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Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis

In this study, we aimed to determine the association between gastroesophageal reflux disease (GERD) and subsequent coronary heart disease (CHD) development, if any, and to evaluate whether longer use of proton pump inhibitors (PPIs) increases the risk of CHD. Patients diagnosed with GERD between 200...

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Autores principales: Chen, Chien-Hua, Lin, Cheng-Li, Kao, Chia-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058831/
https://www.ncbi.nlm.nih.gov/pubmed/27399102
http://dx.doi.org/10.1097/MD.0000000000004089
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author Chen, Chien-Hua
Lin, Cheng-Li
Kao, Chia-Hung
author_facet Chen, Chien-Hua
Lin, Cheng-Li
Kao, Chia-Hung
author_sort Chen, Chien-Hua
collection PubMed
description In this study, we aimed to determine the association between gastroesophageal reflux disease (GERD) and subsequent coronary heart disease (CHD) development, if any, and to evaluate whether longer use of proton pump inhibitors (PPIs) increases the risk of CHD. Patients diagnosed with GERD between 2000 and 2011 were identified as the study cohort (n = 12,960). Patients without GERD were randomly selected from the general population, frequency-matched with the study group according to age, sex, and index year, and evaluated as the comparison cohort (n = 51,840). Both cohorts were followed up until the end of 2011 to determine the incidence of CHD. The risk of CHD was evaluated in both groups by using Cox proportional hazards regression models. The GERD patients had a greater probability of CHD than the cohort without GERD did (log-rank test, P < 0.001 and 11.8 vs 6.5 per 1000 person-years). The GERD cohort had a higher risk of CHD than the comparison cohort did after adjustment for age, sex, hypertension, diabetes, hyperlipidemia, alcohol-related illness, stroke, chronic obstructive pulmonary disease, asthma, biliary stone, anxiety, depression, chronic kidney disease, and cirrhosis (adjusted hazard ratio [aHR]: 1.49, 95% confidence interval [CI]: 1.34–1.66). The risk of CHD was greater for the patients treated with PPIs for more than 1 year (aHR = 1.67, 95% CI = 1.34–2.08) than for those treated with PPIs for <1 year (aHR = 1.56, 95% CI = 1.39–1.74). Our population-based cohort study results indicate that GERD was associated with an increased risk of developing CHD, and that PPI use for more than 1 year might increase the risk of CHD.
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spelling pubmed-50588312016-11-18 Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis Chen, Chien-Hua Lin, Cheng-Li Kao, Chia-Hung Medicine (Baltimore) 4500 In this study, we aimed to determine the association between gastroesophageal reflux disease (GERD) and subsequent coronary heart disease (CHD) development, if any, and to evaluate whether longer use of proton pump inhibitors (PPIs) increases the risk of CHD. Patients diagnosed with GERD between 2000 and 2011 were identified as the study cohort (n = 12,960). Patients without GERD were randomly selected from the general population, frequency-matched with the study group according to age, sex, and index year, and evaluated as the comparison cohort (n = 51,840). Both cohorts were followed up until the end of 2011 to determine the incidence of CHD. The risk of CHD was evaluated in both groups by using Cox proportional hazards regression models. The GERD patients had a greater probability of CHD than the cohort without GERD did (log-rank test, P < 0.001 and 11.8 vs 6.5 per 1000 person-years). The GERD cohort had a higher risk of CHD than the comparison cohort did after adjustment for age, sex, hypertension, diabetes, hyperlipidemia, alcohol-related illness, stroke, chronic obstructive pulmonary disease, asthma, biliary stone, anxiety, depression, chronic kidney disease, and cirrhosis (adjusted hazard ratio [aHR]: 1.49, 95% confidence interval [CI]: 1.34–1.66). The risk of CHD was greater for the patients treated with PPIs for more than 1 year (aHR = 1.67, 95% CI = 1.34–2.08) than for those treated with PPIs for <1 year (aHR = 1.56, 95% CI = 1.39–1.74). Our population-based cohort study results indicate that GERD was associated with an increased risk of developing CHD, and that PPI use for more than 1 year might increase the risk of CHD. Wolters Kluwer Health 2016-07-08 /pmc/articles/PMC5058831/ /pubmed/27399102 http://dx.doi.org/10.1097/MD.0000000000004089 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 4500
Chen, Chien-Hua
Lin, Cheng-Li
Kao, Chia-Hung
Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title_full Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title_fullStr Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title_full_unstemmed Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title_short Association between gastroesophageal reflux disease and coronary heart disease: A nationwide population-based analysis
title_sort association between gastroesophageal reflux disease and coronary heart disease: a nationwide population-based analysis
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058831/
https://www.ncbi.nlm.nih.gov/pubmed/27399102
http://dx.doi.org/10.1097/MD.0000000000004089
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