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ABSTRACT: Aim
To assess the impact of the HbA1c levels achieved with antidiabetic therapies (ADTs) on the risk of MACE.Methods
A systematic search was performed in PubMed, Cochrane, and ClinicalTrials. gov for RCTs published up to March 2022 reporting the occurrence of MACE and all-cause mortality in individuals with T2DM treated with all marketed ADTs, including a sample size ≥100 individuals in each study arm and follow-up ≥24 weeks. A systematic review and additive-effects network meta-analysis with random effects and a multivariate meta-regression were utilized to assess the impact of achieved HbA1c on incident MACE.Results
We included 126 RCTs with 143 treatment arms, 270,874 individuals, and 740,295 individuals-years who were randomized to an active treatment vs. control group. Among all ADTs, only therapy with SGLT2i, GLP1-RA, or pioglitazone similarly reduced the risk of MACE compared to placebo. The achievement of HbA1c ≤ 7.0% in RCTs with the 3 drug classes in the active arm was associated with an adjusted HR of 0.91 (95% CI 0.80, 0.97; p = 0.017) compared with HbA1c>7.0%, without affecting all-cause mortality. These results, however, were not maintained among all ADTs.Conclusions
Achieving lower glucose levels with SGLT2i, GLP1-RA, or pioglitazone is linearly associated with a reduced risk of MACEs, without affecting all-cause mortality.Systematic review registration
www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020213127, identifier: CRD42020213127.
SUBMITTER: de Carvalho LSF
PROVIDER: S-EPMC9098935 | biostudies-literature | 2022
REPOSITORIES: biostudies-literature
de Carvalho Luiz Sergio Fernandes LSF Nogueira Ana Claudia Cavalcante ACC Bonilha Isabella I Luchiari Beatriz B Benchimol Alexander A Couri Carlos Eduardo Barra CEB Borges Jairo Lins JL Barreto Joaquim J Sposito Andrei C AC
Frontiers in cardiovascular medicine 20220429
<h4>Aim</h4>To assess the impact of the HbA1c levels achieved with antidiabetic therapies (ADTs) on the risk of MACE.<h4>Methods</h4>A systematic search was performed in PubMed, Cochrane, and ClinicalTrials. gov for RCTs published up to March 2022 reporting the occurrence of MACE and all-cause mortality in individuals with T2DM treated with all marketed ADTs, including a sample size ≥100 individuals in each study arm and follow-up ≥24 weeks. A systematic review and additive-effects network meta- ...[more]