Effects of SGLT2 inhibitors on cardiovascular outcomes and mortality in type 2 diabetes A meta-analysis

被引:73
作者
Zou, Cai-Yan [1 ,2 ]
Liu, Xue-Kui [1 ,2 ]
Sang, Yi-Quan [1 ,2 ]
Wang, Ben [1 ,2 ]
Liang, Jun [1 ,2 ,3 ]
机构
[1] Xuzhou Med Univ, Xuzhou Cent Hosp, Dept Endocrinol, Xuzhou Clin Sch, Xuzhou, Jiangsu, Peoples R China
[2] Southeast Univ, Med Sch, Xuzhou, Jiangsu, Peoples R China
[3] Xuzhou Inst Med Sci, Xuzhou Inst Diabet, Xuzhou, Jiangsu, Peoples R China
关键词
cardiovascular outcomes; meta-analysis; mortality; SGLT2; inhibitors; type; 2; diabetes; ADD-ON THERAPY; METFORMIN PLUS SULFONYLUREA; INADEQUATE GLYCEMIC CONTROL; COTRANSPORTER; INHIBITORS; LONG-TERM EFFICACY; DOUBLE-BLIND; JAPANESE PATIENTS; EMPAGLIFLOZIN MONOTHERAPY; BACKGROUND METFORMIN; ADIPOSE-TISSUE;
D O I
10.1097/MD.0000000000018245
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Optimal glycemic control is required to restrain the increase of cardiovascular events in patients with type 2 diabetes. The effects of sodium-glucose cotransporter-2 (SGLT-2) inhibitors on cardiovascular events and mortality in those patients are not well established. This meta-analysis was conducted to assess the effects of SGLT2 inhibitors on cardiovascular events and mortality in patients with type 2 diabetes. Methods: We conducted a systematic literature search of Medline, Embase and Cochrane Library and included randomized controlled trials (RCTs) of 3 different SGLT2 inhibitors (canagliflozin, dapagliflozin and empagliflozin) that evaluated the effects on cardiovascular outcomes and mortality in the final meta-analysis. The intervention arm was defined either as SGLT2 inhibitor monotherapy or as SGLT2 inhibitor add-on to other non-SGLT2 inhibitor antidiabetic agents (ADAs). Results: Forty-two trials with a total of 61,076 patients with type 2 diabetes were included in the meta-analysis. Compared with the control, SGLT2 inhibitor treatment was associated with a reduction in the incidence of major adverse cardiovascular events (MACEs) (OR=0.86, 95% CI 0.80-0.93, P<.0001), myocardial infarction (OR=0.86, 95% CI 0.79-0.94, P=.001), cardiovascular mortality (OR=0.74, 95% CI 0.67-0.81, P<.0001) and all cause mortality (OR=0.85, 95% CI 0.79-0.92, P<.0001). However, the risk of ischemic stroke was not reduced after SGLT2 inhibitor treatment in patients with type 2 diabetes (OR=0.95, 95% CI 0.85-1.07, P=.42). Conclusion: These data suggest a decreased risk of harm with SGLT2 inhibitor as a class with respect to cardiovascular events and mortality.
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页数:14
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