Biology and Pathophysiology of Placenta Accreta Spectrum Disorder
Биология и патофизиология расстройств спектра placenta accreta
2025-04-10
SCID: 54.1/39hhud2n
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extravillous trophoblast invasionplacenta accreta spectrumsingle-cell RNA sequencingspiral artery remodelinguterine scarring
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Abstract (AI)
Placenta accreta spectrum (PAS) disorders present a significant clinical challenge, characterized by abnormal placental adherence to the uterine wall secondary to uterine scarring. With the rising global cesarean delivery rates, the incidence of this iatrogenic disorder has increased, underscoring the critical need for an understanding of its pathophysiology to inform management and prevention strategies. Normal placentation depends on tightly regulated extravillous trophoblast invasion into the decidua, spiral artery remodeling, interactions with the extracellular matrix, and immune modulation. Uterine scarring disrupts this balance, creating an environment deficient in key regulatory signals required for coordinated implantation and decidualization. In PAS, the loss of inhibitory decidual cues and deficient boundary limits permits unrestrained trophoblast into the abnormal decidual environment. Dysregulated signaling, along with an inflammatory milieu in scarred tissues, exacerbates abnormal placental development. Current prenatal imaging focuses on the appearance of excessive fibrinoid deposition, extracellular matrix remodeling, and incomplete spiral artery transformation as surrogates of PAS risk stratification. Emerging single-cell RNA sequencing and proteomic profiling offer insights into biomarkers and pathways that enable targeted interventions. Preventive efforts should prioritize reducing cesarean delivery rates to limit uterine scarring. Advances in regenerative medicine and bioengineering, including extracellular matrix-modulating biomaterials, growth factor therapies, and antifibrotic interventions, hold promise for improving scar healing and reducing PAS risk. This review bridges foundational science and clinical application, emphasizing the importance of the underlying placental biology and pathophysiology to make a clinical difference in detecting, treating, and preventing PAS. Addressing drivers of abnormal placentation is critical for improving maternal and neonatal outcomes with this increasingly prevalent iatrogenic condition.
Key Findings
1
Inflammatory signaling and dysregulated pathways in scarred tissues exacerbate abnormal placental development and contribute to PAS pathophysiology.
2
Loss of inhibitory decidual signals and deficient boundary limits permits unrestrained extravillous trophoblast invasion into abnormal scarred tissue.
3
Placenta accreta spectrum results from abnormal placental adherence associated with uterine scarring, with incidence rising alongside global cesarean delivery rates.
4
Prenatal imaging uses excessive fibrinoid deposition, extracellular-matrix remodeling, and incomplete spiral-artery transformation as surrogate indicators of PAS risk.
5
Single-cell RNA sequencing and proteomic profiling may identify biomarkers and pathways for targeted interventions, while regenerative, antifibrotic, and biomaterial-based approaches could improve scar healing and reduce risk.
6
Uterine scarring disrupts decidualization, trophoblast-invasion regulation, spiral-artery remodeling, extracellular-matrix interactions, and immune modulation during placentation.
Research Object
placenta accreta spectrum disorder in scarred uterus
Research Subject
the pathophysiological mechanisms of abnormal placental implantation, including dysregulated trophoblast invasion, decidualization, spiral artery remodeling, extracellular matrix interactions, and immune modulation
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2025-04-10
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