土耳其儿童维生素D受体基因多态性与肥胖、代谢综合征、肝纤维化的关系

B. Özhan, Elif Bi̇lgi̇han, Ozan Çetin, Kadir Ağladıoğlu
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引用次数: 0

摘要

目的:探讨儿童TaqI (rs731236)、ApaI (rs7975232)、BsmI (rs1544410)、FokI (rs10735810)的维生素D受体基因(VDR)多态性与肥胖、代谢综合征和肝纤维化的关系。材料与方法:本研究纳入10-16岁肥胖儿童130例,健康儿童130例。所有患儿均进行了人体测量、生化评价和腹部USG。采用限制性内切片段长度多态性技术对肥胖儿童和健康儿童进行了VDR基因最常见的多态性分析。代谢综合征的诊断采用国际糖尿病联合会的标准。结果:肥胖患者与对照组的BsmI、FokI、TaqI多态性基因型分布有统计学差异,而肥胖合并代谢综合征和肝骨病患者的所有研究多态性基因型分布无统计学差异。结论:BsmI多态性(rs1544410)在肥胖、代谢综合征和肝赘肉病的发生中具有显著的积极作用。携带儿童肥胖危险因素的儿童可以在发展为肥胖和相关代谢并发症之前使用VDR基因的BsmI多态性进行筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The relations of vitamin D receptor gene polymorphisms with risk of obesity, metabolic syndrome, hepatostetosis in Turkish children
Purpose: The aim of study was to determine the relation of vitamin D receptor gene (VDR) polymorphisms of TaqI (rs731236), ApaI (rs7975232), BsmI (rs1544410), FokI (rs10735810) with the risk of obesity, metabolic syndrome and hepatosteatosis in children.Materials and methods: 130 obese and 130 healthy children of age range between 10-16 years included in this study. Anthropometric measurements, biochemical evaluations and abdominal USG of all children were done. Obese and healty children were analyzed for the most common polymorphisms of the VDR gene by restriction fragment length polymorphism’s technique. The diagnosis of metabolic syndrome was made using the International Diabetes Federation criteria.Results: Genotypic distribution of BsmI, FokI, and TaqI polymorphism were found statistically different between obese patients and control group, but genotypic distribution of all studied polymorphisms were not found statistically different in obese patients with metabolic syndrome or hepatosteotosis. Conclusion: BsmI polymorphism (rs1544410) was found to have a significant positive effect on the development of obesity, metabolic syndrome and hepatosteatosis. Children who carry risk factors for childhood obesity could be screened before the development of obesity and associated metabolic complications using the BsmI polymorphism of the VDR gene.
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