Preimplantation genetic diagnosis significantly improves the pregnancy outcome of translocation carriers with a history of recurrent miscarriage and unsuccessful pregnancies

被引:81
作者
Otani, Tetsuo
Roche, Muriel
Mizuike, Miho
Colls, Pere
Escudero, Tomas
Munne, Santiago
机构
[1] Otani Womens Clin, Kobe, Hyogo, Japan
[2] Reprogenet Japan LLC, Kobe, Hyogo, Japan
[3] Reprogenetics LLC, Hoboken, NJ USA
[4] Reprogenet Calif LLC, W San Francisco, CA USA
关键词
chromosome imbalance; PGD; pregnancy outcome; recurrent miscarriage; translocation;
D O I
10.1016/S1472-6483(10)61037-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Preimplantation genetic diagnosis (PGD) for translocations has been shown to significantly reduce the risk of recurrent miscarriage, but because the majority of embryos produced are unbalanced, pregnancy rate is relatively low since 20% or more cycles have no normal or balanced embryos to transfer. The purpose of this study was to evaluate whether PGD could improve pregnancy outcome in translocation carriers with a history of two or more consecutive miscarriages and no live births. PGD for translocations was offered to translocation carriers with two or more previous miscarriages (average 3.5) and no live births (0/117 pregnancies) using a combination of distal and proximal probes to the breakpoints. After PGD, only 18.3% of embryos were normal or balanced. Only 5.3% of pregnancies were lost after PGD compared with 100% before PGD (P < 0.001). The cumulative pregnancy rate was 57.6% and the cumulative ongoing pregnancy rate was 54.5% in the short period of time of 1.24 IVF cycles, or 46.3% and 43.9% respectively per cycle. In conclusion, PGD significantly reduced losses and increased the number of viable pregnancies (P < 0.001). IVF plus PGD are a faster method of conceiving a live child than natural conception, at least for translocation carriers with recurrent miscarriages and no previous live births.
引用
收藏
页码:869 / 874
页数:6
相关论文
共 32 条
[1]  
[Anonymous], HUMAN EMBRYONIC FETA
[2]  
BOUE JG, 1976, CURR TOPICS PATHOL, V62, P193
[3]   A longitudinal study of pregnancy outcome following idiopathic recurrent miscarriage [J].
Brigham, SA ;
Conlon, C ;
Farquharson, RG .
HUMAN REPRODUCTION, 1999, 14 (11) :2868-2871
[4]  
Burgoyne P S, 1984, Symp Soc Exp Biol, V38, P349
[5]   Parental karyotype and subsequent live births in recurrent miscarriage [J].
Carp, H ;
Feldman, B ;
Oelsner, G ;
Schiff, E .
FERTILITY AND STERILITY, 2004, 81 (05) :1296-1301
[6]   Genetic contribution to male infertility [J].
Chandley, AC .
HUMAN REPRODUCTION, 1998, 13 :76-83
[7]   CHROMOSOMAL BASIS OF HUMAN INFERTILITY [J].
CHANDLEY, AC .
BRITISH MEDICAL BULLETIN, 1979, 35 (02) :181-186
[8]   Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions [J].
Conn, CM ;
Harper, JC ;
Winston, RML ;
Delhanty, JDA .
HUMAN GENETICS, 1998, 102 (01) :117-123
[9]   Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities [J].
Fridström, M ;
Ährlund-Richter, L ;
Iwarsson, E ;
Malmgren, H ;
Inzunza, J ;
Rosenlund, B ;
Sjöblom, P ;
Nordenskjöld, M ;
Blennow, E ;
Hovatta, O .
PRENATAL DIAGNOSIS, 2001, 21 (09) :781-787
[10]   Clinical value of preimplantation genetic diagnosis [J].
Gianaroli, L ;
Magli, MC ;
Fiorentino, F ;
Baldi, M ;
Ferraretti, AP .
PLACENTA, 2003, 24 :S77-S83