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Lifetime Smoking and Asthma: A Mendelian Randomization Study

Evidence from clinical and epidemiological studies indicates that asthma is associated with allergic diseases including hay fever, allergic rhinitis, and eczema. Genetic analysis demonstrated that asthma had a positive genetic correlation with allergic diseases. A Mendelian randomization (MR) analys...

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Autores principales: Shen, Ming, Liu, Xin, Li, Guoqi, Li, Zhun, Zhou, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438748/
https://www.ncbi.nlm.nih.gov/pubmed/32903690
http://dx.doi.org/10.3389/fgene.2020.00769
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author Shen, Ming
Liu, Xin
Li, Guoqi
Li, Zhun
Zhou, Hongyu
author_facet Shen, Ming
Liu, Xin
Li, Guoqi
Li, Zhun
Zhou, Hongyu
author_sort Shen, Ming
collection PubMed
description Evidence from clinical and epidemiological studies indicates that asthma is associated with allergic diseases including hay fever, allergic rhinitis, and eczema. Genetic analysis demonstrated that asthma had a positive genetic correlation with allergic diseases. A Mendelian randomization (MR) analysis using the rs16969968 single-nucleotide variant as the instrumental variable indicated that smoking was associated with increased risk of asthma. However, in a different MR analysis, smoking was significantly associated with reduced hay fever and reduced allergic sensitization risk. These findings revealed inconsistencies in the association of smoking with asthma and allergic diseases. Hence, we conducted an updated MR analysis to investigate the causal association between lifetime smoking and asthma risk by using 124 genetic variants as the instrumental variables. No significant pleiotropy was detected using the MR–Egger intercept test. We found that increased lifetime smoking was significantly associated with decreased asthma risk by using the inverse variance weighted (IVW) method (OR = 0.97, 95% CI 0.956–0.986, and P = 1.77E-04), the weighted median regression method (OR = 0.976, 95% CI 0.96–0.994, and P = 8.00E-03), and the MR–Egger method (OR = 0.919, 95% CI 0.847–0.998, and P = 4.5E-02). Importantly, MR pleiotropy residual sum and outlier (MR-PRESSO) MR analysis also indicated a significant association between increased lifetime smoking and decreased asthma risk with OR = 0.971, 95% CI 0.956–0.986, and P = 2.69E-04. After the outlier was removed, MR-PRESSO outlier test further supported the significant association with OR = 0.971, 95% CI 0.959–0.984, P = 1.57E-05.
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spelling pubmed-74387482020-09-03 Lifetime Smoking and Asthma: A Mendelian Randomization Study Shen, Ming Liu, Xin Li, Guoqi Li, Zhun Zhou, Hongyu Front Genet Genetics Evidence from clinical and epidemiological studies indicates that asthma is associated with allergic diseases including hay fever, allergic rhinitis, and eczema. Genetic analysis demonstrated that asthma had a positive genetic correlation with allergic diseases. A Mendelian randomization (MR) analysis using the rs16969968 single-nucleotide variant as the instrumental variable indicated that smoking was associated with increased risk of asthma. However, in a different MR analysis, smoking was significantly associated with reduced hay fever and reduced allergic sensitization risk. These findings revealed inconsistencies in the association of smoking with asthma and allergic diseases. Hence, we conducted an updated MR analysis to investigate the causal association between lifetime smoking and asthma risk by using 124 genetic variants as the instrumental variables. No significant pleiotropy was detected using the MR–Egger intercept test. We found that increased lifetime smoking was significantly associated with decreased asthma risk by using the inverse variance weighted (IVW) method (OR = 0.97, 95% CI 0.956–0.986, and P = 1.77E-04), the weighted median regression method (OR = 0.976, 95% CI 0.96–0.994, and P = 8.00E-03), and the MR–Egger method (OR = 0.919, 95% CI 0.847–0.998, and P = 4.5E-02). Importantly, MR pleiotropy residual sum and outlier (MR-PRESSO) MR analysis also indicated a significant association between increased lifetime smoking and decreased asthma risk with OR = 0.971, 95% CI 0.956–0.986, and P = 2.69E-04. After the outlier was removed, MR-PRESSO outlier test further supported the significant association with OR = 0.971, 95% CI 0.959–0.984, P = 1.57E-05. Frontiers Media S.A. 2020-08-04 /pmc/articles/PMC7438748/ /pubmed/32903690 http://dx.doi.org/10.3389/fgene.2020.00769 Text en Copyright © 2020 Shen, Liu, Li, Li and Zhou. http://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 Genetics
Shen, Ming
Liu, Xin
Li, Guoqi
Li, Zhun
Zhou, Hongyu
Lifetime Smoking and Asthma: A Mendelian Randomization Study
title Lifetime Smoking and Asthma: A Mendelian Randomization Study
title_full Lifetime Smoking and Asthma: A Mendelian Randomization Study
title_fullStr Lifetime Smoking and Asthma: A Mendelian Randomization Study
title_full_unstemmed Lifetime Smoking and Asthma: A Mendelian Randomization Study
title_short Lifetime Smoking and Asthma: A Mendelian Randomization Study
title_sort lifetime smoking and asthma: a mendelian randomization study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438748/
https://www.ncbi.nlm.nih.gov/pubmed/32903690
http://dx.doi.org/10.3389/fgene.2020.00769
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