Relationship between Polygenetic Risk Score of BrainAge and plasma biomarkers in the A4/LEARN studies

Genetic factors associated with increased propensity for accelerated brain aging in the grey matter is associated with p-tau<sub>217</sub>, an early and sensitive marker of AD. These genetic predispositions were more pronounced in older age, highlighting the importance of age as a critical factor that may interact with genetic susceptibility to brain aging, potentially through cumulative lifetime exposures, increasing vascular burden, or age-related declines in cellular repair mechanisms. Associations solely with BrainAge GM PRS implies the specificity of accelerated brain aging in grey matter as a potential early marker of AD risk.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-12-01
DOI
https://doi.org/10.1002/alz70855_106684
Primary Topic
Functional Brain Connectivity Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Relationship between Polygenetic Risk Score of BrainAge and plasma biomarkers in the A4/LEARN studies

Aaron P. Schultz, Rachel F. Buckley, Ibai Díez, Jorge García Condado et al.
Alzheimer s & Dementia
Functional Brain Connectivity Studies
article

Relationship between Polygenetic Risk Score of BrainAge and plasma biomarkers in the A4/LEARN studies

Aaron P. Schultz, Rachel F. Buckley, Ibai Díez, Jorge García Condado, Gillian Coughlan, Colin Birkenbihl, Asier Erramuzpe, Jasmeer P. Chhatwal, Hannah M Klinger, Cortes Jesús, K. A. Johnson, R. Sperling, Hyun‐Sik Yang, Michael J. Properzi, Dorene M. Rentz, Mabel Seto
article en

Abstract

Genetic factors associated with increased propensity for accelerated brain aging in the grey matter is associated with p-tau<sub>217</sub>, an early and sensitive marker of AD. These genetic predispositions were more pronounced in older age, highlighting the importance of age as a critical factor that may interact with genetic susceptibility to brain aging, potentially through cumulative lifetime exposures, increasing vascular burden, or age-related declines in cellular repair mechanisms. Associations solely with BrainAge GM PRS implies the specificity of accelerated brain aging in grey matter as a potential early marker of AD risk.

Alzheimer s & DementiaVol. 21(S1)
Ikerbasque (ES), Brigham and Women's Hospital (US), Harvard University (US), The University of Melbourne (AU), University of the Basque Country (ES), Massachusetts General Hospital (US), BioCruces Health research Institute (ES)
Openalex Percentile: Top 33%
Functional Brain Connectivity Studies
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Relationship between Polygenetic Risk Score of BrainAge and plasma biomarkers in the A4/LEARN studies — Aaron P. Schultz, Rachel F. Buckley, et al. · Alzheimer s & Dementia (2025) | TGRS Research Map | TGRS