TY - JOUR
T1 - Estimates of age-related memory decline are inflated by unrecognized Alzheimer's disease
AU - AIBL Research Group
AU - Harrington, Karra D.
AU - Schembri, Adrian
AU - Lim, Yen Ying
AU - Dang, Christa
AU - Ames, David
AU - Hassenstab, Jason
AU - Laws, Simon M.
AU - Rainey-Smith, Stephanie
AU - Robertson, Joanne
AU - Rowe, Christopher C.
AU - Sohrabi, Hamid R.
AU - Salvado, Olivier
AU - Weinborn, Michael
AU - Villemagne, Victor L.
AU - Masters, Colin L.
AU - Maruff, Paul
N1 - Funding Information:
KDH received a PhD Scholarship cofunded by the Alzheimer's Australia Dementia Research Foundation and the Florey Institute of Neuroscience and Mental Health. The authors acknowledge the financial support of the CRC for Mental Health. The Cooperative Research Centre (CRC) program is an Australian Government Initiative.
Funding Information:
Funding for the AIBL study was provided in part by the study partners [Australian Commonwealth Scientific Industrial and Research Organization (CSIRO), Edith Cowan University (ECU), Mental Health Research Institute (MHRI), Alzheimer's Australia (AA), National Ageing Research Institute (NARI), Austin Health, CogState Ltd, Hollywood Private Hospital, Sir Charles Gardner Hospital]. The study also received support from the National Health and Medical Research Council (NHMRC) and the Dementia Collaborative Research Centres program (DCRC2), as well as ongoing funding from the Science and Industry Endowment Fund (SIEF).
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/10
Y1 - 2018/10
N2 - Cognitive decline is considered an inevitable consequence of aging; however, estimates of cognitive aging may be influenced negatively by undetected preclinical Alzheimer's disease (AD). This study aimed to determine the extent to which estimates of cognitive aging were biased by preclinical AD. Cognitively normal older adults (n = 494) with amyloid-β status determined from positron emission tomography neuroimaging underwent serial neuropsychological assessment at 18-month intervals over 72 months. Estimates of the effects of age on verbal memory, working memory, executive function, and processing speed were derived using linear mixed models. The presence of preclinical AD and clinical progression to mild cognitive impairment or dementia during the study were then added to these models as covariates. Initially, age was associated with decline across all 4 cognitive domains. With the effects of elevated amyloid-β and clinical progression controlled, age was no longer associated with decline in verbal or working memory. However, the magnitude of decline was reduced only slightly for executive function and was unchanged for processing speed. Thus, considered together, the results of the study indicate that undetected preclinical AD negatively biases estimates of age-related cognitive decline for verbal and working memory.
AB - Cognitive decline is considered an inevitable consequence of aging; however, estimates of cognitive aging may be influenced negatively by undetected preclinical Alzheimer's disease (AD). This study aimed to determine the extent to which estimates of cognitive aging were biased by preclinical AD. Cognitively normal older adults (n = 494) with amyloid-β status determined from positron emission tomography neuroimaging underwent serial neuropsychological assessment at 18-month intervals over 72 months. Estimates of the effects of age on verbal memory, working memory, executive function, and processing speed were derived using linear mixed models. The presence of preclinical AD and clinical progression to mild cognitive impairment or dementia during the study were then added to these models as covariates. Initially, age was associated with decline across all 4 cognitive domains. With the effects of elevated amyloid-β and clinical progression controlled, age was no longer associated with decline in verbal or working memory. However, the magnitude of decline was reduced only slightly for executive function and was unchanged for processing speed. Thus, considered together, the results of the study indicate that undetected preclinical AD negatively biases estimates of age-related cognitive decline for verbal and working memory.
KW - Aging
KW - Alzheimer
KW - Amyloid-β
KW - Cognition
KW - Preclinical
UR - http://www.scopus.com/inward/record.url?scp=85049740168&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2018.06.005
DO - 10.1016/j.neurobiolaging.2018.06.005
M3 - Article
C2 - 30015036
AN - SCOPUS:85049740168
SN - 0197-4580
VL - 70
SP - 170
EP - 179
JO - Neurobiology of Aging
JF - Neurobiology of Aging
ER -