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Noninvasive pre-transfer identification of women with recurrent implantation failure using a plasma microRNA-based machine learning model

生物 植入失败 小RNA 胚胎 逻辑回归 实时聚合酶链反应 机器学习 生物信息学 排卵 计算生物学 鉴定(生物学) 曲线下面积 人工智能 内科学 接收机工作特性 聚合酶链反应 子宫内膜 风险评估 弗雷明翰风险评分 选择(遗传算法) 肿瘤科 胚胎移植 男科 阶段(地层学) 氯米芬 妇科 子宫
作者
Lingyin Kong,Ying Ju,Xiao He,Xiuyu Feng,Lu Wang,Hongya Yang,Ying Kang,Li Hai,Fan Wang,Jing Wu,Juan Zhou,Jun Wang,Xingqing Gou,Xiyi Wang,Xiyi Wang,Bo Liang,Keping Chen,Xiang Xiao,Xiaohong Wang,Xiaohong Wang
出处
期刊:Biology of Reproduction [Oxford University Press]
卷期号:115 (1): 264-279
标识
DOI:10.1093/biolre/ioag070
摘要

Recurrent implantation failure (RIF) refers to patients who have undergone at least three implantation failures with several high-quality embryos. Identifying patients with RIF in advance is crucial for effective clinical managements. However, uterine biopsy, the primary research approach, is not only invasive but also poses a risk to the integrity of the endometrial microenvironment. Here, we provided a novel, safe, and immediate methodology for RIF populations identification through plasma microRNA (miRNA) profiles. Peripheral blood samples of 163 women were collected and sequenced to quantify the relative expression levels of plasma miRNAs. Through a comparative analysis of the temporal expression between patients with RIF and those with successful embryo implantation during the peri-implantation period, we determined that the RIF-associated miRNA signature was established at the early stage of the window of implantation. By global screening, we identified 217 miRNAs that were differentially expressed between groups on the ovulation day (D0), using a threshold of |fold change| ≥ 1.5. Through refining selection criteria, 10 eligible miRNAs were ultimately selected and further validated through real-time quantitative polymerase chain reaction. These miRNAs were employed to construct a logistic regression-based RIF model. The model demonstrated robust performance in the validation and test cohorts, with area under the curve of 0.947 and 0.912, respectively. We also demonstrated that miRNAs maintain relative stability within a specific phase, making them suitable as clinical biomarkers. This study provides a noninvasive methodology for identifying women with RIF and suggests a potential role in predicting RIF risk before embryo transfer.
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