Adverse pregnancy outcome associations among women prior to a diagnosis of systemic lupus erythematosus.

Frontiers in lupus Pub Date : 2026-01-01 Epub Date: 2026-06-08 DOI:10.3389/flupu.2026.1806496
Jessica A English, Bethany J Wolf, Diane L Kamen
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Abstract

Background: Immune dysregulation years prior to a clinical diagnosis of systemic lupus erythematosus (SLE) may include a range of asymptomatic autoantibody positivity to clinically evident disease. The effect of this spectrum of immune dysregulation on pregnancy outcomes, including pregnancies in women prior to a diagnosis of SLE, is poorly understood. We sought to identify associations of adverse pregnancy outcomes across groups along this spectrum.

Methods: Utilizing a large longitudinal cohort at a single center, we evaluated pregnancy outcomes among the following four groups: antinuclear antibody (ANA) negative controls, ANA-positive controls, pregnancies before a diagnosis of SLE, and pregnancies after a diagnosis of SLE. The pregnancy outcomes considered were live birth rate, preeclampsia, low birth weight, premature birth, spontaneous abortion, and stillbirth. Generalized estimating equation models were used to evaluate key associations and confounders.

Results: We included 811 participants and 2,209 pregnancies. Of these, 198 participants were ANA-positive controls and 369 were diagnosed with SLE, with their first pregnancy occurring before diagnosis. Overall, 81.5% self-identified as Black and 31% had resided in areas with high social vulnerability. The median number of pregnancies between the groups was similar, with the majority of participants having at least one live birth. The lowest median number of pregnancies occurred in the pregnancy after SLE diagnosis group. The adverse outcome rate did not differ between the ANA-positive and ANA-negative controls. The risk of any adverse outcome was greatest in those with pregnancies after an SLE diagnosis [OR (95% CI): 3.33 (2.35, 4.71)], but was also increased in those with pregnancies before a diagnosis of SLE as compared to the ANA-positive controls [OR (95% CI): 1.78 (1.28, 2.47)]. When grouped by time prior to diagnosis, the risk of any adverse outcome remained increased in pregnancies occurring both 2-5 years or greater than 5 years prior to SLE diagnosis as compared to the ANA-positive controls [OR (95% CI): 1.64 (1.01, 2.67) and OR (95% CI): 1.65 (1.17, 2.32), respectively].

Conclusion: The risk of adverse pregnancy outcomes appears to increase along the SLE spectrum, with the highest risk occurring after diagnosis. ANA positivity alone is not sufficient to impact pregnancy outcomes.

在诊断为系统性红斑狼疮的妇女中不良妊娠结局的关联。
背景:系统性红斑狼疮(SLE)临床诊断前几年的免疫失调可能包括一系列无症状自身抗体阳性到临床明显疾病。这一系列免疫失调对妊娠结局的影响,包括在SLE诊断前怀孕的妇女,目前尚不清楚。我们试图在这一范围内确定各组不良妊娠结局的关联。方法:利用单一中心的大型纵向队列,我们评估了以下四组的妊娠结局:抗核抗体(ANA)阴性对照组、ANA阳性对照组、SLE诊断前妊娠和SLE诊断后妊娠。考虑的妊娠结局包括活产率、先兆子痫、低出生体重、早产、自然流产和死产。使用广义估计方程模型来评估关键关联和混杂因素。结果:我们纳入了811名参与者和2209名孕妇。其中,198名参与者为ana阳性对照,369名被诊断为SLE,在诊断前首次怀孕。总体而言,81.5%的人认为自己是黑人,31%的人居住在社会脆弱性高的地区。两组之间怀孕的中位数相似,大多数参与者至少有一次活产。SLE诊断后妊娠组中位妊娠数最低。ana阳性对照和ana阴性对照的不良转归率无差异。任何不良后果的风险在SLE诊断后怀孕的患者中最大[OR (95% CI): 3.33(2.35, 4.71)],但与ana阳性对照相比,SLE诊断前怀孕的患者也增加了[OR (95% CI): 1.78(1.28, 2.47)]。当按诊断前时间分组时,与ana阳性对照相比,在SLE诊断前2-5年或5年以上怀孕的任何不良结果的风险仍然增加[or (95% CI): 1.64(1.01, 2.67)和or (95% CI): 1.65(1.17, 2.32)]。结论:不良妊娠结局的风险似乎随着SLE谱系的增加而增加,诊断后发生的风险最高。单是ANA阳性并不足以影响妊娠结局。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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