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Severe teratozoospermia and its influence on pronuclear morphology, embryonic cleavage and compaction

机译:严重畸形精子症及其对前核形态,胚胎分裂和压实的影响

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Background Fertilization, cell division and embryo development depend on genomic contributions from male and female gametes. We hypothesize that teratozoospermic sperm influences early embryo development and embryo compaction. Methods We conducted a retrospective analysis of embryos derived from intracytoplasmic sperm injection (ICSI) cycles. Two hundred thirty-five consecutive ICSI cycles were included in the study; all treatment was provided at the Cleveland Clinic Fertility Center. Patient cycles were divided by sperm morphology based on Kruger's strict criteria: Group A, embryos where teratozoospermic sperm (0-2% normal) were used for ICSI and Group B, embryos where dysmorphic sperm (5-13% normal) were used for ICSI. All cycles analyzed were of patients doing day 3 embryo transfers. Outcome measures assessed included pronuclear (PN) pattern, syngamy, early cleavage, cell number, rate of compaction and blastulation of embryos left in culture and not transferred on day 3. Results A total of 1762 embryos were analyzed. PN patterns were similar in Group A and Group B embryos. No differences were noted in syngamy, cleavage, cell number or blastulation rate. Studying the development of embryos in culture after day 3 transfer revealed a difference in the timeline for compaction. By day 4, 25% of Group A embryos had compacted compared to 36% in Group B (P = 0.0007). There was no difference found between Group A and Group B embryos in regards to blastulation. Conclusions We did not find an association between sperm morphology and clinical outcomes. The impact of teratozoospermia may be masked in ICSI cycles where fertilization, implantation rate and clinical pregnancy rate are the primary outcome measures. However, by examining the timeline of development, we were better able to discern a potential paternal effect at critical transition points from fertilization through activation.
机译:背景受精,细胞分裂和胚胎发育取决于雄性和雌性配子的基因组贡献。我们假设畸胎动物的精子会影响早期胚胎发育和胚致密。方法我们对细胞质内精子注射(ICSI)周期衍生的胚胎进行了回顾性分析。这项研究包括了235个连续的ICSI周期。克利夫兰诊所生育中心提供了所有治疗方法。根据克鲁格的严格标准,将患者周期按精子形态进行划分:A组,使用畸胎精子(0-2%正常)的胚胎用于ICSI,B组,畸形的精子(5-13%的正常)用于ICSI 。分析的所有周期均为进行第3天胚胎移植的患者。评估的结果指标包括原核(PN)模式,共生,早期卵裂,细胞数量,在培养中留存且在第3天未转移的胚的紧实率和成球率。结果共分析了1762个胚。 PN模式在A组和B组胚胎中相似。在同性,分裂,细胞数或成囊率上没有差异。研究第3天转移后培养物中胚胎的发育,发现压实时间的差异。到第4天,A组胚胎已压缩了25%,而B组则为36%(P = 0.0007)。 A组和B组胚胎的囊胚形成没有区别。结论我们没有发现精子形态与临床结局之间存在关联。在以受精,着床率和临床妊娠率为主要结果指标的ICSI周期中,可以掩盖畸形精子症的影响。但是,通过检查发育的时间表,我们能够更好地识别从受精到激活的关键过渡点的潜在父本效应。

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