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提高非侵入性植入前非整倍体基因检测准确性的条件:聚焦透明带和早期囊胚

Conditions for improved accuracy of noninvasive preimplantation genetic testing for aneuploidy: Focusing on the zona pellucida and early blastocysts.

作者信息

Takeuchi Hiroki, Morishita Midori, Uemura Midori, Maezawa Tadashi, Shibahara Takashi, Takayama Erina, Nishioka Mikiko, Kondo Eiji, Minoura Hiroyuki, Ikeda Tomoaki

机构信息

Department of Obstetrics and Gynecology, Graduate School of Medicine Mie University Tsu Japan.

Center of Advanced Reproductive Medicine Mie University Hospital Tsu Japan.

出版信息

Reprod Med Biol. 2024 Sep 10;23(1):e12604. doi: 10.1002/rmb2.12604. eCollection 2024 Jan-Dec.

Abstract

PURPOSE

Recently, noninvasive preimplantation genetic testing for aneuploidy (niPGT-A) using cell-free deoxyribonucleic acid has been developed; however, there are few reports on this and the results are inconsistent. This study was conducted to optimize the cultural environment.

METHODS

We used 35 blastocysts that had been discarded after in-vitro fertilization. The concordance rate of karyotype analysis results between whole embryos (WEs), spent culture mediums (SCMs), and trophectoderms after 8, 16, and 24 h of culture was examined. Next, zona pellucida (ZP)-free blastocysts and then early blastocysts were cultured for 24 h each.

RESULTS

Regarding the optimal culture times, the concordance rate between WEs and SCMs was 20%, 60%, and 100% at 8, 16, and 24 h, respectively. Significant differences were found between 8 and 24 h. The concordance rate with ZP cultures was 40.0%, and no significant differences were found. The concordance rate of early blastocysts thawed and cultured for 24 h was 40.0%, which was significantly lower than that of day 5 blastocysts.

CONCLUSIONS

The optimal culture times for niPGT-A were 24 h, and the concordance rate with free ZP was higher. The concordance rate for early blastocysts was low, suggesting that optimization of the conditions may be necessary.

摘要

目的

最近,利用游离脱氧核糖核酸进行非侵入性胚胎植入前非整倍体基因检测(niPGT-A)技术已得到发展;然而,关于此技术的报道较少且结果不一致。本研究旨在优化培养环境。

方法

我们使用了35枚体外受精后被丢弃的囊胚。检测了培养8、16和24小时后全胚胎(WEs)、废弃培养基(SCMs)和滋养外胚层之间核型分析结果的一致性率。接下来,分别对无透明带(ZP)囊胚和早期囊胚进行24小时培养。

结果

关于最佳培养时间,WEs与SCMs之间的一致性率在8、16和24小时分别为20%、60%和100%。在8小时和24小时之间发现了显著差异。与ZP培养的一致性率为40.0%,未发现显著差异。解冻并培养24小时的早期囊胚的一致性率为40.0%,显著低于第5天囊胚。

结论

niPGT-A的最佳培养时间为24小时,与无ZP培养的一致性率更高。早期囊胚的一致性率较低,表明可能需要优化条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e1/11387587/f5f93e5aef63/RMB2-23-e12604-g005.jpg

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