Abnormal placental development induced by repeated cesarean sections: Investigating an animal model of placenta accreta spectrum disorders.

Placenta

Department of Obstetrics and Gynecology and Reproductive Medicine, Peking University First Hospital, Beijing, China; Beijing Key Laboratory of Maternal Fetal Medicine of Gestational Diabetes Mellitus, Beijing, China. Electronic address:

Published: December 2024

AI Article Synopsis

  • Placenta accreta spectrum (PAS) is a serious health issue that can cause severe bleeding after childbirth, often requiring emergency surgery; however, the underlying mechanisms are not well understood due to limitations in animal research.
  • In this study, researchers performed multiple cesarean sections on pregnant mice to create a model that mimics the risk factors for PAS, examining various aspects of pregnancy outcomes and placental health.
  • Results showed that repeated cesarean sections led to significant complications in pregnancy, including abnormal placental development and fetal issues, indicating that this mouse model closely resembles the clinical features of PAS and can be useful for future research and prevention strategies.

Article Abstract

Introduction: Placenta accreta spectrum (PAS) is a serious condition associated with severe postpartum hemorrhage, leading to emergency hysterectomy. Research has predominantly focused on clinical diagnosis and the prevention of adverse maternal outcomes, but the underlying pathological mechanisms remain poorly understood, partly due to the limitations of animal models.

Methods: In this study, we conducted up to three cesarean sections (CS) on full-term pregnant mice, since a history of multiple CS is an independent risk factor for PAS. We evaluated pregnancy outcomes, placental development, morphology, trophoblast invasion, and angiogenesis at the maternal-fetal interface to assess the impact of repeated CS.

Results: Following repeated CS, the model mice displayed adverse pregnancy outcomes, including placental dysplasia, incomplete remodeling of spiral arteries, deep trophoblast invasion at the maternal-fetal interface, and reduced placental perfusion. Additionally, the mice exhibited abnormal fetal development, imbalances in angiogenic and anti-angiogenic both within the placenta and in peripheral blood.

Conclusion: The pathological phenotypes of placenta and adverse pregnancy outcomes observed in mice with a history of three CSs closely resemble the clinical features of PAS. This model offers a valuable tool for studying the pathogenesis of PAS and could serve as a foundation for the development of early prevention strategies.

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Source
http://dx.doi.org/10.1016/j.placenta.2024.11.008DOI Listing

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