人着床前胚胎分泌的microrna与体外受精结果。

Shintaro Kamijo, Toshio Hamatani, Hiroyuki Sasaki, Hiroki Suzuki, Akane Abe, Osamu Inoue, Maki Iwai, Seiji Ogawa, Kei Odawara, Kanako Tanaka, Mutsumi Mikashima, Masami Suzuki, Kenji Miyado, Ryo Matoba, Yasushi Odawara, Mamoru Tanaka
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引用次数: 5

摘要

目的:通过分析胚胎培养基中的microrna (miRNAs),建立有效的胚胎预测模型,并确定一种无创评估方法。设计:分析从形态学良好的囊胚废培养基中提取的microRNA图谱,这些囊胚有或没有导致怀孕。单位:临床及实验研究。患者:60例接受卵浆内单精子注射后的囊胚解冻胚胎移植。干预:无。主要观察指标:培养基中囊胚分泌的miRNA丰度水平与着床成功的相关性。结果:我们的RNA测序分析发现妊娠组和非妊娠组培养液中共有53个差异表达的mirna。分析了21个mirna预测植入成功的潜力。进一步从qPCR Ct值的逻辑回归分析结果中提取8个mirna (hsa-miR-191-5p、hsa-miR-320a、hsa-miR-92a-3p、hsa-miR-509-3p、hsa-miR-378a-3p、hsa-miR-28-3p、hsa-miR-512-5p和hsa-miR-181a-5p)。利用这8个mirna生成了一个高质量囊胚的预测模型,经过5次交叉验证,平均准确率为0.82。结论:我们分离到了可以预测着床成功的囊胚mirna,并建立了预测存活胚胎的模型。需要增加研究病例的数量并进一步研究每种miRNA对胚胎发育的影响,以完善基于miRNA的预测模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MicroRNAs secreted by human preimplantation embryos and IVF outcome.

MicroRNAs secreted by human preimplantation embryos and IVF outcome.

MicroRNAs secreted by human preimplantation embryos and IVF outcome.

MicroRNAs secreted by human preimplantation embryos and IVF outcome.

Objective: To generate an effective embryo prediction model and identify a non-invasive evaluation method by analyzing microRNAs (miRNAs) in embryo culture medium.

Design: Analysis of microRNA profiles from spent culture medium of blastocysts with good morphology that did or did not result in pregnancy.

Setting: Clinical and experimental research.

Patients: Sixty patients who underwent thawed embryo transfer of blastocysts after intracytoplasmic sperm injection.

Intervention(s): None.

Main outcome measure(s): The association of miRNA abundance levels secreted by blastocysts in culture medium and implantation success.

Results: Our RNA sequencing analysis found a total of 53 differentially expressed miRNAs in the culture media of pregnancy and non-pregnancy groups. Twenty-one miRNAs were analyzed for their potential to predict implantation success. Eight miRNAs (hsa-miR-191-5p, hsa-miR-320a, hsa-miR-92a-3p, hsa-miR-509-3p, hsa-miR-378a-3p, hsa-miR-28-3p, hsa-miR-512-5p, and hsa-miR-181a-5p) were further extracted from the results of a logistic regression analysis of qPCR Ct values. A prediction model for high-quality blastocysts was generated using the eight miRNAs, with an average accuracy of 0.82 by 5-fold cross validation.

Conclusion: We isolated blastocyst miRNAs that may predict implantation success and created a model to predict viable embryos. Increasing the number of investigated cases and further studying the effect of each miRNA on embryonic development is needed to refine the miRNA-based predictive model.

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