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Discovery of a Metabolic Signature Predisposing High Risk Patients with Mild Cognitive Impairment to Converting to Alzheimer's Disease.
Huang, Yi-Long; Lin, Chao-Hsiung; Tsai, Tsung-Hsien; Huang, Chen-Hua; Li, Jie-Ling; Chen, Liang-Kung; Li, Chun-Hsien; Tsai, Ting-Fen; Wang, Pei-Ning.
Affiliation
  • Huang YL; Aging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Lin CH; Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Tsai TH; Aging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Huang CH; Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Li JL; Advanced Tech BU, Acer Inc., New Taipei City 221, Taiwan.
  • Chen LK; Department of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Li CH; Aging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Tsai TF; Aging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
  • Wang PN; Center for Geriatrics and Gerontology, Taipei Veterans General Hospital, Taipei 112, Taiwan.
Int J Mol Sci ; 22(20)2021 Oct 09.
Article in En | MEDLINE | ID: mdl-34681563
ABSTRACT
Assessing dementia conversion in patients with mild cognitive impairment (MCI) remains challenging owing to pathological heterogeneity. While many MCI patients ultimately proceed to Alzheimer's disease (AD), a subset of patients remain stable for various times. Our aim was to characterize the plasma metabolites of nineteen MCI patients proceeding to AD (P-MCI) and twenty-nine stable MCI (S-MCI) patients by untargeted metabolomics profiling. Alterations in the plasma metabolites between the P-MCI and S-MCI groups, as well as between the P-MCI and AD groups, were compared over the observation period. With the help of machine learning-based stratification, a 20-metabolite signature panel was identified that was associated with the presence and progression of AD. Furthermore, when the metabolic signature panel was used for classification of the three patient groups, this gave an accuracy of 73.5% using the panel. Moreover, when specifically classifying the P-MCI and S-MCI subjects, a fivefold cross-validation accuracy of 80.3% was obtained using the random forest model. Importantly, indole-3-propionic acid, a bacteria-generated metabolite from tryptophan, was identified as a predictor of AD progression, suggesting a role for gut microbiota in AD pathophysiology. Our study establishes a metabolite panel to assist in the stratification of MCI patients and to predict conversion to AD.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propionates / Metabolomics / Alzheimer Disease / Cognitive Dysfunction Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Taiwan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Propionates / Metabolomics / Alzheimer Disease / Cognitive Dysfunction Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Int J Mol Sci Year: 2021 Type: Article Affiliation country: Taiwan