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A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction
Metformin improves cardiovascular prognosis in patients with diabetes mellitus, compared to alternative glucose-lowering drugs, despite similar glycemic control. Direct cardiovascular protective properties have therefore been proposed, and studied in preclinical models of myocardial infarction. We n...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568412/ https://www.ncbi.nlm.nih.gov/pubmed/28832637 http://dx.doi.org/10.1371/journal.pone.0183664 |
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author | Hesen, Nienke A. Riksen, Niels P. Aalders, Bart Ritskes-Hoitinga, Merel El Messaoudi, Saloua Wever, Kimberley E. |
author_facet | Hesen, Nienke A. Riksen, Niels P. Aalders, Bart Ritskes-Hoitinga, Merel El Messaoudi, Saloua Wever, Kimberley E. |
author_sort | Hesen, Nienke A. |
collection | PubMed |
description | Metformin improves cardiovascular prognosis in patients with diabetes mellitus, compared to alternative glucose-lowering drugs, despite similar glycemic control. Direct cardiovascular protective properties have therefore been proposed, and studied in preclinical models of myocardial infarction. We now aim to critically assess the quality and outcome of these studies. We present a systematic review, quality assessment and meta-analysis of the effect of metformin in animal studies of experimental myocardial infarction. Through a comprehensive search in Pubmed and EMBASE, we identified 27 studies, 11 reporting on ex vivo experiments and 18 reporting on in vivo experiments. The primary endpoint infarct size as percentage of area at risk was significantly reduced by metformin in vivo (MD -18.11[-24.09,-12.14]) and ex vivo (MD -18.70[-25.39, -12.02]). Metformin improved the secondary endpoints left ventricular ejection fraction (LVEF) and left ventricular end systolic diameter. A borderline significant effect on mortality was observed, and there was no overall effect on cardiac hypertrophy. Subgroup analyses could be performed for comorbidity and timing of treatment (infarct size and mortality) and species and duration of ischemia (LVEF), but none of these variables accounted for significant amounts of heterogeneity. Reporting of possible sources of bias was extremely poor, including randomization (reported in 63%), blinding (33%), and sample size calculation (0%). As a result, risk of bias (assessed using SYRCLE’s risk of bias tool) was unclear in the vast majority of studies. We conclude that metformin limits infarct-size and improves cardiac function in animal models of myocardial infarction, but our confidence in the evidence is lowered by the unclear risk of bias and residual unexplained heterogeneity. We recommend an adequately powered, high quality confirmatory animal study to precede a randomized controlled trial of acute administration of metformin in patients undergoing reperfusion for acute myocardial infarction. |
format | Online Article Text |
id | pubmed-5568412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55684122017-09-09 A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction Hesen, Nienke A. Riksen, Niels P. Aalders, Bart Ritskes-Hoitinga, Merel El Messaoudi, Saloua Wever, Kimberley E. PLoS One Research Article Metformin improves cardiovascular prognosis in patients with diabetes mellitus, compared to alternative glucose-lowering drugs, despite similar glycemic control. Direct cardiovascular protective properties have therefore been proposed, and studied in preclinical models of myocardial infarction. We now aim to critically assess the quality and outcome of these studies. We present a systematic review, quality assessment and meta-analysis of the effect of metformin in animal studies of experimental myocardial infarction. Through a comprehensive search in Pubmed and EMBASE, we identified 27 studies, 11 reporting on ex vivo experiments and 18 reporting on in vivo experiments. The primary endpoint infarct size as percentage of area at risk was significantly reduced by metformin in vivo (MD -18.11[-24.09,-12.14]) and ex vivo (MD -18.70[-25.39, -12.02]). Metformin improved the secondary endpoints left ventricular ejection fraction (LVEF) and left ventricular end systolic diameter. A borderline significant effect on mortality was observed, and there was no overall effect on cardiac hypertrophy. Subgroup analyses could be performed for comorbidity and timing of treatment (infarct size and mortality) and species and duration of ischemia (LVEF), but none of these variables accounted for significant amounts of heterogeneity. Reporting of possible sources of bias was extremely poor, including randomization (reported in 63%), blinding (33%), and sample size calculation (0%). As a result, risk of bias (assessed using SYRCLE’s risk of bias tool) was unclear in the vast majority of studies. We conclude that metformin limits infarct-size and improves cardiac function in animal models of myocardial infarction, but our confidence in the evidence is lowered by the unclear risk of bias and residual unexplained heterogeneity. We recommend an adequately powered, high quality confirmatory animal study to precede a randomized controlled trial of acute administration of metformin in patients undergoing reperfusion for acute myocardial infarction. Public Library of Science 2017-08-23 /pmc/articles/PMC5568412/ /pubmed/28832637 http://dx.doi.org/10.1371/journal.pone.0183664 Text en © 2017 Hesen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hesen, Nienke A. Riksen, Niels P. Aalders, Bart Ritskes-Hoitinga, Merel El Messaoudi, Saloua Wever, Kimberley E. A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title | A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title_full | A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title_fullStr | A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title_full_unstemmed | A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title_short | A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
title_sort | systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568412/ https://www.ncbi.nlm.nih.gov/pubmed/28832637 http://dx.doi.org/10.1371/journal.pone.0183664 |
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