目的 探讨精子DNA碎片指数(DFI)对体外受精-胚胎移植(IVF-ET)胚胎发育及妊娠结局的影响,为优化男性生育力评估及辅助生殖治疗策略提供依据。方法 回顾性分析2023年1月—2024年1月于徐州市妇幼保健院接受IVF-ET治疗的126对不孕夫妇,根据男方DFI检测结果分为低碎片组(DFI≤15%,n=42)、临界组(15%<DFI<30%,n=45)和高碎片组(DFI≥30%,n=39)。比较三组患者受精相关指标、胚胎发育指标及妊娠结局指标的差异,并分析DFI与各指标的相关性。结果 低碎片组双原核率(2PN)率、优质胚胎率及囊胚形成率均高于临界组和高碎片组(P<0.001),低碎片组1PN率、多PN率均低于临界组和高碎片组(P<0.001);三组种植率、临床妊娠率、早期流产率比较差异无统计学意义(P>0.05),但高碎片组活产率低于低碎片组(P<0.05)。相关性分析结果表明,DFI与优质胚胎率(r=-0.412,P<0.001)、囊胚形成率(r=-0.387,P<0.001)、活产率(r=-0.287,P=0.012)呈负相关,与早期流产率(r=0.206,P=0.059)、种植率(r=-0.215,P=0.058)、临床妊娠率(r=-0.203,P=0.072)无显著相关性。结论 精子DNA碎片指数是影响IVF-ET胚胎发育及妊娠结局的重要因素,高DFI主要通过降低胚胎发育潜能及增加流产风险导致活产率下降,临床需对高DFI患者进行干预以改善治疗结局。
Objective To investigate the impact of sperm DNA fragmentation index(DFI)on embryo development and pregnancy outcomes of in vitro fertilization-embryo transfer(IVF-ET),and to provide a basis for optimizing male fertility assessment and assisted reproductive treatment strategies.Methods A retrospective analysis was performed on 126 infertile couples undergoing IVF-ET treatment at the Reproductive Medicine Center of Xuzhou Maternal and Child Health Hospital from January 2023 to January 2024.According to the male DFI test results,they were divided into three groups:low fragmentation group(DFI≤15%,n=42),critical group(15% < DFI < 30%,n=45),and high fragmentation group(DFI≥30%,n=39).Differences in fertilization-related indicators,embryo development indicators,and pregnancy outcome indicators were compared among the three groups,and the correlation between DFI and each indicator was analyzed.Results The 2 pronuclei rate(PN)rate,high-quality embryo rate,and blastocyst formation rate in the low fragmentation group were significantly higher than those in the critical and high fragmentation groups(P<0.001).The 1PN rate and multi-PN rate in the low fragmentation group were significantly lower than those in the critical and high fragmentation groups(P<0.001).There was no significant difference in the three groups of implantation rate,clinical pregnancy rate and early abortion rate(P>0.05),but the live birth rate of high fragment group was significantly lower than that of low fragment group(P<0.05).The results of correlation analysis showed that DFI was significantly negatively correlated with the rate of high quality embryos(r=-0.412,P<0.001),blastocyst formation rate(r=-0.387,P<0.001)and live birth rate(r=-0.287,P=0.012),but not with the rate of early abortion(r=0.206,P=0.059),implantation rate(r=-0.215,P=0.058)and clinical pregnancy rate(r=-0.203,P=0.072).Conclusions Sperm DFI is an important factor affecting embryo development and pregnancy maintenance in IVF-ET.High DFI leads to a decrease in live birth rate mainly by reducing embryo developmental potential and increasing the risk of early abortion.Clinically,early intervention is needed for patients with high DFI to improve treatment outcomes.
目的 探讨体外受精治疗中第3天(D3)不同质量卵裂期胚胎培养至囊胚的发育潜能,为囊胚培养提供实验室依据。方法 对2015年4月—2019年4月D3移植或冷冻后剩余行囊胚培养的5 510枚胚胎进行了回顾性分析。按D3胚胎质量、卵裂球数目、均一性及碎片率分组,比较囊胚形成率,优质囊胚形成率及可利用囊胚形成率,并分析各因素与可利用囊胚形成的相关性。结果 D3优质胚胎的囊胚形成率,优质囊胚形成率及可利用囊胚形成率与非优质胚胎组相比有统计学差异(P<0.05);4-6细胞组及<4细胞组与7-9细胞组相比有统计学差异(P<0.05),但融合期胚胎(CP)组及> 9细胞组与7-9细胞组相比差异无统计学意义;卵裂球大小差异(+)组和(++/+++)组与卵裂球大小均匀(-)相比有统计学差异(P<0.05); 10%~25%组及碎片>25%组与碎片≤10%组相比有统计学差异(P<0.05)。 Logistic分析结果表明,D3胚胎质量、卵裂球数目、均一性及胚胎碎片率与可利用囊胚形成显著相关(P<0.05)。 结论 D3胚胎质量、卵裂球数目、均一性及胚胎碎片均会影响到囊胚的形成及质量,其中胚胎质量和卵裂球数目对可利用囊胚形成的影响较大。
Objective To explore the developmental potential of day 3(D3) different quality embryos cultured to blastocyst in vitro fertilization treatment, and to provide laboratory basis for blastocyst culture. Methods A total of 5 510 embryos with blastocyst culture remained after D3 transplantation or freezing from April 2015 to April 2019 were analyzed retrospectively. They were divided into groups according to embryo quality, blastomere number, blastomere homogeneity and fragment rate in D3. And the blastocyst formation rate, high quality blastocyst formation rate and available blastocyst formation rate were compared between the groups.The correlation within each factor and available blastocyst formation was analyzed. Results The blastocyst formation rate, high quality blastocyst formation rate and available blastocyst formation rate of D3 high quality embryo group were higher than those of non-high quality embryo group (P<0.05); compared with 7- 9 cell group, 4- 6 cell group and<4 cell group were lower (P<0.05), but there was no significant difference in CP group or >9 cell group. Compared with the normal size of the blastomere (-), the difference in the size of the blastomere (+) group and the (++/+++) group decreased (P<0.05); compared with the fragment ≤ 10%, the difference in the size of the blastomere between the 10%~25% group and the fragment>25% group decreased (P<0.05). The results of logistic analysis suggested that the embryo quality, blastomere number, homogeneity and fragment rate of D3 were correlated with available blastocyst formation (P<0.05). Conclusion D3 embryo quality, blastomere number, homogeneity and embryo fragment may affect the formation and quality of blastocyst, especially the embryo quality and blastomere number.