Suppr超能文献

植入前基因诊断通过避免移植染色体异常胚胎,提高了人类体外受精的着床率。

Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos.

作者信息

Gianaroli L, Magli M C, Ferraretti A P, Fiorentino A, Garrisi J, Munné S

机构信息

Società Italiana Studi Medicina della Riproduzione, Bologna, Italy.

出版信息

Fertil Steril. 1997 Dec;68(6):1128-31. doi: 10.1016/s0015-0282(97)00412-3.

Abstract

OBJECTIVE

To verify the percentage of chromosomally abnormal preimplantation embryos in patients with a poor prognosis and possibly to increase the chance of implantation by selecting chromosomally normal embryos.

DESIGN

A prospective, randomized, controlled study.

SETTING

In vitro fertilization program at the Reproductive Medicine Unit of the Società Italiana Studi Medicina della Riproduzione, Bologna, Italy.

PATIENT(S): In a total of 28 stimulated cycles, the maternal age was > or = 38 years and/or the patient had > or = 3 previous IVF failures, factors that indicated a poor prognosis. After consent, 11 patients underwent preimplantation genetic diagnosis for aneuploidy, whereas 17 controls underwent assisted zona hatching.

INTERVENTION(S): Simultaneous analysis of chromosomes X, Y, 13, 18, and 21 in a blastomere biopsied from day-3 embryos. Chromosomal analysis was performed with fluorescence in situ hybridization. Assisted zona hatching was performed on day-3 embryos from the control-group patients.

MAIN OUTCOME MEASURE(S): Embryo morphology, results of fluorescence in situ hybridization, clinical pregnancies, and implantation.

RESULT(S): In the study group, a total of 61 embryos were analyzed by fluorescence in situ hybridization, and 55% were chromosomally abnormal. Embryo transfer with at least one normal embryo was performed in 10 cycles. Four clinical pregnancies resulted, with a 28.0% implantation rate. In the control group, 41 embryos were transferred in 17 cycles after the assisted zona hatching procedure, yielding four clinical pregnancies and an 11.9% implantation rate.

CONCLUSION(S): Infertile patients classified as having a poor prognosis have a high percentage of chromosomally abnormal embryos. The advantage of selecting and transferring embryos with normal fluorescence in situ hybridization results has an immediate impact on implantation.

摘要

目的

验证预后不良患者中染色体异常的植入前胚胎的比例,并通过选择染色体正常的胚胎可能增加植入机会。

设计

一项前瞻性、随机、对照研究。

地点

意大利博洛尼亚意大利生殖医学学会生殖医学科的体外受精项目。

患者

在总共28个促排卵周期中,产妇年龄≥38岁和/或患者既往有≥3次体外受精失败,这些因素表明预后不良。在获得同意后,11例患者接受了非整倍体植入前基因诊断,而17例对照患者接受了辅助透明带打孔。

干预措施

对从第3天胚胎活检的一个卵裂球同时进行X、Y、13、18和21号染色体分析。采用荧光原位杂交进行染色体分析。对对照组患者的第3天胚胎进行辅助透明带打孔。

主要观察指标

胚胎形态、荧光原位杂交结果、临床妊娠和植入情况。

结果

在研究组中,共对61个胚胎进行了荧光原位杂交分析,其中55%染色体异常。10个周期进行了至少有一个正常胚胎的胚胎移植。获得了4例临床妊娠,植入率为28.0%。在对照组中,辅助透明带打孔术后17个周期移植了41个胚胎,获得了4例临床妊娠,植入率为11.9%。

结论

被归类为预后不良的不孕患者染色体异常胚胎的比例很高。选择并移植荧光原位杂交结果正常的胚胎的优势对植入有直接影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验