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Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort

BACKGROUND: Both genetic and lifestyle factors contribute to the development of asthma, but whether unfavourable lifestyle is associated with similar increases in risk of developing asthma among individuals with varying genetic risk levels remains unknown. METHODS: A healthy lifestyle score was cons...

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Autores principales: Liang, Huaying, Jing, Danrong, Zhu, Yiqun, Li, Dianwu, Zhou, Xin, Tu, Wei, Liu, Hong, Pan, Pinhua, Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086697/
https://www.ncbi.nlm.nih.gov/pubmed/37057096
http://dx.doi.org/10.1183/23120541.00499-2022
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author Liang, Huaying
Jing, Danrong
Zhu, Yiqun
Li, Dianwu
Zhou, Xin
Tu, Wei
Liu, Hong
Pan, Pinhua
Zhang, Yan
author_facet Liang, Huaying
Jing, Danrong
Zhu, Yiqun
Li, Dianwu
Zhou, Xin
Tu, Wei
Liu, Hong
Pan, Pinhua
Zhang, Yan
author_sort Liang, Huaying
collection PubMed
description BACKGROUND: Both genetic and lifestyle factors contribute to the development of asthma, but whether unfavourable lifestyle is associated with similar increases in risk of developing asthma among individuals with varying genetic risk levels remains unknown. METHODS: A healthy lifestyle score was constructed using body mass index, smoking status, physical activities and dietary pattern to further categorise into ideal, intermediate and poor groups. Genetic risk of asthma was also categorised as three groups based on the tertiles of polygenic risk score established using 212 reported and verified single-nucleotide polymorphisms of European ancestry in the UK Biobank study. We examined the risk of incident asthma related with each lifestyle level in each genetic risk group by Cox regression models. RESULTS: Finally, 327 124 participants without baseline asthma were included, and 157 320 (48.1%) were male. During follow-up, 6238 participants (1.9%) developed asthma. Compared to ideal lifestyle in a low genetic risk group, poor lifestyle was associated with a hazard ratio of up to 3.87 (95% CI, 2.98–5.02) for developing asthma in a high genetic risk group. There was interaction between genetic risk and lifestyle, and the population-attributable fraction of lifestyle and genetic risk were 30.2% and 30.0% respectively. CONCLUSION: In this large contemporary population, lifestyle and genetic factors jointly play critical roles in the development of asthma, and the effect values of lifestyle on incident adult-onset asthma were greater than that of genetic risk. Our findings highlighted the necessity of a comprehensive intervention for the prevention of asthma despite the genetic risk.
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spelling pubmed-100866972023-04-12 Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort Liang, Huaying Jing, Danrong Zhu, Yiqun Li, Dianwu Zhou, Xin Tu, Wei Liu, Hong Pan, Pinhua Zhang, Yan ERJ Open Res Original Research Articles BACKGROUND: Both genetic and lifestyle factors contribute to the development of asthma, but whether unfavourable lifestyle is associated with similar increases in risk of developing asthma among individuals with varying genetic risk levels remains unknown. METHODS: A healthy lifestyle score was constructed using body mass index, smoking status, physical activities and dietary pattern to further categorise into ideal, intermediate and poor groups. Genetic risk of asthma was also categorised as three groups based on the tertiles of polygenic risk score established using 212 reported and verified single-nucleotide polymorphisms of European ancestry in the UK Biobank study. We examined the risk of incident asthma related with each lifestyle level in each genetic risk group by Cox regression models. RESULTS: Finally, 327 124 participants without baseline asthma were included, and 157 320 (48.1%) were male. During follow-up, 6238 participants (1.9%) developed asthma. Compared to ideal lifestyle in a low genetic risk group, poor lifestyle was associated with a hazard ratio of up to 3.87 (95% CI, 2.98–5.02) for developing asthma in a high genetic risk group. There was interaction between genetic risk and lifestyle, and the population-attributable fraction of lifestyle and genetic risk were 30.2% and 30.0% respectively. CONCLUSION: In this large contemporary population, lifestyle and genetic factors jointly play critical roles in the development of asthma, and the effect values of lifestyle on incident adult-onset asthma were greater than that of genetic risk. Our findings highlighted the necessity of a comprehensive intervention for the prevention of asthma despite the genetic risk. European Respiratory Society 2023-04-11 /pmc/articles/PMC10086697/ /pubmed/37057096 http://dx.doi.org/10.1183/23120541.00499-2022 Text en Copyright ©The authors 2023 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org)
spellingShingle Original Research Articles
Liang, Huaying
Jing, Danrong
Zhu, Yiqun
Li, Dianwu
Zhou, Xin
Tu, Wei
Liu, Hong
Pan, Pinhua
Zhang, Yan
Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title_full Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title_fullStr Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title_full_unstemmed Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title_short Association of genetic risk and lifestyle with incident adult-onset asthma in the UK Biobank cohort
title_sort association of genetic risk and lifestyle with incident adult-onset asthma in the uk biobank cohort
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086697/
https://www.ncbi.nlm.nih.gov/pubmed/37057096
http://dx.doi.org/10.1183/23120541.00499-2022
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