Suppr超能文献

植入前胚胎染色体数目和结构异常的基因诊断

Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities.

作者信息

Munné Santiago

机构信息

Saint Barnabas Medical Centre, 101 Old Short Hills Road, Suite 501, West Orange, NJ 07052, USA.

出版信息

Reprod Biomed Online. 2002 Mar-Apr;4(2):183-96. doi: 10.1016/s1472-6483(10)61938-4.

Abstract

The causes of the decline in implantation rates observed with increasing maternal age are still a matter for debate. Data from oocyte donation strongly suggest that in women of advanced reproductive age, the ability to become pregnant is largely unaffected while oocyte quality is compromised. The incidence of chromosomal abnormalities in embryos is considerably higher than that reported in spontaneous abortions, suggesting that a sizable percentage of chromosomally abnormal embryos are eliminated before any prenatal diagnosis. Such loss may partly account for the decline in implantation in older women. Because of the correlation between aneuploidy and reduced implantation, it has been postulated that selection of chromosomally normal embryos could reverse this trend. Preimplantation genetic diagnosis (PGD) for aneuploidy had three objectives relevant to the present paper: (i) to increase rates of implantation, (ii) to reduce risks of spontaneous abortion, and (iii) to avoid chromosomally abnormal births. Implantation rates did not increase when only five chromosomes were analysed in blastomeres. With eight chromosomes, a significant increase in implantation was achieved. PGD can significantly reduce the incidence of spontaneous abortion. In our clinic, a significant decrease in spontaneous abortions was found, from 23 to 11% after PGD. Currently in cases diagnosed at Saint Barnabas, 0.8% chromosomally abnormal conceptions have been observed after PGD versus an expected 3.2% in a control age-matched group. It seems clear that PGD reduces the possibility of trisomic conceptions under all conditions. If a couple's main interest is to improve their chances of conceiving (improve implantation), then one should consider maternal age and number of available embryos. Improvements in conception after PGD again increase after 37 years of age with eight or nine probes. Carriers of translocations are at a high risk of miscarriage or chromosomally unbalanced offspring, and a high proportion have secondary infertility. PGD of translocations has been approached through a variety of methods, here reviewed, and has resulted in a significant reduction in spontaneous abortions. However, implantation rates in translocation carriers are directly correlated with the proportion of normal gametes, and male patients with 70% or more unbalanced spermatozoa have great difficulty in achieving pregnancy with PGD.

摘要

随着母亲年龄增长,着床率下降的原因仍存在争议。卵母细胞捐赠的数据有力地表明,在高龄生育女性中,怀孕能力在很大程度上未受影响,而卵母细胞质量却受到损害。胚胎中染色体异常的发生率显著高于自然流产报告中的发生率,这表明相当大比例的染色体异常胚胎在进行任何产前诊断之前就被淘汰了。这种损失可能部分解释了老年女性着床率下降的原因。由于非整倍体与着床率降低之间存在关联,因此有人推测选择染色体正常的胚胎可以扭转这一趋势。针对非整倍体的植入前基因诊断(PGD)有三个与本文相关的目标:(i)提高着床率,(ii)降低自然流产风险,(iii)避免染色体异常的婴儿出生。当仅对卵裂球中的五条染色体进行分析时,着床率并未提高。分析八条染色体时,着床率显著提高。PGD可以显著降低自然流产的发生率。在我们的诊所中,发现自然流产率显著下降,PGD后从23%降至11%。目前在圣巴纳巴斯医院诊断的病例中,PGD后观察到0.8%的染色体异常妊娠,而在年龄匹配的对照组中预期为3.2%。显然,PGD在所有情况下都降低了三体妊娠的可能性。如果一对夫妇的主要兴趣是提高受孕几率(提高着床率),那么应该考虑母亲年龄和可用胚胎数量。37岁以后,使用八条或九条探针进行PGD后,受孕成功率再次提高。易位携带者有很高的流产风险或生出染色体不平衡后代的风险,并且很大一部分人存在继发性不孕。本文回顾了通过多种方法进行易位的PGD,其结果是自然流产率显著降低。然而,易位携带者的着床率与正常配子的比例直接相关,精子不平衡率达到70%或更高的男性患者通过PGD怀孕的难度很大。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验