Literature DB >> 28987776

Bile acid profiles in neonatal intrahepatic cholestasis caused by citrin deficiency.

Ching-Hsuan Yang1, Chiung-Yu Chen2, Yen-Yin Chou3, Hung-Chih Chiu2, Wei-Lun Tsai4, Shu-Chu Shiesh5.   

Abstract

BACKGROUND: Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) is characterized by conjugated hyperbilirubinemia and increased plasma bile acid concentrations. However, the underlying mechanisms remain unclear. We established a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for simultaneously quantifying plasma bile acids and examined bile acid profiles in NICCD infants.
METHODS: We measured 15 bile acids within 15min and found a wide linear range for individual bile acids.
RESULTS: The within-run and run-to-run CV of all bile acids was 1.2-10.9% and 3.1-10.8%, respectively, with a mean recovery of 90.5-112.6%. Compared to infants with citrullinemia without mutations in SLC25A13 (non-NICCD), NICCD infants showed increased plasma total bile acid concentrations (mean: 201 vs. 42μM, p<0.001), with a distinct bile acid profile characterized by increased conjugated primary bile acid concentrations. The calculated ratios, including primary/secondary bile acid (714 vs. 235, p<0.05) and conjugated/free bile acid (371 vs. 125, p<0.05) ratios, were higher in NICCD infants. The area under receiver operating characteristic curve for conjugated/free bile acid ratio to identify infants with NICCD was 0.871 (95% confidence interval, 0.713-1.0).
CONCLUSIONS: Together, our findings indicated plasma bile acid profile as a potential noninvasive diagnostic biomarker for NICCD.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bile acid profile; Cholestasis; Citrin; Citrullinemia

Mesh:

Substances:

Year:  2017        PMID: 28987776     DOI: 10.1016/j.cca.2017.10.005

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  5 in total

1.  Clinical characteristics and genetic analysis of neonatal intrahepatic cholestasis caused by citrin deficiency in comparison with idiopathic neonatal cholestasis.

Authors:  Hao Liu; Chun Li; Xiaowen Li; Chaowen Yu; Xiaoyan He; Jingkun Miao
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2021-08-25

2.  Genetic Analysis of Peroxisomal Genes Required for Longevity in a Yeast Model of Citrin Deficiency.

Authors:  Chalongchai Chalermwat; Thitipa Thosapornvichai; Laran T Jensen; Duangrurdee Wattanasirichaigoon
Journal:  Diseases       Date:  2020-01-09

3.  Changes in plasma bile acid profiles after partial internal biliary diversion in PFIC2 patients.

Authors:  Teng Liu; Ren-Xue Wang; Jun Han; Yi-Ling Qiu; Christoph H Borchers; Victor Ling; Jian-She Wang
Journal:  Ann Transl Med       Date:  2020-03

4.  Development and validation of bile acid profile-based scoring system for identification of biliary atresia: a prospective study.

Authors:  Dongying Zhao; Kejun Zhou; Yan Chen; Wei Xie; Yongjun Zhang
Journal:  BMC Pediatr       Date:  2020-05-27       Impact factor: 2.125

5.  Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn.

Authors:  Yiming Lin; Weihua Lin; Yanru Chen; Chunmei Lin; Zhenzhu Zheng; Jianlong Zhuang; Qingliu Fu
Journal:  BMC Pediatr       Date:  2020-10-13       Impact factor: 2.125

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.