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Longitudinal untargeted metabolomics of cognitive impairment in Parkinson's disease.

Created on 06 Oct 2026

Authors

Yuyuan Lin, Yu Yu, Keren Zhang, Irish Del Rosario, Aline Duarte Folle, Elizabeth Rose Mayeda, Dean P Jones, Douglas I Walker, Jeff Bronstein, Adrienne M Keener, Kimberly C Paul, Beate Ritz

Published in

Alzheimer's & dementia : the journal of the Alzheimer's Association. Volume 22. Issue 10. Pages e71890.

Abstract

Cognitive impairment is a common non-motor symptom of Parkinson's disease (PD), yet the mechanism remains unclear.
Longitudinal serum samples from PD patients in a community-based case-control study were profiled, with cognition assessed by the Mini-Mental State Examination at baseline and follow-up. We performed three metabolome-wide association studies: a baseline cross-sectional analysis (n = 632), a time-to-event analysis (n = 412), and a repeated measures analysis (n = 265), followed by "Mummichog" pathway analysis.
Of the 4762 metabolomic features, four reached statistical significance in the baseline analysis, 22 in the time-to-event analysis, and none in the repeated measures analysis. Dysregulated pathways included purine metabolism, the pentose phosphate pathway, fatty acid pathways, and C21-steroid hormone biosynthesis and metabolism.
Disruptions in core metabolic pathways may contribute to PD-related cognitive impairments. Disturbances in pentose and purine pathways may occur before clinical cognitive decline is observed, suggesting early metabolic markers.

PMID:
42836749
Bibliographic data and abstract were imported from PubMed on 06 Oct 2026.

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