Differences between multimodal brain-age and chronological-age are linked to telomere shortening

Neurobiol Aging. 2022 Jul:115:60-69. doi: 10.1016/j.neurobiolaging.2022.03.015. Epub 2022 Mar 31.

Abstract

Telomere shortening is theorized to accelerate biological aging, however, this has not been tested in the brain and cognitive contexts. We used machine learning age-prediction models to determine brain/cognitive age and quantified the degree of accelerated aging as the discrepancy between brain and/or cognitive and chronological ages (i.e., age gap). We hypothesized these age gaps are associated with telomere length (TL). Using healthy participants from the ADNI-3 cohort (N = 196, Agemean=70.7), we trained age-prediction models using 4 modalities of brain features and cognitive scores, as well as a 'stacked' model combining all brain modalities. Then, these 6 age-prediction models were applied to an independent sample diagnosed with mild cognitive impairment (N = 91, Agemean=71.3) to determine, for each subject, the model-specific predicted age and age gap. TL was most strongly associated with age gaps from the resting-state functional connectivity model after controlling for confounding variables. Overall, telomere shortening was significantly related to older brain but not cognitive age gaps. In particular, functional relative to structural brain-age gaps, were more strongly implicated in telomere shortening.

Keywords: Brain-age; Cognitive-age; Cortical thickness; Resting-state functional connectivity; Structural connectivity; Subcortical gray matter; Telomere.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics
  • Aging / psychology
  • Brain
  • Cognitive Dysfunction*
  • Humans
  • Machine Learning
  • Telomere / genetics
  • Telomere Shortening*