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Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study
BACKGROUND: As atopic dermatitis (AD) has been found to be related to various comorbidities as well as substantial patient burden, questions of a possible relationship between AD and nonallergic diseases beyond allergic diseases have also been raised. OBJECTIVE: The aim of this nationwide matched co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937456/ https://www.ncbi.nlm.nih.gov/pubmed/36800327 http://dx.doi.org/10.1371/journal.pone.0281883 |
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author | Lee, Seung Won Park, Jiwon Kim, Hayeon Jung, Yong Woo Baek, Yoo Sang Lim, Yejee Kim, Kyungim |
author_facet | Lee, Seung Won Park, Jiwon Kim, Hayeon Jung, Yong Woo Baek, Yoo Sang Lim, Yejee Kim, Kyungim |
author_sort | Lee, Seung Won |
collection | PubMed |
description | BACKGROUND: As atopic dermatitis (AD) has been found to be related to various comorbidities as well as substantial patient burden, questions of a possible relationship between AD and nonallergic diseases beyond allergic diseases have also been raised. OBJECTIVE: The aim of this nationwide matched cohort study was to evaluate whether AD would increase the development of gastroesophageal reflux disease (GERD). METHODS: Patients diagnosed with AD were identified from the National Health Insurance Service-National Sample Cohort (NHIS-NSC) 2.0 database in South Korea from 2002 to 2015. Finally, 9,164 adults with AD (≥20 years old) and age, sex, household income, region of residence, disability, and baseline year-matched 9,164 controls were included in the analysis. Hazard ratio (HR) with 95% confidence interval (CI) for the development of GERD was estimated using a Cox proportional hazard regression model. RESULTS: Overall, 12.3% of the patients in the AD group developed GERD, whereas 10.4% of the individuals in the control group developed GERD. The results of the adjusted model revealed that patients with AD had a significantly increased risk of developing GERD (adjusted HR, 1.15; 95% CI, 1.06–1.26) compared with the matched controls. Increased risk of developing GERD was consistent in subgroup analyses by sex or age groups under 60 years old as well as all the sensitivity analyses performed. CONCLUSIONS: This study suggested that appropriate management should be considered in adults with AD to prevent GERD, because AD was found to be associated with an increased risk of subsequent GERD. |
format | Online Article Text |
id | pubmed-9937456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99374562023-02-18 Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study Lee, Seung Won Park, Jiwon Kim, Hayeon Jung, Yong Woo Baek, Yoo Sang Lim, Yejee Kim, Kyungim PLoS One Research Article BACKGROUND: As atopic dermatitis (AD) has been found to be related to various comorbidities as well as substantial patient burden, questions of a possible relationship between AD and nonallergic diseases beyond allergic diseases have also been raised. OBJECTIVE: The aim of this nationwide matched cohort study was to evaluate whether AD would increase the development of gastroesophageal reflux disease (GERD). METHODS: Patients diagnosed with AD were identified from the National Health Insurance Service-National Sample Cohort (NHIS-NSC) 2.0 database in South Korea from 2002 to 2015. Finally, 9,164 adults with AD (≥20 years old) and age, sex, household income, region of residence, disability, and baseline year-matched 9,164 controls were included in the analysis. Hazard ratio (HR) with 95% confidence interval (CI) for the development of GERD was estimated using a Cox proportional hazard regression model. RESULTS: Overall, 12.3% of the patients in the AD group developed GERD, whereas 10.4% of the individuals in the control group developed GERD. The results of the adjusted model revealed that patients with AD had a significantly increased risk of developing GERD (adjusted HR, 1.15; 95% CI, 1.06–1.26) compared with the matched controls. Increased risk of developing GERD was consistent in subgroup analyses by sex or age groups under 60 years old as well as all the sensitivity analyses performed. CONCLUSIONS: This study suggested that appropriate management should be considered in adults with AD to prevent GERD, because AD was found to be associated with an increased risk of subsequent GERD. Public Library of Science 2023-02-17 /pmc/articles/PMC9937456/ /pubmed/36800327 http://dx.doi.org/10.1371/journal.pone.0281883 Text en © 2023 Lee et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Lee, Seung Won Park, Jiwon Kim, Hayeon Jung, Yong Woo Baek, Yoo Sang Lim, Yejee Kim, Kyungim Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title | Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title_full | Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title_fullStr | Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title_full_unstemmed | Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title_short | Atopic dermatitis and risk of gastroesophageal reflux disease: A nationwide population-based study |
title_sort | atopic dermatitis and risk of gastroesophageal reflux disease: a nationwide population-based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937456/ https://www.ncbi.nlm.nih.gov/pubmed/36800327 http://dx.doi.org/10.1371/journal.pone.0281883 |
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