Carlon N, Navarro A, Giorgetti C, Roulier R
Laboratoire de Génétique, Faculté de Médecine, Marseille, France.
J Assist Reprod Genet. 1992 Oct;9(5):475-81. doi: 10.1007/BF01204054.
Failure of in vitro fertilization or very low cleavage rates may occur even though oocyte and semen parameters seem satisfactory. Quantified ultrastructural study of spermatozoa was performed in such cases of failure (n = 6) or low cleavage rate (< 20%; n = 4). Through 1 to 11 retrievals, the number of inseminated oocytes ranged from 14 to 145. The results were compared to those of six fertile men. Quantification was achieved by cataloguing cell defects of the spermatozoon heads and mid-/principal pieces of the flagella. Using the data from each specimen, the percentages of total cellular abnormalities in the head/mid-/principal pieces were established. At the level of the head overall percentages for six groups of defects were determined. The overall percentage of combined head abnormalities, defined as the presence of at least three of these six defects on the same spermatozoon head, was established. Statistical differences among control and patient groups were analyzed by nonparametric Mann-Whitney U test. The percentages of anomalies of the midpiece and of the principal piece were not significantly different between patients and controls. Motility assessed by spermogram was considered "functionally uncompromised." In eight patients the percentage of cell alterations of the head (93-100 vs 77.3 +/- 6.4%) and the percentage of combined anomalies of the head (78.1-100 vs 60.8 +/- 8.5%) were significantly different between patients and controls. In two cases, the percentages established for all head parameters considered were not globally different from those observed in controls. Thus in 8 cases of 10, electron microscopy with quantified analysis supplied valuable evidence about the poor quality of these sperm samples judged as normal under light microscopy and may provide an explanation for their impaired fertilizability.(ABSTRACT TRUNCATED AT 250 WORDS)
即使卵母细胞和精液参数看似令人满意,体外受精仍可能失败或出现极低的卵裂率。对这类受精失败的病例(n = 6)或低卵裂率(< 20%;n = 4)进行了精子的超微结构定量研究。经1至11次取卵,受精的卵母细胞数量在14至145个之间。将结果与6名有生育能力男性的结果进行比较。通过对精子头部和鞭毛中段/主段的细胞缺陷进行分类来实现定量。利用每个样本的数据,确定头部/中段/主段细胞异常的总百分比。在头部水平确定了六组缺陷的总体百分比。确定了合并头部异常的总体百分比,即同一精子头部至少存在这六种缺陷中的三种。通过非参数曼-惠特尼U检验分析对照组和患者组之间的统计学差异。患者和对照组之间中段和主段异常的百分比没有显著差异。通过精子活力检测评估的运动能力被认为“功能未受损”。在8名患者中,患者和对照组之间头部细胞改变的百分比(93 - 100对77.3 +/- 6.4%)以及头部合并异常的百分比(78.1 - 100对60.8 +/- 8.5%)有显著差异。在两例中,所考虑的所有头部参数的百分比与对照组观察到的百分比总体上没有差异。因此,在10例中的8例中,电子显微镜定量分析为这些在光学显微镜下被判定为正常的精子样本质量差提供了有价值的证据,并可能解释它们受精能力受损的原因。(摘要截断于250字)