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ABS1028 (2025)
PREGNANCY OUTCOMES IN SYSTEMIC LUPUS ERYTHEMATOSUS: INSIGHTS FROM A MULTICENTER SPANISH STUDY ON THE IMPACT OF ANTIPHOSPHOLIPID ANTIBODIES AND APS
Keywords: Autoantibodies, Pregnancy and reproduction
C. Sieiro Santos1, J. Ordas Martínez1, A. Merino2, H. M. Amar Muñoz3, S. Burger4, I. Braña Abascal4, C. San José Méndez5,6, R. Dos-Santos Sobrín7, J. L. Puga-Guzmán7, E. Diez Álvarez1, V. Martinez-Taboada2
1Complejo Asistencial Universitario de León, Rheumatology, León, Spain
2Hospital Universitario Marqués de Valdecilla, Santader, Spain
3Hospital General Universitario Gregorio Marañón, Rheumatology, Madrid, Spain
4Hospital Universitario Central de Asturias, Rheumatology, Oviedo, Spain
5Complexo Hospitalario Universitario A Coruña, Rheumatology, A Coruña, Spain
6Instituto de Investigación Biomédica A Coruña (INIBIC), A Coruña, Spain
7Hospital Universitario de Santiago de Compostela, Rheumatology, Santiago de Compostela, Spain

Background: Pregnancy in patients with systemic lupus erythematosus (SLE) is associated with significant maternal and obstetric risks, particularly in the context of antiphospholipid syndrome (APS). While these risks are well-documented, the impact of isolated antiphospholipid antibodies (aPL) without overt APS remains unclear. Bridging this knowledge gap is critical to tailoring management strategies for this subgroup of patients, who may face unique clinical challenges.


Objectives: This study aimed to compare clinical characteristics, maternal comorbidities, obstetric complications, and pregnancy outcomes among three groups of SLE patients: those without aPL, those with isolated aPL, and those with secondary APS, using data from a multicenter Spanish registry of pregnancies.


Methods: A multicenter retrospective cohort study included pregnancies in women fulfilling the 2012 SLICC or 2019 ACR/EULAR classification criteria for SLE. Patients were classified into three subgroups: SLE without aPL, SLE with isolated aPL, and SLE with secondary APS. Data were collected at preconception visits, during each trimester, and post-delivery. Key variables included clinical and immunological profiles, maternal comorbidities, obstetric history, pregnancy complications, and delivery outcomes. Comparative analyses were performed to evaluate maternal and fetal outcomes across the subgroups.


Results: A total of 201 pregnancies were analyzed across three groups: SLE without aPL (n=43), SLE with isolated aPL (n=31), and SLE-APS (n=20). While the groups were similar in demographic characteristics and comorbidities, there were striking differences in pregnancy outcomes. The SLE-APS group, experienced the highest rates of adverse pregnancy outcomes. In fact, 60% of pregnancies in this group faced complications, a stark contrast to only 20% in the SLE without aPL group and 5% in the SLE with isolated aPL group ( p <0.0001). The SLE-APS group also had significantly higher rates of preterm delivery (27%) and fetal death before 10 weeks (30%) compared to SLE without aPL (14% and 9%, respectively) and SLE with isolated aPL (6% and 5%, respectively, p =0.04 and p =0.02). The risk of fetal death before 10 weeks was particularly concerning in the SLE-APS group, with nearly one-third of pregnancies affected. Interestingly, despite the increased risk of complications, live birth rates remained relatively similar across all groups, with 70–77% of pregnancies resulting in live births ( p =0.34). However, the SLE-APS group showed a notable trend towards higher IVF failure rates (30% compared to 3% in the SLE without aPL group), which may suggest a more complex reproductive challenge for women with APS ( p =0.06).


Conclusion: This multicenter study highlights the increased risk of adverse pregnancy outcomes in women with SLE-APS, particularly fetal death before 10 weeks and preterm delivery. Although women with isolated aPL also face higher pregnancy risks compared to those without aPL, their outcomes are less severe than those with APS. These findings underscore the importance of closely monitoring and managing pregnancies in women with SLE, particularly in those with APS, to mitigate risks and improve maternal and fetal health outcomes. Further studies are needed to explore tailored interventions for this subgroup of patients.

Demographic characteristics, cardiovascular risk factors and main comorbidities in the different groups

SLE without APL SLE with APL SLE-APS P value
Age (years), m ± SD 32.5±3.8 33.2±3.4 34.2±5.2 0.83
Time to diagnosis, mean (IQR) 30 (14.2-57.3) 28.4 (9.7-54.3) 32 (15.2-57.2) 0.65
Follow-up (months), m±SD 120 (81.4-206.8) 98 (34.2-201) 194 (78-234) 0.04
Obesity (n, %) 5 (12%) 2 (6%) 5 (20%) 0.14
Smoking (n, %) 15 (35%) 12 (39%) 9 (45%) 0.35
Hypertension (n, %) 5 (12%) 3 (9.7%) 5 (11%) 0.57
Diabetes (n, %) 3 (7%) 3 (10%) 2 (10%) 0.45
Dyslipidemia (n, %) 4 (13%) 4 (13%) 3 (10%) 0.67
Hereditary thrombophilia (n, %) 5 (12%) 5 (16%) 6 (30%) 0.42
Thyroid disease (n, %) 7 (16%) 1 (3%) 3 (15%) 0.52
Obstetric comorbidity (n, %) 10 (23%) 10 (32%) 6 (20%) 0.49

Maternal and Pregnancy Outcomes in SLE Patients Stratified by aPL and APS Status

SLE without APL SLE with APL SLE-APS P value
Damage by SLICC (n, %) 14 (13%) 12 (18%) 6 (20%) 0.24
SLEDAI before pregnancy (mean±SD) 2.1 + 3.37 2.5 + 3.60 2.6 + 3.44 0.61
Adverse pregnancy outcomes (n, %) 21 (20%) 3 (5%) 18 (60% ) <0.0001
Live births (n, %) 82 (77%) 47 (72%) 21 (70%) 0.34
Preterm delivery <37 weeks (n, %) 15 (14%) 4 (6%) 8 (27%) 0.04
Fetal death <10 weeks (n, %) 10 (9%) 3 (5%) 9 (30%) 0.02
Fetal death >10 weeks (n, %) 5 (5%) 2 (3%) 3 (10%) 0.45
Preeclampsia/Eclampsia (n, %) 3 (3%) 1 (2%) 2 (7%) 0.38
Abruption placentae (n, %) - 1 (2%) - 0.78
IVF Failures (more than 2) (n, %) 3 (3%) 9 (14%) 1 (30%) 0.06
Intrauterine growth restriction (n, %) 3 (3%) 1 (2%) 2 (7%) 0.08
Ectopic pregnancies (n, %) 5 (5%) 1 (2%) 0 0.15

REFERENCES: NIL.


Acknowledgements: NIL.


Disclosure of Interests: None declared.

© The Authors 2025. This abstract is an open access article published in Annals of Rheumatic Diseases under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ). Neither EULAR nor the publisher make any representation as to the accuracy of the content. The authors are solely responsible for the content in their abstract including accuracy of the facts, statements, results, conclusion, citing resources etc.


DOI: annrheumdis-2025-eular.B3984
Keywords: Autoantibodies, Pregnancy and reproduction
Citation: , volume 84, supplement 1, year 2025, page 2250
Session: Systemic lupus erythematosus (Publication Only)