A1 Journal article (refereed)
Mortality associations with DNA methylation-based biological aging and physical functioning measures across a 20-year follow-up period (2023)


Föhr, T., Waller, K., Viljanen, A., Rantanen, T., Kaprio, J., Ollikainen, M., & Sillanpää, E. (2023). Mortality associations with DNA methylation-based biological aging and physical functioning measures across a 20-year follow-up period. Journals of Gerontology Series A : Biological Sciences and Medical Sciences, 78(8), 1489-1496. https://doi.org/10.1093/gerona/glad026


JYU authors or editors


Publication details

All authors or editorsFöhr, Tiina; Waller, Katja; Viljanen, Anne; Rantanen, Taina; Kaprio, Jaakko; Ollikainen, Miina; Sillanpää, Elina

Journal or seriesJournals of Gerontology Series A : Biological Sciences and Medical Sciences

ISSN1079-5006

eISSN1758-535X

Publication year2023

Publication date22/01/2023

Volume78

Issue number8

Pages range1489-1496

PublisherOxford University Press (OUP)

Publication countryUnited States

Publication languageEnglish

DOIhttps://doi.org/10.1093/gerona/glad026

Publication open accessOpenly available

Publication channel open accessPartially open access channel

Publication is parallel published (JYX)https://jyx.jyu.fi/handle/123456789/88431


Abstract

Background
Measures of biological aging range from DNA methylation (DNAm)-based estimates to measures of physical abilities. The purpose of this study was to compare DNAm- and physical functioning-based measures of biological aging in predicting mortality.

Methods
We studied 63- to 76-year-old women (N = 395) from the Finnish Twin Study on Aging (FITSA). Participants’ biological age (epigenetic clocks DNAm GrimAge and DunedinPACE) was estimated using blood DNAm data. Tests of physical functioning conducted under standardized laboratory conditions included the Timed Up and Go (TUG) test and 10-m walk test. Mortality hazard ratios (HRs) were calculated per every one standard deviation (SD) increase in the predictor. Cox regression models were conducted for individuals and twin pairs, the latter controlling for underlying genetic effects. The models were adjusted for known lifestyle predictors of mortality.

Results
During the follow-up period (mean 17.0 years, range 0.2–20.3), 187 participants died. In both the individual-based and pairwise analyses, GrimAge and both functional biomarkers of aging were associated with mortality independent of family relatedness, chronological age, physical activity, body mass index, smoking, education, or chronic diseases. In a model including both the DNAm-based measures and functional biomarkers of aging, GrimAge and TUG remained predictive.

Conclusions
The findings suggest that DNAm GrimAge and the TUG test are strong predictors of mortality independent of each other’s and genetic influences. DNAm-based measures and functional tests capture different aspects of the aging process and thus complement each other as measures of biological aging in predicting mortality.


Keywordstwinsepigeneticsepigenetic inheritancewalking (motion)ageingmortalitygenome

Free keywordsepigenetic clock; Timed Up and Go test; walking speed; twins


Contributing organizations


Related projects


Ministry reportingYes

Reporting Year2023

Preliminary JUFO rating3


Last updated on 2024-22-04 at 18:37