Mass spectrometric profiling of oxidized lipid products in human nonalcoholic fatty liver disease and nonalcoholic steatohepatitis

被引:259
作者
Feldstein, Ariel E. [1 ,2 ,3 ]
Lopez, Rocio [5 ]
Tamimi, Tarek Abu-Rajab [7 ]
Yerian, Lisa [4 ]
Chung, Yoon-Mi [1 ,2 ]
Berk, Michael [1 ,2 ]
Zhang, Renliang [1 ,2 ]
McIntyre, Thomas M. [1 ,2 ]
Hazen, Stanley L. [1 ,2 ,6 ]
机构
[1] Case Western Reserve Univ, Cleveland Clin, Coll Med, Dept Cell Biol,Lerner Res Inst, Cleveland, OH 44106 USA
[2] Cleveland Clin, Ctr Cardiovasc Diagnost Prevent, Cleveland, OH 44106 USA
[3] Cleveland Clin, Dept Pediat Gastroenterol, Cleveland, OH 44106 USA
[4] Cleveland Clin, Dept Anat Pathol, Cleveland, OH 44106 USA
[5] Cleveland Clin, Dept Quantitat Hlth Sci, Cleveland, OH 44106 USA
[6] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44106 USA
[7] Cleveland Clin, Dept Gastroenterol & Hepatol, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
oxidized fatty acids; mass spectrometry; chiral mass spectrometry; OXIDATIVE STRESS; POPULATION; PATHOGENESIS; PEROXIDATION; PREVALENCE; MECHANISMS; DIAGNOSIS;
D O I
10.1194/jlr.M007096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Oxidative stress is a core abnormality responsible for disease progression in nonalcoholic fatty liver disease (NAFLD). However, the pathways that contribute to oxidative damage in vivo are poorly understood. Our aims were to define the circulating profile of lipid oxidation products in NAFLD patients, the source of these products, and assess whether their circulating levels reflect histological changes in the liver. The levels of multiple structurally specific oxidized fatty acids, including individual hydroxy-eicosatetraenoic acids (HETE), hydroxy-octadecadenoicacids (HODE), and oxo-octadecadenoic acids (oxoODE), were measured by mass spectrometry in plasma at time of liver biopsy in an initial cohort of 73 and a validation cohort of 49 consecutive patients. Of the markers monitored, 9- and 13-HODEs and 9- and 13-oxoODEs, products of free radical-mediated oxidation of linoleic acid (LA), were significantly elevated in patients with nonalcoholic steatohepatitis (NASH), compared with patients with steatosis. A strong correlation was revealed between these oxidation products and liver histopathology (inflammation, fibrosis, and steatosis). Further analyses of HODEs showed equivalent R and S chiral distribution. A risk score for NASH (oxNASH) was developed in the initial clinical cohort and shown to have high diagnostic accuracy for NASH versus steatosis in the independent validation cohort. Subjects with elevated oxNASH levels (top tertile) were 9.7-fold (P < 0.0001) more likely to have NASH than those with low levels (bottom tertile). Collectively, these findings support a key role for free radical-mediated linoleic acid oxidation in human NASH and define a risk score, oxNASH, for noninvasive detection of the presence of NASH.-Feldstein, A. E., R. Lopez, T. A-R. Tamimi, L. Yerian, Y-M. Chung, M. Berk, R. Zhang, T.M. McIntyre, and S. L. Hazen. Mass spectrometric profiling of oxidized lipid products in human nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. J. Lipid Res. 2010. 51: 3046-3054.
引用
收藏
页码:3046 / 3054
页数:9
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