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Profiles of Serum Bile Acids in Liver Diseases

Cholylglycine (CG) and sulfolithocholylglycine (SLCG) in fasting and postprandial serum were determined in patients with liver diseases by radioimmunoassay. In normal controls, fasting CG and SLCG were 54.67±68.66ng/100ml and 16.61 ±12.84ng/100ml respectively, while postprandial CG and SLCG were 61....

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Detalles Bibliográficos
Autores principales: Kim, Min Ja, Suh, Dong Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534900/
https://www.ncbi.nlm.nih.gov/pubmed/15759374
http://dx.doi.org/10.3904/kjim.1986.1.1.37
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author Kim, Min Ja
Suh, Dong Jin
author_facet Kim, Min Ja
Suh, Dong Jin
author_sort Kim, Min Ja
collection PubMed
description Cholylglycine (CG) and sulfolithocholylglycine (SLCG) in fasting and postprandial serum were determined in patients with liver diseases by radioimmunoassay. In normal controls, fasting CG and SLCG were 54.67±68.66ng/100ml and 16.61 ±12.84ng/100ml respectively, while postprandial CG and SLCG were 61.21 ±37.29ng/100ml and 21.95± 15.9ng/100ml respectively. In liver disease, serum bile acids were elevated. The greatest increase was found in acute viral hepatitis but moderate or slight increase was also found in chronic active hepatitis, liver cirrhosis, and hepatoma. Fasting bile acids seem to be a sensitive index for hepatocellular dysfunction but not for differential diagnosis of liver diseases. In liver diseases except hepatoma, fasting CG and SLCG correlated significantly with total bilirubin, albumin, GOT, GPT, and alkaline phosphatase but not with cholesterol. Insignificant elevation of bile acids was found postprandially in patients with liver diseases as well as normal controls and postprandial bile acids were not more sensitive than fasting ones.
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spelling pubmed-45349002015-10-02 Profiles of Serum Bile Acids in Liver Diseases Kim, Min Ja Suh, Dong Jin Korean J Intern Med Original Article Cholylglycine (CG) and sulfolithocholylglycine (SLCG) in fasting and postprandial serum were determined in patients with liver diseases by radioimmunoassay. In normal controls, fasting CG and SLCG were 54.67±68.66ng/100ml and 16.61 ±12.84ng/100ml respectively, while postprandial CG and SLCG were 61.21 ±37.29ng/100ml and 21.95± 15.9ng/100ml respectively. In liver disease, serum bile acids were elevated. The greatest increase was found in acute viral hepatitis but moderate or slight increase was also found in chronic active hepatitis, liver cirrhosis, and hepatoma. Fasting bile acids seem to be a sensitive index for hepatocellular dysfunction but not for differential diagnosis of liver diseases. In liver diseases except hepatoma, fasting CG and SLCG correlated significantly with total bilirubin, albumin, GOT, GPT, and alkaline phosphatase but not with cholesterol. Insignificant elevation of bile acids was found postprandially in patients with liver diseases as well as normal controls and postprandial bile acids were not more sensitive than fasting ones. Korean Association of Internal Medicine 1986-01 /pmc/articles/PMC4534900/ /pubmed/15759374 http://dx.doi.org/10.3904/kjim.1986.1.1.37 Text en © 1986 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Min Ja
Suh, Dong Jin
Profiles of Serum Bile Acids in Liver Diseases
title Profiles of Serum Bile Acids in Liver Diseases
title_full Profiles of Serum Bile Acids in Liver Diseases
title_fullStr Profiles of Serum Bile Acids in Liver Diseases
title_full_unstemmed Profiles of Serum Bile Acids in Liver Diseases
title_short Profiles of Serum Bile Acids in Liver Diseases
title_sort profiles of serum bile acids in liver diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534900/
https://www.ncbi.nlm.nih.gov/pubmed/15759374
http://dx.doi.org/10.3904/kjim.1986.1.1.37
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