Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: clinical outcome until delivery of 312 cycles

被引:28
|
作者
Keymolen, Kathelijn [1 ]
Staessen, Catherine [1 ]
Verpoest, Willem [2 ]
Liebaers, Inge [1 ]
Bonduelle, Maryse [1 ]
机构
[1] Vrije Univ Brussel, Ctr Med Genet, Univ Ziekenhuis Brussel, B-1090 Brussels, Belgium
[2] Vrije Univ Brussel, Ctr Reprod Med, Univ Ziekenhuis Brussel, B-1090 Brussels, Belgium
关键词
preimplantation genetic diagnosis; PGD; reciprocal translocations; reproductive counseling; PREGNANCY FOLLOW-UP; ESHRE PGD; CONSORTIUM; COHORT; REARRANGEMENTS; EXPERIENCE; JANUARY; INFANTS; EMBRYOS; COUPLES;
D O I
10.1038/ejhg.2011.208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Carriers of reciprocal translocations (rcp) are known to be at risk for reproductive difficulties. Preimplantation genetic diagnosis (PGD) is one of the options these carriers have to try in order to fulfil their desire to have a child. In the present study, we retrospectively looked at the results of 11 years (1997-2007) of PGD for rcp in our center to improve the reproductive counseling of these carriers. During this period 312 cycles were performed for 69 male and 73 female carriers. The mean female age was 32.8 years, the mean male age 35.8 years. Most carriers were diagnosed with a translocation because of fertility problems or recurrent miscarriages, and most of them opted for PGD to avoid these problems. In 150 of the 312 cycles, embryo transfer (ET) was feasible and 40 women had a successful singleton or twin pregnancy. This gives a live birth delivery rate of 12.8% per started cycle and of 26.7% per cycle with ET. Owing to the large number of abnormal embryos, PGD cycles for rcp often lead to cancellation of ET, explaining the low success rate when expressed per cycle with oocyte pick-up. Once ET was feasible, the live birth delivery rate was similar to that of PGD in general at our center. PGD is therefore an established option for specific reciprocal translocation carriers. European Journal of Human Genetics (2012) 20, 376-380; doi: 10.1038/ejhg.2011.208; published online 9 November 2011
引用
收藏
页码:376 / 380
页数:5
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