Biomarkers of NAFLD progression: a lipidomics approach to an epidemic

被引:275
作者
Gorden, D. Lee [1 ,2 ]
Myers, David S. [3 ]
Ivanova, Pavlina T. [3 ]
Fahy, Eoin [7 ]
Maurya, Mano R. [7 ]
Gupta, Shakti [7 ]
Min, Jun [7 ]
Spann, Nathanael J. [8 ,9 ]
McDonald, Jeffrey G. [10 ]
Kelly, Samuel L. [11 ,12 ,13 ,14 ]
Duan, Jingjing [11 ,12 ,13 ,14 ]
Sullards, M. Cameron [11 ,12 ,13 ,14 ]
Leiker, Thomas J. [15 ]
Barkley, Robert M. [15 ]
Quehenberger, Oswald [16 ,17 ]
Armando, Aaron M. [17 ]
Milne, Stephen B. [3 ]
Mathews, Thomas P. [3 ]
Armstrong, Michelle D. [3 ]
Li, Chijun
Melvin, Willie V. [1 ]
Clements, Ronald H. [1 ]
Washington, M. Kay [4 ]
Mendonsa, Alisha M. [2 ]
Witztum, Joseph L. [16 ]
Guan, Ziqiang [19 ]
Glass, Christopher K. [8 ,9 ]
Murphy, Robert C. [15 ]
Dennis, Edward A. [17 ,18 ]
Merrill, Alfred H., Jr. [11 ,12 ,13 ,14 ]
Russell, David W. [10 ]
Subramaniam, Shankar [7 ,18 ]
Brown, H. Alex [3 ,5 ,6 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Surg, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, Dept Canc Biol, Nashville, TN USA
[3] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[5] Vanderbilt Univ, Med Ctr, Dept Biochem, Nashville, TN USA
[6] Vanderbilt Univ, Med Ctr, Vanderbilt Inst Chem Biol, Nashville, TN USA
[7] Univ Calif San Diego, Sch Engn, Dept Bioengn, La Jolla, CA 92093 USA
[8] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[9] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[10] Univ Texas SW Med Ctr Dallas, Dept Mol Genet, Dallas, TX 75390 USA
[11] Georgia Inst Technol, Sch Biol, Atlanta, GA 30332 USA
[12] Georgia Inst Technol, Sch Chem, Atlanta, GA 30332 USA
[13] Georgia Inst Technol, Sch Biochem, Atlanta, GA 30332 USA
[14] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[15] Univ Colorado Denver, Dept Pharmacol, Aurora, CO USA
[16] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
[17] Univ Calif San Diego, Sch Med, Dept Pharmacol, La Jolla, CA 92093 USA
[18] Univ Calif San Diego, Sch Med, Dept Chem & Biochem, La Jolla, CA 92093 USA
[19] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
diagnostic tools; mass spectrometry; phospholipids; sphingolipids; nonalcoholic fatty liver disease; nonalcoholic steatohepatitis; NONALCOHOLIC FATTY LIVER; LIQUID-CHROMATOGRAPHY; QUANTITATIVE-ANALYSIS; GENETIC-VARIATION; MOUSE MODEL; DE-NOVO; FIBROSIS; ACCUMULATION; STEATOHEPATITIS; METABOLITES;
D O I
10.1194/jlr.P056002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:722 / 736
页数:15
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