Scholarlink

Purpose <p>To evaluate whether the inflammatory proteomics of uterine fluid is feasible in defining the endometrial receptivity phase.</p> Methods <p>Inflammatory proteomics of uterine fluid was measured using the OLINK Target-96 Inflammation panel. Endometrial receptivity testing (ERT) combined with endometrial dating was used to define the phase of endometrial receptivity. A predictive model based on proteomics of uterine fluid was established to predict the endometrial receptivity phase.</p> Results <p>The inflammatory factors in uterine fluid were differentially expressed between the window of implantation (WOI) and displaced WOI groups; the displaced WOI group was characterized by increased expression of a variety of inflammatory factors. The predictive model established based on the top five differential proteins could classify the endometrial receptive phase. Transcriptomic data from endometrial tissues showed that the differential gene sets between different receptive phases were mostly enriched in immune-related processes, and the expression of immune-related genes in the WOI group was significantly lower than that in the displaced WOI group.</p> Conclusions <p>Detecting inflammatory proteins from the uterine fluid using the OLINK inflammation panel is feasible and holds&#xa0;promise as&#xa0;a novel non-invasive method to define endometrial receptivity phases.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Inflammatory proteomics of uterine fluid is potentially a non-invasive predictor for endometrial receptivity: a pilot study

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年11月1日

查看全文
  • Hong Zeng,
  • Yahan Chang,
  • Jing Fu,
  • Hongying Tang,
  • Nenghui Liu,
  • Baihua Luo,
  • Shuyi Li

摘要

Purpose

To evaluate whether the inflammatory proteomics of uterine fluid is feasible in defining the endometrial receptivity phase.

Methods

Inflammatory proteomics of uterine fluid was measured using the OLINK Target-96 Inflammation panel. Endometrial receptivity testing (ERT) combined with endometrial dating was used to define the phase of endometrial receptivity. A predictive model based on proteomics of uterine fluid was established to predict the endometrial receptivity phase.

Results

The inflammatory factors in uterine fluid were differentially expressed between the window of implantation (WOI) and displaced WOI groups; the displaced WOI group was characterized by increased expression of a variety of inflammatory factors. The predictive model established based on the top five differential proteins could classify the endometrial receptive phase. Transcriptomic data from endometrial tissues showed that the differential gene sets between different receptive phases were mostly enriched in immune-related processes, and the expression of immune-related genes in the WOI group was significantly lower than that in the displaced WOI group.

Conclusions

Detecting inflammatory proteins from the uterine fluid using the OLINK inflammation panel is feasible and holds promise as a novel non-invasive method to define endometrial receptivity phases.