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DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936

BACKGROUND: The biological mechanisms underlying frailty in older people are poorly understood. There is some evidence to suggest that DNA methylation patterns may be altered in frail individuals. METHODS: Participants were 791 people aged 70 years from the Lothian Birth Cohort 1936. DNA methylation...

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Autores principales: Gale, Catharine R., Marioni, Riccardo E., Harris, Sarah E., Starr, John M., Deary, Ian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091041/
https://www.ncbi.nlm.nih.gov/pubmed/30075802
http://dx.doi.org/10.1186/s13148-018-0538-4
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author Gale, Catharine R.
Marioni, Riccardo E.
Harris, Sarah E.
Starr, John M.
Deary, Ian J.
author_facet Gale, Catharine R.
Marioni, Riccardo E.
Harris, Sarah E.
Starr, John M.
Deary, Ian J.
author_sort Gale, Catharine R.
collection PubMed
description BACKGROUND: The biological mechanisms underlying frailty in older people are poorly understood. There is some evidence to suggest that DNA methylation patterns may be altered in frail individuals. METHODS: Participants were 791 people aged 70 years from the Lothian Birth Cohort 1936. DNA methylation was measured in whole blood. Biological age was estimated using two measures of DNA methylation-based age acceleration-extrinsic and intrinsic epigenetic age acceleration. We carried out an epigenome-wide association study of physical frailty, as defined by the Fried phenotype. Multinomial logistic regression was used to calculate relative risk ratios for being physically frail or pre-frail according to epigenetic age acceleration. RESULTS: There was a single significant (P = 1.16 × 10–7) association in the epigenome-wide association study comparing frail versus not frail. The same CpG was not significant when comparing pre-frail versus not frail. Greater extrinsic epigenetic age acceleration was associated with an increased risk of being physically frail, but not of being pre-frail. For a year increase in extrinsic epigenetic age acceleration, age- and sex-adjusted relative risk ratios (95% CI) for being physically frail or pre-frail were 1.06 (1.02, 1.10) and 1.02 (1.00, 1.04), respectively. After further adjustment for smoking and chronic disease, the association with physical frailty remained significant. Intrinsic epigenetic age acceleration was not associated with physical frailty status. CONCLUSIONS: People who are biologically older, as indexed by greater extrinsic epigenetic age acceleration, are more likely to be physically frail. Future research will need to investigate whether epigenetic age acceleration plays a causal role in the onset of physical frailty. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0538-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-60910412018-08-17 DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936 Gale, Catharine R. Marioni, Riccardo E. Harris, Sarah E. Starr, John M. Deary, Ian J. Clin Epigenetics Short Report BACKGROUND: The biological mechanisms underlying frailty in older people are poorly understood. There is some evidence to suggest that DNA methylation patterns may be altered in frail individuals. METHODS: Participants were 791 people aged 70 years from the Lothian Birth Cohort 1936. DNA methylation was measured in whole blood. Biological age was estimated using two measures of DNA methylation-based age acceleration-extrinsic and intrinsic epigenetic age acceleration. We carried out an epigenome-wide association study of physical frailty, as defined by the Fried phenotype. Multinomial logistic regression was used to calculate relative risk ratios for being physically frail or pre-frail according to epigenetic age acceleration. RESULTS: There was a single significant (P = 1.16 × 10–7) association in the epigenome-wide association study comparing frail versus not frail. The same CpG was not significant when comparing pre-frail versus not frail. Greater extrinsic epigenetic age acceleration was associated with an increased risk of being physically frail, but not of being pre-frail. For a year increase in extrinsic epigenetic age acceleration, age- and sex-adjusted relative risk ratios (95% CI) for being physically frail or pre-frail were 1.06 (1.02, 1.10) and 1.02 (1.00, 1.04), respectively. After further adjustment for smoking and chronic disease, the association with physical frailty remained significant. Intrinsic epigenetic age acceleration was not associated with physical frailty status. CONCLUSIONS: People who are biologically older, as indexed by greater extrinsic epigenetic age acceleration, are more likely to be physically frail. Future research will need to investigate whether epigenetic age acceleration plays a causal role in the onset of physical frailty. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0538-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-03 /pmc/articles/PMC6091041/ /pubmed/30075802 http://dx.doi.org/10.1186/s13148-018-0538-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Gale, Catharine R.
Marioni, Riccardo E.
Harris, Sarah E.
Starr, John M.
Deary, Ian J.
DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title_full DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title_fullStr DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title_full_unstemmed DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title_short DNA methylation and the epigenetic clock in relation to physical frailty in older people: the Lothian Birth Cohort 1936
title_sort dna methylation and the epigenetic clock in relation to physical frailty in older people: the lothian birth cohort 1936
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091041/
https://www.ncbi.nlm.nih.gov/pubmed/30075802
http://dx.doi.org/10.1186/s13148-018-0538-4
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