4.4 Article

Serum and Fecal Oxylipins in Patients with Alcohol-Related Liver Disease

Journal

DIGESTIVE DISEASES AND SCIENCES
Volume 64, Issue 7, Pages 1878-1892

Publisher

SPRINGER
DOI: 10.1007/s10620-019-05638-y

Keywords

AA; EPA; DHA; PUFA; Lipid mediator; Metabolomics

Funding

  1. NIH [R01 AA020703, R01 AA24726, U01 AA021856, U01 AA026939]
  2. Biomedical Laboratory Research & Development Service of the VA Office of Research and Development [BX004594]
  3. Fond National de Recherche Scientifique (FNRS) Belgium [CDR J.0146.17, PDR T.0217.18]

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BackgroundAlcohol-related liver disease is one of the most prevalent chronic liver diseases worldwide. Mechanisms involved in the pathogenesis of alcohol-related liver disease are not well understood. Oxylipins play a crucial role in numerous biological processes and pathological conditions. Nevertheless, oxylipins are not well studied in alcohol-related liver disease.Aims(1) To characterize the patterns of bioactive -3 and -6 polyunsaturated fatty acid metabolites in alcohol use disorder and alcoholic hepatitis patients and (2) to identify associations of serum oxylipins with clinical parameters in patients with alcohol-related liver disease.MethodsWe performed a comprehensive liquid chromatography with tandem mass spectrometry (LC-MS/MS) analysis of serum and fecal oxylipins derived from -6 arachidonic acid, -3 eicosapentaenoic acid, and docosahexaenoic acid in a patient cohort with alcohol-related liver disease.ResultsOur results show profound alterations in the serum oxylipin profile of patients with alcohol use disorder and alcoholic hepatitis compared to nonalcoholic controls. Spearman correlation of the oxylipins with clinical parameters shows a link between different serum oxylipins and intestinal permeability, aspartate aminotransferase, bilirubin, albumin, international normalized ratio, platelet count, steatosis, fibrosis and model for end-stage liver disease score. Especially, higher level of serum 20-HETE was significantly associated with decreased albumin, increased hepatic steatosis, polymorphonuclear infiltration, and 90-day mortality.ConclusionsPatients with alcohol-related liver disease have different oxylipin profiles. Future studies are required to confirm oxylipins as disease biomarker or to connect oxylipins to disease pathogenesis.

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