Subjective memory decline predicts greater rates of clinical progression in preclinical Alzheimer's disease

被引:144
作者
Buckley, Rachel F. [1 ]
Maruff, Paul [2 ]
Ames, David [3 ]
Bourgeat, Pierrick [4 ]
Martins, Ralph N. [5 ,6 ,7 ,8 ]
Masters, Colin L. [9 ]
Rainey-Smith, Stephanie [5 ,8 ]
Lautenschlager, Nicola [3 ,6 ,7 ]
Rowe, Christopher C. [10 ,11 ,12 ]
Savage, Greg [13 ]
Villemagne, Victor L. [9 ,10 ,11 ,12 ]
Ellis, Kathryn A. [3 ]
机构
[1] Univ Melbourne, Melbourne Sch Psychol Sci, Melbourne, Vic, Australia
[2] Cogstate Ltd, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Psychiat, St Vincents Hlth, Acad Unit Psychiat Old Age, Melbourne, Vic 3010, Australia
[4] CSIRO Hlth & Biosecur Flagship, Australian eHlth Res Ctr, Brisbane, Qld, Australia
[5] Edith Cowan Univ, Sch Med Sci, Ctr Excellence Alzheimers Dis Res & Care, Churchlands, WA 6018, Australia
[6] Univ Western Australia, Sch Psychiat & Clin Neurosci, Nedlands, WA 6009, Australia
[7] Univ Western Australia, West Australian Ctr Hlth & Ageing, Nedlands, WA 6009, Australia
[8] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Perth, WA, Australia
[9] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[10] Austin Hlth, Dept Nucl Med, Heidelberg, Vic, Australia
[11] Austin Hlth, Ctr PET, Heidelberg, Vic, Australia
[12] Univ Melbourne, Dept Med, Austin Hlth, Melbourne, Vic, Australia
[13] Macquarie Univ, ARC Ctr Excellence Cognit & Its Disorders, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Preclinical AD; Prodromal AD; Subjective cognitive decline; Subjective memory decline cognitively normal older adults; Amyloid; PET imaging; MILD COGNITIVE IMPAIRMENT; AMYLOID BURDEN; OLDER-ADULTS; HEALTHY-ADULTS; A-BETA; COMPLAINTS; DEMENTIA; MCI; INDIVIDUALS; BIOMARKERS;
D O I
10.1016/j.jalz.2015.12.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The objective of this study was to determine the utility of subjective memory decline (SMD) to predict episodic memory change and rates of clinical progression in cognitively normal older adults with evidence of high beta-amyloid burden (CN A beta+). Methods: Fifty-eight CN A beta+ participants from the Australian Imaging, Biomarkers, and Lifestyle study responded to an SMD questionnaire and underwent comprehensive neuropsychological assessments. Participant data for three follow-up assessments were analyzed. Results: In CN A beta+, subjects with high SMD did not exhibit significantly greater episodic memory decline than those with low SMD. High SMD was related to greater rates of progression to mild cognitive impairment or Alzheimer's disease (AD) dementia (hazard ratio = 5.1; 95% confidence interval, 1.4-20.0, P = .02) compared with low SMD. High SMD was associated with greater depressive symptomatology and smaller left hippocampal volume. Discussion: High SMD is a harbinger of greater rates of clinical progression in preclinical AD. Although SMD reflects broader diagnostic implications for CN A beta+, more sensitive measures may be required to detect early subtle cognitive change. (C) 2016 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:796 / 804
页数:9
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