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脂联素基因多态性与儿童肥胖的关联

[Association of adiponectin gene polymorphism with obesity in children].

作者信息

Wu Jing, Yan Wei-Jian, Mo Juan, Yang Hao-Bo, Wang Zhao-Zhao, Lei Min-Xiang, Peng Lie-Wu

机构信息

Department of Endocrinology, Xiangya Hospital of Central South University, Changsha 410008, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2011 Jul;13(7):539-42.

PMID:21752317
Abstract

OBJECTIVE

To study the distribution characteristics of adiponectin gene +45 single nucleotide polymorphisms (SNP) in Chinese children, and to determine the role of adiponectin gene +45 polymorphisms in the pathogenesis of childhood obesity.

METHODS

A total of 147 Chinese obese and 118 healthy children were randomly selected and enrolled to identify adiponectin gene SNP+45 polymorphism by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. Plasma adiponectin levels were determined using ELISA. Waist circumference (WC), waist to hip ratio (WHR), percentage of body fat (%BF), systolic blood pressure (SBP), diastolic blood pressure (DBP), fasting plasma glucose (FPG), serum triglycerides (TG), total cholesterol (TC), high density lipoprotein-cholesterol (HDL-C), low density lipoprotein-cholesterol (LDL-C), plasma fasting insulin (FINS), and homeostasis model assessment of insulin resistance (HOMA-IR) were measured.

RESULTS

The allelic frequency of adiponectin gene SNP+45 in children with obesity and healthy controls were 40.5% and 25.4%, respectively. There were significant differences in the distribution of genotypes and the allelic frequency between the two groups (P<0.05). The plasma adiponectin levels were significantly higher, in contrast, %BF, HOMA-IR, TC and LDL-C levels were significantly lower in obese children with TT genotype than those in obese children with TG or GG genotype.

CONCLUSIONS

The adiponectin gene SNP+45 polymorphism may be associated with pathogenesis of obesity in children. T→G variance may be associated an increased risk of childhood obesity and result in a decreased level of adiponectin.

摘要

目的

研究脂联素基因+45单核苷酸多态性(SNP)在中国儿童中的分布特征,确定脂联素基因+45多态性在儿童肥胖发病机制中的作用。

方法

随机选取147名中国肥胖儿童和118名健康儿童,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法鉴定脂联素基因SNP+45多态性。采用酶联免疫吸附测定法(ELISA)测定血浆脂联素水平。测量腰围(WC)、腰臀比(WHR)、体脂百分比(%BF)、收缩压(SBP)、舒张压(DBP)、空腹血糖(FPG)、血清甘油三酯(TG)、总胆固醇(TC)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、血浆空腹胰岛素(FINS)以及胰岛素抵抗稳态模型评估(HOMA-IR)。

结果

肥胖儿童和健康对照儿童脂联素基因SNP+45的等位基因频率分别为40.5%和25.4%。两组间基因型分布和等位基因频率存在显著差异(P<0.05)。相比之下,TT基因型肥胖儿童的血浆脂联素水平显著较高,而%BF、HOMA-IR、TC和LDL-C水平显著低于TG或GG基因型肥胖儿童。

结论

脂联素基因SNP+45多态性可能与儿童肥胖的发病机制有关。T→G变异可能与儿童肥胖风险增加有关,并导致脂联素水平降低。

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