The Association Between the Dosage of SGLT2 Inhibitor and Weight Reduction in Type 2 Diabetes Patients: A Meta‐Analysis

Objective Sodium glucose cotransporter 2 (SGLT2) inhibitors may induce urinary glucose excretion via the inhibition of renal glucose reabsorption, improve glycemic control, and lower body weight. The aim of this meta‐analysis was to evaluate weight changes in patients who received different dosages...

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Published inObesity (Silver Spring, Md.) Vol. 26; no. 1; pp. 70 - 80
Main Authors Cai, Xiaoling, Yang, Wenjia, Gao, Xueying, Chen, Yifei, Zhou, Lingli, Zhang, Simin, Han, Xueyao, Ji, Linong
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2018
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Summary:Objective Sodium glucose cotransporter 2 (SGLT2) inhibitors may induce urinary glucose excretion via the inhibition of renal glucose reabsorption, improve glycemic control, and lower body weight. The aim of this meta‐analysis was to evaluate weight changes in patients who received different dosages of SGLT2 inhibitors. Methods Overall, 55 placebo‐controlled trials were included. Results The results indicated that treatment with 2.5 mg, 5 mg, 10 mg, and 20 mg of dapagliflozin led to significant decreases in body weight compared with a placebo (weighted mean difference [WMD], −1.30 kg, −1.51 kg, −1.79 kg, −2.24 kg, respectively; P < 0.001). Treatment with 50 mg, 100 mg, 200 mg, and 300 mg of canagliflozin also led to significant decreases in weight (WMD, −1.20 kg, −1.82 kg, −1.83 kg, −2.37 kg, respectively; P < 0.001). In the treatment with empagliflozin, ipragliflozin, tofogliflozin, and luseogliflozin, body weight also significantly decreased. The decrease in weight was associated with the dosage of dapagliflozin (P < 0.05). Conclusions Body weight significantly decreased in patients with type 2 diabetes who received different dosages of SGLT2 inhibitors compared with patients who received a placebo. Moreover, in patients treated with dapagliflozin, there was a statistically significant dosage‐dependent trend in body weight reduction.
Bibliography:This study was supported by AstraZeneca Ltd. (China). The funding agencies had no role in the study design, data collection or analysis, decision to publish, or preparation of the manuscript.
Design of this meta‐analysis: LNJ and XLC; study selection and data extraction: WJY, XYG, and YFC; statistical analyses: XLC and XYH; manuscript writing: XLC, LLZ, SMZ, and LNJ. All authors contributed to the manuscript drafts and gave final approval for this manuscript.
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Funding agencies
LNJ has received fees for consultations and meeting presentations from AstraZeneca, Sanofi‐Aventis, Eli Lilly, Novartis, Merck, Roche, Abbott, and Takeda. The other authors declared no conflict of interest.
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ISSN:1930-7381
1930-739X
DOI:10.1002/oby.22066