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首页> 外文期刊>Journal of assisted reproduction and genetics >A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM)
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A prospective study of non-invasive preimplantation genetic testing for aneuploidies (NiPGT-A) using next-generation sequencing (NGS) on spent culture media (SCM)

机译:使用下一代测序(NGS)对废培养培养基(SCM)的非侵入性预致癌遗传学试验的前瞻性研究(NIPGT-A)

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Purpose This study was to evaluate if spent culture media (SCM) of embryos could be used as a non-invasive tool to achieve aneuploidy screening. Ploidy calls, as well as concordance rates between PGT-A results from trophectoderm (TE) and SCM, were compared. Clinical outcomes of single euploid transfers were also evaluated. Methods The study was conducted from March 2017 to June 2018 in a university-based ART center. SCM of day 3 to the day(s) of TE biopsy of all biopsied blastocysts were collected for testing. PGT-A results of SCM were compared with the standard results of TE, with clinical relevance and outcomes examined. Results NiPGT-A using SCM gave a sensitivity of 81.6%, specificity of 48.3%, positive predictive value of 82.6%, and negative predictive value of 46.7% in ploidy calling. The concordance rates for autosomes and sex determination were 62.1% and 82.4%, respectively. There were 14 single embryo transfer cycles of euploids as determined by TE biopsy. Clinical outcomes not only confirmed 3 false positive results from SCM but also reflected the true ploidy status of the transferred embryo in one case. If ploidy calls were dichotomized without mosaic embryos, the sensitivity and NPV would increase to 91.0% and 66.7% (p = 0.60 and p = 0.25), respectively. Conclusions Cell-free DNA found in SCM could provide ploidy information of an embryo as in PGT-A from its TE. Given its potential to reflect the comprehensive chromosomal profile of the whole embryo, more research based on clinical outcomes is required to determine if SCM could be a reliable selection tool in PGT-A.
机译:目的本研究是评估胚胎的培养介质(SCM)是否可以用作非侵入性工具来实现非稀释性筛选。比较倍增性呼叫,以及PGT-A来自琐事胚胎(TE)和SCM的结果之间的一致性速率。还评估了单层转移的临床结果。方法从2017年3月至2018年6月在一所大学艺术中心进行。收集所有活检胚泡的TE活检的第3天的第3天的SCM进行测试。 PGT-A的结果与TE的标准结果进行了比较,临床相关性和结果。结果NIPGT-A使用SCM的灵敏度为81.6%,特异性为48.3%,阳性预测值82.6%,倍增性呼叫中的负预测值为46.7%。常染色体和性别测定的一致性率分别为62.1%和82.4%。通过TE活组织检查测定,有14个单倍体的胚胎转移循环。临床结果不仅确认了SCM的3个假阳性结果,而且还反映了一种情况下转移胚胎的真正倍增性状态。如果没有马赛克胚胎的倍频性调用,敏感性和NPV分别会增加到91.0%和66.7%(p = 0.60和p = 0.25)。结论SCM中发现的无细胞DNA可以从其TE中提供胚胎的倍频信息。鉴于其潜力来反映整个胚胎的综合染色体剖面,需要根据临床结果的更多研究来确定SCM是否可以是PGT-A中的可靠选择工具。

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