首页> 外文期刊>Journal of Reproductive Immunology >Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis.
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Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis.

机译:FCRL3 C-169T启动子单核苷酸多态性与特发性不孕症和与不孕症相关的子宫内膜异位症的关联。

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摘要

An aberrant immunological mechanism is thought to be involved in the pathogenesis of endometriosis. The present study aimed to determine whether there is a relationship between endometriosis and/or infertility and the FCRL3 C-169T polymorphism. This case-control study included 167 infertile women with endometriosis, 60 women with idiopathic infertility and 167 fertile women. Detection of the FCRL3 C-169T polymorphism was performed using TaqMan PCR. A significant difference in the genotype and allele frequencies of the FCRL3 C-169T polymorphism between endometriosis-related infertility (p=0.003 and p=0.001) and idiopathic infertility (p=0.027 and p=0.0185) versus controls was demonstrated. In conclusion, the results suggest that the FCRL3 C-169T polymorphism may play an important role in the pathogenesis of endometriosis and/or infertility.
机译:异常的免疫机制被认为与子宫内膜异位症的发病机制有关。本研究旨在确定子宫内膜异位和/或不育与FCRL3 C-169T多态性之间是否存在关系。这项病例对照研究包括167名子宫内膜异位症不育妇女,60名特发性不育妇女和167名可育妇女。使用TaqMan PCR对FCRL3 C-169T多态性进行检测。与子宫内膜异位症相关的不育症(p = 0.003和p = 0.001)和特发性不育症(p = 0.027和p = 0.0185)之间,FCRL3 C-169T多态性的基因型和等位基因频率存在显着差异。总之,结果表明,FCRL3 C-169T多态性可能在子宫内膜异位和/或不孕症的发病机理中起重要作用。

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