Midlife Stress in Relation to Late-Life Cerebrospinal Fluid Biomarkers of Alzheimer's Disease: A 25-Year Follow-Up Study

被引:10
作者
Johansson, Lena [1 ]
Kern, Silke [1 ]
Zetterberg, Henrik [1 ,2 ]
Blennow, Kaj [1 ]
Borjesson-Hansson, Anne [1 ]
Rosengren, Lars [3 ]
Guo, Xinxin [1 ]
Skoog, Ingmar [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Ctr Ageing & Hlth AgeCap, Dept Psychiat & Neurochem, Gothenburg, Sweden
[2] UCL Inst Neurol, Dept Mol Neurosci, London, England
[3] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Clin Neurosci, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
Amyloid; Dementia; Neuropathology; Stress; Tau protein; Population study; CHRONIC DISTRESS; AMYLOID-BETA; DEMENTIA; CSF; RISK; TAU; PERSONALITY; POPULATION; PROTEIN; BRAIN;
D O I
10.1159/000490885
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
Background/Aims: Psychological stress has previously been associated with higher risk of developing late-life dementia, especially Alzheimer's disease (AD). This study tested whether longstanding midlife stress is related to cerebrospinal fluid (CSF) biomarkers of late-life AD, such as tau protein and amyloid beta (A beta). Methods: The study included 79 nondemented females from the Prospective Population Study of Women in Gothenburg, Sweden, who responded to a standardized stress question at baseline (mean age 49 years) and underwent a lumbar puncture at follow-up 25 years later. Multiple linear regression models analyzed the relationships between midlife psychological stress and late-life CSF measures of total tau (t-tau), phosphorylated tau (p-tau), A beta 40, and A beta 42. Results: Longstanding stress in midlife was associated with higher levels of CSF t-tau (beta = 0.64, p = 0.01) and A beta 40 (beta = 0.60, p = 0.02) in late life. No associations were found between midlife stress and levels of p-tau or A beta 42. Conclusion: The findings suggest that longstanding stress stimulates unspecific neurodegenerative processes, but not the core processes of AD, at least not in the early phase of the disease. The association with higher concentration of CSF t-tau may reflect neural degeneration and the association with higher A beta 40 may be an early sign of A beta overproduction or cerebro- vascular processes in the brain. (C) 2018 S. Karger AG, Basel
引用
收藏
页码:90 / 99
页数:10
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