Association of dietary fatty acids with longitudinal change in plasma-based biomarkers of Alzheimer’s disease

dc.contributor.authorHoost, Serena S.
dc.contributor.authorHonig, Lawrence S.
dc.contributor.authorKang, Min Suk
dc.contributor.authorBahl, Aanya
dc.contributor.authorLee, Annie J.
dc.contributor.authorSanchez, Danurys
dc.contributor.authorReyes-Dumeyer, Dolly
dc.contributor.authorLantigua, Rafael A.
dc.contributor.authorDage, Jeffrey L.
dc.contributor.authorBrickman, Adam M.
dc.contributor.authorManly, Jennifer J.
dc.contributor.authorMayeux, Richard
dc.contributor.authorGu, Yian
dc.contributor.departmentNeurology, School of Medicine
dc.date.accessioned2025-06-16T09:39:16Z
dc.date.available2025-06-16T09:39:16Z
dc.date.issued2025
dc.description.abstractBackground: Elevated intake of omega-3 polyunsaturated fatty acids is linked to a reduced risk of dementia in some prospective studies. However, few studies have examined the relationship between nutrient intake and plasma biomarkers of Alzheimer's disease. Objectives: We explored whether omega-3, omega-6, and monounsaturated fat intakes were associated with changes in plasma biomarkers of Alzheimer's disease over time. Design: The Washington Heights-Inwood Columbia Aging Project is a prospective cohort study (1994-2021); the data set used here includes a mean follow-up of 7.0 years. Setting: Community-based in New York City. Participants: 599 dementia-free individuals at baseline who completed a 61-item food frequency questionnaire and had biomarkers measured in plasma from at least two different time points. Measurements: Fatty acid intake tertiles were computed from participant-completed 61-item Willett semi-quantitative food frequency questionnaires (Channing Laboratory, Cambridge, Massachusetts) obtained once at their baseline visit. Plasma-based biomarker assays were performed, using the single molecule array technology Quanterix Simoa HD-X platform, at baseline and follow-up visits. Generalized Estimating Equations (GEE) models were used to evaluate the association between baseline nutrient intake tertile and changes in biomarkers including phospho-tau181, amyloid-beta 42/40 ratio, phospho-tau181/amyloid-beta42 ratio, glial fibrillary acidic protein, neurofilament light chain, and two biomarker patterns derived from Principal Component Analysis (PCA1 and PCA2), with higher scores indicating a high level of neurodegeneration and low level of Alzheimer's disease burden, respectively). Models were adjusted for age, sex, race/ethnicity, education, and calculated total energy intake initially, and additionally for cerebrovascular risk factors. Results: Higher baseline omega-3 intake tertile was associated with lesser decline in PCA2 (β = 0.221, p < 0.001) and amyloid-beta 42/40 ratio (β = 0.022, p = 0.003), and a lesser rise in phospho-tau181 (β = -0.037, p = 0.001). Higher omega-6 intake tertile was linked to a lesser rise in phospho-tau181 (β = -0.050, p < 0.001) and glial fibrillary acidic protein (β = -0.028, p = 0.002). Most associations persisted after adjusting for cardiovascular risk factors. Conclusions: Higher relative baseline intake of omega-3 and omega-6 fatty acids is associated with lesser progression of blood-based biomarkers of Alzheimer's disease. Consuming healthy fatty acids may help prevent accumulation of Alzheimer's disease-related pathological changes.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationHoost SS, Honig LS, Kang MS, et al. Association of dietary fatty acids with longitudinal change in plasma-based biomarkers of Alzheimer's disease. J Prev Alzheimers Dis. 2025;12(5):100117. doi:10.1016/j.tjpad.2025.100117
dc.identifier.urihttps://hdl.handle.net/1805/48717
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.tjpad.2025.100117
dc.relation.journalThe Journal of Prevention of Alzheimer's Disease
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectAlzheimer's disease
dc.subjectAmyloid
dc.subjectBlood-based biomarker
dc.subjectDiet
dc.subjectOmega-3
dc.titleAssociation of dietary fatty acids with longitudinal change in plasma-based biomarkers of Alzheimer’s disease
dc.typeArticle
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