Thanh Hoa N, Thanh Hoa N, Khanh Trang H N, Minh Duc N, Manh Ha N
Department of Histology and Embryology, Hanoi Medical University,Hanoi, Vietnam.
IVF and Tissue Engineering Center, Hanoi Medical University Hospital,Hanoi, Vietnam.
Clin Ter. 2023 Mar-Apr;174(2):189-194. doi: 10.7417/CT.2023.2518.
We assessed the morphologies of meiotic spindles in oocytes that failed to fertilize following intracytoplasmic sperm injection (ICSI) and identified factors contributing to failed fertilization.
A total of 225 unfertilized oocytes were collected after ICSI. Oocytes were fixed and stained for tubulin and chromosomes. Meiotic spindle morphologies, chromosome alignment, and sperm nuclear decondensation were assessed to identify contributing factors to fertilization failure. We identified relationships between several factors and both abnormal spindle morphologies and sperm nuclear decondensation in oocytes that failed to fertilize.
Three causes for unfertilized oocytes after ICSI were identified: (I) the absence of a sperm nucleus in the ooplasm; (II) failed oocyte activation; and (III) defects in pronucleus formation or migration. The rate of disarranged polar spindles in oocytes collected from women older than 35 years (73.3%; 33/45 oocytes) was significantly higher than that of those collected from women 35 years and younger (50.4%; 68/135 oocytes; odds ratio [OR]: 2.71, 95% confidence interval [CI]: 1.29-5.69, p = 0.009). The proportion of unfertilized oocytes with abnormal spindles and chromosome misalignment was significantly higher in oocytes collected from women older than 35 years than those from women 35 years and younger (62.2% vs. 41.5%, p = 0.016). The proportion of partially decondensed chromatin in the abnormal sperm morphology group was significantly higher than in the normal sperm morphology group (66.7% versus 52.9%, OR: 1.78, 95% CI: 1.01-3.11, p = 0.044).
The main contributor to the failure of oocytes to fertilize after ICSI is failed oocyte activation. The ICSI technique used, the maternal age, and sperm morphology are also contributing factors in fertilization failure after ICSI.
我们评估了卵胞浆内单精子注射(ICSI)后未受精的卵母细胞中减数分裂纺锤体的形态,并确定了导致受精失败的因素。
ICSI后共收集225个未受精卵母细胞。将卵母细胞固定并用微管蛋白和染色体进行染色。评估减数分裂纺锤体形态、染色体排列和精子核去浓缩情况,以确定受精失败的相关因素。我们确定了几个因素与未受精卵母细胞中异常纺锤体形态和精子核去浓缩之间的关系。
确定了ICSI后未受精卵母细胞的三个原因:(I)卵质中无精子核;(II)卵母细胞激活失败;(III)原核形成或迁移缺陷。从35岁以上女性收集的卵母细胞中极性纺锤体排列紊乱的比例(73.3%;45个卵母细胞中的33个)显著高于35岁及以下女性收集的卵母细胞(50.4%;135个卵母细胞中的68个;优势比[OR]:2.71,95%置信区间[CI]:1.29 - 5.69,p = 0.009)。从35岁以上女性收集的卵母细胞中纺锤体异常和染色体排列错误的未受精卵母细胞比例显著高于35岁及以下女性(62.2%对41.5%,p = 0.016)。异常精子形态组中部分去浓缩染色质的比例显著高于正常精子形态组(66.7%对52.9%,OR:1.78,95% CI:1.01 - 3.11,p = 0.044)。
ICSI后卵母细胞受精失败的主要原因是卵母细胞激活失败。所使用的ICSI技术、产妇年龄和精子形态也是ICSI后受精失败的影响因素。