Lifetime Stressful Events Associated with Alzheimer's Pathologies, Neuroinflammation and Brain Structure in a Risk Enriched Cohort

被引:4
作者
Palpatzis, Eleni [1 ,2 ,3 ]
Akinci, Muge [1 ,2 ,3 ]
Aguilar-Dominguez, Pablo [1 ,2 ]
Garcia-Prat, Marina [3 ]
Blennow, Kaj [4 ,5 ]
Zetterberg, Henrik [4 ,5 ,6 ,7 ,8 ,9 ]
Carboni, Margherita [10 ]
Kollmorgen, Gwendlyn [11 ]
Wild, Norbert [11 ]
Fauria, Karine [3 ,12 ,13 ]
Falcon, Carles [3 ,12 ,13 ]
Gispert, Juan Domingo [3 ,12 ,14 ]
Suarez-Calvet, Marc [3 ,12 ,14 ,15 ]
Grau-Rivera, Oriol [3 ,12 ,14 ,15 ]
Sanchez-Benavides, Gonzalo [3 ,12 ,14 ]
Arenaza-Urquijo, Eider M. [1 ,3 ,12 ,14 ]
机构
[1] Barcelona Inst Global Hlth ISGlobal, Barcelona, Spain
[2] Univ Pompeu Fabra UPF, Barcelona, Spain
[3] Pasqual Maragall Fdn, Barcelonabeta Brain Res Ctr, Barcelona, Spain
[4] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Molndal, Sweden
[5] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[6] UCL, Dementia Res Inst, London, England
[7] UCL, Dept Neurodegenerat Dis, Inst Neurol, London, England
[8] Hong Kong Ctr Neurodegenerat Dis, Clear Water Bay, Hong Kong, Peoples R China
[9] Univ Wisconsin, Wisconsin Alzheimers Dis Res Ctr, Sch Med & Publ Hlth, Madison, WI USA
[10] Roche Diagnost Int Ltd, Rotkreuz, Switzerland
[11] Roche Diagnost GmbH, Penzberg, Germany
[12] IMIM Hosp del Mar Med Res Inst, Barcelona, Spain
[13] Inst Salud Carlos III, Ctr Invest Biomed Red Bioingn Biomat & Nanomed, Madrid, Spain
[14] Ctr Invest Biomed Red Fragilidad & Envejecimiento, Madrid, Spain
[15] Hosp del Mar, Serv Neurol, Barcelona, Spain
关键词
CEREBROSPINAL-FLUID BIOMARKERS; COGNITIVE DECLINE; DISEASE; INFLAMMATION; DEPRESSION; MODEL; ADAPTATION; HEALTH; TAU;
D O I
10.1002/ana.26881
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveAlong with the known effects of stress on brain structure and inflammatory processes, increasing evidence suggest a role of chronic stress in the pathogenesis of Alzheimer's disease (AD). We investigated the association of accumulated stressful life events (SLEs) with AD pathologies, neuroinflammation, and gray matter (GM) volume among cognitively unimpaired (CU) individuals at heightened risk of AD.MethodsThis cross-sectional cohort study included 1,290 CU participants (aged 48-77) from the ALFA cohort with SLE, lumbar puncture (n = 393), and/or structural magnetic resonance imaging (n = 1,234) assessments. Using multiple regression analyses, we examined the associations of total SLEs with cerebrospinal fluid (1) phosphorylated (p)-tau181 and A beta 1-42/1-40 ratio, (2) interleukin 6 (IL-6), and (3) GM volumes voxel-wise. Further, we performed stratified and interaction analyses with sex, history of psychiatric disease, and evaluated SLEs during specific life periods.ResultsWithin the whole sample, only childhood and midlife SLEs, but not total SLEs, were associated with AD pathophysiology and neuroinflammation. Among those with a history of psychiatric disease SLEs were associated with higher p-tau181 and IL-6. Participants with history of psychiatric disease and men, showed lower A beta 1-42/1-40 with higher SLEs. Participants with history of psychiatric disease and women showed reduced GM volumes in somatic regions and prefrontal and limbic regions, respectively.InterpretationWe did not find evidence supporting the association of total SLEs with AD, neuroinflammation, and atrophy pathways. Instead, the associations appear to be contingent on events occurring during early and midlife, sex and history of psychiatric disease. ANN NEUROL 2024
引用
收藏
页码:1058 / 1068
页数:11
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