Mineralocorticoid Receptor Antagonist Combined with SGLT2 Inhibitor versus SGLT2 Inhibitor Alone in Chronic Kidney Disease: A Meta-Analysis of Randomized Trials

医学 盐皮质激素受体 肾脏疾病 随机对照试验 内科学 盐皮质激素 荟萃分析 敌手 药理学 血管紧张素转换酶抑制剂 内分泌学 醛固酮 泌尿科 受体 血管紧张素转换酶 血压
作者
João Pedro Ferreira,Ana Oliveira,Francisco Vasques‐Nóvoa,Ana Rita Leite,Luís Mendonça,Faı̈ez Zannad,Javed Butler,Adelino Leite‐Moreira,Francisca Saraiva,João Sérgio Neves
出处
期刊:American Journal of Nephrology [S. Karger AG]
卷期号:56 (2): 1-7 被引量:7
标识
DOI:10.1159/000541686
摘要

Introduction: Sodium glucose co-transporter 2 inhibitors (SGLT2i) and mineralocorticoid receptor antagonists (MRAs) reduce the progression of kidney disease. Whether the combination of these agents provides additional benefits compared to SGLT2i alone is worth exploring using data from randomized trials designed for this purpose. The aim of the study was to assess the randomized treatment effect of MRAs combined with SGLT2i versus SGLT2i alone on markers of kidney and cardiovascular health. Methods: Random-effects meta-analysis of randomized trials testing the combination of MRAs with SGLT2i versus SGLT2i alone on albuminuria, blood pressure, estimated glomerular filtration rate (eGFR), and serum potassium among patients with chronic kidney disease (CKD). Results: Four randomized trials were included with a total of 272 patients with CKD: eGFR varying between 30 and 60 mL/min/1.73 m2 and urinary albumin-to-creatinine ratio (UACR) between 90 and 500 mg/g, with >60% having type 2 diabetes. Treatment with MRAs plus SGLT2i versus SGLT2i alone reduced UACR by −33.6% (−42.6 to −24.7%), p < 0.001, I2 = 0%. MRAs plus SGLT2i versus SGLT2i alone reduced systolic blood pressure by −6.1 mm Hg (−8.9 to −3.3) mm Hg, eGFR by −3.4 mm Hg (−5.2 to −1.6) mm Hg, and increased serum potassium by + 0.23 mmol/L (0.15–0.34) mmol/L; p < 0.001 for all, without significant heterogeneity between trials (I2 <25%). Conclusion: In this meta-analysis, MRAs plus SGLT2i provided greater reductions in albuminuria and blood pressure compared to SGLT2i alone. Larger randomized trials with longer follow-up should test whether MRA/SGLT2i combination therapies improve cardiovascular and renal outcomes compared to SGLT2i alone.

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