Literature DB >> 32860942

SGLT2 inhibitors for prevention of cardiorenal events in people with type 2 diabetes without cardiorenal disease: A meta-analysis of large randomized trials and cohort studies.

Mei Qiu1, Liang-Liang Ding2, Miao Zhang3, Jin-Hao Lin4, Jin-Song Gu5, Xian Zhou6, Ying-Xi Tang7, Xu-Bin Wei8, Shu-Yan Liu9.   

Abstract

To investigate whether sodium glucose cotransporter 2 inhibitors (SGLT2is) can reduce important cardiorenal endpoints in type 2 diabetic adults without established cardiovascular disease (ECD), in those without heart failure (HF), and in those without chronic kidney disease (CKD). We searched PubMed, Embase, Cochrane Central Register of Controlled Trials (CENTRAL) and clinicaltrials.gov. Event-driven randomized controlled trials (RCTs) and cohort studies were included. We conducted random-effects meta-analysis, respectively based on RCTs and cohort studies, on eight cardiorenal endpoints in three type 2 diabetic subgroups. Thirteen large studies were included. Meta-analysis of RCTs showed the high quality evidences: compared with placebo, SGLT2is significantly reduced the risk of major adverse cardiovascular events, cardiovascular death or hospitalization for HF, and progression of CKD in type 2 diabetic adults without ECD [HRs (95 % CIs): 0.88 (0.82, 0.94), 0.76 (0.70, 0.82), and 0.59 (0.52, 0.66), respectively; risk differences (95 % CIs): -1.6 (-2.4, -0.8), -2.6 (-3.3, -2.0), and -2.4 (-2.8, -2.0) per 1000 patient-years, respectively], in those without HF [HRs (95 % CIs): 0.89 (0.82, 0.95), 0.74 (0.67, 0.81), and 0.61 (0.55, 0.67), respectively; risk differences (95 % CIs): -1.7 (-2.9, -0.8), -5.8 (-7.3, -4.2), and -2.3 (-2.6, -1.9) per 1000 patient-years, respectively], and in those without CKD [HRs (95 % CIs): 0.88 (0.82, 0.94), 0.77 (0.71, 0.83), and 0.63 (0.57, 0.70), respectively; risk differences (95 % CIs): -2.4 (-3.6, -1.2), -6.1 (-7.6, -4.5), and -2.2 (-2.6, -1.8) per 1000 patient-years, respectively]. Meta-analysis of cohort studies also showed the benefits of SGLT2is on the three composite outcomes in the three diabetic subgroups. SGLT2is also significantly reduced some other cardiorenal endpoints in these diabetic subgroups. SGLT2is can significantly reduce important cardiorenal events in type 2 diabetic adults without ECD, in those without HF, and in those without CKD; which supports SGLT2is used in these diabetic subpopulations to prevent cardiorenal events.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cardiorenal events; Cardiovascular disease; Chronic kidney disease; Heart failure; SGLT2 inhibitors; Type 2 diabetes

Year:  2020        PMID: 32860942     DOI: 10.1016/j.phrs.2020.105175

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  4 in total

1.  Cardiorenal outcomes with sodium/glucose cotransporter-2 inhibitors in patients with type 2 diabetes and low kidney risk: real world evidence.

Authors:  Meir Schechter; Cheli Melzer-Cohen; Aliza Rozenberg; Ilan Yanuv; Gabriel Chodick; Avraham Karasik; Mikhail Kosiborod; Ofri Mosenzon
Journal:  Cardiovasc Diabetol       Date:  2021-08-18       Impact factor: 9.951

2.  Impact of demographic characteristics and antihyperglycemic and cardiovascular drugs on the cardiorenal benefits of SGLT2 inhibitors in patients with type 2 diabetes mellitus: A protocol for systematic review and meta-analysis.

Authors:  Rong Chang; Shu-Yan Liu; Li-Min Zhao
Journal:  Medicine (Baltimore)       Date:  2021-11-24       Impact factor: 1.817

Review 3.  Preventing all-cause hospitalizations in type 2 diabetes with sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists: A narrative review and proposed clinical approach.

Authors:  Meir Schechter; Matan Fischer; Ofri Mosenzon
Journal:  Diabetes Obes Metab       Date:  2022-03-24       Impact factor: 6.408

4.  Sodium Glucose Cotransporter Type 2 Inhibitors Improve Cardiorenal Outcome of Patients With Coronary Artery Disease: A Meta-Analysis.

Authors:  Wen Wei; Jin Liu; Shiqun Chen; Xinghao Xu; Dachuan Guo; Yibo He; Zhidong Huang; Bo Wang; Haozhang Huang; Qiang Li; Jiyan Chen; Hong Chen; Ning Tan; Yong Liu
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-07       Impact factor: 5.555

  4 in total

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