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Serum Metabolic Profiling Reveals Altered Metabolic Pathways in Patients with Post-traumatic Cognitive Impairments

Overview
Journal Sci Rep
Specialty Science
Date 2016 Feb 18
PMID 26883691
Citations 29
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Abstract

Cognitive impairment, the leading cause of traumatic brain injury (TBI)-related disability, adversely affects the quality of life of TBI patients, and exacts a personal and economic cost that is difficult to quantify. The underlying pathophysiological mechanism is currently unknown, and an effective treatment of the disease has not yet been identified. This study aimed to advance our understanding of the mechanism of disease pathogenesis; thus, metabolomics based on gas chromatography/mass spectrometry (GC-MS), coupled with multivariate and univariate statistical methods were used to identify potential biomarkers and the associated metabolic pathways of post-TBI cognitive impairment. A biomarker panel consisting of nine serum metabolites (serine, pyroglutamic acid, phenylalanine, galactose, palmitic acid, arachidonic acid, linoleic acid, citric acid, and 2,3,4-trihydroxybutyrate) was identified to be able to discriminate between TBI patients with cognitive impairment, TBI patients without cognitive impairment and healthy controls. Furthermore, associations between these metabolite markers and the metabolism of amino acids, lipids and carbohydrates were identified. In conclusion, our study is the first to identify several serum metabolite markers and investigate the altered metabolic pathway that is associated with post-TBI cognitive impairment. These markers appear to be suitable for further investigation of the disease mechanisms of post-TBI cognitive impairment.

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References
1.
Adibhatla R, Hatcher J . Altered lipid metabolism in brain injury and disorders. Subcell Biochem. 2008; 49:241-68. PMC: 2293298. DOI: 10.1007/978-1-4020-8831-5_9. View

2.
Wortzel H, Arciniegas D . Treatment of post-traumatic cognitive impairments. Curr Treat Options Neurol. 2012; 14(5):493-508. PMC: 3437653. DOI: 10.1007/s11940-012-0193-6. View

3.
Wang J, Byun J, Pennathur S . Analytical approaches to metabolomics and applications to systems biology. Semin Nephrol. 2010; 30(5):500-11. PMC: 2989741. DOI: 10.1016/j.semnephrol.2010.07.007. View

4.
Ellis J, Athersuch T, Thomas L, Teichert F, Perez-Trujillo M, Svendsen C . Metabolic profiling detects early effects of environmental and lifestyle exposure to cadmium in a human population. BMC Med. 2012; 10:61. PMC: 3391181. DOI: 10.1186/1741-7015-10-61. View

5.
Hashimoto K, Fukushima T, Shimizu E, Okada S, Komatsu N, Okamura N . Possible role of D-serine in the pathophysiology of Alzheimer's disease. Prog Neuropsychopharmacol Biol Psychiatry. 2004; 28(2):385-8. DOI: 10.1016/j.pnpbp.2003.11.009. View