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Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease

BACKGROUND: Whether the associations of time spent in screen-based sedentary activities with CHD vary by genetic susceptibility is currently unknown. The objective of this study was to examine the interplay of genetic susceptibility to CHD and two prevalent types of screen-based sedentary activities...

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Autores principales: Kim, Youngwon, Yeung, Shiu Lun Au, Sharp, Stephen J., Wang, Mengyao, Jang, Haeyoon, Luo, Shan, Brage, Soren, Wijndaele, Katrien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126635/
https://www.ncbi.nlm.nih.gov/pubmed/35606845
http://dx.doi.org/10.1186/s12916-022-02380-7
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author Kim, Youngwon
Yeung, Shiu Lun Au
Sharp, Stephen J.
Wang, Mengyao
Jang, Haeyoon
Luo, Shan
Brage, Soren
Wijndaele, Katrien
author_facet Kim, Youngwon
Yeung, Shiu Lun Au
Sharp, Stephen J.
Wang, Mengyao
Jang, Haeyoon
Luo, Shan
Brage, Soren
Wijndaele, Katrien
author_sort Kim, Youngwon
collection PubMed
description BACKGROUND: Whether the associations of time spent in screen-based sedentary activities with CHD vary by genetic susceptibility is currently unknown. The objective of this study was to examine the interplay of genetic susceptibility to CHD and two prevalent types of screen-based sedentary activities (television [TV] viewing and computer use) for CHD incidence. METHODS: This prospective cohort study included 373,026 individuals of European ancestry without prevalent CHD/stroke from UK Biobank data. Genetic susceptibility to CHD was assessed using weighted polygenic risk scores, calculated by summing the number of risk-increasing alleles among 300 single-nucleotide polymorphisms, multiplied by their corresponding effect estimates. TV viewing and computer use were assessed through touch-screen questionnaires. CHD incidence (n=9185) was adjudicated over a median 12.6-year follow-up. RESULTS: Compared with ≥4h/day of TV viewing, the hazard ratio of CHD was 0.84 (95% confidence interval [CI] 0.79–0.90) and 0.94 (0.90–0.99) for ≤1h/day and 2–3h/day of TV viewing, respectively, after adjusting for confounders including the genetic risk. CHD hazards were higher for medium and high genetic risk than for low genetic risk. Across all levels of genetic risk including high-genetic risk, ≤1h/day of TV viewing had lower CHD hazards, compared with ≥4h/day: no evidence of interaction between genetic risk and TV viewing (p value: 0.362). Estimates of the population attributable fraction (PAF) suggested that 10.9% (95% CI 6.1–15.3%) of CHD could be prevented if TV viewing time were reduced to ≤1h/day, assuming causality. The PAF values were relatively larger for medium-to-high genetic risk than for low genetic risk, although the CIs were wide and overlapping. No associations were observed for computer use. CONCLUSIONS: Less TV viewing time was associated with lower CHD risk independently of genetic risk. Clinical trials targeted at individuals with high genetic susceptibility should consider reducing TV viewing as as a behavioural target for prevention of an early onset of cardiovascular events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02380-7.
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spelling pubmed-91266352022-05-24 Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease Kim, Youngwon Yeung, Shiu Lun Au Sharp, Stephen J. Wang, Mengyao Jang, Haeyoon Luo, Shan Brage, Soren Wijndaele, Katrien BMC Med Research Article BACKGROUND: Whether the associations of time spent in screen-based sedentary activities with CHD vary by genetic susceptibility is currently unknown. The objective of this study was to examine the interplay of genetic susceptibility to CHD and two prevalent types of screen-based sedentary activities (television [TV] viewing and computer use) for CHD incidence. METHODS: This prospective cohort study included 373,026 individuals of European ancestry without prevalent CHD/stroke from UK Biobank data. Genetic susceptibility to CHD was assessed using weighted polygenic risk scores, calculated by summing the number of risk-increasing alleles among 300 single-nucleotide polymorphisms, multiplied by their corresponding effect estimates. TV viewing and computer use were assessed through touch-screen questionnaires. CHD incidence (n=9185) was adjudicated over a median 12.6-year follow-up. RESULTS: Compared with ≥4h/day of TV viewing, the hazard ratio of CHD was 0.84 (95% confidence interval [CI] 0.79–0.90) and 0.94 (0.90–0.99) for ≤1h/day and 2–3h/day of TV viewing, respectively, after adjusting for confounders including the genetic risk. CHD hazards were higher for medium and high genetic risk than for low genetic risk. Across all levels of genetic risk including high-genetic risk, ≤1h/day of TV viewing had lower CHD hazards, compared with ≥4h/day: no evidence of interaction between genetic risk and TV viewing (p value: 0.362). Estimates of the population attributable fraction (PAF) suggested that 10.9% (95% CI 6.1–15.3%) of CHD could be prevented if TV viewing time were reduced to ≤1h/day, assuming causality. The PAF values were relatively larger for medium-to-high genetic risk than for low genetic risk, although the CIs were wide and overlapping. No associations were observed for computer use. CONCLUSIONS: Less TV viewing time was associated with lower CHD risk independently of genetic risk. Clinical trials targeted at individuals with high genetic susceptibility should consider reducing TV viewing as as a behavioural target for prevention of an early onset of cardiovascular events. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02380-7. BioMed Central 2022-05-24 /pmc/articles/PMC9126635/ /pubmed/35606845 http://dx.doi.org/10.1186/s12916-022-02380-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kim, Youngwon
Yeung, Shiu Lun Au
Sharp, Stephen J.
Wang, Mengyao
Jang, Haeyoon
Luo, Shan
Brage, Soren
Wijndaele, Katrien
Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title_full Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title_fullStr Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title_full_unstemmed Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title_short Genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
title_sort genetic susceptibility, screen-based sedentary activities and incidence of coronary heart disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126635/
https://www.ncbi.nlm.nih.gov/pubmed/35606845
http://dx.doi.org/10.1186/s12916-022-02380-7
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