A Multidomain Lifestyle Intervention Is Associated With Improved Functional Trajectories and Favorable Changes in Epigenetic Aging Markers in Frail Older Adults: A Randomized Controlled Trial
Gloria Olaso‐Gonzalez, Fernando Millan‐Domingo, Luis Garcia‐Fernandez, Elisa Garcia‐Tercero, Monica Cebrian, Cristina Garcia‐Dominguez, Juan Antonio Carbonell, German Casabo‐Valles, Jose Luis Garcia‐Gimenez, Eva Tamayo‐Torres, Juan Gambini, Francisco Jose Tarazona‐Santabalbina

TL;DR
A 6-month lifestyle intervention improved physical function and slowed biological aging in frail older adults.
Contribution
The study shows that a multidomain lifestyle intervention can slow epigenetic aging and improve functional outcomes in frail older adults.
Findings
The intervention group showed significant reductions in frailty and improvements in grip strength, gait speed, and balance.
The intervention was associated with reduced DNA methylation-based PhenoAge and preserved telomere length.
The control group showed accelerated epigenetic aging as measured by DNAm PhenoAge.
Abstract
Frailty emerges as the intermediate stage preceding disability, but there is a gap in molecular signatures for early detection of subclinical cellular changes, which could help predict frailty onset or the effectiveness of interventions. In this randomized, controlled study, we assessed phenotypical and functional changes in frail individuals before and after a 6‐month multidomain lifestyle intervention (nutritional supplement and supervised exercise) vs habitual care. We also analyzed whole‐blood methylome, including five epigenetic clocks, a DNA methylation‐based telomere length estimator, and the Rate of Epigenetic Aging (REA). Between October 2019 and July 2022, we recruited 47 frail, community‐dwelling individuals in Spain. Mean age was 80.2 years (SD 3.1) in the control group (CG; n = 19) and 80.5 years (4.3) in the intervention group (IG; n = 28). Compared with the CG, a…
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Taxonomy
TopicsEpigenetics and DNA Methylation · Frailty in Older Adults · Telomeres, Telomerase, and Senescence
