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在一家三级医疗中心就诊的不育男性中Y染色体微缺失的患病率:明斯特经验

Prevalence of Y chromosome microdeletions in infertile men who consulted a tertiary care medical centre: the Münster experience.

作者信息

Maurer B, Gromoll J, Simoni M, Nieschlag E

机构信息

Institute of Reproductive Medicine of the University, Münster, Germany.

出版信息

Andrologia. 2001 Jan;33(1):27-33. doi: 10.1046/j.1439-0272.2001.00406.x.

Abstract

The long arm of the human Y chromosome is required for male fertility. Microdeletions in three different regions of the human Y chromosome, designated AZFa, AZFb and AZFc, respectively, are frequently associated with male infertility. The varying frequency of Y microdeletions found in cohorts of infertile men (0.4-55.5%) is probably related to the criteria by which the patients are selected. We report the diagnosis of Y chromosomal microdeletion in a total of 1,470 men who attended our infertility clinic, the largest sample of infertile patients to have been analysed to date. This cohort consists of three populations. The first subgroup comprises 228 selected patients with severely impaired spermatogenesis. Since microdeletions had also been reported in patients with less severe defects in spermatogenesis, we then intended to define the deletion frequency in unselected patients (population II: 378 patients). Population III comprises 864 prospectively selected patients and intracytoplasmic sperm injection candidates. Altogether, 19 patients with microdeletions were found (1.3%). The microdeletion frequencies in populations I, II and III were 3.5%, 0.3% and 1.2%, respectively. Our study helps to define a subgroup of infertile men at risk of Y chromosomal microdeletions, and strongly supports the recommendation that Y microdeletion analysis should be limited to azoospermic and severely oligozoospermic men and candidates for intracytoplasmic sperm injection.

摘要

人类Y染色体的长臂对男性生育能力至关重要。人类Y染色体上三个不同区域的微缺失,分别命名为AZFa、AZFb和AZFc,常与男性不育相关。在不育男性群体中发现的Y微缺失频率各异(0.4 - 55.5%),这可能与患者的入选标准有关。我们报告了对1470名前来我们不育症诊所就诊的男性进行Y染色体微缺失诊断的情况,这是迄今为止分析的不育患者最大样本。该群体由三部分人群组成。第一亚组包括228名经挑选的精子发生严重受损的患者。由于在精子发生缺陷较轻的患者中也有微缺失的报道,我们接着打算确定未挑选患者中的缺失频率(第二群体:378名患者)。第三群体包括864名经前瞻性挑选的患者及胞浆内单精子注射候选者。总共发现19名患者存在微缺失(1.3%)。第一、第二和第三群体中的微缺失频率分别为3.5%、0.3%和1.2%。我们的研究有助于确定有Y染色体微缺失风险的不育男性亚组,并有力支持以下建议:Y微缺失分析应限于无精子症和严重少精子症男性以及胞浆内单精子注射候选者。

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