Literature DB >> 33859329

Plasma fetal bile acids 7α-hydroxy-3-oxochol-4-en-24-oic acid and 3-oxachola-4,6-dien-24-oic acid indicate severity of liver cirrhosis.

Tudor Mocan1, Dong Wook Kang2, Billy J Molloy3, Hyeonho Jeon2, Zeno A Spârchez1, Diren Beyoğlu4, Jeffrey R Idle5,6.   

Abstract

Two 3-oxo-Δ4 fetal bile acids, 3-oxachola-4,6-dien-24-oic acid (1) and 7α-hydroxy-3-oxochol-4-en-24-oic acid (2), occur normally in the human fetus but remain elevated in neonates and children with severe cholestatic liver disease due to an autosomal recessive inborn error of metabolism affecting Δ4-3-oxo-steroid 5β-reductase (AKR1D1). Relatively little is known about 1 and 2 in adult patients with liver disease. The chemical synthesis of 1 and 2 is therefore described and their quantitation in plasma by ultrarapid chromatography-triple quadrupole mass spectrometry. Plasma concentrations of 1 and 2 were investigated in 25 adult patients with varying degrees of liver cirrhosis with and without hepatocellular carcinoma (HCC). Highly statistically significant correlations (P < 0.0001) were found between severity of liver cirrhosis, determined by the Child-Pugh and MELD scores, with plasma 1 and 2 concentrations, both alone and combined. The presence of HCC did not influence these correlations. Plasma cholic, chenodeoxycholic, deoxycholic, lithocholic or ursodeoxycholic acids, free and as their glycine or taurine conjugates, did not correlate with Child-Pugh or MELD score when corrected for multiple comparisons. These findings demonstrate that plasma levels of fetal bile acids 3-oxachola-4,6-dien-24-oic acid and 7α-hydroxy-3-oxochol-4-en-24-oic acid and likely deteriorating AKR1D1 activity indicate the severity of liver cirrhosis measured by the Child-Pugh and MELD scores.

Entities:  

Year:  2021        PMID: 33859329     DOI: 10.1038/s41598-021-87921-5

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  20 in total

Review 1.  Assessment of the prognosis of cirrhosis: Child-Pugh versus MELD.

Authors:  François Durand; Dominique Valla
Journal:  J Hepatol       Date:  2004-12-24       Impact factor: 25.083

Review 2.  Metabolomic and Lipidomic Biomarkers for Premalignant Liver Disease Diagnosis and Therapy.

Authors:  Diren Beyoğlu; Jeffrey R Idle
Journal:  Metabolites       Date:  2020-01-28

3.  Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis.

Authors:  K D Setchell; F J Suchy; M B Welsh; L Zimmer-Nechemias; J Heubi; W F Balistreri
Journal:  J Clin Invest       Date:  1988-12       Impact factor: 14.808

4.  Superiority of the Child-Pugh classification to quantitative liver function tests for assessing prognosis of liver cirrhosis.

Authors:  I Albers; H Hartmann; J Bircher; W Creutzfeldt
Journal:  Scand J Gastroenterol       Date:  1989-04       Impact factor: 2.423

5.  Aberrant lipid metabolism in hepatocellular carcinoma revealed by plasma metabolomics and lipid profiling.

Authors:  Andrew D Patterson; Olivier Maurhofer; Diren Beyoglu; Christian Lanz; Kristopher W Krausz; Thomas Pabst; Frank J Gonzalez; Jean-François Dufour; Jeffrey R Idle
Journal:  Cancer Res       Date:  2011-09-07       Impact factor: 12.701

Review 6.  Global liver disease burdens and research trends: Analysis from a Chinese perspective.

Authors:  Jia Xiao; Fei Wang; Nai-Kei Wong; Jinhan He; Rui Zhang; Ruijuan Sun; Yanying Xu; Yingxia Liu; Wei Li; Kazuo Koike; Weiling He; Hong You; Yinglei Miao; Xiaowei Liu; Mingming Meng; Bin Gao; Hua Wang; Cui Li
Journal:  J Hepatol       Date:  2019-03-12       Impact factor: 25.083

Review 7.  Clinical epidemiology and disease burden of nonalcoholic fatty liver disease.

Authors:  Brandon J Perumpail; Muhammad Ali Khan; Eric R Yoo; George Cholankeril; Donghee Kim; Aijaz Ahmed
Journal:  World J Gastroenterol       Date:  2017-12-21       Impact factor: 5.742

8.  The acidic pathway of bile acid synthesis: Not just an alternative pathway.

Authors:  William M Pandak; Genta Kakiyama
Journal:  Liver Res       Date:  2019-05-21

9.  AKR1D1 is a novel regulator of metabolic phenotype in human hepatocytes and is dysregulated in non-alcoholic fatty liver disease.

Authors:  Nikolaos Nikolaou; Laura L Gathercole; Lea Marchand; Sara Althari; Niall J Dempster; Charlotte J Green; Martijn van de Bunt; Catriona McNeil; Anastasia Arvaniti; Beverly A Hughes; Bruno Sgromo; Richard S Gillies; Hanns-Ulrich Marschall; Trevor M Penning; John Ryan; Wiebke Arlt; Leanne Hodson; Jeremy W Tomlinson
Journal:  Metabolism       Date:  2019-07-19       Impact factor: 8.694

10.  Obesity and accumulation of subcutaneous adipose tissue are poor prognostic factors in patients with alcoholic liver cirrhosis.

Authors:  Akira Sakamaki; Kunihiko Yokoyama; Kyutaro Koyama; Shinichi Morita; Hiroyuki Abe; Kenya Kamimura; Masaaki Takamura; Shuji Terai
Journal:  PLoS One       Date:  2020-11-17       Impact factor: 3.240

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  2 in total

Review 1.  Novel approaches in search for biomarkers of cholangiocarcinoma.

Authors:  Lavinia-Patricia Mocan; Maria Ilieș; Carmen Stanca Melincovici; Mihaela Spârchez; Rareș Crăciun; Iuliana Nenu; Adelina Horhat; Cristian Tefas; Zeno Spârchez; Cristina Adela Iuga; Tudor Mocan; Carmen Mihaela Mihu
Journal:  World J Gastroenterol       Date:  2022-04-21       Impact factor: 5.374

Review 2.  Bile acids as drivers and biomarkers of hepatocellular carcinoma.

Authors:  Santo Colosimo; Jeremy W Tomlinson
Journal:  World J Hepatol       Date:  2022-09-27
  2 in total

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