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首页> 外文期刊>Trends in Medical Research >Molecular Screening for Y Chromosome Microdeletions in Egyptian Infertile Men with Severe Oligozoospermia
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Molecular Screening for Y Chromosome Microdeletions in Egyptian Infertile Men with Severe Oligozoospermia

机译:严重少精症埃及不育男子Y染色体微缺失的分子筛查

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摘要

Background: Male infertility is a multifactorial syndrome. Genetic factors contribute about 10-15% of cases. Among these factors, Y chromosome microdeletions are the second most frequent genetic cause after Klinefelter’s syndrome. Objective: The aim of the study was to detect azoospermia factor (AZF) region microdeletions and their locations on Y chromosome in infertile men with severe oligozoospermia and to correlate these microdeletions with the patient’s semen analysis, hormonal profile and testicular volume. Materials and Methods: In this cross sectional study, 50 infertile severe oligozoospermic patients (<5 million) were included, their ages ranged from 20-50 years. The patients included in this study were selected from Damietta Outpatient Clinic of Dermatology and Andrology Department, Al-Azhar Faculty of Medicine from March, 2014-2016 and were subjected for history, general and local examinations, semen analysis, FSH, LH and testosterone levels and PCR examination. Results: The mean age of studied cases was 34.26 years with mean duration of infertility 8.16 years. Normal FSH, LH and testosterone was found in 74, 96 and 88%, respectively. The AZF deletion was reported in 4 cases. Regarding relation to studied hormones and testicular size, there was significant association between AZF deletion with both FSH (p = 0.02) and LH (p = 0.025), while there was no significant association with testosterone (p = 0.44) or testicular size (p = 0.12). Conclusion: Microdeletions of the Y chromosome in the study were 8% among severe oligozoospermic males. There was no statistically significant relation between testicular size, semen volume, testosterone and LH with the Y chromosome microdeletions. The detection of a deletion in an infertile man provides a proper diagnosis of the disease, allow the clinician to avoid empirical, unnecessary or often expensive treatments to improve fertility. A molecular diagnostic test of Y chromosome microdeletions should be at least performed in all men with a sperm concentration of <5×106 mL–1, regardless of the presence of other apparent concomitant cause of testicular damage.
机译:背景:男性不育是一种多因素综合症。遗传因素占病例的约10-15%。在这些因素中,Y染色体微缺失是仅次于Klinefelter综合征的第二大遗传原因。目的:该研究的目的是检测重症少精症不育男性无精子症因子(AZF)区的微缺失及其在Y染色体上的位置,并将这些微缺失与患者的精液分析,激素水平和睾丸体积相关联。材料和方法:在这项横断面研究中,纳入了50例不育的严重少精子症患者(<500万),其年龄在20至50岁之间。该研究纳入的患者选自2014年3月至2016年3月在Al-Azhar医学院皮肤科和男科Damietta门诊接受的患者的病史,常规和局部检查,精液分析,FSH,LH和睾丸激素水平和PCR检查。结果:研究病例的平均年龄为34.26岁,平均不育时间为8。16年。正常的FSH,LH和睾丸激素分别占74%,96%和88%。据报道有4例AZF缺失。关于研究激素和睾丸大小的关系,AZF缺失与FSH(p = 0.02)和LH(p = 0.025)均存在显着关联,而与睾丸激素(p = 0.44)或睾丸大小(p = 0.12)。结论:该研究中Y染色体的微缺失在严重少精症男性中为8%。睾丸大小,精液量,睾丸激素和LH与Y染色体微缺失之间无统计学意义的相关性。在不育男子中检测到缺失可正确诊断疾病,使临床医生避免进行经验,不必要或通常昂贵的治疗以提高生育能力。不论是否存在其他明显的睾丸损伤伴随原因,至少应对所有精子浓度<5×106 mL-1的男性进行Y染色体微缺失的分子诊断测试。

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