Your browser doesn't support javascript.
loading
Biomarkers of NAFLD progression: a lipidomics approach to an epidemic.
Gorden, D Lee; Myers, David S; Ivanova, Pavlina T; Fahy, Eoin; Maurya, Mano R; Gupta, Shakti; Min, Jun; Spann, Nathanael J; McDonald, Jeffrey G; Kelly, Samuel L; Duan, Jingjing; Sullards, M Cameron; Leiker, Thomas J; Barkley, Robert M; Quehenberger, Oswald; Armando, Aaron M; Milne, Stephen B; Mathews, Thomas P; Armstrong, Michelle D; Li, Chijun; Melvin, Willie V; Clements, Ronald H; Washington, M Kay; Mendonsa, Alisha M; Witztum, Joseph L; Guan, Ziqiang; Glass, Christopher K; Murphy, Robert C; Dennis, Edward A; Merrill, Alfred H; Russell, David W; Subramaniam, Shankar; Brown, H Alex.
Afiliação
  • Gorden DL; Departments of Surgery, Vanderbilt University Medical Center, Nashville, TN; Cancer Biology, Vanderbilt University Medical Center, Nashville, TN.
  • Myers DS; Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
  • Ivanova PT; Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
  • Fahy E; Department of Bioengineering, School of Engineering, University of California, San Diego, La Jolla, CA.
  • Maurya MR; Department of Bioengineering, School of Engineering, University of California, San Diego, La Jolla, CA.
  • Gupta S; Department of Bioengineering, School of Engineering, University of California, San Diego, La Jolla, CA.
  • Min J; Department of Bioengineering, School of Engineering, University of California, San Diego, La Jolla, CA.
  • Spann NJ; Departments of Cellular and Molecular Medicine and Medicine, University of California, San Diego, La Jolla, CA.
  • McDonald JG; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX.
  • Kelly SL; Schools of Biology, Chemistry, and Biochemistry, and the Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA.
  • Duan J; Schools of Biology, Chemistry, and Biochemistry, and the Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA.
  • Sullards MC; Schools of Biology, Chemistry, and Biochemistry, and the Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA.
  • Leiker TJ; Department of Pharmacology, University of Colorado at Denver, Aurora, CO.
  • Barkley RM; Department of Pharmacology, University of Colorado at Denver, Aurora, CO.
  • Quehenberger O; Departments of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA; Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA.
  • Armando AM; Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA.
  • Milne SB; Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
  • Mathews TP; Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
  • Armstrong MD; Pharmacology, Vanderbilt University Medical Center, Nashville, TN.
  • Li C; Department of Biochemistry, Duke University Medical Center, Durham, NC.
  • Melvin WV; Departments of Surgery, Vanderbilt University Medical Center, Nashville, TN.
  • Clements RH; Departments of Surgery, Vanderbilt University Medical Center, Nashville, TN.
  • Washington MK; Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.
  • Mendonsa AM; Cancer Biology, Vanderbilt University Medical Center, Nashville, TN.
  • Witztum JL; Departments of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA.
  • Guan Z; Department of Biochemistry, Duke University Medical Center, Durham, NC.
  • Glass CK; Departments of Cellular and Molecular Medicine and Medicine, University of California, San Diego, La Jolla, CA.
  • Murphy RC; Department of Pharmacology, University of Colorado at Denver, Aurora, CO.
  • Dennis EA; Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA; Chemistry and Biochemistry, School of Medicine, University of California, San Diego, La Jolla, CA.
  • Merrill AH; Schools of Biology, Chemistry, and Biochemistry, and the Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA.
  • Russell DW; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX.
  • Subramaniam S; Department of Bioengineering, School of Engineering, University of California, San Diego, La Jolla, CA; Chemistry and Biochemistry, School of Medicine, University of California, San Diego, La Jolla, CA. Electronic address: shankar@ucsd.edu.
  • Brown HA; Pharmacology, Vanderbilt University Medical Center, Nashville, TN; Biochemistry, and the Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical Center, Nashville, TN. Electronic address: alex.brown@vanderbilt.edu.
J Lipid Res ; 56(3): 722-736, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25598080
ABSTRACT
The spectrum of nonalcoholic fatty liver disease (NAFLD) includes steatosis, nonalcoholic steatohepatitis (NASH), and cirrhosis. Recognition and timely diagnosis of these different stages, particularly NASH, is important for both potential reversibility and limitation of complications. Liver biopsy remains the clinical standard for definitive diagnosis. Diagnostic tools minimizing the need for invasive procedures or that add information to histologic data are important in novel management strategies for the growing epidemic of NAFLD. We describe an "omics" approach to detecting a reproducible signature of lipid metabolites, aqueous intracellular metabolites, SNPs, and mRNA transcripts in a double-blinded study of patients with different stages of NAFLD that involves profiling liver biopsies, plasma, and urine samples. Using linear discriminant analysis, a panel of 20 plasma metabolites that includes glycerophospholipids, sphingolipids, sterols, and various aqueous small molecular weight components involved in cellular metabolic pathways, can be used to differentiate between NASH and steatosis. This identification of differential biomolecular signatures has the potential to improve clinical diagnosis and facilitate therapeutic intervention of NAFLD.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Hepatopatia Gordurosa não Alcoólica / Lipídeos Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Hepatopatia Gordurosa não Alcoólica / Lipídeos Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article