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Meta-Analysis
. 2022 Jan;24(1):106-114.
doi: 10.1111/dom.14555. Epub 2021 Oct 4.

Sotagliflozin for patients with type 2 diabetes: A systematic review and meta-analysis

Affiliations
Meta-Analysis

Sotagliflozin for patients with type 2 diabetes: A systematic review and meta-analysis

Ioannis Avgerinos et al. Diabetes Obes Metab. 2022 Jan.

Abstract

Aim: To assess the efficacy and safety of sotagliflozin in patients with type 2 diabetes.

Methods: We searched Medline, Embase, the Cochrane Library, and grey literature sources up to August 2021 for randomized controlled trials (RCTs) that compared sotagliflozin with placebo or other antidiabetic agents in patients with type 2 diabetes. Our primary outcome was change in HbA1c from baseline. We additionally assessed three secondary efficacy and 15 safety outcomes. We synthesized data using weighted mean differences (WMDs) and odds ratios (ORs), along with 95% confidence intervals (CIs).

Results: We included 11 RCTs comprising 16 411 subjects in the meta-analysis. Compared with placebo, sotagliflozin reduced HbA1c (WMD -0.42%, 95% CI -0.56 to -0.29), body weight (WMD -1.33 kg, 95% CI -1.57 to -1.09), and systolic blood pressure (WMD -2.44 mmHg, 95% CI -2.81 to -2.07). No difference was evident against other active comparators. Sotagliflozin reduced myocardial infarction (OR 0.72, 95% CI 0.54 to 0.97) and heart failure (OR 0.68, 95% CI 0.58 to 0.79) compared with placebo, and had a neutral effect on all-cause mortality, cardiovascular mortality, and stroke. Treatment with sotagliflozin was safe regarding the incidence of serious adverse events, hypoglycaemia, and diabetic ketoacidosis. Nevertheless, it was associated with an increased incidence of diarrhoea, genital infections, and volume depletion events.

Conclusions: Sotagliflozin reduces blood glucose, body weight, and systolic blood pressure, and demonstrates a beneficial effect on heart failure and myocardial infarction. Its overall safety profile is comparable with other sodium-glucose co-transporter-2 inhibitors.

Keywords: SGLT2 inhibitor; glycaemic control; macrovascular disease; meta-analysis; type 2 diabetes.

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References

REFERENCES

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