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

Author:

Palpatzis Eleni123ORCID,Akinci Muge123,Aguilar‐Dominguez Pablo12,Garcia‐Prat Marina3,Blennow Kaj45,Zetterberg Henrik45678,Carboni Margherita9,Kollmorgen Gwendlyn10,Wild Norbert10,Fauria Karine31112,Falcon Carles31112,Gispert Juan Domingo31113,Suárez‐Calvet Marc3111314ORCID,Grau‐Rivera Oriol3111314,Sánchez‐Benavides Gonzalo31113,Arenaza‐Urquijo Eider M.131113ORCID,

Affiliation:

1. Barcelona Institute for Global Health (ISGlobal) Barcelona Spain

2. University of Pompeu Fabra (UPF) Barcelona Spain

3. Barcelonaβeta Brain Research Center (BBRC) Pasqual Maragall Foundation Barcelona Spain

4. Department of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology, University of Gothenburg Mölndal Sweden

5. Clinical Neurochemistry Laboratory Sahlgrenska University Hospital Mölndal Sweden

6. UK Dementia Research Institute at UCL London United Kingdom

7. Department of Neurodegenerative Disease UCL Institute of Neurology London United Kingdom

8. Hong Kong Center for Neurodegenerative Diseases, Clear Water Bay Hong Kong China

9. Roche Diagnostics International Ltd Rotkreuz Switzerland

10. Roche Diagnostics GmbH Penzberg Germany

11. IMIM (Hospital del Mar Medical Research Institute) Barcelona Spain

12. Centro de Investigación Biomédica en Red Bioingeniería Biomateriales y Nanomedicina, Instituto de Salud Carlos III Madrid Spain

13. Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable (CIBERFES) Madrid Spain

14. Servei de Neurologia Hospital del Mar Barcelona Spain

Abstract

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 Aβ1–42/1–40 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 Aβ1–42/1–40 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;95:1058–1068

Funder

'la Caixa' Foundation

Alzheimer's Association

Ministerio de Ciencia e Innovación

Publisher

Wiley

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