Osmania University, Hyderabad, India.
J Assist Reprod Genet. 2013 Nov;30(11):1493-503. doi: 10.1007/s10815-013-0080-4. Epub 2013 Aug 23.
Tumor Necrosis Factor Alpha (TNF-α), is a proinflammatory cytokine in the pathogenesis of Polycystic Ovary Syndrome (PCOS). In order to investigate the role of rs1800629 and rs1799964 polymorphisms in relation to anthropometric measures, family history of complex diseases, diet and clinical features, we performed a case control study in PCOS women from South India.
A total of 589 samples comprising of 283 patients and 306 controls were enrolled in the present study. Patients were selected based on Rotterdam criteria and ultrasound scanned normal women were selected as controls. Following extraction of DNA, genotyping for rs1800629 and rs1799964 was performed by polymerase chain reaction using tetra primers and PCR-RFLP respectively.
The distribution of genotypes for rs1799964 was significantly different between the groups (p = 0.001), however it was not for rs1800629. Haplotype analysis revealed a significant difference between patients and controls. The predisposing and protective role of haplotype with mutant allele at both loci (combination 3) and haplotype with mutant allele at either loci was reflected by the over representation of combination 3 in patients and combination 2 in controls respectively. In addition, rs1799964 showed an association with dietary habit, clinical hyperandrogenism and AAO. The modifying role of TT genotype on age at onset was noted in quartile analysis.
Replicative studies on the influence of TNF-α polymorphism in different ethnic groups may identify the potentiality of these polymorphisms as markers of inflammation and in turn may help the clinicians for the better management of the condition.
肿瘤坏死因子-α(TNF-α)是多囊卵巢综合征(PCOS)发病机制中的一种促炎细胞因子。为了研究 rs1800629 和 rs1799964 多态性与人体测量指标、复杂疾病家族史、饮食和临床特征的关系,我们在印度南部的 PCOS 女性中进行了病例对照研究。
本研究共纳入 589 例样本,包括 283 例患者和 306 例对照。根据 Rotterdam 标准选择患者,选择超声扫描正常的女性作为对照。提取 DNA 后,采用四引物聚合酶链反应(PCR)对 rs1800629 和 rs1799964 进行基因分型,PCR-RFLP 分别用于 rs1799964。
rs1799964 的基因型分布在两组间差异有统计学意义(p=0.001),但 rs1800629 无差异。单体型分析显示患者与对照组之间存在显著差异。携带两个突变等位基因的单体型(组合 3)和携带任一突变等位基因的单体型具有易感性和保护作用,分别表现为组合 3 在患者中过度表达,组合 2 在对照组中过度表达。此外,rs1799964 与饮食、临床高雄激素血症和 AAO 相关。在四分位分析中,TT 基因型对发病年龄的修饰作用。
在不同种族群体中对 TNF-α 多态性影响的复制研究可能会发现这些多态性作为炎症标志物的潜力,从而有助于临床医生更好地管理病情。