Effects of Dietary Fructose Restriction on Liver Fat, De Novo Lipogenesis, and Insulin Kinetics in Children With Obesity

被引:204
作者
Schwarz, Jean-Marc [1 ,2 ]
Noworolski, Susan M. [3 ]
Erkin-Cakmak, Ayca [4 ]
Korn, Natalie J. [3 ]
Wen, Michael J. [2 ]
Tai, Viva W. [5 ]
Jones, Grace M. [1 ]
Palii, Sergiu P. [1 ]
Velasco-Alin, Moises [1 ,2 ]
Pan, Karen [2 ]
Patterson, Bruce W. [6 ]
Gugliucci, Alejandro [1 ]
Lustig, Robert H. [4 ]
Mulligan, Kathleen [1 ,2 ]
机构
[1] Touro Univ Calif, Coll Osteopath Med, Vallejo, CA USA
[2] Univ Calif San Francisco, Zuckerberg San Francisco Gen Hosp, Dept Med, Div Endocrinol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Benioff Childrens Hosp, Dept Pediat, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Clin & Translat Sci Inst, Clin Res Serv, San Francisco, CA 94143 USA
[6] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
Dietary Treatment; NAFLD; Pediatric; Overweight; HEPATIC STEATOSIS; VISCERAL FAT; ECTOPIC FAT; WEIGHT-LOSS; DISEASE; RESISTANCE; GLUCOSE; ADOLESCENTS; SENSITIVITY; DYSREGULATION;
D O I
10.1053/j.gastro.2017.05.043
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Consumption of sugar is associated with obesity, type 2 diabetes mellitus, nonalcoholic fatty liver disease, and cardiovascular disease. The conversion of fructose to fat in liver (de novo lipogenesis [DNL]) may be a modifiable pathogenetic pathway. We determined the effect of 9 days of isocaloric fructose restriction on DNL, liver fat, visceral fat (VAT), subcutaneous fat, and insulin kinetics in obese Latino and African American children with habitual high sugar consumption (fructose intake >50 g/d). METHODS: Children (9-18 years old; n=41) had all meals provided for 9 days with the same energy and macronutrient composition as their standard diet, but with starch substituted for sugar, yielding a final fructose content of 4% of total kilocalories. Metabolic assessments were performed before and after fructose restriction. Liver fat, VAT, and subcutaneous fat were determined by magnetic resonance spectroscopy and imaging. The fractional DNL area under the curve value was measured using stable isotope tracers and gas chromatography/mass spectrometry. Insulin kinetics were calculated from oral glucose tolerance tests. Paired analyses compared change from day 0 to day 10 within each child. RESULTS: Compared with baseline, on day 10, liver fat decreased from a median of 7.2% (interquartile range [IQR], 2.5%-14.8%) to 3.8% (IQR, 1.7%-15.5%) (P<.001) and VAT decreased from 123 cm(3) (IQR, 85-145 cm(3)) to 110 cm(3) (IQR, 84-134 cm(3)) (P<.001). The DNL area under the curve decreased from 68% (IQR, 46%-83%) to 26% (IQR, 16%-37%) (P<.001). Insulin kinetics improved (P<.001). These changes occurred irrespective of baseline liver fat. CONCLUSIONS: Short-term (9 days) isocaloric fructose restriction decreased liver fat, VAT, and DNL, and improved insulin kinetics in children with obesity. These findings support efforts to reduce sugar consumption. ClinicalTrials.gov Number: NCT01200043.
引用
收藏
页码:743 / 752
页数:10
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