The Cardiovascular Benefits and Infections Risk of SGLT2i versus Metformin in Type 2 Diabetes: A Systemic Review and Meta-Analysis

被引:4
作者
Xu, Chunmei [1 ,2 ,3 ]
He, Liping [4 ,5 ]
Zhang, Jing [4 ,5 ]
Xu, Lusi [6 ]
Dong, Jianjun [7 ]
Liao, Lin [4 ,5 ,6 ]
机构
[1] Shandong First Med Univ, Shandong Prov Hosp, Dept Endocrinol, Jinan 250021, Peoples R China
[2] Shandong Prov Hosp, Shandong Key Lab Endocrinol & Lipid Metab, Jinan 250021, Peoples R China
[3] Shandong Univ, Shandong Prov Hosp, Dept Endocrinol, Jinan 250021, Peoples R China
[4] Shandong First Med Univ, Affiliated Hosp 1, Dept Endocrinol & Metabol, Jinan 250014, Peoples R China
[5] Shandong Prov Qianfoshan Hosp, Shandong Inst Nephrol, Shandong Key Lab Rheumat Dis & Translat Med, Jinan 250014, Peoples R China
[6] Shandong Univ, Shandong Prov Qianfoshan Hosp, Dept Endocrinol & Metabol, Jinan 250014, Peoples R China
[7] Shandong Univ, Qilu Hosp, Dept Internal Med, Div Endocrinol, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
sodium-glucose cotransporter 2 inhibitors; genitourinary tract infections; cardiovascular benefits; metformin; randomized controlled trials; meta-analysis; COTRANSPORTER; 2; INHIBITORS; INADEQUATE GLYCEMIC CONTROL; DOUBLE-BLIND; DAPAGLIFLOZIN MONOTHERAPY; INITIAL COMBINATION; JAPANESE PATIENTS; SAFETY OUTCOMES; OPEN-LABEL; EFFICACY; EMPAGLIFLOZIN;
D O I
10.3390/metabo12100979
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) and metformin are both widely accepted anti-hyperglycemic agents. However, there is still no systematic review evaluating the cardiovascular benefits and risk of infections of SGLT2i versus metformin. To make that clear, we designed this study. Public databases, including the Cochrane library database, PubMed, and Embase were searched for randomized clinical trials (RCTs) fitting the inclusion criteria. Two reviewers extracted the data and appraised the study quality independently. Thirteen RCTs enrolling 4189 patients were eligible for this analysis. Our results showed that compared with metformin, SGLT2i increased the risk of genitourinary tract infections (p < 0.00001). Further subgroup analysis suggested that the occurrence of urinary tract infections (UTI) was not statistically significant (p = 0.18), but the incidence of reproductive tract infections (RTI) was significantly increased in patients in the SGLT2i group compared with that in the metformin group (p < 0.00001). In addition, SGLT2i markedly decreased the levels of cardiovascular risk factor, including body weight, blood pressure, and triglyceride level, and significantly increased the HDL-cholesterol level (p < 0.00001) in patients versus that of metformin. For type 2 diabetes patients with obesity, SGLT2i was associated with more significant reductions in weight and blood pressure compared to metformin without an increased risk of genitourinary infections, and the reduction in fasting plasma glucose was superior in the SGLT2i group; the decrease in HbA1c was similar in both groups. Additionally, no significant publication bias was seen. Based on these findings, SGLT2i provided the similar antihyperglycemic effects, additional cardiovascular benefits, and a potential RTI risk compared with that of metformin. Our results indicate that SGLT2i is a good choice for those patients with metformin intolerance or resistance.
引用
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页数:28
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