Mechanistic insights into intrauterine adhesions.

Semin Immunopathol

Department of Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Published: November 2024

AI Article Synopsis

  • Intrauterine adhesions (IUA), also known as Asherman's syndrome, occur due to damage to the endometrial layer, often from medical procedures, leading to fibrous tissue formation that can block the uterine cavity or cervical canal.
  • Diagnosis of IUA is best performed through hysteroscopy, but predicting future live birth rates remains uncertain.
  • New research on the underlying causes of IUA, including inflammation, cellular balance issues, autophagy defects, and ferroptosis, is essential for developing improved treatment strategies.

Article Abstract

Intrauterine adhesions (IUA), also known as Asherman's syndrome, arise from damage to the basal layer of the endometrium, frequently caused by intrauterine interventions. This damage leads to nonregenerative healing of endometrium resulting in replacement by fibrous connective tissue, which bring about the adherence of opposing endometrium to render the uterine cavity and/or cervical canal partially or completely obliterated. IUA is a common cause of the refractory uterine infertility. Hysteroscopy is the gold standard for diagnosis of IUA. However, the method of accurately predicting the likelihood of achieving a live birth in the future remains established. Classical treatments have shown limited success, particularly in severe cases. Therefore, utilizing new research methods to deepen the understanding of the pathogenesis of IUA will facilitate the new treatment approaches to be found. In this article we briefly described the advances in the pathogenesis of IUA, with focus on inflammation and parenchymal cellular homeostasis disruption, defects in autophagy and the role of ferroptosis, and we also outlined the progress in IUA therapy.

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Source
http://dx.doi.org/10.1007/s00281-024-01030-9DOI Listing

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