核型正常且无微缺失y染色体的非阻塞性无精子症男性不育患者的减数分裂研究为临床夫妻管理提供了参考

Marie-Odile North , Ilona Lellei , Edit Erdei , Jacques Patrick Barbet , Joseph Tritto
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引用次数: 3

摘要

为了确定非阻塞性无精子症男性不孕症治疗的减数分裂标准,在法国巴黎、意大利罗马和匈牙利布达佩斯的男科组织了一项前瞻性多中心研究。对117例核型正常、无y染色体微缺失的无梗阻性无精子男性进行双侧睾丸活检组织学和减数分裂研究。组织学上,40例(34%)患者出现精母细胞或精子细胞阻滞,39例(33%)出现精子发育不足,而其余患者(33%)未观察到减数分裂细胞。细胞遗传学上,减数分裂图像只能从两个前组织学组获得。共有44例(37.6%)患者观察到减数分裂异常,其中9例(7.7%)为严重I级和IIB级异常,19例(16.2%)为IIC级环境相关减数分裂异常。这些结果为准确的临床处理提供了重要的线索。对于无减数分裂数字的患者和I类和IIB类异常患者,激素刺激是虚幻的,应直接提出精子赠予。对于出现IIC类异常的患者,应直接或在睾丸微环境治疗后对所有其他患者进行激素刺激。在所有存在IIA、III或IV型异常的情况下,应向所有夫妇清楚地说明妊娠的遗传风险和产前染色体分析的可能性。这种治疗策略已应用于我们系列的所有患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meiotic studies of infertile men in case of non-obstructive azoospermia with normal karyotype and no microdeleted Y-chromosome precise the clinical couple management

To identify meiotic criteria for infertility management in non-obstructive azoospermic men, a prospective and multicentric study was organized in Andrological Departments of Paris (France), Roma (Italy) and Budapest (Hungary). In 117 non-obstructive azoospermic men with normal karyotype and no Y-chromosome microdeletion, histology and meiotic studies on bilateral bipolar testicular biopsies were done. Histologically, 40 patients (34%) presented spermatocyte or spermatid arrest, 39 (33%) hypospermatogenesis whereas no meiotic cell could be observed in the remaining patients (33%). Cytogenetically, meiotic figures could only be obtained from the two first histological groups. Meiotic abnormalities were observed in a total of 44 patients (37.6%) including nine patients (7.7%) with severe class I and class IIB anomalies and 19 patients (16.2%) with class IIC environmentally linked meiotic abnormalities. These results provided essential clues for an accurate clinical management. For patients with no meiotic figures and patients with class I and class IIB anomalies, an hormonal stimulation is illusory and a sperm gift should be directly proposed. An hormonal stimulation should be proposed to all the other patients, either directly or following the treatment of the testicular microenvironment for the patients presenting class IIC anomalies. The genetic risk and possibility of prenatal chromosomal analysis in case of pregnancy should be clearly exposed to all the couples in all the cases where type IIA, III or IV anomalies are present. This therapeutical strategy has been applied to all the patients in our series.

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