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Depressive Symptoms and Plasma Markers of Alzheimer's Disease and Neurodegeneration: A Coordinated Meta-Analysis of 8 Cohort Studies.

Authors :
Twait EL
Kamarioti M
Verberk IMW
Teunissen CE
Nooyens ACJ
Monique Verschuren WM
Visser PJ
Huisman M
Kok AAL
Eline Slagboom P
Beekman M
Vojinovic D
Lakenberg N
Arfan Ikram M
Schuurmans IK
Wolters FJ
Moonen JEF
Gerritsen L
van der Flier WM
Geerlings MI
Source :
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry [Am J Geriatr Psychiatry] 2024 Sep; Vol. 32 (9), pp. 1141-1153. Date of Electronic Publication: 2024 Mar 11.
Publication Year :
2024

Abstract

Background: Depressive symptoms are associated with an increased risk of Alzheimer's disease (AD). There has been a recent emergence in plasma biomarkers for AD pathophysiology, such as amyloid-beta (Aβ) and phosphorylated tau (p-tau), as well as for axonal damage (neurofilament light, NfL) and astrocytic activation (glial fibrillary acidic protein, GFAP). Hypothesizing that depressive symptoms may occur along the AD process, we investigated associations between plasma biomarkers of AD with depressive symptoms in individuals without dementia.<br />Methods: A two-stage meta-analysis was performed on 2 clinic-based and 6 population-based cohorts (N = 7210) as part of the Netherlands Consortium of Dementia Cohorts. Plasma markers (Aβ42/40, p-tau181, NfL, and GFAP) were measured using Single Molecular Array (Simoa; Quanterix) assays. Depressive symptoms were measured with validated questionnaires. We estimated the cross-sectional association of each standardized plasma marker (determinants) with standardized depressive symptoms (outcome) using linear regressions, correcting for age, sex, education, and APOE ε4 allele presence, as well as subgrouping by sex and APOE ε4 allele. Effect estimates were entered into a random-effects meta-analysis.<br />Results: Mean age of participants was 71 years. The prevalence of clinically relevant depressive symptoms ranged from 1% to 22%. None of the plasma markers were associated with depressive symptoms in the meta-analyses. However, NfL was associated with depressive symptoms only in APOE ε4 carriers (β 0.11; 95% CI: 0.05-0.17).<br />Conclusions: Late-life depressive symptoms did not show an association to plasma biomarkers of AD pathology. However, in APOE ε4 allele carriers, a more profound role of neurodegeneration was suggested with depressive symptoms.<br />Competing Interests: DISCLOSURES No disclosures to report.<br /> (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1545-7214
Volume :
32
Issue :
9
Database :
MEDLINE
Journal :
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
Publication Type :
Academic Journal
Accession number :
38553327
Full Text :
https://doi.org/10.1016/j.jagp.2024.03.004