TY - JOUR
T1 - Regional age-related atrophy after screening for preclinical alzheimer disease
AU - Dominantly Inherited Alzheimer Network (DIAN)
AU - Koenig, Lauren N.
AU - LaMontagne, Pamela
AU - Glasser, Matthew F.
AU - Bateman, Randall
AU - Holtzman, David
AU - Yakushev, Igor
AU - Chhatwal, Jasmeer
AU - Day, Gregory
AU - Jack, Clifford
AU - Mummery, Catherine
AU - Perrin, Richard J.
AU - Gordon, Brian A.
AU - Morris, John C.
AU - Shimony, Joshua S.
AU - Benzinger, Tammie L.S.
N1 - Publisher Copyright:
© 2021
PY - 2022/1
Y1 - 2022/1
N2 - Brain atrophy occurs in aging even in the absence of dementia, but it is unclear to what extent this is due to undetected preclinical Alzheimer disease. Here we examine a cross-sectional cohort (ages 18-88) free from confounding influence of preclinical Alzheimer disease, as determined by amyloid PET scans and three years of clinical evaluation post-imaging. We determine the regional strength of age-related atrophy using linear modeling of brain volumes and cortical thicknesses with age. Age-related atrophy was seen in nearly all regions, with greatest effects in the temporal lobe and subcortical regions. When modeling age with the estimated derivative of smoothed aging curves, we found that the temporal lobe declined linearly with age, subcortical regions declined faster at later ages, and frontal regions declined slower at later ages than during midlife. This age-derivative pattern was distinct from the linear measure of age-related atrophy and significantly associated with a measure of myelin. Atrophy did not detectably differ from a preclinical Alzheimer disease cohort when age ranges were matched.
AB - Brain atrophy occurs in aging even in the absence of dementia, but it is unclear to what extent this is due to undetected preclinical Alzheimer disease. Here we examine a cross-sectional cohort (ages 18-88) free from confounding influence of preclinical Alzheimer disease, as determined by amyloid PET scans and three years of clinical evaluation post-imaging. We determine the regional strength of age-related atrophy using linear modeling of brain volumes and cortical thicknesses with age. Age-related atrophy was seen in nearly all regions, with greatest effects in the temporal lobe and subcortical regions. When modeling age with the estimated derivative of smoothed aging curves, we found that the temporal lobe declined linearly with age, subcortical regions declined faster at later ages, and frontal regions declined slower at later ages than during midlife. This age-derivative pattern was distinct from the linear measure of age-related atrophy and significantly associated with a measure of myelin. Atrophy did not detectably differ from a preclinical Alzheimer disease cohort when age ranges were matched.
KW - Magnetic Resonance Imaging (MRI)
KW - Normal Aging
KW - Preclinical Alzheimer disease
KW - Volumetrics
UR - http://www.scopus.com/inward/record.url?scp=85120933920&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2021.09.010
DO - 10.1016/j.neurobiolaging.2021.09.010
M3 - Article
C2 - 34655980
AN - SCOPUS:85120933920
SN - 0197-4580
VL - 109
SP - 43
EP - 51
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -