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植入前遗传学诊断与人类着床——综述

Preimplantation genetic diagnosis and human implantation--a review.

作者信息

Munné S

机构信息

The Institute for Reproductive Medicine and Science of Saint Barnabas, Livingston, NJ 07030, USA.

出版信息

Placenta. 2003 Oct;24 Suppl B:S70-6. doi: 10.1016/s0143-4004(03)00177-2.

Abstract

By selecting chromosomally normal embryos for replacement, PGD for aneuploidy can (i) increase implantation rates, (ii) reduce spontaneous abortion rates, and (iii) avoid aneuploid conceptions. When eight chromosomes are analysed, a significant increase in implantation is achieved. PGD is also found to significantly reduce the incidence of spontaneous abortion and chromosomally abnormal conceptions. PGD for patients of advanced maternal age with an adequate number of embryos will improve their chances of childbirth via improved implantation and sustained gestation. PGD has also been used to help other specific groups of patients with high rates of chromosome abnormalities such as patients with recurrent spontaneous abortions, non-obstructive azoospermia, repeated IVF failure, and patients previous trisomic offspring. Recently, PGD has been performed using comparative genome hybridization, which counts all chromosomes; but time constraints require embryo cryopreservation, which reduces the potential of improved implantation

摘要

通过选择染色体正常的胚胎进行移植,针对非整倍体的胚胎植入前遗传学诊断(PGD)可以:(i)提高着床率;(ii)降低自然流产率;(iii)避免非整倍体妊娠。当分析八条染色体时,着床率会显著提高。研究还发现,PGD能显著降低自然流产率和染色体异常妊娠的发生率。对于高龄产妇且有足够数量胚胎的患者,PGD可通过提高着床率和维持妊娠来增加其分娩几率。PGD还被用于帮助其他染色体异常率较高的特定患者群体,如复发性自然流产患者、非梗阻性无精子症患者、反复体外受精失败患者以及曾生育过三体后代的患者。最近,已采用比较基因组杂交技术进行PGD,该技术可对所有染色体进行计数;但由于时间限制需要对胚胎进行冷冻保存,这降低了提高着床率的可能性

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