Key result
Non-steroidal mineralocorticoid receptor antagonists significantly reduced the urinary albumin-to-creatinine ratio (WMD -0.40) compared to placebo in patients with chronic kidney disease and type 2 diabetes.
Why the study?
Non-steroidal mineralocorticoid receptor antagonists are promising treatments in patients with chronic kidney disease and type 2 diabetes, but differences among individual agents remained to be explored.
Do non-steroidal MRAs improve renal and blood pressure outcomes in patients with chronic kidney disease and type 2 diabetes?
Meta-Analysis (n=14,450)
Yes
Do non-steroidal MRAs improve renal and blood pressure outcomes in patients with chronic kidney disease and type 2 diabetes?
Effect estimate: WMD -0.40 (95% CI -0.48 to -0.32)
p-value: p=<0.001
Non-steroidal MRAs effectively reduce proteinuria and blood pressure in patients with CKD and T2D, though they increase the risk of hyperkalemia, with indirect comparisons suggesting potential differences in antihypertensive efficacy among agents.
Reduces albuminuria in CKD with T2D; reinforces non-steroidal MRA efficacy across pooled trials.
Background: The non-steroidal mineralocorticoid receptor antagonists (MRAs) are promising treatments in patients with chronic kidney disease (CKD) and type 2 diabetes (T2D). We conducted a meta-analysis to explore the efficacy and safety of the non-steroidal MRAs (finerenone, apararenone, esaxerenone) and detect the differences among them. Methods: We searched several databases for eligible randomized controlled trials (RCTs) investigating non-steroidal MRAs versus placebo in patients with CKD and T2D. We performed a conventional meta-analysis separately, and then indirect comparisons for efficacy and safety outcomes were conducted among these included drugs. Results: Eight RCTs with 14,450 subjects were enrolled. In patients with CKD and T2D, a greater reduction in urinary albumin-to-creatinine ratio (UACR) (WMD −0.40, 95% CI −0.48 to −0.32, p < 0.001), estimated glomerular filtration rate (eGFR) (WMD −2.69, 95% CI −4.47 to −0.91, p = 0.003), systolic blood pressure (SBP) (WMD −4.84, 95% CI −5.96 to −3.72, p < 0.001) and a higher risk of hyperkalemia (RR 2.07, 95% CI 1.86 to 2.30, p < 0.001) were observed in the non-steroidal MRAs versus placebo; there is no significant difference in the incidence of serious adverse events between two groups (RR 1.32, 95% CI 0.98 to 1.79, p = 0.067). Compared with finerenone, esaxerenone showed no significant difference in UACR reduction (WMD 0.24, 95% CI −0.016 to 0.496, p = 0.869); apararenone and esaxerenone showed greater decreases in SBP (WMD 1.37, 95% CI 0.456 to 2.284, p = 0.010; WMD 3.11, 95% CI 0.544 to 5,676, p = 0.021). Conclusions: Despite the moderate increased risk of hyperkalemia, use of non-steroidal MRAs could reduce proteinuria and SBP in patients with CKD and T2D. In terms of renoprotection, esaxerenone and finerenone may have similar effects. Esaxerenone and apararenone may have better antihypertensive effects than finerenone. The head-to-head RCTs are still needed to compare the differences of the efficacy and safety in these non-steroidal MRAs.
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Jiang et al. (2022) conducted a meta-analysis in Chronic Kidney Disease and Type 2 Diabetes (n=14,450). Non-steroidal mineralocorticoid receptor antagonists (finerenone, apararenone, esaxerenone) vs. Placebo was evaluated on Changes in urinary albumin-to-creatinine ratio (UACR) from baseline (WMD -0.40, 95% CI -0.48 to -0.32, p=<0.001). Non-steroidal mineralocorticoid receptor antagonists significantly reduced the urinary albumin-to-creatinine ratio (WMD -0.40) compared to placebo in patients with chronic kidney disease and type 2 diabetes.
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