4.2 Article

Current perspectives on endometrial receptivity: A comprehensive overview of etiology and treatment

Journal

Publisher

WILEY
DOI: 10.1111/jog.15759

Keywords

assisted reproductive technology; embryo implantation; endometrial receptivity; female infertility; recurrent implantation failure

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Recurrent implantation failure (RIF) is a challenging problem in assisted reproductive technology (ART), and understanding the effects of uterine abnormalities on endometrial receptivity is important. This review discusses the impact of various uterine pathologies on defective embryo implantation and suggests potential treatments for RIF patients. Further studies are needed to fully understand the pathophysiology of abnormal endometrial receptivity and optimize ART treatments.
Recurrent implantation failure (RIF) remains a challenging problem in assisted reproductive technology (ART). Further insights into uterine abnormalities that can disturb embryo implantation should be obtained. This review provides an overview of the effects of organic and non-organic uterine disorders on endometrial receptivity. The results suggest that various uterine pathologies can lead to defective embryo implantation via multiple mechanisms. In particular, uterine adenomyosis dysregulates molecular and cellular interactions that are vital for successful embryo implantation with a background of chronic inflammation, which may be alleviated by pretreatment with a gonadotropin-releasing hormone agonist. Uterine myomas can cause endometrial deformation and adverse alterations in uterine contractility. Nonetheless, the effectiveness of myomectomy remains debated, and endometrial polyp removal may be considered, particularly in patients with RIF. Chronic endometritis abrogates the appropriate uterine immunological environment critical for embryo implantation. Abnormal endometrial microbiota have been suggested to influence endometrial receptivity; however, supporting evidence is currently scarce. Platelet-rich plasma therapy may be a potential treatment for thin endometria; nevertheless, further validation is required. Endometrial receptivity analysis can detect dysregulation of the window of implantation, and new non-invasive methods for predicting endometrial receptivity have recently been proposed. However, numerous issues still need to be fully clarified. Further clinical and basic studies are necessary to investigate the pathophysiology of defective endometrial receptivity and identify optimal treatments for patients undergoing ART, especially those with RIF.

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