Key result
GLP-1 agonists or SGLT2 inhibitors cut MACE ~12% vs. placebo in type 2 diabetes.
Why the study?
Differences in cardiovascular outcomes with SGLT2 inhibitors and GLP-1 receptor agonists by age, sex, race, BMI, and diabetes duration in type 2 diabetes were unclear.
Meta-Analysis (n=96,580)
Yes
Hazard Ratio: 0.88 (95% CI 0.85–0.92)
Supports adding GLP-1RAs or SGLT2is for MACE prevention in type 2 diabetes; confirms consistent benefit across 11 major trials.
Background: ), and duration of diabetes (< 10 years vs. ≥ 10 years). Methods: We performed a MEDLINE database search from inception up to July 31, 2022 to identify all placebo-controlled phase 3 CVOTs that evaluated the efficacy of SGLT2i and GLP-1 RAs on vascular events at least 1-year after randomisation in participants with type 2 diabetes, and we selected those reporting hazard ratios (HRs) for the specific risk groups for MACE. Differences on MACE in risk groups were examined using a random-effect meta-analysis. The study protocol was registered on PROSPERO (CRD42022347901). Findings: values ranging from 0% to 54%. Interpretation: In patients with type 2 diabetes at highest risk of cardiovascular disease or established cardiovascular disease, a greater benefit on MACE was found for elderly patients and for Asian individuals compared with White individuals with GLP-1 RAs, and those with a long duration of diabetes with SGLT2i. These findings could help in providing guidance for treatment prescription and facilitate selection and stratification of patients for future CVOTs. Furthermore, pooled individual patient-level data are urgently needed to support our conclusions, and to derive definitive evidence. Funding: None.
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Diallo et al. (2022) conducted a meta-analysis in Type 2 diabetes (n=96,580). SGLT2 inhibitors and GLP-1 receptor agonists vs. Placebo was evaluated on MACE-3 (composite of cardiovascular death, non-fatal stroke, and non-fatal myocardial infarction) (HR 0.88, 95% CI 0.85-0.92). Adding GLP-1 receptor agonists or SGLT2 inhibitors to standard care reduced the risk of major adverse cardiovascular events by 12% (HR 0.88) compared to placebo in patients with type 2 diabetes.
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