The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study

Traumatic brain injury is one of the major causes of morbidity and ‍mortality worldwide. With the development of bile acids as a ‍potential treatment, to identify the influence of traumatic brain ‍injury on bile acid metabolism shows growing importance. This present study did a preliminary explorati...

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Published inJournal of Clinical Biochemistry and Nutrition Vol. 73; no. 1; pp. 97 - 102
Main Authors Zhu, Yuanrun, Zheng, Peidong, Lin, Yajun, Wang, Juehan, You, Wendong, Wang, Yadong, Zheng, Huiqing, Wen, Liang, Yang, Xiaofeng
Format Journal Article
LanguageEnglish
Published Japan SOCIETY FOR FREE RADICAL RESEARCH JAPAN 2023
Japan Science and Technology Agency
the Society for Free Radical Research Japan
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Summary:Traumatic brain injury is one of the major causes of morbidity and ‍mortality worldwide. With the development of bile acids as a ‍potential treatment, to identify the influence of traumatic brain ‍injury on bile acid metabolism shows growing importance. This present study did a preliminary exploration of the bile acid ‍profile alteration among traumatic brain injury patients. In total, 14 patients and 7 healthy volunteers were enrolled. The bile ‍acid profile of the blood samples were detected by an Ultra-‍performance Liquid Chromatography Mass Spectrometer/Mass Spectrometer system. It was found that 6 bile acids were statistically decreased in traumatic brain injury patients comparing with healthy volunteers: glycocholic acid (median level 44.4 ng/ml vs 98.7 ng/ml, p = 0.003), taurocholic acid (median level 10.9 ng/ml vs 19.5 ng/ml, p = 0.006), glycoursodeoxycholic acid (median level 17.4 ng/ml vs 71.4 ng/ml, p = 0.001), ursodeoxycholic acid (median level <1 ng/ml vs 32.4 ng/ml, p = 0.002), taurochenodeoxycholic acid (median level <1 ng/ml vs 53.6 ng/ml, p = 0.003) and glycochenodeoxycholic acid (GCDCA, median level 160 ng/ml vs ‍364 ng/ml, p<0.001). In conclusion, traumatic brain injury events are able to induce bile acid metabolism alteration in plasma and might cause reduction in glycocholic, taurocholic, glycoursodeoxycholic, ursodeoxycholic, taurochenodeoxycholic and glycochenodeoxycholic acid levels.
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These authors contributed equally to this work.
ISSN:0912-0009
1880-5086
DOI:10.3164/jcbn.23-10