Amyloid burden and incident depressive symptoms in cognitively normal older adults

被引:45
|
作者
Harrington, Karra D. [1 ,2 ,3 ]
Gould, Emma [1 ]
Lim, Yen Ying [2 ]
Ames, David [3 ,4 ]
Pietrzak, Robert H. [5 ,6 ]
Rembach, Alan [2 ]
Rainey-Smith, Stephanie [7 ,8 ]
Martins, Ralph N. [7 ,8 ]
Salvado, Olivier [9 ]
Villemagne, Victor L. [2 ,10 ,11 ]
Rowe, Christopher C. [10 ,11 ]
Masters, Colin L. [2 ]
Maruff, Paul [2 ,12 ]
机构
[1] Deakin Univ, Sch Psychol, Geelong, Vic, Australia
[2] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[3] Univ Melbourne, Acad Unit Psychiat Old Age, Dept Psychiat, Parkville, Vic, Australia
[4] Natl Ageing Res Inst, Parkville, Vic, Australia
[5] VA Connecticut Healthcare Syst, Clin Neurosci Div, Natl Ctr Posttraumat Stress Disorder, US Dept Vet Affairs, West Haven, CT USA
[6] Yale Sch Med, Dept Psychiat, New Haven, CT USA
[7] Edith Cowan Univ, Sch Exercise Biomed & Hlth Sci, Ctr Excellence Alzheimers Dis Res & Care, Perth, WA, Australia
[8] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Nedlands, WA, Australia
[9] Australian E Hlth Res Ctr BioMedIA, CSIRO Preventat Hlth Natl Res Flagship, Herston, Qld, Australia
[10] Austin Hlth, Ctr PET, Dept Nucl Med, Heidelberg, Vic, Australia
[11] Univ Melbourne, Dept Med, Austin Hlth, Heidelberg, Vic, Australia
[12] CogState Ltd, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
amyloid; depression; Alzheimer's disease; cognitively normal; LATE-LIFE DEPRESSION; ALZHEIMERS ASSOCIATION WORKGROUPS; BETA PROTEIN; DIAGNOSTIC GUIDELINES; ELDERLY DEPRESSION; NATIONAL INSTITUTE; A-BETA; DISEASE; BIOMARKERS; HISTORY;
D O I
10.1002/gps.4489
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
ObjectiveSeveral studies have reported that non-demented older adults with clinical depression show changes in amyloid- (A) levels in blood, cerebrospinal fluid and on neuroimaging that are consistent with those observed in patients with Alzheimer's disease. These findings suggest that A may be one of the mechanisms underlying the relation between the two conditions. We sought to determine the relation between elevated cerebral A and the presence of depression across a 54-month prospective observation period. MethodsCognitively normal older adults from the Australian Imaging Biomarkers and Lifestyle study who were not depressed and had undergone a positron emission tomography scan to classify them as either high A (n=81) or low A (n=278) participated. Depressive symptoms were assessed using the Geriatric Depression Scale Short Form at 18-month intervals over 54months. ResultsWhilst there was no difference in probable depression between groups at baseline, incidence was 4.5 (95% confidence interval [CI] 1.3-16.4) times greater within the high A group (9%) than the low A group (2%) by the 54-month assessment. ConclusionsResults of this study suggest that elevated A levels are associated with a 4.5-fold increased likelihood of developing clinically significant depressive symptoms on follow-up in preclinical Alzheimer's disease. This underscores the importance of assessing, monitoring and treating depressive symptoms in older adults with elevated A. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:455 / 463
页数:9
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