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[胰岛素受体基因(INSR)rs2252673单核苷酸多态性与多囊卵巢综合征的关联]

[Association between single nucleotide polymorphism of rs2252673 of INSR gene and polycystic ovarian syndrome].

作者信息

Du Jing, Wang Ze, Zhang Jiangtao, Jia Lili, Zhang Fengli, Shi Yuhua, Chen Zijiang

机构信息

Hospital for Reproductive Medicine Affiliated to Shandong University, Jinan 250021, China.

Email:

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2014 Dec;49(12):919-24.

Abstract

OBJECTIVE

This study is designed to determine whether an association exists between single nucleotide polymorphism (SNP) variant rs2252673 of insulin receptor (INSR) gene and polycystic ovarian syndrome (PCOS) in Han Chinese in order to identify INSR as a genetic susceptibility factor for PCOS.

METHODS

A total of 224 women with PCOS, 192 controls and 672 participants consisting of 224 trios (mother, father and offspring with PCOS) were recruited from the Hospital for Reproductive Medicine Affiliated to Shandong University, from July 2007 to April 2013. Genomic DNA was extracted according to the manufacturer's protocol. SNP rs2252673 of INSR gene was amplified by PCR and then sequenced on an automated sequencer. Moreover, clinical and metabolic features of the patients with PCOS were compared according to the genotypes. The subjects were divided into twot groups according to body mass index (BMI), and then the results were compared between two groups. And the transmitted disequilibrium test (TDT) was applied for data analysis.

RESULTS

(1) There were three kinds of genotype of CC, CG and GG. Genotype frequencies of rs2252673 were 8.0%, 38.8%, 53.1% and 14.6%, 42.2%, 43.2% in the PCOS group and the control group, respectively. The allele frequencies of C and G were 27.5%, 72.5% and 35.7%, 64.3% in the PCOS group and the control group, respectively. There were statistical differences in genotype frequencies and allele frequencies between two groups (all P < 0.05 ). (2)No significant differences were observed in the different genotype according to clinical and metabolic characteristics of women with PCOS(P > 0.05). But when merging the genotype CG and GG, carriers of the CG and GG genotypes in women with PCOS were slightly associated with total cholesterol (TC) levels (t = 2.072, P = 0.048) and lower high-density lipoprotein (HDL) levels (t = 2.274, P = 0.026). Although statistical significance was not achieved, there was an increased tendency in fasting blood glucose (FBG) and fasting insulin (FINS) levels in CG and GG genotypes in PCOS cases.(3)Between the obesity and the non-obesity with PCOS, there was no statistical significance in the genotype and allele frequencies (χ(2) = 0.054, P = 0.974; χ(2) = 0.022, P = 0.883 ). (4) The results of families based analysis shown that genotype distribution of the SNP rs2252673 was in Hardy-Weinberg equilibrium (P > 0.05). After the TDT, the G allele in SNP rs2252673 was over transmitted in families (transmitted:non-transmitted = 120:88; χ(2) = 4.923, P = 0.027). There was a transmitted disequilibrium in rs2252673, which implies the association of INSR and PCOS were independent of population stratification.

CONCLUSIONS

There were a association between the SNP variant rs2252673 of INSR gene and the susceptibility to PCOS in Han Chinese women, which was independently of body mass index. The carrier of G allele frequency of rs2252673 may have higher risk of PCOS.

摘要

目的

本研究旨在确定胰岛素受体(INSR)基因的单核苷酸多态性(SNP)变体rs2252673与中国汉族多囊卵巢综合征(PCOS)之间是否存在关联,以确定INSR作为PCOS的遗传易感性因素。

方法

2007年7月至2013年4月,从山东大学附属生殖医院招募了224例PCOS女性、192例对照以及由224个三联体(母亲、父亲和患PCOS的后代)组成的672名参与者。按照制造商的方案提取基因组DNA。通过聚合酶链反应(PCR)扩增INSR基因的SNP rs2252673,然后在自动测序仪上进行测序。此外,根据基因型比较PCOS患者的临床和代谢特征。根据体重指数(BMI)将受试者分为两组,然后比较两组结果。并应用传递不平衡检验(TDT)进行数据分析。

结果

(1)存在CC、CG和GG三种基因型。rs2252673的基因型频率在PCOS组和对照组中分别为8.0%、38.8%、53.1%和14.6%、42.2%、43.2%。PCOS组和对照组中C和G的等位基因频率分别为27.5%、72.5%和35.7%、64.3%。两组间基因型频率和等位基因频率存在统计学差异(均P<0.05)。(2)根据PCOS女性的临床和代谢特征,不同基因型之间未观察到显著差异(P>0.05)。但当合并基因型CG和GG时,PCOS女性中CG和GG基因型携带者与总胆固醇(TC)水平(t=2.072,P=0.048)和较低的高密度脂蛋白(HDL)水平(t=2.274,P=0.026)略有相关。尽管未达到统计学显著性,但PCOS病例中CG和GG基因型的空腹血糖(FBG)和空腹胰岛素(FINS)水平有升高趋势。(3)在肥胖和非肥胖的PCOS患者之间,基因型和等位基因频率无统计学差异(χ²=0.054,P=0.974;χ²=0.022,P=0.883)。(4)基于家系分析的结果表明,SNP rs2252673的基因型分布处于哈迪-温伯格平衡(P>0.05)。经过TDT分析,SNP rs2252673中的G等位基因在家族中过度传递(传递:未传递=120:88;χ²=4.923,P=0.027)。rs2252673存在传递不平衡,这意味着INSR与PCOS的关联独立于人群分层。

结论

INSR基因的SNP变体rs2252673与中国汉族女性PCOS易感性之间存在关联,且独立于体重指数。rs2252673的G等位基因携带者可能患PCOS的风险更高。

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