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Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study

We investigated the association between the current use of individual sulphonylureas and the risk of a first‐ever acute myocardial infarction (AMI) and all‐cause mortality, in a population‐based cohort study, using primary care data from the Clinical Practice Research Datalink database (2004‐2012)....

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Autores principales: van Dalem, Judith, Brouwers, Martijn C. G. J., Stehouwer, Coen D. A., Krings, André, Klungel, Olaf H., Driessen, Johanna H. M., de Vries, Frank, Burden, Andrea M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873381/
https://www.ncbi.nlm.nih.gov/pubmed/29171906
http://dx.doi.org/10.1111/dom.13168
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author van Dalem, Judith
Brouwers, Martijn C. G. J.
Stehouwer, Coen D. A.
Krings, André
Klungel, Olaf H.
Driessen, Johanna H. M.
de Vries, Frank
Burden, Andrea M.
author_facet van Dalem, Judith
Brouwers, Martijn C. G. J.
Stehouwer, Coen D. A.
Krings, André
Klungel, Olaf H.
Driessen, Johanna H. M.
de Vries, Frank
Burden, Andrea M.
author_sort van Dalem, Judith
collection PubMed
description We investigated the association between the current use of individual sulphonylureas and the risk of a first‐ever acute myocardial infarction (AMI) and all‐cause mortality, in a population‐based cohort study, using primary care data from the Clinical Practice Research Datalink database (2004‐2012). New users (N = 121 869), aged ≥18 years, with at least one prescription for a non‐insulin antidiabetic agent were included. The first prescription defined start of follow‐up. Time‐dependent Cox proportional hazard models were used to estimate the risk of a first‐ever AMI and all‐cause mortality associated with the use of individual sulphonylureas, and other non‐insulin glucose‐lowering drugs. No differences in risk of a first‐ever AMI (adjusted hazard ratio [HR] 1.02, 95% confidence interval [CI] 0.70‐1.50) or all‐cause mortality (adjusted HR 0.97, 95% CI 0.80‐1.17) were observed when comparing gliclazide use with non‐gliclazide sulphonylurea use. Similar results were found for each individual sulphonylurea. As evidence is accumulating that gliclazide is no safer than other sulphonylureas, current guidelines suggesting superiority should be carefully evaluated.
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spelling pubmed-58733812018-03-31 Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study van Dalem, Judith Brouwers, Martijn C. G. J. Stehouwer, Coen D. A. Krings, André Klungel, Olaf H. Driessen, Johanna H. M. de Vries, Frank Burden, Andrea M. Diabetes Obes Metab Brief Reports We investigated the association between the current use of individual sulphonylureas and the risk of a first‐ever acute myocardial infarction (AMI) and all‐cause mortality, in a population‐based cohort study, using primary care data from the Clinical Practice Research Datalink database (2004‐2012). New users (N = 121 869), aged ≥18 years, with at least one prescription for a non‐insulin antidiabetic agent were included. The first prescription defined start of follow‐up. Time‐dependent Cox proportional hazard models were used to estimate the risk of a first‐ever AMI and all‐cause mortality associated with the use of individual sulphonylureas, and other non‐insulin glucose‐lowering drugs. No differences in risk of a first‐ever AMI (adjusted hazard ratio [HR] 1.02, 95% confidence interval [CI] 0.70‐1.50) or all‐cause mortality (adjusted HR 0.97, 95% CI 0.80‐1.17) were observed when comparing gliclazide use with non‐gliclazide sulphonylurea use. Similar results were found for each individual sulphonylurea. As evidence is accumulating that gliclazide is no safer than other sulphonylureas, current guidelines suggesting superiority should be carefully evaluated. Blackwell Publishing Ltd 2017-12-27 2018-04 /pmc/articles/PMC5873381/ /pubmed/29171906 http://dx.doi.org/10.1111/dom.13168 Text en © 2017 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Reports
van Dalem, Judith
Brouwers, Martijn C. G. J.
Stehouwer, Coen D. A.
Krings, André
Klungel, Olaf H.
Driessen, Johanna H. M.
de Vries, Frank
Burden, Andrea M.
Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title_full Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title_fullStr Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title_full_unstemmed Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title_short Risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: A population‐based cohort study
title_sort risk of a first‐ever acute myocardial infarction and all‐cause mortality with sulphonylurea treatment: a population‐based cohort study
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5873381/
https://www.ncbi.nlm.nih.gov/pubmed/29171906
http://dx.doi.org/10.1111/dom.13168
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