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土耳其特拉凯地区不育男性患者亚甲基四氢叶酸还原酶c.677TT基因型与少精子症的关系。

The relationship between methylenetetrahydrofolate reductase c.677TT genotype and oligozoospermia in infertile male patients living in the Trakya region of Turkey.

作者信息

Gurkan H, Tozkır H, Göncü E, Ulusal S, Yazar M

机构信息

Department of Medical Genetics, Medical Faculty, Trakya University, Edirne, Turkey.

出版信息

Andrologia. 2015 Nov;47(9):1068-74. doi: 10.1111/and.12380. Epub 2014 Nov 26.

Abstract

Methylenetetrahydrofolate reductase (MTHFR), the key enzyme of the folate metabolic pathway, has been reported to be five times more active in the testicles compared to other organs in adult mice. The aim of this study was to investigate the relationship between MTHFR c.677C>T and c.1298A>C polymorphisms and infertility in nonobstructive azoospermic and oligozoospermic male patients living in the Trakya region of Turkey. The study population included 75 nonobstructive azoospermic and 62 oligozoospermic, nonconsanguineous patients who were referred to the Department of Medical Genetics of Trakya University between 01.03.2012 and 01.06.2013 due to infertility and who had been diagnosed based on clinical examinations and spermiograms. All of the patients had a normal karyotype without a Y chromosome microdeletion. Melting curve analysis with labelled probes and primers that were designed by the manufacturers and the real-time polymerase chain reaction method were used. The MTHFR c.677TT genotype frequency in the oligozoospermic infertile male patient group was greater than that of the fertile control group [odds ratio (OR) = 2.675 (95% CI: 0.979-7.305), (P < 0.048)]. The MTHFR c.677TT genotype may be a genetic risk factor for oligozoospermic infertile male patients who live in the Trakya region of Turkey.

摘要

亚甲基四氢叶酸还原酶(MTHFR)是叶酸代谢途径的关键酶,据报道,在成年小鼠中,该酶在睾丸中的活性比其他器官高五倍。本研究的目的是调查居住在土耳其特拉凯地区的非阻塞性无精子症和少精子症男性患者中,MTHFR基因c.677C>T和c.1298A>C多态性与不育症之间的关系。研究人群包括75例非阻塞性无精子症患者和62例少精子症患者,这些非近亲患者于2012年3月1日至2013年6月1日因不育症转诊至特拉凯大学医学遗传学系,并根据临床检查和精子图谱进行了诊断。所有患者的染色体核型均正常,无Y染色体微缺失。使用由制造商设计的标记探针和引物进行熔解曲线分析以及实时聚合酶链反应方法。少精子症不育男性患者组中MTHFR基因c.677TT基因型频率高于生育对照组[比值比(OR)=2.675(95%置信区间:0.979 - 7.305),(P<0.048)]。MTHFR基因c.677TT基因型可能是居住在土耳其特拉凯地区的少精子症不育男性患者的遗传危险因素。

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