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通过阵列比较基因组杂交进行植入前基因诊断和筛查:单中心100多例病例的经验。

Preimplantation genetic diagnosis and screening by array comparative genomic hybridisation: experience of more than 100 cases in a single centre.

作者信息

Chow J Fc, Yeung W Sb, Lee V Cy, Lau E Yl, Ho P C, Ng E Hy

机构信息

Department of Obstetrics and Gynaecology, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong.

Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong.

出版信息

Hong Kong Med J. 2017 Apr;23(2):129-33. doi: 10.12809/hkmj164883. Epub 2017 Feb 17.

Abstract

INTRODUCTION

Preimplantation genetic screening has been proposed to improve the in-vitro fertilisation outcome by screening for aneuploid embryos or blastocysts. This study aimed to report the outcome of 133 cycles of preimplantation genetic diagnosis and screening by array comparative genomic hybridisation.

METHODS

This study of case series was conducted in a tertiary assisted reproductive centre in Hong Kong. Patients who underwent preimplantation genetic diagnosis for chromosomal abnormalities or preimplantation genetic screening between 1 April 2012 and 30 June 2015 were included. They underwent in-vitro fertilisation and intracytoplasmic sperm injection. An embryo biopsy was performed on day-3 embryos and the blastomere was subject to array comparative genomic hybridisation. Embryos with normal copy numbers were replaced. The ongoing pregnancy rate, implantation rate, and miscarriage rate were studied.

RESULTS

During the study period, 133 cycles of preimplantation genetic diagnosis for chromosomal abnormalities or preimplantation genetic screening were initiated in 94 patients. Overall, 112 cycles proceeded to embryo biopsy and 65 cycles had embryo transfer. The ongoing pregnancy rate per transfer cycle after preimplantation genetic screening was 50.0% and that after preimplantation genetic diagnosis was 34.9%. The implantation rates after preimplantation genetic screening and diagnosis were 45.7% and 41.1%, respectively and the miscarriage rates were 8.3% and 28.6%, respectively. There were 26 frozen-thawed embryo transfer cycles, in which vitrified and biopsied genetically transferrable embryos were replaced, resulting in an ongoing pregnancy rate of 36.4% in the screening group and 60.0% in the diagnosis group.

CONCLUSIONS

The clinical outcomes of preimplantation genetic diagnosis and screening using comparative genomic hybridisation in our unit were comparable to those reported internationally. Genetically transferrable embryos replaced in a natural cycle may improve the ongoing pregnancy rate and implantation rate when compared with transfer in a stimulated cycle.

摘要

引言

植入前基因筛查已被提出用于通过筛查非整倍体胚胎或囊胚来改善体外受精的结局。本研究旨在报告133个采用阵列比较基因组杂交技术进行植入前基因诊断和筛查周期的结果。

方法

本病例系列研究在香港一家三级辅助生殖中心进行。纳入了2012年4月1日至2015年6月30日期间接受染色体异常植入前基因诊断或植入前基因筛查的患者。他们接受了体外受精和卵胞浆内单精子注射。在第3天的胚胎上进行胚胎活检,将卵裂球进行阵列比较基因组杂交。替换具有正常拷贝数的胚胎。研究持续妊娠率、着床率和流产率。

结果

在研究期间,94例患者开始了133个染色体异常植入前基因诊断或植入前基因筛查周期。总体而言,112个周期进行了胚胎活检,65个周期进行了胚胎移植。植入前基因筛查后每个移植周期的持续妊娠率为50.0%,植入前基因诊断后为34.9%。植入前基因筛查和诊断后的着床率分别为45.7%和41.1%,流产率分别为8.3%和28.6%。有26个冻融胚胎移植周期,其中替换了经玻璃化处理和活检的可基因转移胚胎,筛查组的持续妊娠率为36.4%,诊断组为60.0%。

结论

我们单位使用比较基因组杂交技术进行植入前基因诊断和筛查的临床结果与国际上报道的结果相当。与在促排卵周期中移植相比,在自然周期中替换可基因转移胚胎可能会提高持续妊娠率和着床率。

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