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体外受精和卵胞浆内单精子注射产生的未受精卵母细胞的细胞遗传学异常:一项双盲研究。

Cytogenetic abnormalities of unfertilized oocytes generated from in-vitro fertilization and intracytoplasmic sperm injection: a double-blind study.

作者信息

Edirisinghe W R, Murch A, Junk S, Yovich J L

机构信息

PIVET Medical Centre, Leederville, Perth, Western Australia.

出版信息

Hum Reprod. 1997 Dec;12(12):2784-91. doi: 10.1093/humrep/12.12.2784.

Abstract

In the present study we have assessed the cytogenetic abnormalities of unfertilized oocytes from in-vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) programmes during a one year period (July 1995 to July 1996) with the cytogenetic analysis being carried out in a double-blind manner. A total of 88 unfertilized ICSI and 85 unfertilized IVF oocytes were used for the study and of these 51 and 62 oocytes, in each respective group, were suitable for analysis. The haploidy, diploidy and aneuploidy rates between ICSI (62.7, 7.8 and 5.9%) and IVF (61.3, 9.7 and 14.5%) groups were similar. A significant inter-patient variation in the incidence of hypohaploidy was observed within the IVF group. Chromosomal fragmentation or breakage was observed at a similar rate in both groups of unfertilized oocytes (23.5 and 14.5% for ICSI and IVF respectively). A significantly higher proportion of ICSI oocytes contained sperm nuclei (27/51, 52.9%) than did IVF oocytes (20/62, 32.3%, P < 0.01). The distribution and state of sperm head chromatin in relation to oocyte chromosomal complement was studied in both groups. ICSI oocytes contained decondensed or swollen sperm nuclei in association with haploid oocyte chromosomes (12/27, 44.4%) or condensed sperm heads in oocytes showing no chromosomal complements (7/27, 25.9%). In IVF oocytes sperm heads were either arrested in the condensed state (5/20, 25%), metaphase stage (3/20, 15%) or had undergone premature chromosome condensation (PCC; 6/20, 30%) in association with haploid oocyte chromosomes. The incidence of PCC was similar in the two groups. A marked variation in the incidence of total chromosomal abnormality was observed between patients within both ICSI (0-75%) and IVF (0-71%) groups indicating a possible similarity in oocyte quality between the majority of male factor and tubal infertility patients. The type of sperm used in the two fertilization procedures showed an increased incidence of chromosomal breakage with ICSI-MESA (microepididymal sperm aspiration) spermatozoa (4/6, 67%) compared to the ICSI-ejaculated (6/35, 17.1%; P < 0.05), ICSI-testicular biopsy (2/10, 20%) and IVF-normospermic (9/62, 14.5%; P < 0.01) spermatozoa. Chromosomal fragmentation may be associated with the degree of difficulty experienced at sperm injection, especially with sperm retrieved from the reproductive tract. Thus chromosomal fragmentation in ICSI may need further investigation using a larger sample size in order to assess the possible causative factors.

摘要

在本研究中,我们评估了1995年7月至1996年7月这一年期间,体外受精(IVF)和卵胞浆内单精子注射(ICSI)项目中未受精卵子的细胞遗传学异常情况,细胞遗传学分析以双盲方式进行。本研究共使用了88个ICSI未受精卵和85个IVF未受精卵,其中每组分别有51个和62个卵子适合进行分析。ICSI组(62.7%、7.8%和5.9%)和IVF组(61.3%、9.7%和14.5%)的单倍体、二倍体和非整倍体率相似。在IVF组中观察到患者间单倍体发生率存在显著差异。两组未受精卵中观察到染色体断裂或破碎的发生率相似(ICSI组和IVF组分别为23.5%和14.5%)。ICSI卵子中含有精核的比例(27/51,52.9%)显著高于IVF卵子(20/62,32.3%,P<0.01)。研究了两组中精子头部染色质相对于卵母细胞染色体组成的分布和状态。ICSI卵子中,去浓缩或肿胀的精核与单倍体卵母细胞染色体相关(12/27,44.4%),或在无染色体组成的卵母细胞中含有浓缩的精子头部(7/27,25.9%)。在IVF卵子中,精子头部要么停滞在浓缩状态(5/20,25%)、中期阶段(3/20,15%),要么与单倍体卵母细胞染色体相关发生了早熟染色体凝集(PCC;6/20,30%)。两组中PCC的发生率相似。在ICSI组(0 - 75%)和IVF组(0 - 71%)的患者之间观察到总染色体异常发生率存在显著差异,这表明大多数男性因素和输卵管性不孕患者的卵母细胞质量可能相似。与ICSI - 射出精子(6/35,17.1%;P<0.05)、ICSI - 睾丸活检精子(2/10,20%)和IVF - 正常精子(9/62,14.5%;P<0.01)相比,两种受精程序中使用的ICSI - MESA(显微附睾精子抽吸)精子的染色体断裂发生率增加(4/6,67%)。染色体断裂可能与精子注射时遇到的困难程度有关,尤其是从生殖道获取的精子。因此,可能需要使用更大样本量对ICSI中的染色体断裂进行进一步研究,以评估可能的致病因素。

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