The rs72613567: TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children.

A. Di Sessa, G. R. Umano, G. Cirillo, P. Marzuillo, M. Arienzo, M. Pedullà, E. M. Giudice
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引用次数: 21

Abstract

We first investigated in obese children the protective role of the hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13) rs72613567:TA variant in liver damage. Six hundred eighty-five obese children were genotyped for HSD17B13, patatin-like phospholipase domain containing 3 (PNPLA3), transmembrane 6 superfamily member 2 (TM6SF2), and membrane bound O-acyltransferase domain containing 7 (MBOAT7) polymorphisms and underwent anthropometrical, ultrasonographic, and biochemical evaluation. Indirect measurement of liver fibrosis (Pediatric NAFLD Fibrosis Index [PNFI]) was calculated. The population was clustered in two genetic risk groups based on the numbers of steatogenic alleles (low: carriers up to 3 risk alleles, high:4-6 risk alleles).Carriers of the HSD17B13 rare A allele showed lower percentage of hepatic steatosis and both lower serum transaminase and PNFI levels than noncarriers, even after adjustments for confounders. These findings were also confirmed in both risk groups.We demonstrated the protective effect of the rs72613567:TA HSD17B13 variant in reducing liver damage in obese children regardless of genetic predisposition.
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羟基类固醇17- β脱氢酶13基因的rs72613567: TA变异可减少肥胖儿童的肝损伤
我们首先在肥胖儿童中研究了羟基类固醇17- β脱氢酶13 (HSD17B13) rs72613567:TA变异对肝损伤的保护作用。685名肥胖儿童进行了HSD17B13、含patin -like磷脂酶结构域3 (PNPLA3)、跨膜6超家族成员2 (TM6SF2)和膜结合o -酰基转移酶结构域7 (MBOAT7)多态性的基因分型,并进行了人体测量、超声和生化评价。计算肝纤维化间接测量(小儿NAFLD纤维化指数[PNFI])。根据致脂性等位基因的数量,将人群分为两个遗传风险组(低:携带多达3个风险等位基因,高:携带4-6个风险等位基因)。HSD17B13罕见A等位基因的携带者比非携带者的肝脂肪变性率更低,血清转氨酶和PNFI水平也更低,即使在混杂因素调整后也是如此。这些发现在两个风险群体中也得到了证实。我们证明了rs72613567:TA HSD17B13变异在减轻肥胖儿童肝损伤方面的保护作用,而不考虑遗传易感性。
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