AI Article Synopsis

  • Landmark trials show SGLT2 inhibitors (SGLT2-Is) are beneficial for cardiovascular and renal diseases, but research on their effects on metabolic syndrome (MetS) is limited.
  • This study aimed to analyze how SGLT2-Is affect the components of MetS by reviewing various trials and conducting a meta-analysis.
  • Results indicated that SGLT2-Is significantly reduced fasting plasma glucose, systolic blood pressure, and waist circumference, with no notable effect on HDL cholesterol, suggesting their potential in managing MetS.

Article Abstract

Background: Landmark trials have established the benefits of sodium-glucose cotransporter-2 inhibitors (SGLT2-Is) in cardiovascular disease including heart failure with reduced and preserved ejection fraction and renal diseases regardless of the presence of diabetes mellitus. However, studies evaluating the role of SGLT2-Is in metabolic syndrome (MetS) are limited.

Aim: This study primarily aimed to evaluate the impact of SGLT2-Is on the components of MetS.

Methods: Two independent reviewers and an experienced librarian searched Medline, Scopus and the Cochrane central from inception to December 9, 2021 to identify placebo controlled randomized controlled trials that evaluated the impact of SGLT2-Is on the components of MetS as an endpoint. Pre- and post-treatment data of each component were obtained. A meta-analysis was performed using the RevMan (version 5.3; Copenhagen: The Nordic Cochrane Center, The Cochrane Collaboration).

Results: Treatment with SGLT2-Is resulted in a decrease in fasting plasma glucose (-18.07 mg/dL; 95%CI: -25.32 to -10.82), systolic blood pressure (-1.37 mmHg; 95%CI: -2.08 to -0.65), and waist circumference (-1.28 cm; 95%CI: -1.39 to -1.18) compared to placebo. The impact on high-density lipoprotein cholesterol was similar to placebo (0.01 mg/dL; 95%CI: -0.05 to 0.07).

Conclusion: SGLT2-Is have a promising role in the management of MetS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724001PMC
http://dx.doi.org/10.4330/wjc.v14.i11.599DOI Listing

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