Key result
Greater HbA1c reduction correlates with lower MACE risk across CVOTs, driven by fewer strokes with GLP-1RAs.
Meta-Analysis
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AIM: In order to disclose relations between reduction of haemoglobin A1c (HbA1c) levels and risk of major cardiovascular events (MACE), we performed a meta-analysis with metaregression of all cardiovascular outcome trials (CVOTs) so far published in patients with type 2 diabetes (T2D). MATERIALS AND METHODS: An electronic search up to February 10, 2020 was conducted to determine eligible trials. Pooled summary estimates and 95% confidence intervals (CI) were calculated according to the random effects model using the Paule-Mandel method; restricted maximum likelihood estimators were used to estimate model parameters in the metaregression. RESULTS: = 44%, P = 0.060) There was a robust relation between the reduction in achieved HbA1c at the end of the trial and the HR reduction for MACE (beta = -0.3169, P = 0.029), explaining most (78%) of the between-study variance; this relation was totally driven by the risk reduction of non-fatal stroke only, which explained 100% of between-study variance, and apparently restricted to the class of glucagon-like peptide 1 receptor agonists (GLP-1RAs). There was no relation between the reduction in achieved HbA1c and the HR for heart failure (variance explained = 0%) or all-cause mortality (variance explained = 6%). CONCLUSION: The blood glucose reduction observed in CVOTs may play some role in reducing the risk of non-fatal stroke, at least during treatment with GLP-1RAs, without affecting the other two components of MACE.
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Giugliano et al. (2020) conducted a meta-analysis in Type 2 diabetes. Reduction of haemoglobin A1c (HbA1c) levels was evaluated on Major cardiovascular events (MACE) (beta -0.3169, p=0.029). Reduction in achieved HbA1c across 15 CVOTs significantly correlated with MACE HR reduction (beta = -0.3169, P = 0.029), driven entirely by non-fatal stroke reduction in GLP-1RA trials.
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