Abstract | Objective: Methods: We searched the PubMed, Embase and Cochrane Library from inception until October 15, 2021. We included randomized controlled trials (RCTs) reporting the effect of SGLT-2i on major adverse cardiovascular event ( MACE), hospitalization for heart failure (HHF), cardiovascular (CV) death and cardiorenal parameters in CAD patients. Hazard ratio (HR) with 95% confidence interval (CI) and mean difference (MD) from trials were meta-analyzed using fixed-effects models. Results: Nine trials enrolling 15,301 patients with CAD were included in the analyses. Overall, SGLT2i were associated with a reduced risk of MACE (HR: 0.84; 95% CI 0.74-0.95; I2 = 0%), HHF (HR: 0.69; 95% CI 0.58-0.83; I2 = 0%) and a composite of CV death or HHF (HR: 0.78; 95% CI 0.71-0.86; I2 = 37%) in CAD patients. Compared with control group, estimated glomerular filtration rate (eGFR) level decreased less in SGLT-2i group (mean difference [MD] = -3.60, 95% CI, -5.90 to -1.30, p = 0.002; I2 = 0%). Conclusions: SGLT-2i can improve cardiorenal outcomes in CAD patients. Further RCTs and real world studies are need to investigate the effect of SGLT2i on CAD patients. Systematic Review Registration: PROSPERO, CRD42021258237.
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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 | Frontiers in endocrinology
(Front Endocrinol (Lausanne))
Vol. 13
Pg. 850836
( 2022)
ISSN: 1664-2392 [Print] Switzerland |
PMID | 35330914
(Publication Type: Meta-Analysis, Research Support, Non-U.S. Gov't, Systematic Review)
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Copyright | Copyright © 2022 Wei, Liu, Chen, Xu, Guo, He, Huang, Wang, Huang, Li, Chen, Chen, Tan and Liu. |
Chemical References |
- Sodium-Glucose Transport Proteins
- Sodium-Glucose Transporter 2 Inhibitors
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Topics |
- Coronary Artery Disease
(complications, drug therapy)
- Diabetes Mellitus, Type 2
(complications, drug therapy)
- Heart Failure
(complications)
- Humans
- Sodium-Glucose Transport Proteins
- Sodium-Glucose Transporter 2 Inhibitors
(pharmacology, therapeutic use)
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