TY - JOUR
T1 - Differences between multimodal brain-age and chronological-age are linked to telomere shortening
AU - Yu, Junhong
AU - Mathi Kanchi, Madhu
AU - Rawtaer, Iris
AU - Feng, Lei
AU - Kumar, Alan Prem
AU - Kua, Ee Heok
AU - Mahendran, Rathi
N1 - Publisher Copyright:
© 2022
PY - 2022/7
Y1 - 2022/7
N2 - 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.
AB - 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.
KW - Brain-age
KW - Cognitive-age
KW - Cortical thickness
KW - Resting-state functional connectivity
KW - Structural connectivity
KW - Subcortical gray matter
KW - Telomere
UR - http://www.scopus.com/inward/record.url?scp=85130862814&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2022.03.015
DO - 10.1016/j.neurobiolaging.2022.03.015
M3 - Article
SN - 0197-4580
VL - 115
SP - 60
EP - 69
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -