Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease

Objectives. We determined the serum bile acid (BA) composition in patients with liver diseases and healthy volunteers to investigate the relationship between the etiologies of liver disease and BA metabolism. Material and Methods. Sera from 150 patients with liver diseases and 46 healthy volunteers...

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Main Authors: Tomonori Sugita, Katsushi Amano, Masanori Nakano, Noriko Masubuchi, Masahiro Sugihara, Tomokazu Matsuura
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2015/717431
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author Tomonori Sugita
Katsushi Amano
Masanori Nakano
Noriko Masubuchi
Masahiro Sugihara
Tomokazu Matsuura
author_facet Tomonori Sugita
Katsushi Amano
Masanori Nakano
Noriko Masubuchi
Masahiro Sugihara
Tomokazu Matsuura
author_sort Tomonori Sugita
collection DOAJ
description Objectives. We determined the serum bile acid (BA) composition in patients with liver diseases and healthy volunteers to investigate the relationship between the etiologies of liver disease and BA metabolism. Material and Methods. Sera from 150 patients with liver diseases and 46 healthy volunteers were obtained. The serum concentrations of the 16 different BAs were determined according to the LC-MS/MS method and were compared between the different liver diseases. Results. A total of 150 subjects, including patients with hepatitis C virus (HCV) (n=44), hepatitis B virus (HBV) (n=23), alcoholic liver disease (ALD) (n=21), biliary tract disease (n=20), nonalcoholic fatty liver disease (NAFLD) (n=13), and other liver diseases (n=29), were recruited. The levels of UDCA and GUDCA were significantly higher in the ALD group, and the levels of DCA and UDCA were significantly lower in the biliary tract diseases group than in viral hepatitis group. In the UDCA therapy (−) subgroup, a significantly lower level of TLCA was observed in the ALD group, with lower levels of CDCA, DCA, and GLCA noted in biliary tract diseases group compared to viral hepatitis group. Conclusions. Analysis of the BA composition may be useful for differential diagnosis in liver disease.
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spelling doaj-art-97256ef983154b01800b45602e231bc32025-02-03T01:01:13ZengWileyGastroenterology Research and Practice1687-61211687-630X2015-01-01201510.1155/2015/717431717431Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver DiseaseTomonori Sugita0Katsushi Amano1Masanori Nakano2Noriko Masubuchi3Masahiro Sugihara4Tomokazu Matsuura5Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato, Tokyo 105-8461, JapanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato, Tokyo 105-8461, JapanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-shinbashi, Minato, Tokyo 105-8461, JapanDrug Metabolism & Pharmacokinetics Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, JapanClinical Data & Biostatistics Department, R&D Division, Daiichi Sankyo Co., Ltd., Tokyo, JapanDepartment of Laboratory Medicine, The Jikei University School of Medicine, Tokyo, JapanObjectives. We determined the serum bile acid (BA) composition in patients with liver diseases and healthy volunteers to investigate the relationship between the etiologies of liver disease and BA metabolism. Material and Methods. Sera from 150 patients with liver diseases and 46 healthy volunteers were obtained. The serum concentrations of the 16 different BAs were determined according to the LC-MS/MS method and were compared between the different liver diseases. Results. A total of 150 subjects, including patients with hepatitis C virus (HCV) (n=44), hepatitis B virus (HBV) (n=23), alcoholic liver disease (ALD) (n=21), biliary tract disease (n=20), nonalcoholic fatty liver disease (NAFLD) (n=13), and other liver diseases (n=29), were recruited. The levels of UDCA and GUDCA were significantly higher in the ALD group, and the levels of DCA and UDCA were significantly lower in the biliary tract diseases group than in viral hepatitis group. In the UDCA therapy (−) subgroup, a significantly lower level of TLCA was observed in the ALD group, with lower levels of CDCA, DCA, and GLCA noted in biliary tract diseases group compared to viral hepatitis group. Conclusions. Analysis of the BA composition may be useful for differential diagnosis in liver disease.http://dx.doi.org/10.1155/2015/717431
spellingShingle Tomonori Sugita
Katsushi Amano
Masanori Nakano
Noriko Masubuchi
Masahiro Sugihara
Tomokazu Matsuura
Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
Gastroenterology Research and Practice
title Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
title_full Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
title_fullStr Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
title_full_unstemmed Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
title_short Analysis of the Serum Bile Acid Composition for Differential Diagnosis in Patients with Liver Disease
title_sort analysis of the serum bile acid composition for differential diagnosis in patients with liver disease
url http://dx.doi.org/10.1155/2015/717431
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