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Cardiovascular outcomes after initiating GLP-1 receptor agonist or basal insulin for the routine treatment of type 2 diabetes: a region-wide retrospective study.
Longato, Enrico; Di Camillo, Barbara; Sparacino, Giovanni; Tramontan, Lara; Avogaro, Angelo; Fadini, Gian Paolo.
  • Longato E; Department of Information Engineering, University of Padova, 35100, Padova, Italy.
  • Di Camillo B; Department of Information Engineering, University of Padova, 35100, Padova, Italy.
  • Sparacino G; Department of Information Engineering, University of Padova, 35100, Padova, Italy.
  • Tramontan L; Arsenàl.IT, Veneto's Research Centre for eHealth Innovation, 31100, Treviso, Italy.
  • Avogaro A; Department of Medicine, University of Padova, Via Giustiniani 2, 35100, Padova, Italy.
  • Fadini GP; Department of Medicine, University of Padova, Via Giustiniani 2, 35100, Padova, Italy. gianpaolo.fadini@unipd.it.
Cardiovasc Diabetol ; 20(1): 222, 2021 11 13.
Article en En | MEDLINE | ID: mdl-34774054
ABSTRACT

AIM:

We aimed to compare cardiovascular outcomes of patients with type 2 diabetes (T2D) who initiated GLP-1 receptor agonists (GLP-1RA) or basal insulin (BI) under routine care.

METHODS:

We accessed the administrative claims database of the Veneto Region (Italy) to identify new users of GLP-1RA or BI in 2014-2018. Propensity score matching (PSM) was implemented to obtain two cohorts of patients with superimposable characteristics. The primary endpoint was the 3-point major adverse cardiovascular events (3P-MACE). Secondary endpoints included 3P-MACE components, hospitalization for heart failure, revascularizations, and adverse events.

RESULTS:

From a background population of 5,242,201 citizens, 330,193 were identified as having diabetes. PSM produced two very well matched cohorts of 4063 patients each, who initiated GLP-1RA or BI after an average of 2.5 other diabetes drug classes. Patients were 63-year-old and only 15% had a baseline history of cardiovascular disease. During a median follow-up of 24 months in the intention-to-treat analysis, 3P-MACE occurred less frequently in the GLP-1RA cohort (HR versus BI 0.59; 95% CI 0.50-0.71; p < 0.001). All secondary cardiovascular endpoints were also significantly in favor of GLP-1RA. Results were confirmed in the as-treated approach and in several stratified analyses. According to the E-value, confounding by unmeasured variables were unlikely to entirely explain between-group differences in cardiovascular outcomes.

CONCLUSIONS:

Patients with T2D who initiated a GLP-1RA experienced far better cardiovascular outcomes than did matched patients who initiated a BI in the same healthcare system. These finding supports prioritization of GLP-1RA as the first injectable regimen for the management of T2D.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Incretinas / Receptor del Péptido 1 Similar al Glucagón / Hipoglucemiantes / Insulina Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Incretinas / Receptor del Péptido 1 Similar al Glucagón / Hipoglucemiantes / Insulina Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País como asunto: Europa Idioma: En Año: 2021 Tipo del documento: Article