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Published on: January 26, 2024
Obstetric antiphospholipid syndrome: Advances in pathogenesis
Shumin Wang1, Huimin Liu1, Wanrong Huang2
1Reproductive Medical Center, Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu 610041, China; Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
The 2023 ACR-EULAR criteria refine antiphospholipid syndrome (APS) understanding, highlighting obstetric APS (OAPS) as a distinct subtype. OAPS pathogenesis involves multifactorial causes beyond thrombosis, including placental and immune dysfunction.
Area of Science:
- Rheumatology
- Immunology
- Obstetrics
Background:
- The 2023 ACR-EULAR classification criteria for antiphospholipid syndrome (APS) mark a paradigm shift from a generalized approach to a subphenotype-based understanding.
- Obstetric APS (OAPS) is now recognized as a distinct subtype with unique pathophysiology, moving beyond a singular focus on thrombosis.
Purpose of the Study:
- To summarize the multifactorial pathogenesis of Obstetric APS (OAPS).
- To provide a comprehensive overview facilitating research and clinical management of OAPS.
Main Methods:
- Review of recent evidence on OAPS pathogenesis.
- Analysis of the shift in classification criteria and its implications.
Main Results:
- OAPS is understood as a multifactorial autoimmune disorder.
- Pathogenesis involves trophoblast dysfunction, inflammation, and decidual microenvironmental dysfunction, in addition to placental vascular issues.
Conclusions:
- The evolving understanding of OAPS pathogenesis is critical for advancing research and clinical practice.
- A comprehensive summary of OAPS pathogenesis is essential for future progress.
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