Development of a Predictive Model for Optimization of Embryo Transfer Timing Using Blood-Based microRNA Expression Profile

Author:

Chen Ming-Jer1ORCID,Hsu An2ORCID,Lin Pei-Yi2,Chen Yu-Ling2,Wu Ko-Wen2ORCID,Chen Kuan-Chun2,Wang Tiffany2,Yi Yu-Chiao1,Kung Hsiao-Fan1,Chang Jui-Chun1,Yang Wen-Jui3,Lu Farn3,Guu Hwa-Fen1,Chen Ya-Fang1,Chuan Shih-Ting1,Chen Li-Yu1,Chen Ching-Hung3ORCID,Yang Pok Eric2,Huang Jack Yu-Jen34

Affiliation:

1. Division of Reproductive Endocrinology and Infertility, Department of Obstetrics Gynecology & Women’s Health, Taichung Veterans General Hospital, Taichung 40764, Taiwan

2. Inti Labs, Hsinchu 30261, Taiwan

3. Taiwan IVF Group Center for Reproductive Medicine and Infertility, Hsinchu 30274, Taiwan

4. Department of Obstetrics & Gynecology, Stanford University, Stanford, CA 94305, USA

Abstract

MicroRNAs (miRNAs) can regulate the expression of genes involved in the establishment of the window of implantation (WOI) in the endometrium. Recent studies indicated that cell-free miRNAs in uterine fluid and blood samples could act as alternative and non-invasive sample types for endometrial receptivity analysis. In this study, we attempt to systematically evaluate whether the expression levels of cell-free microRNAs in blood samples could be used as non-invasive biomarkers for assessing endometrial receptivity status. We profiled the miRNA expression levels of 111 blood samples using next-generation sequencing to establish a predictive model for the assessment of endometrial receptivity status. This model was validated with an independent dataset (n = 73). The overall accuracy is 95.9%. Specifically, we achieved accuracies of 95.9%, 95.9%, and 100.0% for the pre-receptive group, the receptive group, and the post-respective group, respectively. Additionally, we identified a set of differentially expressed miRNAs between different endometrial receptivity statuses using the following criteria: p-value < 0.05 and fold change greater than 1.5 or less than −1.5. In conclusion, the expression levels of cell-free miRNAs in blood samples can be utilized in a non-invasive manner to distinguish different endometrial receptivity statuses.

Funder

Inti Labs, Taiwan, Inc.

Quark Biosciences, Inc.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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