Genetics and Immunology · Reproductive Immunology

Antiphospholipid syndrome in pregnancy: a comprehensive literature review

Murvai VR, Galiș R, Panaitescu A, Radu CM, Ghitea TC, Trif P, Onița-Avram M, Vesa AA, Huniadi A

Published March 24, 2025 BMC pregnancy and childbirth, 25(1), 337
DOI 10.1186/s12884-025-07471-w PMID 40128683 PMC PMC11934569

Abstract

Background

Antiphospholipid syndrome (APS) is an autoimmune disorder associated with thrombotic events and adverse obstetric outcomes, particularly in its obstetric form (OAPS). Affecting approximately 0.5% of the population, APS is a leading contributor to recurrent pregnancy loss (RPL), preeclampsia (PE), and fetal growth restriction ((FGR). Despite advancements in understanding its pathophysiology and management, optimal treatment strategies for APS in pregnancy remain challenging and require systematic evaluation. This review synthesizes current evidence on APS mechanisms, diagnostic criteria, and therapeutic interventions, with a focus on maternal and fetal outcomes in OAPS.

Methods

A comprehensive search of PubMed, was conducted to identify studies exploring APS pathogenesis, diagnostic standards, and treatment efficacy in obstetric settings. Inclusion criteria prioritized randomized controlled trials, cohort studies, and systematic reviews with a clear focus on APS and pregnancy.

Results

The review confirmed that APS current accepted pathogenesis is governed by a "two-hit" model, where antiphospholipid antibodies (aPLs) initiate endothelial damage, culminating in thrombosis and placental insufficiency. Epidemiological analysis underscores the prevalence and severity of APS in obstetric contexts, with lupus anticoagulant (LA) emerging as a significant predictor of adverse outcomes. Evidence supports the use of low-dose aspirin (LDA) and heparin to reduce miscarriage rates, while adjunctive treatments, such as hydroxychloroquine (HCQ), have shown promise in improving live birth rates and reducing preterm delivery in high-risk cases. Emerging therapies, including tumoral necrosis factor (TNF-alpha) inhibitors and nitric oxide modulators, may offer additional benefits in refractory cases.

Conclusion

APS remains a critical determinant of adverse pregnancy outcomes, necessitating precise diagnostic criteria and tailored management approaches. This systematic review emphasizes the importance of individualized therapeutic regimens to optimize maternal and fetal health in OAPS and highlights areas for future research, particularly regarding novel pharmacological approaches. Further studies are essential to refine treatment protocols and improve clinical guidelines for managing APS in pregnancy.

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Genetics and Immunology › Reproductive Immunology › Antiphospholipid Syndrome and Thrombophilia · Pregnancy › Pregnancy Complications › Hypertensive Disorders · Autoimmune and Inflammatory Disease › Autoimmune Conditions › Systemic Autoimmune Disease
PMID 40128683 40128683 DOI 10.1186/s12884-025-07471-w 10.1186/s12884-025-07471-w Murvai et al. 2025, Murvai 2025