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All-cause mortality and cardiovascular events in patients with type 2 diabetes treated with alpha-glucosidase inhibitors: A meta-analysis of randomized controlled trials.
Mannucci, Edoardo; Gallo, Marco; Pintaudi, Basilio; Targher, Giovanni; Candido, Riccardo; Giaccari, Andrea; Monami, Matteo.
Afiliación
  • Mannucci E; Diabetology, Careggi Hospital and University of Florence, Italy.
  • Gallo M; Endocrinology and Metabolic Diseases Unit, AO SS. Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
  • Pintaudi B; SSD Diabetes Unit, Niguarda Ca' Granda Hospital, Milan, Italy.
  • Targher G; Endocrinology, Diabetes and Metabolism, University of Verona, Italy.
  • Candido R; Diabetes Centre District 3, Azienda Sanitaria Universitaria Integrata di Trieste, Via Puccini 48/50, 34100, Trieste, Italy.
  • Giaccari A; Centro per le Malattie Endocrine e Metaboliche, Fondazione Policlinico Universitario A. Gemelli UCSC and Università Cattolica del Sacro Cuore, Rome, Italy.
  • Monami M; Diabetology, Careggi Hospital and University of Florence, Italy. Electronic address: matteo.monami@unifi.it.
Nutr Metab Cardiovasc Dis ; 32(2): 511-514, 2022 02.
Article en En | MEDLINE | ID: mdl-34893404
ABSTRACT

AIM:

Alpha-glucosidase inhibitors are approved drugs for treating type 2 diabetes (T2DM); however, their effects on mortality and cardiovascular safety are unclear. This meta-analysis was aimed at evaluating the effects of alpha-glucosidase inhibitors on all-cause mortality and major cardiovascular events (MACE). DATA

SYNTHESIS:

A Medline, Embase, Cochrane database searching for alpha-glucosidase inhibitors was performed up to July 1st, 2021. All randomized controlled trials (RCT) with a duration ≥52 weeks and comparing the effects of alpha-glucosidase inhibitors with placebo or active drugs were collected. Further inclusion criteria were RCT reporting MACE within their primary outcome, or as pre-defined secondary outcome; and RCT enrolling at least 100 patients with T2DM. Mantel-Haenszel odds ratio (MH-OR) with 95% confidence intervals were calculated for the aforementioned outcomes. A total of eight RCTs, enrolling 1124 and 908 patients on alpha-glucosidase inhibitors and comparators, respectively, were identified. No trials reported information on MACE. Treatment with alpha-glucosidase inhibitors was not associated with a significant increase of all-cause mortality compared with other therapies or no therapy/placebo (MH-OR 0.76 [0.28; 2.05]).

CONCLUSIONS:

The evidence of beneficial or detrimental effects of alpha-glucosidase inhibitors on all-cause mortality and cardiovascular events is not sufficient to draw any conclusions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Inhibidores de Glicósido Hidrolasas / Hipoglucemiantes Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Inhibidores de Glicósido Hidrolasas / Hipoglucemiantes Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article