TY - JOUR
T1 - Predicting brain age from functional connectivity in symptomatic and preclinical Alzheimer disease
AU - for the Dominantly Inherited Alzheimer Network
AU - Millar, Peter R.
AU - Luckett, Patrick H.
AU - Gordon, Brian A.
AU - Benzinger, Tammie L.S.
AU - Schindler, Suzanne E.
AU - Fagan, Anne M.
AU - Cruchaga, Carlos
AU - Bateman, Randall J.
AU - Allegri, Ricardo
AU - Jucker, Mathias
AU - Lee, Jae Hong
AU - Mori, Hiroshi
AU - Salloway, Stephen P.
AU - Yakushev, Igor
AU - Morris, John C.
AU - Ances, Beau M.
AU - Adams, Sarah
AU - Araki, Aki
AU - Barthelemy, Nicolas
AU - Bechara, Jacob
AU - Berman, Sarah
AU - Bodge, Courtney
AU - Brandon, Susan
AU - Brooks, William (Bill)
AU - Brosch, Jared
AU - Buck, Jill
AU - Buckles, Virginia
AU - Carter, Kathleen
AU - Cash, Lisa
AU - Chen, Charlie
AU - Chhatwal, Jasmeer
AU - Mendez, Patricio Chrem
AU - Chua, Jasmin
AU - Chui, Helena
AU - Courtney, Laura
AU - Day, Gregory S.
AU - DeLaCruz, Chrismary
AU - Denner, Darcy
AU - Diffenbacher, Anna
AU - Dincer, Aylin
AU - Donahue, Tamara
AU - Douglas, Jane
AU - Duong, Duc
AU - Egido, Noelia
AU - Esposito, Bianca
AU - Farlow, Marty
AU - Feldman, Becca
AU - Fitzpatrick, Colleen
AU - Goate, Alison
AU - Renton, Alan
N1 - Publisher Copyright:
© 2022
PY - 2022/8/1
Y1 - 2022/8/1
N2 - “Brain-predicted age” quantifies apparent brain age compared to normative neuroimaging trajectories. Advanced brain-predicted age has been well established in symptomatic Alzheimer disease (AD), but is underexplored in preclinical AD. Prior brain-predicted age studies have typically used structural MRI, but resting-state functional connectivity (FC) remains underexplored. Our model predicted age from FC in 391 cognitively normal, amyloid-negative controls (ages 18–89). We applied the trained model to 145 amyloid-negative, 151 preclinical AD, and 156 symptomatic AD participants to test group differences. The model accurately predicted age in the training set. FC-predicted brain age gaps (FC-BAG) were significantly older in symptomatic AD and significantly younger in preclinical AD compared to controls. There was minimal correspondence between networks predictive of age and AD. Elevated FC-BAG may reflect network disruption during symptomatic AD. Reduced FC-BAG in preclinical AD was opposite to the expected direction, and may reflect a biphasic response to preclinical AD pathology or may be driven by inconsistency between age-related vs. AD-related networks. Overall, FC-predicted brain age may be a sensitive AD biomarker.
AB - “Brain-predicted age” quantifies apparent brain age compared to normative neuroimaging trajectories. Advanced brain-predicted age has been well established in symptomatic Alzheimer disease (AD), but is underexplored in preclinical AD. Prior brain-predicted age studies have typically used structural MRI, but resting-state functional connectivity (FC) remains underexplored. Our model predicted age from FC in 391 cognitively normal, amyloid-negative controls (ages 18–89). We applied the trained model to 145 amyloid-negative, 151 preclinical AD, and 156 symptomatic AD participants to test group differences. The model accurately predicted age in the training set. FC-predicted brain age gaps (FC-BAG) were significantly older in symptomatic AD and significantly younger in preclinical AD compared to controls. There was minimal correspondence between networks predictive of age and AD. Elevated FC-BAG may reflect network disruption during symptomatic AD. Reduced FC-BAG in preclinical AD was opposite to the expected direction, and may reflect a biphasic response to preclinical AD pathology or may be driven by inconsistency between age-related vs. AD-related networks. Overall, FC-predicted brain age may be a sensitive AD biomarker.
KW - Alzheimer disease
KW - Brain aging
KW - Machine learning
KW - Resting-state functional connectivity
KW - fMRI
UR - http://www.scopus.com/inward/record.url?scp=85129731315&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2022.119228
DO - 10.1016/j.neuroimage.2022.119228
M3 - Article
C2 - 35452806
AN - SCOPUS:85129731315
SN - 1053-8119
VL - 256
JO - NeuroImage
JF - NeuroImage
M1 - 119228
ER -