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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 exploration...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390815/ https://www.ncbi.nlm.nih.gov/pubmed/37534094 http://dx.doi.org/10.3164/jcbn.23-10 |
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author | Zhu, Yuanrun Zheng, Peidong Lin, Yajun Wang, Juehan You, Wendong Wang, Yadong Zheng, Huiqing Wen, Liang Yang, Xiaofeng |
author_facet | Zhu, Yuanrun Zheng, Peidong Lin, Yajun Wang, Juehan You, Wendong Wang, Yadong Zheng, Huiqing Wen, Liang Yang, Xiaofeng |
author_sort | Zhu, Yuanrun |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10390815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-103908152023-08-02 The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study Zhu, Yuanrun Zheng, Peidong Lin, Yajun Wang, Juehan You, Wendong Wang, Yadong Zheng, Huiqing Wen, Liang Yang, Xiaofeng J Clin Biochem Nutr Original Article 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. the Society for Free Radical Research Japan 2023-07 2023-06-13 /pmc/articles/PMC10390815/ /pubmed/37534094 http://dx.doi.org/10.3164/jcbn.23-10 Text en Copyright © 2023 JCBN https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article Zhu, Yuanrun Zheng, Peidong Lin, Yajun Wang, Juehan You, Wendong Wang, Yadong Zheng, Huiqing Wen, Liang Yang, Xiaofeng The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title | The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title_full | The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title_fullStr | The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title_full_unstemmed | The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title_short | The alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
title_sort | alteration of serum bile acid profile among traumatic brain injury patients: a small-scale prospective study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390815/ https://www.ncbi.nlm.nih.gov/pubmed/37534094 http://dx.doi.org/10.3164/jcbn.23-10 |
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