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首页> 外文期刊>The American journal of clinical nutrition. >Increased hepatic fat in overweight Hispanic youth influenced by interaction between genetic variation in PNPLA3 and high dietary carbohydrate and sugar consumption.
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Increased hepatic fat in overweight Hispanic youth influenced by interaction between genetic variation in PNPLA3 and high dietary carbohydrate and sugar consumption.

机译:受PNPLA3遗传变异与高膳食碳水化合物和糖摄入量之间相互作用的影响,超重西班牙裔青年的肝脏脂肪增加。

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BACKGROUND: Recently, a genetic variant (rs738409; C-->G) of the PNPLA3 gene was identified to be associated with increased hepatic fat deposition, and the effect was more pronounced in Hispanics. Animal models have also shown that PNPLA3 expression can be regulated by dietary carbohydrate. OBJECTIVE: The aim of this study was to examine whether the influence of PNPLA3 genotype on hepatic fat is modulated by dietary factors in Hispanic children. DESIGN: PNPLA3 was genotyped in 153 Hispanic children (75 female, ages 8-18 y) by using the TaqMan method. Dietary intake was assessed by using three 24-h dietary recalls or diet records. Visceral adipose tissue (VAT), subcutaneous abdominal adipose tissue (SAAT), and hepatic fat fraction (HFF) were assessed in multiple abdominal slices by magnetic resonance imaging. Analysis of covariance was used to assess the diet x genotype interaction in liver fat, with the following a priori covariates: sex, age, energy, VAT, and SAAT. RESULTS: HFF was influenced by a significant interaction between genotype and diet (genotype x carbohydrate, P = 0.04; genotype x total sugar, P = 0.01). HFF was positively related to carbohydrate (r = 0.31, P = 0.04) and total sugar (r = 0.34, P = 0.02) intakes but only in the GG group, independent of covariates. Dietary variables were not related to HFF in the CC or CG group or to other fat depots in all genotype groups. CONCLUSIONS: These findings suggest that Hispanic children carrying the GG genotype are susceptible to increased hepatic fat when dietary carbohydrate intake, specifically sugar, is high. Specific dietary interventions based on genetic predisposition in this population may lead to more effective therapeutic outcomes for fatty liver. This trial was registered at clinicaltrials.gov as NCT00697580, 195-1642394A1, and NCT00693511.
机译:背景:最近,一个遗传变异(rs738409;PNPLA3基因的C-->G)被鉴定为与肝脏脂肪沉积增加有关,并且该效应在西班牙裔中更为明显。动物模型还表明,PNPLA3的表达可以受膳食碳水化合物的调节。目的: 本研究的目的是检查 PNPLA3 基因型对西班牙裔儿童肝脏脂肪的影响是否受饮食因素的调节。设计:使用 TaqMan 方法对 153 名西班牙裔儿童(75% 女性,年龄 8-18 岁)进行基因分型。通过使用三次 24 小时饮食回忆或饮食记录来评估饮食摄入量。通过磁共振成像评估多个腹部切片的内脏脂肪组织 (VAT)、皮下腹部脂肪组织 (SAAT) 和肝脏脂肪分数 (HFF)。协方差分析用于评估肝脏脂肪中的饮食 x 基因型相互作用,具有以下先验协变量:性别、年龄、能量、VAT 和 SAAT。结果:HFF受到基因型和饮食之间显著相互作用的影响(基因型x碳水化合物,P = 0.04;基因型x总糖,P = 0.01)。HFF与碳水化合物(r = 0.31,P = 0.04)和总糖(r = 0.34,P = 0.02)摄入量呈正相关,但仅在GG组中,与协变量无关。饮食变量与 CC 或 CG 组的 HFF 或所有基因型组的其他脂肪库无关。结论:这些发现表明,当膳食碳水化合物摄入量(特别是糖)较高时,携带GG基因型的西班牙裔儿童容易出现肝脂肪增加。基于该人群遗传易感性的特定饮食干预可能会为脂肪肝带来更有效的治疗结果。该试验在 clinicaltrials.gov 注册为NCT00697580,195-1642394A1和NCT00693511。

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