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The Impact of FSHR Gene Polymorphisms Ala307Thr and Asn680Ser in the Endometriosis Development

机译:FSHR基因多态性Ala30680ser在子宫内膜异位症发育中的影响

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Endometriosis is an estrogen-dependent inflammatory disease that affects a large number of women in reproductive age. Follicle-stimulating hormone (FSH) plays a role in steroidogenesis and acts through a transmembrane glycoprotein, FSH receptor (FSHR). Polymorphisms in FSHR gene were previously associated with variability in FSH serum level and reproductive outcomes, but its relation with endometriosis has not been clarified and demonstrated conflicting results, ranging from strong links to no association to endometriosis. Inspired by these findings, we aimed to investigate the influence of FSHR Ala307Thr and Asn680Ser polymorphisms in the risk of endometriosis development and/or progression and the status of fertility in 352 women with endometriosis and 510 fertile controls. Single-marker analysis revealed no significant difference for both Ala307Thr and Asn680Ser polymorphisms between overall endometriosis and control group. However, when the endometriosis group was subdivided according to fertility status and disease stage, a positive association was found between 680Ser/Ser or GG genotype of the Asn680Ser polymorphism and fertile women with endometriosis (p=0.004). Combined alleles of FSHR polymorphisms revealed that GG/307Ala680Ser was more frequently found in fertile women with endometriosis (haplotype frequency of 45.4% in fertile women with endometriosis and 38.3% in controls, p=0.041). The combined alleles of FSHR polymorphisms disclosed that GG/307Ala680Ser was more frequently found in fertile women with endometriosis (haplotype frequency of 45.4% in fertile women with endometriosis and 38.3% in controls, p=0.049), while GA/307Ala680Asn haplotype was less frequently found in endometriosis group (haplotype frequency of 6.5% in cases and 11.9% in controls, p=& 0.001), regardless of fertility status and stage of the disease. The findings suggest that 680Ser-Ser/GG genotype and GG/307Ala680Ser haplotype increase the risk of endometriosis in fertile women, while GA/307Ala680Asn haplotype decreases the risk of endometriosis development and progression.
机译:子宫内膜异位症是一种雌激素依赖性炎症性疾病,影响繁殖时代的大量妇女。卵泡刺激激素(FSH)在甾体制中发挥作用,并通过跨膜糖蛋白,FSH受体(FSHR)作用。 FSHR基因中的多态性先前与FSH血清水平和生殖结果的可变性相关,但其与子宫内膜异位症的关系尚未澄清并表现出相互矛盾的结果,从强烈的链接到No No.NodeMetriosis。灵感来自这些发现,我们旨在调查FSHR ALA3067TH和ASN680SER多态性对子宫内膜异位症发育和/或进展风险以及352名患有子宫内膜异位症和510种肥沃对照的生育状况的影响。单标分析显示ALA307THSTH和ASN680SER多态性对总子宫内膜异位症和对照组之间的多态性没有显着差异。然而,当子宫内膜异位症组根据生育状态和疾病阶段细分时,在680索尔/ er或GG基因型之间发现了阳性关联,患有子宫内膜异位症的肥沃妇女(P = 0.004)。 FSHR多态性的综合等位基因揭示了GG / 307Ala680ser在具有子宫内膜异位症的肥沃妇女中更常见(单倍型45.4%,肥沃妇女的子宫内膜异位症和38.3%的对照,P = 0.041)。 FSHR多态性的综合等位基因公开了GG / 307Ala680ser更常见的是子宫内膜异位症(单倍型患者在子宫内膜异位症的45.4%的45.4%,对照组中的38.3%),而GA / 307Ala680Asn单倍型频率不太频繁在子宫内膜异位症组(单倍型频率为6.5%,对照组11.9%,P =&amp; <0.001),无论疾病的生育状态和阶段如何。研究结果表明,680ser-ser / gg基因型和gg / 307ala680ser单倍型增加了肥沃女性中子宫内膜异位症的风险,而GA / 307Ala680ASN单倍型降低了子宫内膜异位症发育和进展的风险。

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