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卵裂期活检显著损害人类胚胎着床潜能,而囊胚期活检则不会:一项随机配对临床试验。

Cleavage-stage biopsy significantly impairs human embryonic implantation potential while blastocyst biopsy does not: a randomized and paired clinical trial.

机构信息

Reproductive Medicine Associates of New Jersey, Morristown, New Jersey 07920, USA.

出版信息

Fertil Steril. 2013 Sep;100(3):624-30. doi: 10.1016/j.fertnstert.2013.04.039. Epub 2013 Jun 15.

Abstract

OBJECTIVE

To determine if cleavage- or blastocyst-stage embryo biopsy affects reproductive competence.

DESIGN

Paired randomized clinical trial.

SETTING

Academic-assisted reproduction program.

PATIENT(S): Attempting conception through IVF.

INTERVENTION(S): After selecting two embryos for transfer, one was randomized to biopsy and the other to control. Both were transferred within shortly thereafter. The biopsy was submitted for microarray analysis and single-nucleotide polymorphism (SNP) profiling. Buccal DNA obtained from the neonate after delivery had microarray analysis and SNP profile compared with that of the embryonic DNA. A match confirmed that the biopsied embryo implanted and developed to term, whereas a nonmatch indicated that the control embryo had led to the delivery.

MAIN OUTCOME MEASURE(S): Paired analysis of the delivery rates of the transferred embryos. Either twin delivery or failure to deliver represents equivalent outcomes for the biopsied and control embryos. In contrast, singletons were determined to be from the biopsied or the control embryo.

RESULT(S): Blastomere biopsy on day 3 of development resulted in a significant reduction in sustained implantation. Only 30% of biopsied embryos had sustained implantation and ultimately developed into live-born infants versus 50% of unbiopsied controls, a relative reduction of 39%. In contrast, sustained implantation rates were equivalent (51% vs. 54%) for biopsied and control blastocysts.

CONCLUSION(S): Cleavage-stage biopsy markedly reduced embryonic reproductive potential. In contrast, trophectoderm biopsy had no measurable impact and may be used safely when embryo biopsy is indicated.

CLINICAL TRIAL REGISTRATION NUMBER

NCT01219504.

摘要

目的

确定卵裂期或囊胚期胚胎活检是否影响生殖能力。

设计

配对随机临床试验。

地点

辅助生殖项目的学术环境。

患者

通过试管婴儿技术尝试受孕。

干预

选择两个胚胎进行移植后,一个被随机分为活检组,另一个为对照组。之后不久,两个胚胎都被移植。活检标本被提交进行微阵列分析和单核苷酸多态性(SNP)分析。从新生儿出生后的口腔获得 DNA,与胚胎 DNA 进行微阵列分析和 SNP 分析。如果匹配,则证实活检胚胎着床并发育至足月,而非匹配则表明对照组胚胎导致了分娩。

主要观察指标

移植胚胎的分娩率进行配对分析。无论是双胞胎分娩还是未能分娩,对于活检组和对照组胚胎来说,都是等同的结果。相反,单胎被确定为来自活检或对照组胚胎。

结果

第 3 天的卵裂期胚胎活检导致着床持续减少。只有 30%的活检胚胎着床并最终发育为活产婴儿,而未经活检的对照组为 50%,相对减少了 39%。相比之下,活检和对照组囊胚的着床率相当(51%对 54%)。

结论

卵裂期活检显著降低了胚胎的生殖潜能。相比之下,滋养外胚层活检没有明显影响,在需要胚胎活检时可以安全使用。

临床试验注册号

NCT01219504。

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