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正常和少精子症伊朗患者精子中性染色体三体的频率及其对 ICSI 后受精和着床率的影响。

Frequency of sex chromosomal disomy in spermatozoa of normal and oligozoospermic Iranian patients and its effects on fertilisation and implantation rates after ICSI.

机构信息

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, and Department of Infertility, Shariati Hospital, Tehran, Iran.

出版信息

Andrologia. 2013 Feb;45(1):46-55. doi: 10.1111/j.1439-0272.2012.01309.x. Epub 2012 May 8.

DOI:10.1111/j.1439-0272.2012.01309.x
PMID:22564053
Abstract

Chromosomal aneuploidy is a well-known phenomenon in human gametes including spermatozoa. Success rate of fertilisation and implantation in subfertile patients with male factor has always been shown to be very low. We tried to relate the possible impact of sex chromosomal aneuploidy in spermatozoa used for intracytoplasmic sperm injection (ICSI) on fertilisation and implantation rate. To evaluate the frequency of disomy for X and Y chromosomes in sperm samples retrieved from normal and oligozoospermic individuals, primed in situ labelling (PRINS) technique was used. Following ICSI, the rate of eight-cell embryos for each category was determined and followed up for successful implantation. Results showed a statistically significant higher frequency of disomy for all chromosomes under study in spermatozoa of oligozoospermic patients compared with normal men (P<0.01). The rate of eight-cells embryo formation was significantly lower than in normal group (P<0.01). The number of embryos transferred for both groups were nearly similar. Implantation rate for oligozoospermic patients was much lower than that of the normal group but was not significantly different (P>0.05). These results demonstrate that men especially with severe oligozoospermia have an elevated risk for chromosome abnormalities in their spermatozoa. These abnormalities might affect fertilisation and pre-embryo formation with less impact on implantation.

摘要

染色体非整倍体是人类配子(包括精子)中众所周知的现象。有男性因素的生育能力低下患者的受精和着床成功率一直很低。我们试图将用于胞浆内单精子注射(ICSI)的精子中性染色体非整倍体的可能影响与受精和着床率联系起来。为了评估用于 ICSI 的正常和少精子症个体精子样本中 X 和 Y 染色体的二倍体频率,使用了引物原位标记(PRINS)技术。对每个类别的 8 细胞胚胎进行了评估,并对成功着床进行了随访。结果表明,与正常男性相比,少精子症患者的精子中所有研究染色体的二倍体频率均显著升高(P<0.01)。8 细胞胚胎形成率显著低于正常组(P<0.01)。两组的胚胎转移数量几乎相似。少精子症患者的着床率明显低于正常组,但无显著差异(P>0.05)。这些结果表明,男性,尤其是严重少精子症患者的精子中染色体异常的风险增加。这些异常可能会影响受精和胚胎前体形成,对着床的影响较小。

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