A systematic review and meta-analysis of the protective effects of metformin in experimental myocardial infarction

Autor: Niels P. Riksen, Merel Ritskes-Hoitinga, Kimberley E. Wever, Saloua El Messaoudi, Michelle A. E. Brouwer, Bart Aalders, Nienke A. Hesen
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Critical Care and Emergency Medicine
Swine
Vascular damage Radboud Institute for Health Sciences [Radboudumc 16]
Myocardial Infarction
lcsh:Medicine
030204 cardiovascular system & hematology
Vascular Medicine
law.invention
Mice
0302 clinical medicine
Mathematical and Statistical Techniques
Endocrinology
Randomized controlled trial
law
Ischemia
Clinical endpoint
Medicine and Health Sciences
Myocardial infarction
lcsh:Science
Multidisciplinary
Ejection fraction
Vascular damage Radboud Institute for Molecular Life Sciences [Radboudumc 16]
Heart
Metformin
Meta-analysis
Physical Sciences
Cardiology
Rabbits
Anatomy
Statistics (Mathematics)
medicine.drug
Research Article
Cardiac function curve
medicine.medical_specialty
Endocrine Disorders
Cardiac Ventricles
Cardiac Hypertrophy
In Vitro Techniques
Research and Analysis Methods
03 medical and health sciences
Internal medicine
Diabetes mellitus
medicine
Diabetes Mellitus
Animals
Statistical Methods
business.industry
lcsh:R
Correction
Biology and Life Sciences
medicine.disease
Rats
Reconstructive and regenerative medicine Radboud Institute for Health Sciences [Radboudumc 10]
030104 developmental biology
Metabolic Disorders
Reperfusion
Animal Studies
Cardiovascular Anatomy
lcsh:Q
business
Mathematics
Meta-Analysis
Zdroj: PLoS ONE
PLoS One, 12
PLoS ONE, Vol 12, Iss 8, p e0183664 (2017)
PLoS One, 12, 8
ISSN: 1932-6203
Popis: Contains fulltext : 177026.pdf (Publisher’s version ) (Open Access) 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.
Databáze: OpenAIRE