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Metabolomics of blood reveals age-dependent pathways in Parkinson's Disease.
D'Ascenzo, Nicola; Antonecchia, Emanuele; Angiolillo, Antonella; Bender, Victor; Camerlenghi, Marco; Xie, Qingguo; Di Costanzo, Alfonso.
Afiliación
  • D'Ascenzo N; Huazhong University of Science and Technology, Wuhan, China. ndasc@hust.edu.cn.
  • Antonecchia E; Department of Medical Physics and Engineering, Istituto Neurologico Mediterraneo NEUROMED I.R.C.C.S., Pozzilli, Italy. ndasc@hust.edu.cn.
  • Angiolillo A; Huazhong University of Science and Technology, Wuhan, China.
  • Bender V; Department of Medical Physics and Engineering, Istituto Neurologico Mediterraneo NEUROMED I.R.C.C.S., Pozzilli, Italy.
  • Camerlenghi M; Centre for Research and Training in Medicine of Aging, Department of Medicine and Health Sciences "V. Tiberio", University of Molise, Campobasso, Italy. angiolillo@unimol.it.
  • Xie Q; Department of Medical Physics and Engineering, Istituto Neurologico Mediterraneo NEUROMED I.R.C.C.S., Pozzilli, Italy.
  • Di Costanzo A; NIM Competence Center for Digital Healthcare GmbH, Berlin, Germany.
Cell Biosci ; 12(1): 102, 2022 Jul 06.
Article en En | MEDLINE | ID: mdl-35794650
BACKGROUND: Parkinson's Disease (PD) is the second most frequent degenerative disorder, the risk of which increases with age. A preclinical PD diagnostic test does not exist. We identify PD blood metabolites and metabolic pathways significantly correlated with age to develop personalized age-dependent PD blood biomarkers. RESULTS: We found 33 metabolites producing a receiver operating characteristic (ROC) area under the curve (AUC) value of 97%. PCA revealed that they belong to three pathways with distinct age-dependent behavior: glycine, threonine and serine metabolism correlates with age only in PD patients; unsaturated fatty acids biosynthesis correlates with age only in a healthy control group; and, finally, tryptophan metabolism characterizes PD but does not correlate with age. CONCLUSIONS: The targeted analysis of the blood metabolome proposed in this paper allowed to find specific age-related metabolites and metabolic pathways. The model offers a promising set of blood biomarkers for a personalized age-dependent approach to the early PD diagnosis.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Biosci Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Cell Biosci Año: 2022 Tipo del documento: Article País de afiliación: China