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Dynamic Elevation of Aromatic Amino Acids in Hepatitis C Virus-Induced Cirrhosis After a Standard Meal.
Hill, Kareen L; Haddad, James A; Ali, Rabab O; Zhang, Grace Y; Quinn, Gabriella M; Townsend, Elizabeth; Everson, Gregory T; Helmke, Steve M; Bagheri, Mohammadhadi; Schoenfeld, Megan; Yang, Shanna; Koh, Christopher; Levy, Elliot B; Kleiner, David E; Sacks, David B; Etzion, Ohad; Heller, Theo.
Afiliação
  • Hill KL; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Haddad JA; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Ali RO; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Zhang GY; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Quinn GM; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Townsend E; Translational Hepatology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Everson GT; Section of Hepatology, Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Helmke SM; HepQuant LLC, Greenwood Village, Colorado, USA.
  • Bagheri M; Section of Hepatology, Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Schoenfeld M; HepQuant LLC, Greenwood Village, Colorado, USA.
  • Yang S; Clinical Image Processing Service, Radiology and Imaging Sciences, National Institutes of Health, Bethesda, Maryland, USA.
  • Koh C; Nutrition Department, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
  • Levy EB; Nutrition Department, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
  • Kleiner DE; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Sacks DB; Center for Interventional Oncology, Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
  • Etzion O; Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Heller T; Clinical Chemistry Service, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Clin Transl Gastroenterol ; 15(3): e00666, 2024 03 01.
Article em En | MEDLINE | ID: mdl-38088382
ABSTRACT

INTRODUCTION:

Perturbations in aromatic (AAAs) and branched-chain amino acids (BCAAs) are seen in decompensated liver disease. The aim of this study was to evaluate the dynamic, postprandial relationship between hepatitis C virus-induced liver disease and amino acid concentrations in patients with compensated liver disease.

METHODS:

Patients infected with hepatitis C virus underwent a baseline liver biopsy to determine Ishak Fibrosis Score and evaluate the liver transcriptome. Patients ate a standard meal and underwent peripheral vein sampling at defined intervals. Quantitative analysis of amino acids was performed using liquid chromatography-tandem mass spectrometry.

RESULTS:

At baseline, there was no difference in AAA and BCAA concentrations between patients with cirrhosis and non-cirrhotic patients. After a standard meal, AAAs, but not BCAAs, were elevated in patients with cirrhosis compared with non-cirrhotic patients at every time point. The HepQuant SHUNT fraction was significantly higher in patients with cirrhosis and positively correlated with AAA concentration at all time points, but not BCAA. Analysis of the hepatic transcriptome demonstrated greater downregulation of the AAA degradation pathways than the BCAA degradation pathways.

DISCUSSION:

At baseline, cirrhotic patients with compensated liver disease have adequate reserve liver function to metabolize AAAs and BCAAs. When faced with a metabolic stressor, such as a standard meal, patients with cirrhosis are less able to metabolize the increased load of AAAs. This impairment correlates with portosystemic shunting. Further evaluation of AAA levels in compensated liver disease might further the understanding of the liver-muscle axis and the role it may play in the development of sarcopenia in liver disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Hepatopatias Limite: Humans Idioma: En Revista: Clin Transl Gastroenterol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Hepatopatias Limite: Humans Idioma: En Revista: Clin Transl Gastroenterol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos