原发性不孕症的人类精子染色体分析:初步报告。

S J Lin, C C Hsu, Y R Lien, Y S Yang, T R Wang, S M Chuang, T Y Lee
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引用次数: 0

摘要

人类精子染色体可以使用无带仓鼠卵系统进行分析。为了熟悉这项新技术,了解可育和可能不育男性的染色体畸变频率,我们对39例成功的精子染色体进行了分析。受试者被分成两组。第一组为已证实生育能力的健康男性。第二组是不明原因不孕夫妇的丈夫。精液样品新鲜制备或在test -卵黄缓冲液中保存12 - 72小时。第1组新鲜样品平均渗透率为67.40 +/- 14.08%(平均+/- 2SD),成熟指数为1.33 +/- 0.31。蛋黄缓冲液处理的样品平均渗透率为91.34 +/- 7.42%,成熟指数为1.58 +/- 0.42。卵黄缓冲液处理后,穿透率有统计学意义(p < 0.001)。1组89条单倍体染色体,非整倍体4条(4.5%),结构畸变3条(3.4%)。2组新鲜样品平均渗透率为71.34 +/- 27.96%,成熟指数为1.37 +/- 0.25。蛋黄缓冲液处理的样品,渗透率为86.33 +/- 25.18%,成熟指数为1.40 +/- 0.23。2组单倍体染色体135条,非整倍体6条(4.4%),结构畸变4条(3.0%)。1组与2组在染色体渗透率、成熟指数、染色体异常频率方面差异无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human sperm chromosome analysis in primary infertility: a preliminary report.

Human sperm chromosomes can be analyzed using the zona-free hamster egg system. In order to familiarize ourselves with this new technique and to investigate the chromosome aberration frequency in fertile and possibly infertile men, we performed sperm chromosome analysis in 39 successful experiments. The subjects were divided into two groups. Group 1 was healthy men with proven fertility. Group 2 was husbands of couples with unexplained infertility. Semen samples were prepared freshly or preserved in TEST-yolk buffer for 12 to 72 hours. In group 1 using fresh samples, the mean penetration rate was 67.40 +/- 14.08% (mean +/- 2SD), the maturation index was 1.33 +/- 0.31. For samples treated with yolk buffer, the mean penetration rate was 91.34 +/- 7.42%, and the maturation index was 1.58 +/- 0.42. There was a statistically significant increase in penetration after yolk buffer treatment (p less than 0.001). In group 1 there were 89 haploid chromosomes, four were aneuploidy (4.5%), and three with structural aberrations (3.4%). In group 2, for fresh samples, the mean penetration rate was 71.34 +/- 27.96%, and the maturation index was 1.37 +/- 0.25. For samples treated with yolk buffer, the penetration rate was 86.33 +/- 25.18%, and maturation index 1.40 +/- 0.23. In group 2, there were 135 haploid chromosomes, 6 were aneuploidy (4.4%), and 4 with structural aberrations (3.0%). There was no statistically significant difference between group 1 and group 2 in the penetration rate, maturation index and frequency of chromosome abnormalities.

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