Abstract
Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease that is frequently found in athletes and those who have experienced repetitive head traumas. CTE is associated with a variety of neuropathologies, which cause cognitive and behavioral impairments in CTE patients. However, currently, CTE can only be diagnosed after death via brain autopsy, and it is challenging to distinguish it from other neurodegenerative diseases with similar clinical features. To better understand this multifaceted disease and identify metabolic differences in the postmortem brain tissues of CTE patients and control subjects, we performed ultra-high performance liquid chromatography–mass spectrometry (UPLC-MS)-based non-targeted metabolomics. Through multivariate and pathway analysis, we found that the brains of CTE patients had significant changes in the metabolites involved in astrocyte activation, phenylalanine, and tyrosine metabolism. The unique metabolic characteristics of CTE identified in this study were associated with cognitive dysfunction, amyloid-beta deposition, and neuroinflammation. Altogether, this study provided new insights into the pathogenesis of CTE and suggested appealing targets for both diagnosis and treatment for the disease.
Original language | English |
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Article number | 1718 |
Journal | Biomedicines |
Volume | 10 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2022 Jul |
Bibliographical note
Funding Information:This study was supported by grants from Intramural Research Program of the Korea Institute of Science and Technology (KIST) (2E31623, 2E31504, K-Lab Grant, and 2E31505). This study was supported by Korean National Research Foundation Grants (NRF-2018M3C7A1056894, NRF-2020M3E5D9079742, NRF-2022R1A2C3013138, and 2022R1A2C3003901). This study was also supported by NIH Grant (R01NS109537).
Publisher Copyright:
© 2022 by the authors.
Keywords
- astrocyte activation
- catecholamines
- chronic traumatic encephalopathy (CTE)
- non-targeted metabolomics
- phenylalanine metabolism
- tyrosine metabolism
ASJC Scopus subject areas
- Medicine (miscellaneous)
- General Biochemistry,Genetics and Molecular Biology