Which patients with recurrent implantation failure after lVF benefit from PGD for aneuploidy screening?

被引:24
作者
Platteau, P
机构
[1] Dutch Speaking Brussels Free Univ, Univ Hosp, Ctr Reprod Med, B-1090 Brussels, Belgium
[2] Dutch Speaking Brussels Free Univ, Univ Hosp, Ctr Genet Med, B-1090 Brussels, Belgium
关键词
chromosomal aneuploidy; FISH; ICSI; IVF; PGD; recurrent IVF failure;
D O I
10.1016/S1472-6483(10)61006-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Patients with recurrent IVF failure are defined as patients who are younger than 37 years and who had at least three consecutive unsuccessful IVF/intracytoplasmic sperm injection (ICSI) cycles with good quality embryos. These patients might be predisposed to chromosome errors in their embryos and therefore might benefit from preimplantation genetic diagnosis for aneuploidy screening (PGD-AS). This technique is, however, expensive and some normal embryos might be lost due to the error rate. The aim of this retrospective study was to define those patients who would benefit most from it. One hundred and twenty-one first PGD-AS cycles for recurrent IVF failure were analysed. The aneuploidy rate, 'no embryo transfer' rate, live birth rate per embryo transfer and implantation rate were respectively 48.3, 22.3, 29.7 and 19.5%. A multivariate logistic regression analysis gave us a predictive model demonstrating that to have a 90% probability of having an embryo transfer after PGD-AS, the patient should have at least 10 mature oocytes, eight normally fertilized oocytes and six embryos for biopsy. This study suggests that most patients with recurrent IVF failure may benefit from PGD-AS. Future studies, however, should more strictly define this heterogeneous group of patients, so that comparison is easier.
引用
收藏
页码:334 / 339
页数:6
相关论文
共 38 条
[1]   Preimplantation genetic diagnosis for aneuploidy screening in repeated implantation failure [J].
Caglar, GS ;
Asimakopoulos, B ;
Nikolettos, N ;
Diedrich, K ;
Al-Hasani, S .
REPRODUCTIVE BIOMEDICINE ONLINE, 2005, 10 (03) :381-388
[2]   OPTIMAL PREPARATION OF PREIMPLANTATION EMBRYO INTERPHASE NUCLEI FOR ANALYSIS BY FLUORESCENCE IN-SITU HYBRIDIZATION [J].
COONEN, E ;
DUMOULIN, JCM ;
RAMAEKERS, FCS ;
HOPMAN, AHN .
HUMAN REPRODUCTION, 1994, 9 (03) :533-537
[3]   Aspects of biopsy procedures prior to preimplantation genetic diagnosis [J].
De Vos, A ;
Van Steirteghem, A .
PRENATAL DIAGNOSIS, 2001, 21 (09) :767-780
[4]   A review of ten years experience of ICSI [J].
Devroey, P ;
Van Steirteghem, A .
HUMAN REPRODUCTION UPDATE, 2004, 10 (01) :19-28
[5]   Prognostic role of preimplantation genetic diagnosis for aneuploidy in assisted reproductive technology outcome [J].
Ferraretti, AP ;
Magli, MC ;
Kopcow, L ;
Gianaroli, L .
HUMAN REPRODUCTION, 2004, 19 (03) :694-699
[6]   Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis:: identification of the categories for which it should be proposed [J].
Gianaroli, L ;
Magli, MC ;
Ferraretti, AP ;
Munné, S .
FERTILITY AND STERILITY, 1999, 72 (05) :837-844
[7]   The in vivo and in vitro efficiency and efficacy of PGD for aneuploidy [J].
Gianaroli, L ;
Magli, MC ;
Ferraretti, AP .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2001, 183 :S13-S18
[8]   Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos [J].
Gianaroli, L ;
Magli, MC ;
Ferraretti, AP ;
Fiorentino, A ;
Garrisi, J ;
Munne, S .
FERTILITY AND STERILITY, 1997, 68 (06) :1128-1131
[9]   MOSAICISM OF AUTOSOMES AND SEX-CHROMOSOMES IN MORPHOLOGICALLY NORMAL, MONOSPERMIC PREIMPLANTATION HUMAN EMBRYOS [J].
HARPER, JC ;
COONEN, E ;
HANDYSIDE, AH ;
WINSTON, RML ;
HOPMAN, AHN ;
DELHANTY, JDA .
PRENATAL DIAGNOSIS, 1995, 15 (01) :41-49
[10]   A modified cryopreservation method increases the survival of human biopsied cleavage stage embryos [J].
Jericho, H ;
Wilton, L ;
Gook, DA ;
Edgar, DH .
HUMAN REPRODUCTION, 2003, 18 (03) :568-571