首页> 外文期刊>European Journal of Obstetrics, Gynecology and Reproductive Biology: An International Journal >Luteinizing hormone beta-subunit gene (LHbeta) polymorphism in infertility and endometriosis-associated infertility.
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Luteinizing hormone beta-subunit gene (LHbeta) polymorphism in infertility and endometriosis-associated infertility.

机译:黄体生成激素β-亚基基因(LHbeta)多态性与不孕症和与子宫内膜异位症相关的不育症。

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摘要

OBJECTIVE: To establish the frequency of LHbeta G1502A polymorphism in infertile women with endometriosis, infertile women without endometriosis and a control group. STUDY DESIGN: Case-control study including 110 infertile women with endometriosis, 84 infertile women without endometriosis and a control group consisting 209 healthy fertile women recruited from the ABC School of Medicine. The LHbeta G1502A polymorphism was studied by RPLP-PCR (restriction fragment length polymorphism-polymerase chain reaction). RESULTS: Genotypes GG, GA and AA of the LHbeta G1502A polymorphism presented frequencies of 54.6%, 31.8% and 13.6%, respectively, in the women with endometriosis (p=0.0398); of 52.4%, 38.1% and 9.5% (p=0.0123), respectively, in the infertile women without endometriosis; and of 68.9%, 21.5% and 9.6%, respectively, in the control group. In patients with minimal/mild endometriosis and moderate/severe endometriosis, the GG, GA and AA genotype frequencies were, respectively, 47.3%, 36.4% and 16.3% (p=0.0118); and 61.8%, 27.3% and 10.9% (p=0.5975). Considering the alleles, allele G was present in 70.5% of the patients with endometriosis, 71.4%% of the infertile women without endometriosis and in 79.7% of the controls, whereas allele A was present in 29.5%, 28.6% and 20.3%, respectively, in the infertile women with endometriosis (p=0.0121), infertile women without endometriosis (p=0.0409) and controls. Alleles G and A presented frequencies of 65.5% and 34.5% and 75.5% and 24.5%, respectively, in minimal/mild endometriosis (p=0.0026) and moderate/severe endometriosis (p=0.4062). CONCLUSION: The data suggest that LHbeta G1502A polymorphism may be involved in the predisposition to infertility and minimal/mild endometriosis-associated infertility, although endometriosis might be only a coincidental finding along with infertility.
机译:目的:建立具有子宫内膜异位症的不育妇女,没有子宫内膜异位的不育妇女和对照组的LHbeta G1502A多态性频率。研究设计:病例对照研究包括从ABC医学院招募的110名患有子宫内膜异位的不育妇女,84名没有子宫内膜异位的不育妇女和对照组,包括209名健康的可育妇女。通过RPLP-PCR(限制性片段长度多态性-聚合酶链反应)研究了LHbeta G1502A多态性。结果:LHbeta G1502A多态性的基因型GG,GA和AA在子宫内膜异位症女性中的出现频率分别为54.6%,31.8%和13.6%(p = 0.0398)。无子宫内膜异位症的不育女性分别占52.4%,38.1%和9.5%(p = 0.0123);对照组分别为68.9%,21.5%和9.6%。在轻度/轻度子宫内膜异位症和中度/重度子宫内膜异位症患者中,GG,GA和AA基因型频率分别为47.3%,36.4%和16.3%(p = 0.0118);和61.8%,27.3%和10.9%(p = 0.5975)。考虑到等位基因,等位基因G存在于70.5%的子宫内膜异位患者,71.4 %%的不具子宫内膜异位的不育妇女和对照组的79.7%,而等位基因A分别存在于29.5%,28.6%和20.3%。 ,有子宫内膜异位症的不育妇女(p = 0.0121),无子宫内膜异位症的不育妇女(p = 0.0409)和对照组。在最小/轻度子宫内膜异位症(p = 0.0026)和中度/重度子宫内膜异位症(p = 0.4062)中,等位基因G和A的频率分别为65.5%,34.5%,75.5%和24.5%。结论:数据提示LHbeta G1502A基因多态性可能与易感性以及与子宫内膜异位症相关的最小/轻度不育症有关,尽管子宫内膜异位症可能只是不育症的偶然发现。

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