A Branched-Chain Amino Acid-Related Metabolic Signature Characterizes Obese Adolescents with Non-Alcoholic Fatty Liver Disease

被引:96
作者
Goffredo, Martina [1 ]
Santoro, Nicola [1 ]
Trico, Domenico [2 ,3 ]
Giannini, Cosimo [1 ,4 ]
D'Adamo, Ebe [1 ,4 ]
Zhao, Hongyu [5 ]
Peng, Gang [5 ]
Yu, Xiaoqing [5 ]
Lam, Tukiet T. [6 ]
Pierpont, Bridget [1 ]
Caprio, Sonia [1 ]
Herzog, Raimund I. [2 ]
机构
[1] Yale Univ, Sch Med, Dept Pediat, 330 Cedar St,POB 208064, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Internal Med, 300 Cedar St,POB 208020, New Haven, CT 06520 USA
[3] Univ Pisa, Dept Clin & Expt Med, I-56126 Pisa, PI, Italy
[4] Univ G dAnnunzio, Dept Pediat, I-66100 Chieti, CH, Italy
[5] Yale Sch Publ Hlth, New Haven, CT 06520 USA
[6] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
metabolomics; youth; branched chain amino acids; insulin resistance; nonalcoholic fatty liver disease; obesity; INSULIN SENSITIVITY INDEXES; GLUCOSE-TOLERANCE; HEPATIC STEATOSIS; CHILDHOOD OBESITY; SYSTEM L; RESISTANCE; PROFILES; CHILDREN; ETHNICITY; DISCOVERY;
D O I
10.3390/nu9070642
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Dysregulation of several metabolite pathways, including branched-chain amino acids (BCAAs), are associated with Non-Alcoholic Fatty Liver Disease (NAFLD) and insulin resistance in adults, while studies in youth reported conflicting results. We explored whether, independently of obesity and insulin resistance, obese adolescents with NAFLD display a metabolomic signature consistent with disturbances in amino acid and lipid metabolism. A total of 180 plasma metabolites were measured by a targeted metabolomic approach in 78 obese adolescents with (n = 30) or without (n = 48) NAFLD assessed by magnetic resonance imaging (MRI). All subjects underwent an oral glucose tolerance test and subsets of patients underwent a two-step hyperinsulinemic-euglycemic clamp and/or a second MRI after a 2.2 +/- 0.8-year follow-up. Adolescents with NAFLD had higher plasma levels of valine (p = 0.02), isoleucine (p = 0.03), tryptophan (p = 0.02), and lysine (p = 0.02) after adjustment for confounding factors. Circulating BCAAs were negatively correlated with peripheral and hepatic insulin sensitivity. Furthermore, higher baseline valine levels predicted an increase in hepatic fat content (HFF) at follow-up (p = 0.01). These results indicate that a dysregulation of BCAA metabolism characterizes obese adolescents with NAFLD independently of obesity and insulin resistance and predict an increase in hepatic fat content over time.
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页数:12
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