Abstract
Aims
To identify the impact of sodium-glucose co-transporter-2 (SGLT2) inhibitors on anthropometric indices and metabolic markers in individuals without diabetes who are overweight/obese.
Materials and methods
Clinical trials investigating the safety and efficacy of SGLT2 inhibitors in overweight or obese adults were sought in PubMed, Scopus, Google Scholar, and EMBASE databases. The overall intervention effect was estimated using a random-effect meta-analysis. Jadad scale was used to assess the risk of bias. The heterogeneity of the studies was assessed using the Cochran's test (Q test) and I2 Index. Analyses of meta-regression were carried out to identify possible sources of heterogeneity among the trials. The analyses were all conducted using Stata, and p < .05 was set as the statistically significant level.
Results
Of the five clinical trials that were included in the meta-analysis, five, four, three, and two clinical trials met the eligibility criteria for evaluating the efficacy of SGLT2 inhibitors on the weight, waist circumference (WC) and blood pressure, body mass index (BMI), and lipid and glucose profile, respectively. According to the results, SGLT2 inhibitors lowered BMI (WMD = −0.47 [95% CI: −0.63, −0.31]; p < .001), and WC (WMD = −3.25 [95% CI: −6.36, −0.14]; p = .04), but had no significant influence on blood pressure, lipid, and glucose profile of overweight/obese patients compared to the control groups.
Conclusion
The SGLT2 inhibitors appear to ameliorate some anthropometric and metabolic markers. There is, however, a limited number of studies, and further research is required for a firm conclusion.
Registration code in PROSPERO
CRD42022306415.
Transparency
Declaration of funding
There was no financial support for this work.
Declaration of financial/other relationships
The authors report no relevant financial relationships or otherwise to disclose. Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Author contributions
BA and MV contributed to the design of the study, conducted the searches, screening, quality appraisal, data extraction, analysis, synthesis, drafted, and edited the manuscript. AE conducted the data extraction. FH and ARA contributed to the design of the study, supported screening, and revised the manuscript. MV advised and revised the manuscript. All authors have read and approved the final version of the manuscript. MV has primary responsibility for the final content.
Acknowledgements
The authors sincerely thank Dr. Abidi Pharmaceuticals Company for providing study facilities.
Data availability statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.