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Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk

BACKGROUND: This study was performed to explore the causal association between asthma and chronic obstructive pulmonary disease(COPD). METHODS: We obtained summary statistics for asthma from 408,442 Europeans in an open genome-wide association study (GWAS) from the UK Biobank to select strongly asso...

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Autores principales: Li, Yuanyuan, Wang, Weina, Zhou, Dengfeng, Lu, Qiaofa, Li, Lili, Zhang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473539/
https://www.ncbi.nlm.nih.gov/pubmed/37656706
http://dx.doi.org/10.1371/journal.pone.0291102
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author Li, Yuanyuan
Wang, Weina
Zhou, Dengfeng
Lu, Qiaofa
Li, Lili
Zhang, Bo
author_facet Li, Yuanyuan
Wang, Weina
Zhou, Dengfeng
Lu, Qiaofa
Li, Lili
Zhang, Bo
author_sort Li, Yuanyuan
collection PubMed
description BACKGROUND: This study was performed to explore the causal association between asthma and chronic obstructive pulmonary disease(COPD). METHODS: We obtained summary statistics for asthma from 408,442 Europeans in an open genome-wide association study (GWAS) from the UK Biobank to select strongly associated single nucleotide polymorphisms that could serve as instrumental variables for asthma (P < 5×10(−8)). Additional summary statistics for COPD were obtained from 193,638 individuals of European ancestry in the GWAS published by FinnGen. Univariable Mendelian randomization(UVMR) analysis was performed using inverse variance weighted (IVW) as the primary method of analysis. The reliability of the results was verified by multivariable MR(MVMR), reverse and replication MR analysis, and sensitivity analysis. RESULTS: In the UVMR analysis, asthma increased the risk of COPD, with an odds ratio (OR) of 1.27 (95% confidence interval (CI) = 1.16–1.39, P = 5.44×10(−7)). Estimates were consistent in MVMR analyses by the adjustments of smoking initiation, age of smoking initiation, cigarettes per day, PM 2.5, and the combination of the above factors. In the reverse MR analysis, there was no evidence of a causal effect of COPD on asthma risk(OR = 1.02, 95% CI = 0.97–1.07, P = 0.3643). In the replication MR analysis, asthma still increased the risk of COPD. Sensitivity analyses validated the robustness of the above associations. CONCLUSIONS: We found that genetically predicted asthma was positively associated with the risk of COPD. Additionally, there was no evidence that COPD increases the risk of asthma. Further clarification of this link and underlying mechanisms is needed to identify feasible measures to promote COPD prevention.
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spelling pubmed-104735392023-09-02 Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk Li, Yuanyuan Wang, Weina Zhou, Dengfeng Lu, Qiaofa Li, Lili Zhang, Bo PLoS One Research Article BACKGROUND: This study was performed to explore the causal association between asthma and chronic obstructive pulmonary disease(COPD). METHODS: We obtained summary statistics for asthma from 408,442 Europeans in an open genome-wide association study (GWAS) from the UK Biobank to select strongly associated single nucleotide polymorphisms that could serve as instrumental variables for asthma (P < 5×10(−8)). Additional summary statistics for COPD were obtained from 193,638 individuals of European ancestry in the GWAS published by FinnGen. Univariable Mendelian randomization(UVMR) analysis was performed using inverse variance weighted (IVW) as the primary method of analysis. The reliability of the results was verified by multivariable MR(MVMR), reverse and replication MR analysis, and sensitivity analysis. RESULTS: In the UVMR analysis, asthma increased the risk of COPD, with an odds ratio (OR) of 1.27 (95% confidence interval (CI) = 1.16–1.39, P = 5.44×10(−7)). Estimates were consistent in MVMR analyses by the adjustments of smoking initiation, age of smoking initiation, cigarettes per day, PM 2.5, and the combination of the above factors. In the reverse MR analysis, there was no evidence of a causal effect of COPD on asthma risk(OR = 1.02, 95% CI = 0.97–1.07, P = 0.3643). In the replication MR analysis, asthma still increased the risk of COPD. Sensitivity analyses validated the robustness of the above associations. CONCLUSIONS: We found that genetically predicted asthma was positively associated with the risk of COPD. Additionally, there was no evidence that COPD increases the risk of asthma. Further clarification of this link and underlying mechanisms is needed to identify feasible measures to promote COPD prevention. Public Library of Science 2023-09-01 /pmc/articles/PMC10473539/ /pubmed/37656706 http://dx.doi.org/10.1371/journal.pone.0291102 Text en © 2023 Li 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
Li, Yuanyuan
Wang, Weina
Zhou, Dengfeng
Lu, Qiaofa
Li, Lili
Zhang, Bo
Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title_full Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title_fullStr Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title_full_unstemmed Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title_short Mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
title_sort mendelian randomization study shows a causal effect of asthma on chronic obstructive pulmonary disease risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473539/
https://www.ncbi.nlm.nih.gov/pubmed/37656706
http://dx.doi.org/10.1371/journal.pone.0291102
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