2013年3月26日

高齡不需施行PGD以提高懷孕率

高齡(>37歲)施行試管嬰兒不需要常規施行胚胎著床前基因診斷(PGD)以提高懷孕率,

PGD並無法明顯提高高齡病患胚胎植入後懷孕率‧

http://humrep.oxfordjournals.org/content/19/12/2849.full




Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age: a prospective randomized controlled trial
  1. André Van Steirteghem1
+Author Affiliations
  1. 1Centre for Reproductive Medicine and 2Centre for Medical Genetics, University Hospital, Dutch-speaking Brussels Free University (Vrije Universiteit Brussel), Laarbeeklaan 101, B-1090 Brussels, Belgium
  1. 3To whom correspondence should be addressed. Email:catherine.staessen@az.vub.ac.be

    Abstract

    BACKGROUND: It is generally accepted that the age-related increased aneuploidy rate is correlated with reduced implantation and a higher abortion rate. Therefore, advanced maternal age (AMA) couples are a good target group to assess the possible benefit of preimplantation genetic diagnosis for aneuploidy screening (PGD-AS) on the outcome after assisted reproductive technology (ART). METHODS: A prospective randomized controlled clinical trial (RCT) was carried out comparing the outcome after blastocyst transfer combined with PGD-AS using fluorescence in situ hybridization (FISH) for the chromosomes X, Y, 13, 16, 18, 21 and 22 in AMA couples (aged ≥37 years) with a control group without PGD-AS. From the 400 (200 for PGD-AS and 200 controls) couples that were allocated to the trial, an oocyte pick-up was performed effectively in 289 cycles (148 PGD-AS cycles and 141 control cycles). RESULTS: Positive serum HCG rates per transfer and per cycle were the same for PGD-AS and controls: 35.8% (19.6%) [%/per embryo transfer (per cycle)] and 32.2% (27.7%), respectively (NS). Significantly fewer embryos were transferred in the PGD-AS group than in the control group (P<0.001). The implantation rate (with fetal heart beat) was 17.1% in the PGD-AS group versus 11.5% in the control group (not significant; P=0.09). We observed a normal diploid status in 36.8% of the embryos. CONCLUSIONS: This RCT provides no arguments in favour of PGD-AS for improving clinical outcome per initiated cycle in patients with AMA when there are no restrictions in the number of embryos to be transferred.



    Table II.
    Clinical results
    ControlPGD-ASStatistics
    Cycles (n)141148
    No. of cycles with
        Oocyte retrieval failure02
        Fertilization failure57
        All embryos arrested on day 39
        With biopsy130
        With only genetically abnormal  embryos38
        With no morula or blastocyst  formation from genetically normal  embryos11
        With no blastocyst formation15
    No. of embryo transfers (ETs)12181P<0.001a
        Total number of embryos  transferred338164
        Mean embryos transferredb2.8±1.22.0±0.9P<0.001c
        No. of positive serum HCG3929
        % positive serum HCG per ET32.235.8
        % positive serum HCG per cycle27.719.6
    No. of implantations with fetal  heartbeat (B)3928
        % of B per transferred embryo11.517.1P=0.09a
    Outcome
        Preclinical abortions97
        Clinical abortions and EUG10
        Ongoing ≥12 weeks2922
        Singleton23d18
        Twin63e,f
        Triplet1
        No. of ongoing implantations (C)3527
        % of C per transferred embryo10.416.5P=0.06a


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