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Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging

BACKGROUND: The trajectory of frailty in older adults is important to public health; therefore, markers that may help predict this and other important outcomes could be beneficial. Epigenetic clocks have been developed and are associated with various health-related outcomes and sociodemographic fact...

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Autores principales: Verschoor, Chris P., Lin, David T. S., Kobor, Michael S., Mian, Oxana, Ma, Jinhui, Pare, Guillaume, Ybazeta, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381580/
https://www.ncbi.nlm.nih.gov/pubmed/34425884
http://dx.doi.org/10.1186/s13148-021-01150-1
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author Verschoor, Chris P.
Lin, David T. S.
Kobor, Michael S.
Mian, Oxana
Ma, Jinhui
Pare, Guillaume
Ybazeta, Gustavo
author_facet Verschoor, Chris P.
Lin, David T. S.
Kobor, Michael S.
Mian, Oxana
Ma, Jinhui
Pare, Guillaume
Ybazeta, Gustavo
author_sort Verschoor, Chris P.
collection PubMed
description BACKGROUND: The trajectory of frailty in older adults is important to public health; therefore, markers that may help predict this and other important outcomes could be beneficial. Epigenetic clocks have been developed and are associated with various health-related outcomes and sociodemographic factors, but associations with frailty are poorly described. Further, it is uncertain whether newer generations of epigenetic clocks, trained on variables other than chronological age, would be more strongly associated with frailty than earlier developed clocks. Using data from the Canadian Longitudinal Study on Aging (CLSA), we tested the hypothesis that clocks trained on phenotypic markers of health or mortality (i.e., Dunedin PoAm, GrimAge, PhenoAge and Zhang in Nat Commun 8:14617, 2017) would best predict changes in a 76-item frailty index (FI) over a 3-year interval, as compared to clocks trained on chronological age (i.e., Hannum in Mol Cell 49:359–367, 2013, Horvath in Genome Biol 14:R115, 2013, Lin in Aging 8:394–401, 2016, and Yang Genome Biol 17:205, 2016). RESULTS: We show that in 1446 participants, phenotype/mortality-trained clocks outperformed age-trained clocks with regard to the association with baseline frailty (mean = 0.141, SD = 0.075), the greatest of which is GrimAge, where a 1-SD increase in ΔGrimAge (i.e., the difference from chronological age) was associated with a 0.020 increase in frailty (95% CI 0.016, 0.024), or ~ 27% relative to the SD in frailty. Only GrimAge and Hannum (Mol Cell 49:359–367, 2013) were significantly associated with change in frailty over time, where a 1-SD increase in ΔGrimAge and ΔHannum 2013 was associated with a 0.0030 (95% CI 0.0007, 0.0050) and 0.0028 (95% CI 0.0007, 0.0050) increase over 3 years, respectively, or ~ 7% relative to the SD in frailty change. CONCLUSION: Both prevalence and change in frailty are associated with increased epigenetic age. However, not all clocks are equally sensitive to these outcomes and depend on their underlying relationship with chronological age, healthspan and lifespan. Certain clocks were significantly associated with relatively short-term changes in frailty, thereby supporting their utility in initiatives and interventions to promote healthy aging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01150-1.
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spelling pubmed-83815802021-08-23 Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging Verschoor, Chris P. Lin, David T. S. Kobor, Michael S. Mian, Oxana Ma, Jinhui Pare, Guillaume Ybazeta, Gustavo Clin Epigenetics Research BACKGROUND: The trajectory of frailty in older adults is important to public health; therefore, markers that may help predict this and other important outcomes could be beneficial. Epigenetic clocks have been developed and are associated with various health-related outcomes and sociodemographic factors, but associations with frailty are poorly described. Further, it is uncertain whether newer generations of epigenetic clocks, trained on variables other than chronological age, would be more strongly associated with frailty than earlier developed clocks. Using data from the Canadian Longitudinal Study on Aging (CLSA), we tested the hypothesis that clocks trained on phenotypic markers of health or mortality (i.e., Dunedin PoAm, GrimAge, PhenoAge and Zhang in Nat Commun 8:14617, 2017) would best predict changes in a 76-item frailty index (FI) over a 3-year interval, as compared to clocks trained on chronological age (i.e., Hannum in Mol Cell 49:359–367, 2013, Horvath in Genome Biol 14:R115, 2013, Lin in Aging 8:394–401, 2016, and Yang Genome Biol 17:205, 2016). RESULTS: We show that in 1446 participants, phenotype/mortality-trained clocks outperformed age-trained clocks with regard to the association with baseline frailty (mean = 0.141, SD = 0.075), the greatest of which is GrimAge, where a 1-SD increase in ΔGrimAge (i.e., the difference from chronological age) was associated with a 0.020 increase in frailty (95% CI 0.016, 0.024), or ~ 27% relative to the SD in frailty. Only GrimAge and Hannum (Mol Cell 49:359–367, 2013) were significantly associated with change in frailty over time, where a 1-SD increase in ΔGrimAge and ΔHannum 2013 was associated with a 0.0030 (95% CI 0.0007, 0.0050) and 0.0028 (95% CI 0.0007, 0.0050) increase over 3 years, respectively, or ~ 7% relative to the SD in frailty change. CONCLUSION: Both prevalence and change in frailty are associated with increased epigenetic age. However, not all clocks are equally sensitive to these outcomes and depend on their underlying relationship with chronological age, healthspan and lifespan. Certain clocks were significantly associated with relatively short-term changes in frailty, thereby supporting their utility in initiatives and interventions to promote healthy aging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01150-1. BioMed Central 2021-08-23 /pmc/articles/PMC8381580/ /pubmed/34425884 http://dx.doi.org/10.1186/s13148-021-01150-1 Text en © The Author(s) 2021 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
Verschoor, Chris P.
Lin, David T. S.
Kobor, Michael S.
Mian, Oxana
Ma, Jinhui
Pare, Guillaume
Ybazeta, Gustavo
Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title_full Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title_fullStr Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title_full_unstemmed Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title_short Epigenetic age is associated with baseline and 3-year change in frailty in the Canadian Longitudinal Study on Aging
title_sort epigenetic age is associated with baseline and 3-year change in frailty in the canadian longitudinal study on aging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381580/
https://www.ncbi.nlm.nih.gov/pubmed/34425884
http://dx.doi.org/10.1186/s13148-021-01150-1
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