Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease

Diabetic kidney disease (DKD) is one of the major causes of end-stage renal disease (ESRD). To evaluate the efficacy and safety of different types of mineralocorticoid receptor antagonists (MRAs) in diabetic kidney disease patients, we conducted this network meta-analysis by performing a systematic...

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Main Authors: Yichuan Wu, Huanjia Lin, Yuan Tao, Ying Xu, Jiaqi Chen, Yijie Jia, Zongji Zheng
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2022.967317/full
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author Yichuan Wu
Yichuan Wu
Huanjia Lin
Huanjia Lin
Yuan Tao
Yuan Tao
Ying Xu
Ying Xu
Jiaqi Chen
Jiaqi Chen
Yijie Jia
Yijie Jia
Zongji Zheng
Zongji Zheng
author_facet Yichuan Wu
Yichuan Wu
Huanjia Lin
Huanjia Lin
Yuan Tao
Yuan Tao
Ying Xu
Ying Xu
Jiaqi Chen
Jiaqi Chen
Yijie Jia
Yijie Jia
Zongji Zheng
Zongji Zheng
author_sort Yichuan Wu
collection DOAJ
description Diabetic kidney disease (DKD) is one of the major causes of end-stage renal disease (ESRD). To evaluate the efficacy and safety of different types of mineralocorticoid receptor antagonists (MRAs) in diabetic kidney disease patients, we conducted this network meta-analysis by performing a systematic search in PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Library, and Clinicaltrials.gov. A total of 12 randomized clinical trials with 15,492 patients applying various types of MRAs covering spironolactone, eplerenone, finerenone, esaxerenone, and apararenone were included. The efficacy outcomes were the ratio of urine albumin creatine ratio (UACR) at posttreatment vs. at baseline, change in posttreatment estimated glomerular filtration (eGFR) vs. at baseline, and change in posttreatment systolic blood pressure (SBP) vs. at baseline. The safety outcome was the number of patients suffering from hyperkalemia. High-dose finerenone (MD −0.31, 95% CI: −0.52, −0.11), esaxerenone (MD −0.54, 95% CI: −0.72, −0.30), and apararenone (MD −0.63, 95% CI: −0.90, −0.35) were associated with a superior reduction in proteinuria in patients with DKD. Regarding the change in eGFR, the results of all drugs were similar, and finerenone may have potential superiority in protecting the kidney. Compared with placebo, none of the treatments was associated with a higher probability of controlling systolic blood pressure during treatment. Moreover, spironolactone, esaxerenone, and 20 mg of finerenone presented a higher risk of hyperkalemia. This Bayesian network meta-analysis was the first to explore the optimal alternative among MRAs in the treatment of DKD and revealed the superiority of 20 mg of finerenone among MRAs in treating DKD.Systematic Review Registration: PROSPERO, identifier (CRD42022313826)
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spelling doaj.art-aee5e448735a468da0e9308ac6eb99e72022-12-22T04:04:42ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122022-09-011310.3389/fphar.2022.967317967317Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney diseaseYichuan Wu0Yichuan Wu1Huanjia Lin2Huanjia Lin3Yuan Tao4Yuan Tao5Ying Xu6Ying Xu7Jiaqi Chen8Jiaqi Chen9Yijie Jia10Yijie Jia11Zongji Zheng12Zongji Zheng13Department of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDepartment of Endocrinology and Metabolism, Nanfang Hospital, Southern Medical University, Guangzhou, ChinaDe Feng Academy, Southern Medical University, Guangzhou, ChinaDiabetic kidney disease (DKD) is one of the major causes of end-stage renal disease (ESRD). To evaluate the efficacy and safety of different types of mineralocorticoid receptor antagonists (MRAs) in diabetic kidney disease patients, we conducted this network meta-analysis by performing a systematic search in PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Library, and Clinicaltrials.gov. A total of 12 randomized clinical trials with 15,492 patients applying various types of MRAs covering spironolactone, eplerenone, finerenone, esaxerenone, and apararenone were included. The efficacy outcomes were the ratio of urine albumin creatine ratio (UACR) at posttreatment vs. at baseline, change in posttreatment estimated glomerular filtration (eGFR) vs. at baseline, and change in posttreatment systolic blood pressure (SBP) vs. at baseline. The safety outcome was the number of patients suffering from hyperkalemia. High-dose finerenone (MD −0.31, 95% CI: −0.52, −0.11), esaxerenone (MD −0.54, 95% CI: −0.72, −0.30), and apararenone (MD −0.63, 95% CI: −0.90, −0.35) were associated with a superior reduction in proteinuria in patients with DKD. Regarding the change in eGFR, the results of all drugs were similar, and finerenone may have potential superiority in protecting the kidney. Compared with placebo, none of the treatments was associated with a higher probability of controlling systolic blood pressure during treatment. Moreover, spironolactone, esaxerenone, and 20 mg of finerenone presented a higher risk of hyperkalemia. This Bayesian network meta-analysis was the first to explore the optimal alternative among MRAs in the treatment of DKD and revealed the superiority of 20 mg of finerenone among MRAs in treating DKD.Systematic Review Registration: PROSPERO, identifier (CRD42022313826)https://www.frontiersin.org/articles/10.3389/fphar.2022.967317/fulldiabetic kidney disease (DKD)mineralocorticoid receptor antagonists (MRA)type 2 diabeteshyperkalemianetwork meta-analysis (NMA)
spellingShingle Yichuan Wu
Yichuan Wu
Huanjia Lin
Huanjia Lin
Yuan Tao
Yuan Tao
Ying Xu
Ying Xu
Jiaqi Chen
Jiaqi Chen
Yijie Jia
Yijie Jia
Zongji Zheng
Zongji Zheng
Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
Frontiers in Pharmacology
diabetic kidney disease (DKD)
mineralocorticoid receptor antagonists (MRA)
type 2 diabetes
hyperkalemia
network meta-analysis (NMA)
title Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
title_full Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
title_fullStr Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
title_full_unstemmed Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
title_short Network meta-analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
title_sort network meta analysis of mineralocorticoid receptor antagonists for diabetic kidney disease
topic diabetic kidney disease (DKD)
mineralocorticoid receptor antagonists (MRA)
type 2 diabetes
hyperkalemia
network meta-analysis (NMA)
url https://www.frontiersin.org/articles/10.3389/fphar.2022.967317/full
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