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Systematic transcriptome analysis reveals elevated expression of alcohol-metabolizing genes in NAFLD livers.
Zhu, Ruixin; Baker, Susan S; Moylan, Cynthia A; Abdelmalek, Manal F; Guy, Cynthia D; Zamboni, Fausto; Wu, Dingfeng; Lin, Weili; Liu, Wensheng; Baker, Robert D; Govindarajan, Sugantha; Cao, Zhiwei; Farci, Patrizia; Diehl, Anna Mae; Zhu, Lixin.
Affiliation
  • Zhu R; Department of Bioinformatics, Tongji University, Shanghai, China.
  • Baker SS; Digestive Diseases and Nutrition Center, Department of Pediatrics, The State University of New York at Buffalo, Buffalo, New York, USA.
  • Moylan CA; Division of Gastroenterology and Hepatology, Department of Medicine, Duke University, Durham, North Carolina, USA.
  • Abdelmalek MF; Division of Gastroenterology and Hepatology, Department of Medicine, Durham Veterans Affairs Medical Center, Durham, North Carolina, USA.
  • Guy CD; Division of Gastroenterology and Hepatology, Department of Medicine, Duke University, Durham, North Carolina, USA.
  • Zamboni F; Department of Pathology, Duke University, Durham, North Carolina, USA.
  • Wu D; Liver Transplantation Center, Brotzu Hospital, 09134, Cagliari, Italy.
  • Lin W; Department of Bioinformatics, Tongji University, Shanghai, China.
  • Liu W; Department of Bioinformatics, Tongji University, Shanghai, China.
  • Baker RD; Digestive Diseases and Nutrition Center, Department of Pediatrics, The State University of New York at Buffalo, Buffalo, New York, USA.
  • Govindarajan S; Digestive Diseases and Nutrition Center, Department of Pediatrics, The State University of New York at Buffalo, Buffalo, New York, USA.
  • Cao Z; Department of Pathology, University of Southern California, Los Angeles, California, USA.
  • Farci P; Department of Bioinformatics, Tongji University, Shanghai, China.
  • Diehl AM; Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Zhu L; Division of Gastroenterology and Hepatology, Department of Medicine, Duke University, Durham, North Carolina, USA.
J Pathol ; 238(4): 531-42, 2016 Mar.
Article in En | MEDLINE | ID: mdl-26415102
ABSTRACT
Obese animals and non-alcoholic fatty liver disease (NAFLD) patients exhibit elevated blood alcohol, suggesting potential contributions of alcohol metabolism to the development of NAFLD. Liver gene expression in patients with biopsy-proven mild (N = 40) and severe (N = 32) NAFLD were compared to that in healthy liver donors (N = 7) and alcoholic hepatitis (AH; N = 15) using microarrays. Principal components analyses (PCA) revealed similar gene expression patterns between mild and severe NAFLD which clustered with those of AH but were distinct from those of healthy livers. Differential gene expression between NAFLD and healthy livers was consistent with established NAFLD-associated genes and NAFLD pathophysiology. Alcohol-metabolizing enzymes including ADH, ALDH, CYP2E1, and CAT were up-regulated in NAFLD livers. The expression level of alcohol-metabolizing genes in severe NAFLD was similar to that in AH. The NAFLD gene expression profiles provide new directions for future investigations to identify disease markers and targets for prevention and treatment, as well as to foster our understanding of NAFLD pathogenesis and pathophysiology. Particularly, increased expression of alcohol-metabolizing genes in NAFLD livers supports a role for endogenous alcohol metabolism in NAFLD pathology and provides further support for gut microbiome therapy in NAFLD management. Copyright © 2015 Pathological Society of Great Britain and Ireland. Published by John Wiley © Sons, Ltd.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohols / Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Pathol Year: 2016 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alcohols / Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: J Pathol Year: 2016 Type: Article Affiliation country: China