A prospective study, using sibling oocytes, examining the effect of 30 seconds versus 90 minutes gamete co-incubation in IVF

被引:26
作者
Bungum, M
Bungum, L
Humaidan, P
机构
[1] Viborg Hosp Skive, Fertil Clin, DK-7800 Skive, Denmark
[2] Malmo Univ Hosp, Scanian Androl Ctr, Fertil Ctr, Malmo, Sweden
关键词
fertilization; gamete co-incubation; IVF; polyspermy;
D O I
10.1093/humrep/dei350
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Traditionally oocytes have been exposed to sperm overnight, for 16-20 h. This long period of co-incubation, however, has been shown to create problems with high levels of reactive oxygen species (ROS), which may affect embryo viability and cause hardening of the zona pellucida. Recently, a positive effect of reducing the co-incubation time to 90-120 min was reported. The objective of this study was to evaluate whether a further reduction of the co-incubation period could benefit the outcome of IVF. METHODS: In this prospective study, 777 sibling oocytes from 81 women undergoing IVF were divided via alternate allocation to co-incubation for either 30 s (ultrashort co-incubation) (group A) or for 90 min (standard co-incubation) (group B). Endpoints were normal fertilization (two-pronuclear, 2PN), polyspermy (> 2PN), embryo quality (EQ), clinical pregnancy (CP) and implantation (IR). RESULTS: The normal fertilization rates of the two groups were comparable: group A 58.6% versus group B 58.0%. Significantly lower rates of polyspermy were seen in group A compared to group B (2.8 versus 7.2%, P = 0.008). No statistically significant differences in EQ, CP or IR were seen. CONCLUSION: This is the first study demonstrating the achievement of good fertilization rates in IVF with ultrashort co-incubation. Significantly lower rates of polyspermy were seen in the group with ultrashort compared to the standard co-incubation group. Further studies are, however, needed in order to evaluate whether ultrashort co-incubation has any effect on the outcome of IVF.
引用
收藏
页码:518 / 523
页数:6
相关论文
共 68 条
[1]   Correlation of reactive oxygen species levels with the fertilization rate after in vitro fertilization: a qualified meta-analysis [J].
Agarwal, A ;
Allamaneni, SSR ;
Nallella, KP ;
George, AT ;
Mascha, E .
FERTILITY AND STERILITY, 2005, 84 (01) :228-231
[2]  
Ahmadi A, 1999, J EXP ZOOL, V284, P696, DOI 10.1002/(SICI)1097-010X(19991101)284:6&lt
[3]  
696::AID-JEZ11&gt
[4]  
3.0.CO
[5]  
2-E
[6]  
AITKEN RJ, 1989, J ANDROL, V10, P214
[7]  
AITKEN RJ, 1987, J REPROD FERTIL, V81, P459
[8]  
AITKEN RJ, 1989, BIOL REPROD, V40, P183
[9]   CHROMOSOME-STUDIES IN HUMAN INVITRO FERTILIZATION [J].
ANGELL, RR ;
TEMPLETON, AA ;
AITKEN, RJ .
HUMAN GENETICS, 1986, 72 (04) :333-339
[10]  
[Anonymous], 1999, WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction