Ali Rahmani Seyed, Paknejad Zeynab, Mohammadkhanlou Masoumeh
Ginekol Pol. 2017;88(8):421-7.
Recurrent pregnancy loss (RPL) is a heterogeneous condition consisting of three or more consecutive abortions before the 20 weeks of gestation. The tumor necrosis factor alpha (TNF-α) gene plays a crucial role in immunology and inflammation responses. Interleukin 1 receptor antagonist (IL-1RN) is an important anti-inflammatory molecule which plays important roles in pregnancy. The aim of this study was to investigate effects of TNF-α and IL-1Ra polymorphisms on RPL in Azari women.
The study participants consisted of 100 women with RPL from Iranian Azeri Turkish origin. The control group comprised 100 age and ethnically matched healthy women in the reproductive age. Genomic DNA was extracted from the whole blood and genotype determinations were performed using PCR amplification followed by restriction fragment length polymorphism (RFLP) analysis.
No significant association was indicated between IL-1Ra and RPL among Iranian Azeri Turkish women. Unlike the homozygous state, significantly higher frequency of -857 C/T variant was seen in RPL patients than control subjects. Significantly lower frequency of wild type genotype was observed in RPL patients than of controls. Any association was found between the other TNF-α polymorphisms and RPL.
TNF-α -857 C/C variant might represent protective effect against RPL and the -857 C/T variant might be a genetic risk factor for the occurrence of RPL. Invariant differences in the prevalence of -511 C/T and -31 C/T polymorphisms and IL-1RN VNTR between RPL patients.
复发性流产(RPL)是一种异质性疾病,指妊娠20周前连续发生三次或三次以上流产。肿瘤坏死因子α(TNF-α)基因在免疫和炎症反应中起关键作用。白细胞介素1受体拮抗剂(IL-1RN)是一种重要的抗炎分子,在妊娠过程中发挥重要作用。本研究旨在探讨TNF-α和IL-1Ra基因多态性对阿扎里族女性复发性流产的影响。
研究参与者包括100名来自伊朗阿塞拜疆土耳其族的复发性流产女性。对照组由100名年龄和种族匹配的育龄健康女性组成。从全血中提取基因组DNA,采用聚合酶链反应(PCR)扩增后进行限制性片段长度多态性(RFLP)分析来确定基因型。
在伊朗阿塞拜疆土耳其族女性中,IL-1Ra与复发性流产之间未显示出显著关联。与纯合状态不同,复发性流产患者中-857 C/T变异的频率显著高于对照组。复发性流产患者中野生型基因型的频率显著低于对照组。未发现其他TNF-α基因多态性与复发性流产之间存在任何关联。
TNF-α -857 C/C变异可能对复发性流产具有保护作用,而-857 C/T变异可能是复发性流产发生的遗传危险因素。复发性流产患者中-511 C/T、-31 C/T多态性和IL-1RN VNTR的患病率存在不变的差异。