Amyloid burden and incident depressive symptoms in preclinical Alzheimer's disease

被引:27
作者
Perin, Stephanie [1 ,3 ]
Harrington, Karra D. [2 ]
Lim, Yen Ying [2 ]
Ellis, Kathryn [2 ,3 ]
Ames, David [3 ,4 ]
Pietrzak, Robert H. [5 ,6 ]
Schembri, Adrian [7 ]
Rainey-Smith, Stephanie [8 ,9 ]
Salvado, Olivier [10 ]
Laws, Simon M. [8 ,11 ]
Martins, Ralph N. [8 ,9 ]
Villemagne, Victor L. [2 ,12 ,13 ]
Rowe, Christopher C. [12 ,13 ]
Masters, Colin L. [2 ]
Maruff, Paul [2 ,7 ]
机构
[1] RMIT Univ, Sch Hlth & Biomed Sci, Dept Psychol, Bundoora, 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, US Dept Vet Affairs, Natl Ctr Posttraumat Stress Disorder, Clin Neurosci Div, West Haven, CT USA
[6] Yale Sch Med, Dept Psychiat, New Haven, CT USA
[7] CogState Ltd, Melbourne, Vic, Australia
[8] Edith Cowan Univ, Sch Med & Hlth Sci, Ctr Excellence Alzheimers Dis Res & Care, Perth, WA, Australia
[9] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Nedlands, WA, Australia
[10] Australian E Hlth Res Ctr, CSIRO Hlth & Biosecur, Herston, Qld, Australia
[11] Cooperat Res Ctr Mental Hlth, Carlton, Vic, Australia
[12] Austin Hlth, Ctr PET, Dept Nucl Med, Heidelberg, Vic, Australia
[13] Univ Melbourne, Austin Hlth, Dept Med, Heidelberg, Vic, Australia
基金
英国医学研究理事会;
关键词
Depression; Amyloid-beta; Alzheimer's disease; MILD COGNITIVE IMPAIRMENT; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; SCREENING SCALE; OLDER-ADULTS; RISK; DEMENTIA; APATHY; RECOMMENDATIONS;
D O I
10.1016/j.jad.2017.12.101
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Relationships between depression and Alzheimer's disease (AD) may become clearer if studied in preclinical AD where dementia is not present. Method: The aim of this study was to evaluate prospectively, relationships between brain amyloid-beta (A beta), depressive symptoms and screen positive depression in cognitively normal (CN) older adults. Depressive symptoms were measured with the Geriatric Depression Inventory (GDS-15) in CN adults from the Australian Imaging Biomarkers and Lifestyle (AIBL) study without depression at baseline and classified as having abnormally high (A beta+; n = 136) or low (A beta-; n = 449) A beta according to positron emission tomography at 18-month intervals over 72 months. Results: Incident cases of screen positive depression were not increased in A beta+CN adults although small increases in overall depressive symptoms severity (d = - 0.25; 95% CI, - 0.45, - 0.05) and apathy-anxiety symptoms (d = - 0.28; 95% CI - 0.48, - 0.08) were. Limitations: As the AIBL sample is an experimental sample, no individuals had severe medical illnesses or significant psychiatric disorders. Additionally, individuals who had evidence of screen-positive depression at screening were excluded from enrolment in the AIBL study. Thus, the current data can be considered only as providing a foundation for understanding relationships between A beta and depression in preclinical AD. Conclusions: These results suggest that the presence of a depressive disorder or even increased depressive symptoms are themselves unlikely to be a direct consequence of increasing A beta. New depressive disorders presenting in CN older adults could therefore be investigated for aetiologies beyond AD.
引用
收藏
页码:269 / 274
页数:6
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