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Peripheral serum metabolomic profiles inform central cognitive impairment.

Publication ,  Journal Article
Wang, J; Wei, R; Xie, G; Arnold, M; Kueider-Paisley, A; Louie, G; Mahmoudian Dehkordi, S; Blach, C; Baillie, R; Han, X; De Jager, PL; Jia, W ...
Published in: Sci Rep
August 20, 2020

The incidence of Alzheimer's disease (AD) increases with age and is becoming a significant cause of worldwide morbidity and mortality. However, the metabolic perturbation behind the onset of AD remains unclear. In this study, we performed metabolite profiling in both brain (n = 109) and matching serum samples (n = 566) to identify differentially expressed metabolites and metabolic pathways associated with neuropathology and cognitive performance and to identify individuals at high risk of developing cognitive impairment. The abundances of 6 metabolites, glycolithocholate (GLCA), petroselinic acid, linoleic acid, myristic acid, palmitic acid, palmitoleic acid and the deoxycholate/cholate (DCA/CA) ratio, along with the dysregulation scores of 3 metabolic pathways, primary bile acid biosynthesis, fatty acid biosynthesis, and biosynthesis of unsaturated fatty acids showed significant differences across both brain and serum diagnostic groups (P-value < 0.05). Significant associations were observed between the levels of differential metabolites/pathways and cognitive performance, neurofibrillary tangles, and neuritic plaque burden. Metabolites abundances and personalized metabolic pathways scores were used to derive machine learning models, respectively, that could be used to differentiate cognitively impaired persons from those without cognitive impairment (median area under the receiver operating characteristic curve (AUC) = 0.772 for the metabolite level model; median AUC = 0.731 for the pathway level model). Utilizing these two models on the entire baseline control group, we identified those who experienced cognitive decline in the later years (AUC = 0.804, sensitivity = 0.722, specificity = 0.749 for the metabolite level model; AUC = 0.778, sensitivity = 0.633, specificity = 0.825 for the pathway level model) and demonstrated their pre-AD onset prediction potentials. Our study provides a proof-of-concept that it is possible to discriminate antecedent cognitive impairment in older adults before the onset of overt clinical symptoms using metabolomics. Our findings, if validated in future studies, could enable the earlier detection and intervention of cognitive impairment that may halt its progression.

Duke Scholars

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Published In

Sci Rep

DOI

EISSN

2045-2322

Publication Date

August 20, 2020

Volume

10

Issue

1

Start / End Page

14059

Location

England

Related Subject Headings

  • Proof of Concept Study
  • Neuropsychological Tests
  • Metabolomics
  • Male
  • Longitudinal Studies
  • Humans
  • Female
  • Disease Progression
  • Cognition Disorders
  • Alzheimer Disease
 

Citation

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Wang, J., Wei, R., Xie, G., Arnold, M., Kueider-Paisley, A., Louie, G., … Jia, W. (2020). Peripheral serum metabolomic profiles inform central cognitive impairment. Sci Rep, 10(1), 14059. https://doi.org/10.1038/s41598-020-70703-w
Wang, Jingye, Runmin Wei, Guoxiang Xie, Matthias Arnold, Alexandra Kueider-Paisley, Gregory Louie, Siamak Mahmoudian Dehkordi, et al. “Peripheral serum metabolomic profiles inform central cognitive impairment.Sci Rep 10, no. 1 (August 20, 2020): 14059. https://doi.org/10.1038/s41598-020-70703-w.
Wang J, Wei R, Xie G, Arnold M, Kueider-Paisley A, Louie G, et al. Peripheral serum metabolomic profiles inform central cognitive impairment. Sci Rep. 2020 Aug 20;10(1):14059.
Wang, Jingye, et al. “Peripheral serum metabolomic profiles inform central cognitive impairment.Sci Rep, vol. 10, no. 1, Aug. 2020, p. 14059. Pubmed, doi:10.1038/s41598-020-70703-w.
Wang J, Wei R, Xie G, Arnold M, Kueider-Paisley A, Louie G, Mahmoudian Dehkordi S, Blach C, Baillie R, Han X, De Jager PL, Bennett DA, Kaddurah-Daouk R, Jia W. Peripheral serum metabolomic profiles inform central cognitive impairment. Sci Rep. 2020 Aug 20;10(1):14059.

Published In

Sci Rep

DOI

EISSN

2045-2322

Publication Date

August 20, 2020

Volume

10

Issue

1

Start / End Page

14059

Location

England

Related Subject Headings

  • Proof of Concept Study
  • Neuropsychological Tests
  • Metabolomics
  • Male
  • Longitudinal Studies
  • Humans
  • Female
  • Disease Progression
  • Cognition Disorders
  • Alzheimer Disease