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ABSTRACT: Objective
Motor decline is a hallmark of Parkinson's disease (PD) and biological aging. While epigenetic clocks measure systemic biological aging, their specific relationship with neuromotor function in the context of aging and neurodegeneration remains under-characterized. This study utilized data from the Parkinson's Progression Markers Initiative (PPMI) to examine the relationships between multiple DNA methylation-based epigenetic aging measures and motor impairment across distinct domains.Methods
We utilized longitudinal phenotype and whole-blood DNA methylation data from the PPMI cohort. Seven epigenetic aging measures were calculated, including first-generation clocks (Horvath v1, Hannum), risk-optimized second-generation clocks (PhenoAge, GrimAge v1 and v2), a deep-l
SUBMITTER: Jiang T
PROVIDER: S-EPMC12724155 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature