Estimates of age-related memory decline are inflated by unrecognized Alzheimer's disease

被引:15
作者
Harrington, Karra D. [1 ,2 ]
Schembri, Adrian [3 ]
Lim, Yen Ying [1 ]
Dang, Christa [4 ]
Ames, David [5 ,6 ]
Hassenstab, Jason [7 ,8 ,9 ]
Laws, Simon M. [2 ,10 ,11 ]
Rainey-Smith, Stephanie [12 ,13 ]
Robertson, Joanne [1 ]
Rowe, Christopher C. [14 ,15 ]
Sohrabi, Hamid R. [12 ,16 ]
Salvado, Olivier [17 ]
Weinborn, Michael [12 ,13 ,18 ]
Villemagne, Victor L. [1 ,14 ,15 ]
Masters, Colin L. [1 ]
Maruff, Paul [1 ,3 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, 30 Royal Parade, Parkville, Vic 3052, Australia
[2] Cooperat Res Ctr Mental Hlth, Carlton, Vic, Australia
[3] CogState Ltd, Melbourne, Australia
[4] Univ Melbourne, Melbourne Med Sch, Dept Obstet & Gynaecol, Parkville, Vic, Australia
[5] Univ Melbourne, Acad Unit Psychiat Old Age, Dept Psychiat, Parkville, Vic, Australia
[6] Natl Ageing Res Inst, Parkville, Vic, Australia
[7] Washington Univ, Sch Med, Charles F & Joanne Knight Alzheimers Dis Res Ctr, St Louis, MO USA
[8] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[9] Washington Univ, Dept Psychol & Brain Sci, St Louis, MO USA
[10] Edith Cowan Univ, Sch Exercise Biomed & Hlth Sci, Ctr Excellence Alzheimers Dis Res & Care, Collaborat Genom Grp, Perth, WA, Australia
[11] Curtin Univ, Curtin Hlth Innovat Res Inst, Fac Hlth Sci, Sch Biomed Sci, Western Australia, Australia
[12] Edith Cowan Univ, Sch Exercise Biomed & Hlth Sci, Ctr Excellence Alzheimers Dis Res & Care, Perth, WA, Australia
[13] Hollywood Private Hosp, Australian Alzheimers Dis Res Unit, Perth, WA, Australia
[14] Austin Hlth, Dept Mol Imaging & Therapy, Melbourne, Australia
[15] Univ Melbourne, Dept Med, Austin Hlth, Melbourne, Australia
[16] Univ Western Australia, Sch Psychiat & Clin Neurosci, Nedlands, WA, Australia
[17] Australian eHealth Res Ctr, CSIRO Hlth & Biosecur, Brisbane, Qld, Australia
[18] Univ Western Australia, Sch Psychol Sci, Crawley, WA, Australia
基金
英国医学研究理事会;
关键词
Aging; Amyloid-beta; Preclinical; Alzheimer; Cognition; MINI-MENTAL-STATE; MILD COGNITIVE IMPAIRMENT; PROCESSING SPEED; AMYLOID-BETA; OLDER-ADULTS; LIFE-SPAN; BIOMARKERS; BRAIN; DEMENTIA; POPULATION;
D O I
10.1016/j.neurobiolaging.2018.06.005
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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 ofcognitive aging were biased by preclinical AD. Cognitively normal older adults (n = 494) with amyloid-I3 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-beta 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. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:170 / 179
页数:10
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