Positive outcome after preimplantation diagnosis of aneuploidy in human embryos

被引:262
作者
Munné, S
Magli, C
Cohen, J
Morton, P
Sadowy, S
Gianaroli, L
Tucker, M
Márquez, C
Sable, D
Ferraretti, AP
Massey, JB
Scott, R
机构
[1] St Barnabas Med Ctr, Inst Reprod Med & Sci, Livingston, NJ 07052 USA
[2] SISMeR, Bologna, Italy
[3] Reprod Biol Associates, Atlanta, GA USA
关键词
in-vitro fertilization; preimplantation genetic diagnosis; trisomy; 21; 18; 13; 16;
D O I
10.1093/humrep/14.9.2191
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Chromosomal abnormalities are responsible for a great deal of embryo wastage, which is reflected, at least partially, in decreased implantation and increased miscarriage in older women, To address this problem the transfer of only chromosomally normal embryos previously selected by preimplantation genetic diagnosis (PGD) has been proposed. We designed a multi-centre in-vitro fertilization (IVF) study to compare controls and a test group that underwent embryo biopsy and PGD for aneuploidy, Patients were matched retrospectively, but blindly, for average maternal age, number of previous IVF cycles, duration of stimulation, oestradiol concentrations on day +1, and average mature follicles. All these parameters were similar in test and control groups, Only embryos classified as normal for those chromosomes were transferred after PGD, The results showed that the rates of fetal heart beat (FHB)/embryo transferred between the control and test groups were similar. However, spontaneous abortions, measured as FHB aborted/FHB detected, decreased after PGD (P < 0.05), and ongoing pregnancies and delivered babies increased (P < 0.05) in the PGD group of patients, Two conclusions were obtained: (i) PGD of aneuploidy reduced embryo loss after implantation; (ii) implantation rates were not significantly improved, but the proportion of ongoing and delivered babies was increased.
引用
收藏
页码:2191 / 2199
页数:9
相关论文
共 44 条
  • [1] Human embryo fragmentation in vitro and its implications for pregnancy and implantation
    Alikani, M
    Cohen, J
    Tomkin, G
    Garrisi, GJ
    Mack, C
    Scott, RT
    [J]. FERTILITY AND STERILITY, 1999, 71 (05) : 836 - 842
  • [2] PARENTAL ORIGIN OF THE EXTRA CHROMOSOME IN TRISOMY-21 AS INDICATED BY ANALYSIS OF DNA POLYMORPHISMS
    ANTONARAKIS, SE
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (13) : 872 - 876
  • [3] Preimplantation genetic diagnosis of aneuploidy:: Were we looking at the wrong chromosomes?
    Bahçe, M
    Cohen, J
    Munné, S
    [J]. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 1999, 16 (04) : 176 - 181
  • [4] IMPAIRMENT OF THE HATCHING PROCESS FOLLOWING IVF IN THE HUMAN AND IMPROVEMENT OF IMPLANTATION BY ASSISTING HATCHING USING MICROMANIPULATION
    COHEN, J
    ELSNER, C
    KORT, H
    MALTER, H
    MASSEY, J
    MAYER, MP
    WIEMER, K
    [J]. HUMAN REPRODUCTION, 1990, 5 (01) : 7 - 13
  • [5] Dailey T, 1996, AM J HUM GENET, V59, P176
  • [6] Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients
    Delhanty, JDA
    Harper, JC
    Ao, A
    Handyside, AH
    Winston, RML
    [J]. HUMAN GENETICS, 1997, 99 (06) : 755 - 760
  • [7] Oocyte polarity and cell determination in early mammalian embryos
    Edwards, RG
    Beard, HK
    [J]. MOLECULAR HUMAN REPRODUCTION, 1997, 3 (10) : 863 - 905
  • [8] Egozcue J, 1996, HUM REPROD, V11, P2077
  • [9] FISHER JM, 1995, AM J HUM GENET, V56, P669
  • [10] Garside WT, 1997, MOL REPROD DEV, V47, P99, DOI 10.1002/(SICI)1098-2795(199705)47:1<99::AID-MRD13>3.0.CO