PMID- 37575756 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230815 IS - 2168-8184 (Print) IS - 2168-8184 (Electronic) IS - 2168-8184 (Linking) VI - 15 IP - 7 DP - 2023 Jul TI - A Systematic Review and Meta-Analysis on the Efficacy and Safety of Finerenone Therapy in Patients with Cardiovascular and Chronic Kidney Diseases in Type 2 Diabetes Mellitus. PG - e41746 LID - 10.7759/cureus.41746 [doi] LID - e41746 AB - The purpose of this study is to assess the safety and efficacy of finerenone therapy in type 2 diabetes mellitus (T2DM) patients with cardiovascular and chronic renal diseases. This meta-analysis assesses the efficacy and safety of finerenone in the treatment of diabetic kidney disease (DKD). A comprehensive search of PubMed, Embase, and Google Scholar databases was performed to identify relevant randomized controlled trials (RCTs). To quantify the effects of finerenone, the analysis included the estimation of aggregated mean differences (MDs) and relative risks (RRs), as well as 95% confidence intervals (CIs). This meta-analysis included seven double-blind trials with patients suffering from chronic kidney disease (CKD) and T2D. Participants received finerenone or a placebo was assigned at random. The primary efficacy outcomes were cardiovascular mortality, non-fatal myocardial infarction, non-fatal stroke, hospitalization for heart failure, kidney failure, a sustained 57% decrease in the estimated glomerular filtration rate from baseline over four weeks, or renal death. Among the 39,995 patients included in the analysis, finerenone treatment was associated with a lower risk of cardiovascular and renal-related mortality compared to placebo (RR = 0.86 (0.80, 0.93), p = 0.0002; I-squared statistic (I(2) ) = 0%) and (RR = 0.56 (0.17, 1.82), p = 0.34; I(2 )= 0%). In addition, finerenone treatment was associated with a marginally reduced risk of serious adverse events (RR = 0.95 (0.92, 0.97), p = 0.0001; I(2 )= 0%), although no significant difference in the overall risk of adverse events was observed between the two groups (RR = 1.00 (0.99, 1.01), p = 0.56; I(2 )= 0%). This study's findings suggest that finerenone administration can reduce the risk of end-stage kidney disease, renal failure, cardiovascular mortality, and hospitalization. Patients with both T2DM and CKD are therefore advised to consider finerenone therapy. CI - Copyright (c) 2023, Jyotsna et al. FAU - Jyotsna, Fnu AU - Jyotsna F AD - Medicine, DR. B.R. (Bharatha Rathna) Ambedkar Medical College & Hospital, Bengaluru, IND. FAU - Mahfooz, Kamran AU - Mahfooz K AD - Internal Medicine, Lincoln Medical Center, New York, USA. FAU - Patel, Tirath AU - Patel T AD - Medical Student, American University of Antigua, St. John's, ATG. FAU - Parshant, Fnu AU - Parshant F AD - Medicine, Jinnah Sindh Medical University, Karachi, PAK. FAU - Simran, Fnu AU - Simran F AD - Medicine, Jinnah Sindh Medical University, Karachi, PAK. FAU - Harsha, Fnu AU - Harsha F AD - Medicine, Jinnah Sindh Medical University, Karachi, PAK. FAU - Neha, Fnu AU - Neha F AD - Medicine, Ghulam Muhammad Mahar Medical College, Sukkur, PAK. FAU - Jyotishna, Dev AU - Jyotishna D AD - Cardiology, TU (Tribhuvan University) Teaching Hospital, International Organization for Migration, Mohali, NPL. FAU - Mishra, Dipesh AU - Mishra D AD - Medicine, Chirayu National Hospital and Medical Institute, Kathmandu, NPL. FAU - Subedi, Sirjana AU - Subedi S AD - Medicine, University of Medicine and Health Sciences, Basseterre, NPL. FAU - Khatri, Mahima AU - Khatri M AD - Medicine and Surgery, Dow University of Health Sciences, Karachi, PAK. FAU - Kumar, Satesh AU - Kumar S AD - Medicine and Surgery, Shaheed Mohtarma Benazir Bhutto Medical College, Karachi, PAK. FAU - Varrassi, Giustino AU - Varrassi G AD - Pain Medicine, Paolo Procacci Foundation, Rome, ITA. LA - eng PT - Journal Article PT - Review DEP - 20230711 PL - United States TA - Cureus JT - Cureus JID - 101596737 PMC - PMC10421409 OTO - NOTNLM OT - cardiovascular disease OT - chronic kidney disease OT - ckd OT - diabetes OT - finerenone OT - meta-analysis OT - non-steroidal mineralocorticoid receptor antagonist COIS- The authors have declared that no competing interests exist. EDAT- 2023/08/14 06:42 MHDA- 2023/08/14 06:43 PMCR- 2023/07/11 CRDT- 2023/08/14 04:33 PHST- 2023/07/06 00:00 [received] PHST- 2023/07/11 00:00 [accepted] PHST- 2023/08/14 06:43 [medline] PHST- 2023/08/14 06:42 [pubmed] PHST- 2023/08/14 04:33 [entrez] PHST- 2023/07/11 00:00 [pmc-release] AID - 10.7759/cureus.41746 [doi] PST - epublish SO - Cureus. 2023 Jul 11;15(7):e41746. doi: 10.7759/cureus.41746. eCollection 2023 Jul.