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Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis

BACKGROUND: Atopic diseases and atrial fibrillation (AF) seem to share an underlying inflammatory pathology. To date, some population-based studies have explored the relationship between the two. We aimed to conduct a meta-analysis to examine the role of atopic condition in AF risk. METHODS: All rel...

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Autores principales: Zeng, Rong, Wang, Jing, Liang, Ziting, Zhang, Jintao, Wang, Zihan, Xu, Changjuan, Dong, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468366/
https://www.ncbi.nlm.nih.gov/pubmed/36110420
http://dx.doi.org/10.3389/fcvm.2022.877638
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author Zeng, Rong
Wang, Jing
Liang, Ziting
Zhang, Jintao
Wang, Zihan
Xu, Changjuan
Dong, Liang
author_facet Zeng, Rong
Wang, Jing
Liang, Ziting
Zhang, Jintao
Wang, Zihan
Xu, Changjuan
Dong, Liang
author_sort Zeng, Rong
collection PubMed
description BACKGROUND: Atopic diseases and atrial fibrillation (AF) seem to share an underlying inflammatory pathology. To date, some population-based studies have explored the relationship between the two. We aimed to conduct a meta-analysis to examine the role of atopic condition in AF risk. METHODS: All relevant observational studies in PubMed and EMBASE databases up to November 2021 were searched. In RevMan 5.3, we used random-effects or fixed-effects models to pool the effect sizes of hazard ratio (HR), odds ratio (OR) and their corresponding 95% confidence intervals (95% CI). In addition, I(2) and Cochran Q test were used to evaluate the heterogeneity. RESULTS: A total of 2488 records were retrieved. After screening according to the predetermined criteria, 6 cohort studies and 2 case-control studies were included in this meta-analysis. Herein, the meta-analysis of 6 cohort studies suggested that atopic diseases potentially increased the AF risk with the pooled HR of 1.26 (95%CI,1.14–1.39), while the pooled effect size (OR, 1.04; 95%CI,0.74–1.46) of 2 case-control studies was not statistically significant. Based on the types of atopic diseases, further subgroup analyses of 6 cohort studies revealed that asthma, allergic rhinitis, and atopic dermatitis all potentially increased the risk of subsequent AF with the pooled HR of 1.41 (n = 4; 95%CI, 1.25–1.58), 1.12 (n = 1; 95%CI,1.10–1.14) and 1.06 (n = 3; 95%CI, 1.01–1.12), respectively. CONCLUSION: This meta-analysis demonstrated that patients with atopic diseases have a higher risk of developing AF, particularly those with asthma.
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spelling pubmed-94683662022-09-14 Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis Zeng, Rong Wang, Jing Liang, Ziting Zhang, Jintao Wang, Zihan Xu, Changjuan Dong, Liang Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Atopic diseases and atrial fibrillation (AF) seem to share an underlying inflammatory pathology. To date, some population-based studies have explored the relationship between the two. We aimed to conduct a meta-analysis to examine the role of atopic condition in AF risk. METHODS: All relevant observational studies in PubMed and EMBASE databases up to November 2021 were searched. In RevMan 5.3, we used random-effects or fixed-effects models to pool the effect sizes of hazard ratio (HR), odds ratio (OR) and their corresponding 95% confidence intervals (95% CI). In addition, I(2) and Cochran Q test were used to evaluate the heterogeneity. RESULTS: A total of 2488 records were retrieved. After screening according to the predetermined criteria, 6 cohort studies and 2 case-control studies were included in this meta-analysis. Herein, the meta-analysis of 6 cohort studies suggested that atopic diseases potentially increased the AF risk with the pooled HR of 1.26 (95%CI,1.14–1.39), while the pooled effect size (OR, 1.04; 95%CI,0.74–1.46) of 2 case-control studies was not statistically significant. Based on the types of atopic diseases, further subgroup analyses of 6 cohort studies revealed that asthma, allergic rhinitis, and atopic dermatitis all potentially increased the risk of subsequent AF with the pooled HR of 1.41 (n = 4; 95%CI, 1.25–1.58), 1.12 (n = 1; 95%CI,1.10–1.14) and 1.06 (n = 3; 95%CI, 1.01–1.12), respectively. CONCLUSION: This meta-analysis demonstrated that patients with atopic diseases have a higher risk of developing AF, particularly those with asthma. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9468366/ /pubmed/36110420 http://dx.doi.org/10.3389/fcvm.2022.877638 Text en Copyright © 2022 Zeng, Wang, Liang, Zhang, Wang, Xu and Dong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Zeng, Rong
Wang, Jing
Liang, Ziting
Zhang, Jintao
Wang, Zihan
Xu, Changjuan
Dong, Liang
Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title_full Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title_fullStr Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title_full_unstemmed Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title_short Association of atopic diseases with atrial fibrillation risk: A systematic review and meta-analysis
title_sort association of atopic diseases with atrial fibrillation risk: a systematic review and meta-analysis
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468366/
https://www.ncbi.nlm.nih.gov/pubmed/36110420
http://dx.doi.org/10.3389/fcvm.2022.877638
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