Metabolomic profiling can predict which humans will develop liver dysfunction when deprived of dietary choline

被引:92
作者
Sha, Wei [2 ]
da Costa, Kerry-Ann [4 ,5 ]
Fischer, Leslie M. [4 ,5 ]
Milburn, Michael V. [6 ]
Lawton, Kay A. [6 ]
Berger, Alvin [6 ]
Jia, Wei [3 ]
Zeisel, Steven H. [1 ,4 ,5 ]
机构
[1] Univ N Carolina Chapel Hill, Nutr Res Inst, Kannapolis, NC 28081 USA
[2] Univ N Carolina Charlotte, Bioinformat Res Ctr, Kannapolis, NC USA
[3] Univ N Carolina Greensboro, Dept Nutr, Kannapolis, NC USA
[4] Univ N Carolina, Sch Publ Hlth, Dept Nutr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Sch Med, Chapel Hill, NC 27599 USA
[6] Metabolon Inc, Durham, NC USA
基金
美国国家卫生研究院;
关键词
fatty liver; metabolomics; plasma; PEMT; N-METHYLTRANSFERASE GENE; COA DESATURASE ACTIVITY; NONALCOHOLIC FATTY; HOMOCYSTEINE CONCENTRATION; PARENTERAL-NUTRITION; OSMOTIC REGULATION; FOLATE CONTENT; DEFICIENCY; BETAINE; TRANSPORT;
D O I
10.1096/fj.09-154054
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
Choline is an essential nutrient, and deficiency causes liver and muscle dysfunction. Common genetic variations alter the risk of developing organ dysfunction when choline deficient, probably by causing metabolic inefficiencies that should be detectable even while ingesting a normal choline-adequate diet. We determined whether metabolomic profiling of plasma at baseline could predict whether humans will develop liver dysfunction when deprived of dietary choline. Fifty-three participants were fed a diet containing 550 mg choline/70 kg/d for 10 d and then fed <50 mg choline/70 kg/d for up to 42 d. Participants who developed organ dysfunction on this diet were repleted with a choline-adequate diet for >= 3 d. Plasma samples, obtained at baseline, end of depletion, and end of repletion, were used for targeted and nontargeted metabolomic profiling. Liver fat was assessed using magnetic resonance spectroscopy. Metabolomic profiling and targeted biochemical analyses were highly correlated for the analytes assessed by both procedures. In addition, we report relative concentration changes of other small molecules detected by the nontargeted metabolomic analysis after choline depletion. Finally, we show that metabolomic profiles of participants when they were consuming a control baseline diet could predict whether they would develop liver dysfunction when deprived of dietary choline.-Sha, W., da Costa, K., Fischer, L. M., Milburn, M. V., Lawton, K. A., Berger, A., Jia, W., Zeisel, S. H. Metabolomic profiling can predict which humans will develop liver dysfunction when deprived of dietary choline. FASEB J. 24, 2962-2975 (2010). www.fasebj.org
引用
收藏
页码:2962 / 2975
页数:14
相关论文
共 75 条
[1]  
ACARA M, 1979, AM J PHYSIOL, V236, pF112
[2]   A p53-dependent G1 checkpoint function is not required for induction of apoptosis by acute choline deficiency in immortalized rat hepatocytes in culture [J].
Albright, CD ;
Salganik, RI ;
Kaufmann, WK ;
Vrablic, AS ;
Zeisel, SH .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1998, 9 (08) :476-481
[3]   Effects of orange juice and proline betaine on glycine betaine and homocysteine in healthy male subjects [J].
Atkinson, Wendy ;
Downer, Pamela ;
Lever, Michael ;
Chambers, Stephen T. ;
George, Peter M. .
EUROPEAN JOURNAL OF NUTRITION, 2007, 46 (08) :446-452
[4]   Relationship between stearoyl-CoA desaturase activity and plasma triglycerides in human and mouse hypertriglyceridemia [J].
Attie, AD ;
Krauss, RM ;
Gray-Keller, MP ;
Brownlie, A ;
Miyazaki, M ;
Kastelein, JJ ;
Lusis, AJ ;
Stalenhoef, AFH ;
Stoehr, JP ;
Hayden, MR ;
Ntambi, JM .
JOURNAL OF LIPID RESEARCH, 2002, 43 (11) :1899-1907
[5]  
Barrett T., 2008, U.S. Patent, Patent No. [7,433,787, 7433787]
[6]   Metabolomics approaches for discovering biomarkers of drug-induced hepatotoxicity and nephrotoxicity [J].
Beger, Richard D. ;
Sun, Jinchun ;
Schnackenberg, Laura K. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2010, 243 (02) :154-166
[7]   DEVELOPMENTAL-CHANGES IN THE ACTIVITY OF PHOSPHATIDYLETHANOLAMINE N-METHYLTRANSFERASES IN RAT-BRAIN [J].
BLUSZTAJN, JK ;
ZEISEL, SH ;
WURTMAN, RJ .
BIOCHEMICAL JOURNAL, 1985, 232 (02) :505-511
[8]   Discovery of Metabolomics Biomarkers for Early Detection of Nephrotoxicity [J].
Boudonck, Kurt J. ;
Mitchell, Matthew W. ;
Nemet, Laszlo ;
Keresztes, Lilla ;
Nyska, Abraham ;
Shinar, Doron ;
Rosenstock, Moti .
TOXICOLOGIC PATHOLOGY, 2009, 37 (03) :280-292
[9]   CHOLINE DEFICIENCY - A CAUSE OF HEPATIC STEATOSIS DURING PARENTERAL-NUTRITION THAT CAN BE REVERSED WITH INTRAVENOUS CHOLINE SUPPLEMENTATION [J].
BUCHMAN, AL ;
DUBIN, MD ;
MOUKARZEL, AA ;
JENDEN, DJ ;
ROCH, M ;
RICE, KM ;
GORNBEIN, J ;
AMENT, ME .
HEPATOLOGY, 1995, 22 (05) :1399-1403
[10]   Choline deficiency causes reversible hepatic abnormalities in patients receiving parenteral nutrition: Proof of a human choline requirement: A placebo-controlled trial [J].
Buchman, AL ;
Ament, ME ;
Sohel, M ;
Dubin, M ;
Jenden, DJ ;
Roch, M ;
Pownall, H ;
Farley, W ;
Awal, M ;
Ahn, C .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2001, 25 (05) :260-268