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囊胚滋养外胚层活检及家族性单基因疾病和染色体易位的植入前基因诊断。

Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations.

作者信息

McArthur S J, Leigh D, Marshall J T, Gee A J, De Boer K A, Jansen R P S

机构信息

Sydney IVF, 321 Kent Street, Sydney, Australia.

出版信息

Prenat Diagn. 2008 May;28(5):434-42. doi: 10.1002/pd.1924.

Abstract

OBJECTIVE

Modern in vitro fertilization practices involve transfer of embryos as blastocysts, when anabolic metabolism is well established and pregnancy rates can be maintained while transferring embryos singly to avoid multiple pregnancies. Embryo biopsy for preimplantation genetic diagnosis (PGD), however, is generally performed on day 3, when the embryo comprises just 6 to 8 cells, one or two of which are removed for testing. Implantation rates and clinical pregnancy rates have remained relatively low and a harmful effect from losing one or more cells from such early embryos has not been excluded.

METHODS

We performed a sequential study involving 399 egg retrievals and 1879 embryo biopsies for patients undergoing PGD to avoid a serious monogenic disease or an unbalanced chromosomal translocation. We compared implantation and viable pregnancy rates after biopsies taken on day 3 (cleavage-stage biopsy) with biopsies delayed until day 5 or 6, when the embryo is a blastocyst and 5 or more cells can be sampled from the trophectoderm while the inner cell mass, from which the fetus develops, remains intact. All embryos were transferred as blastocysts.

RESULTS

Despite fewer blastocysts than cleavage embryos biopsied and tested (3.6 compared to 6.6), implantation rates per embryo transferred were 43.4% if biopsied at the blastocyst stage and 25.6% if biopsied at the cleavage stage (P < 0.01), with ongoing or live-birth pregnancy rates per egg retrieval of 34.2% (average transfer number 1.1) for blastocyst biopsies and 25.5% (transfer number 1.6) for cleavage stage biopsies (P < 0.05, 1-tailed). The multiple pregnancy rate for monogenic disease exclusion fell from 16.7% to 2% (P = 0.04, 1-tailed).

CONCLUSIONS

For exclusion of genetic disease, day 5-6 blastocyst-stage biopsies are more likely to be followed by implantation and singleton births than is the case after PGD performed on day 3.

摘要

目的

现代体外受精操作涉及将胚胎作为囊胚进行移植,此时合成代谢已充分建立,并且在单个移植胚胎以避免多胎妊娠的情况下仍可维持妊娠率。然而,用于植入前基因诊断(PGD)的胚胎活检通常在第3天进行,此时胚胎仅由6至8个细胞组成,从中取出一两个细胞进行检测。植入率和临床妊娠率一直相对较低,并且尚未排除早期胚胎丢失一个或多个细胞所产生的有害影响。

方法

我们进行了一项序贯研究,对接受PGD以避免严重单基因疾病或染色体不平衡易位的患者进行了399次取卵和1879次胚胎活检。我们比较了在第3天进行活检(卵裂期活检)与活检推迟至第5天或第6天(此时胚胎为囊胚,可从滋养外胚层取样5个或更多细胞,而发育成胎儿的内细胞团保持完整)后的植入率和活产妊娠率。所有胚胎均作为囊胚进行移植。

结果

尽管活检和检测的囊胚比卵裂期胚胎少(分别为3.6个和6.6个),但在囊胚期活检后每个移植胚胎的植入率为43.4%,而在卵裂期活检后为25.6%(P<0.01),每次取卵的持续妊娠率或活产妊娠率对于囊胚活检为34.2%(平均移植数1.1),对于卵裂期活检为25.5%(移植数1.6)(P<0.05,单尾)。排除单基因疾病的多胎妊娠率从16.7%降至2%(P = 0.04,单尾)。

结论

对于排除遗传疾病,与在第3天进行PGD相比,在第5 - 6天进行囊胚期活检后更有可能实现植入和单胎分娩。

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