosterone antagonists significantly reduced CCV mortality (RR 0.42) and all-cause mortality (RR 0.46).
- Treatment improved left ventricular ejection fraction (LVEF) by 6.35% and decreased left ventricular mass index (LVMI) by -8.69 g/m².
- Increased risks of hyperkalemia (RR 1.70) and gynecomastia (RR 8.01) were observed.
Conclusions:
- Adding aldosterone antagonists to conventional therapy in chronic dialysis patients may reduce CCV mortality.
- This treatment can improve cardiac function and decrease LVMI.
- Careful monitoring for side effects like hyperkalemia and gynecomastia is warranted.
Abstract:
Background and Purpose. Cardiovascular disease is the major cause of death in dialysis patients. Although aldosterone antagonists were considered a treatment for severe heart failure patients to reduce cardiac mortality, whether treating patients undergoing maintenance dialysis with aldosterone antagonists could reduce the risk of cardiocerebrovascular (CCV) remains unclear. We aim to systematically assess the efficacy and tolerability of the addition of aldosterone antagonists to conventional therapy in patients undergoing maintenance dialysis. Materials and Methods. We searched PubMed, EMBASE, the Cochrane Library, the Chinese Biomedical Literature Database (CBM), and the China National Knowledge Infrastructure (CNKI) for relevant articles. The primary endpoint of interest was CCV mortality. The secondary endpoints were all-cause mortality, left ventricular mass index (LVMI), and left ventricular ejection fraction (LVEF). Publication bias was evaluated using funnel plots and Egger's test. The meta-analysis was performed using Review Manager software version 5.3. Results. This analysis included 10 randomized controlled trials (RCTs) with 1172 total chronic dialysis patients. The use of aldosterone antagonists in the dialysis population resulted in a marked reduction in CCV mortality (RR 0.42, 95% CI 0.26-0.65, P=0.0002) and all-cause mortality (RR0.46, 95%CI 0.32-0.66, P<0.0001). The LVEF was improved by treatment with aldosterone antagonists (WMD 6.35%, P<0.00001). Moreover, aldosterone antagonists decreased the LVMI (WMD -8.69 g/m2, P=0.0006), whereas aldosterone antagonists increased the occurrence of hyperkalemia (RR1.70, 95%CI 1-2.88, P=0.05) and gynecomastia (RR 8.01, 95% CI 2.44- 26.27, P=0.0006). Conclusions. Addition of aldosterone antagonists to conventional treatment in chronic dialysis patients may reduce CCV mortality, improve cardiac function, and simultaneously decrease LVMI.
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