日本和非洲不育夫妇y染色体微缺失和生殖结果的前瞻性评估。

Paul E Kihaile, Atsushi Yasui, Yoshihiro Shuto
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引用次数: 26

摘要

背景:比较日本和非洲无精子和少精子男性y染色体微缺失的频率,描述卵胞浆内单精子注射(ICSI)体外受精(IVF)后的胚胎特征和生殖结局。方法:我们的研究在两个中心进行前瞻性研究,一个私立试管婴儿诊所和一个大学医院。对日本和非洲(坦桑尼亚)非阻塞性无精子症(NOA)和少精子症(浓度< 5 × 10(6) /ml)的男性进行y染色体微缺失评估(n = 162)。在47名患有NOA的男性中,26名是日本人,21名非洲人。在115名患有少精症的男性中,87名是日本人,28名非洲人。然后将y染色体微缺失患者的生殖结果与作为对照组的y染色体完整男性/输卵管因素不育夫妇进行的19次IVF+ICSI周期的生殖结果进行比较。结果:7例无精、少精患者存在y染色体缺失;AZFc区域的缺失总数为5个。AZFa区域只有一个缺失,AZF中三个区域(AZFa, b和c)都有一个完全缺失。在我们的研究人群中,日本男性的微缺失频率为6.2% (95% CI, 4.25%-14.45%),而非洲人群中未发现微缺失(95% CI, 0.0%-7.27%)。然而,两组之间的差异没有统计学意义。与y染色体完整组相比,使用y染色体微缺失精子的ICSI胚胎的受精率、囊胚发育率、着床率和妊娠率都有所降低,尽管这些观察到的差异在统计学上并不显著。结论:日本无精子和少精子男性y染色体微缺失率为6.2%;在我们的非洲研究患者中没有发现微缺失。在这组接受IVF+ICSI的夫妇中,y染色体微缺失患者与y染色体完整患者的胚胎特征或妊娠结局无统计学差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prospective assessment of Y-chromosome microdeletions and reproductive outcomes among infertile couples of Japanese and African origin.

Background: To compare the frequency of Y-chromosome microdeletions in Japanese and African azoospermic and oligozoospermic men and describe embryo characteristics and reproductive outcome following in vitro fertilization (IVF) with intracytoplasmic sperm injection (ICSI).

Methods: Our study was performed prospectively at two centers, a private IVF clinic and a university hospital. Japanese and African (Tanzanian) men with nonobstructive azoospermia (NOA) and oligozoospermia (concentration < 5 x 10(6) /ml) were evaluated for Y-chromosome microdeletions (n = 162). Of the 47 men with NOA, 26 were Japanese and 21 were Africans. Of the 115 men with oligozoospermia, 87 were Japanese and 28 were Africans. Reproductive outcomes of patients with Y-chromosome microdeletions were then compared with those of 19 IVF+ICSI cycles performed on couples with Y-chromosome intact males/tubal factor infertility which served as a control group.

Results: Seven azoospermic and oligozoospermic patients had Y-chromosome deletions; the total number of deletions in the AZFc region was five. There was only one deletion in the AZFa region and one complete deletion involving all three regions (AZFa, b, and c) within AZF. In our study population, microdeletion frequency among Japanese men was 6.2% (95% CI, 4.25%-14.45%), whereas no deletions were identified in the African group (95% CI, 0.0%-7.27%). The difference between the two groups was not statistically significant, however. Embryos derived from ICSI utilizing sperm with Y-chromosome microdeletion showed reduced rates of fertilization, blastocyst development, implantation, and pregnancy compared to the Y-chromosome intact group, although these observed differences were not statistically significant.

Conclusion: The observed frequency of Y-chromosome microdeletion was 6.2% among Japanese azoospermic and oligozoospermic males; no microdeletions were identified among our African study patients. In this population of couples undergoing IVF+ICSI, there was no statistically significant difference in embryo characteristics or pregnancy outcome between patients with Y-chromosome microdeletion and those with an intact Y-chromosome.

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