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一种用于植入前基因诊断的胚胎活检简化技术。

A simplified technique for embryo biopsy for preimplantation genetic diagnosis.

作者信息

Wang Wei-Hua, Kaskar Khalied, Gill Jimmy, DeSplinter Traci

机构信息

Houston Fertility Institute, Tomball Regional Hospital, Tomball, Texas 77375, USA.

出版信息

Fertil Steril. 2008 Aug;90(2):438-42. doi: 10.1016/j.fertnstert.2007.06.093. Epub 2007 Sep 19.

Abstract

OBJECTIVE

To report a simplified embryo biopsy method for preimplantation genetic diagnosis (PGD).

DESIGN

Technique and method.

SETTING

A regional hospital in vitro fertilization (IVF) laboratory and private reproductive medicine clinic.

PATIENT(S): Women undergoing IVF and PGD.

INTERVENTION(S): Blastomeres were successfully isolated from day-3 embryos at various stages.

MAIN OUTCOME MEASURE(S): Blastomere integrity after biopsy, time of biopsy procedure, and subsequent blastocyst developmental rate.

RESULT(S): Twenty embryos derived from abnormally fertilized oocytes (one pronucleus or three pronuclei) were used for biopsy at four-cell to 10-cell stages (day 3) by a laser zona drilling and assisted hatching micropipette delivery of culture medium inside the zona to push one blastomere out. Biopsies of all embryos using this method were successful. In two cases for PGD, fourteen 6-9-cell and four 3-4-cell stage embryos were successfully biopsied by this method. Ten out of 14 embryos from the 6-9-cell stage developed to hatching or hatched blastocysts. When two hatched blastocysts were vitrified, warmed, and cultured, both reexpanded, showing normal morphologic features.

CONCLUSION(S): This technique is easy to learn, less damaging to the embryos, and less time consuming. It can be used for all stages of embryos without damage to either embryos or isolated blastomeres. It is an alternative method for embryo biopsy in PGD.

摘要

目的

报告一种用于胚胎植入前遗传学诊断(PGD)的简化胚胎活检方法。

设计

技术与方法。

地点

一家地区医院的体外受精(IVF)实验室及一家私立生殖医学诊所。

患者

接受IVF和PGD的女性。

干预措施

在不同阶段从第3天的胚胎中成功分离出卵裂球。

主要观察指标

活检后卵裂球的完整性、活检操作时间以及随后的囊胚发育率。

结果

20个源自异常受精卵母细胞(一个原核或三个原核)的胚胎在4细胞至10细胞阶段(第3天)通过激光打孔和在透明带内用辅助孵化微吸管输送培养基以推出一个卵裂球的方式进行活检。使用该方法对所有胚胎的活检均成功。在两例PGD病例中,14个6 - 9细胞期胚胎和4个3 - 4细胞期胚胎通过该方法成功活检。14个6 - 9细胞期胚胎中有10个发育为孵化或已孵化的囊胚。当两个已孵化的囊胚被玻璃化、复温并培养时,两者均重新扩张,呈现正常形态特征。

结论

该技术易于学习,对胚胎损伤较小且耗时较少。它可用于胚胎的所有阶段,不会对胚胎或分离出的卵裂球造成损害。它是PGD中胚胎活检的一种替代方法。

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