Effect of pregnancy on scleroderma progression.

Siobhan Deshauer, Mats Junek, Murray Baron, Karen A Beattie, Margaret J Larché
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Abstract

Objective: To explore the trajectory of scleroderma disease activity in women who experienced a pregnancy after systemic sclerosis diagnosis compared to nulliparous women.

Methods: We analyzed data from the Canadian Scleroderma Research Group registry by identifying nulliparous women and women with ⩾1 pregnancy after systemic sclerosis diagnosis. Patient characteristics were compared between groups at registry entry. Controlling for age, smoking, and time since systemic sclerosis diagnosis, generalized estimating equations tested the effect of pregnancy on force vital capacity, diffusing capacity of the lungs for carbon monoxide, right ventricular systolic pressure, glomerular filtration rate, antibody status, active digital ulcers, physician global assessment of activity, and severity over 9 years.

Results: At registry entry, numbers of women in the nulliparous and pregnancy after systemic sclerosis diagnosis groups were 153 and 45, respectively. Corresponding numbers at 6 and 9 years were 48 and 21, and 18 and 9, respectively. The prevalence of anti-topoisomerase positivity was 18.3% in nulliparous and 12.5% in pregnancy after systemic sclerosis diagnosis. Baseline differences included mean (Standard deviation) age of diagnosis (nulliparous: 38.8 (14.0), pregnancy after systemic sclerosis diagnosis: 22.6 (6.8) years, p < 0.001), disease duration (nulliparous: 9.6 (8.9), pregnancy after systemic sclerosis diagnosis: 21.9 (9.6) years; p < 0.001), and inflammatory arthritis (nulliparous: 41 (28%), pregnancy after systemic sclerosis diagnosis: 22 (49%), p = 0.009). There were no significant differences between groups in the change of any outcomes over time.

Conclusion: Results demonstrated that having ⩾1 pregnancy after systemic sclerosis diagnosis did not appear to significantly impact long-term renal, respiratory, or global function outcomes. While this offers a hopeful message to systemic sclerosis patients planning a pregnancy, physicians and patients should remain vigilant for potential post-partum complications.

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妊娠对硬皮病进展的影响。
目的:探讨系统性硬化症诊断后怀孕的妇女与未分娩妇女的硬皮病活动轨迹。方法:我们分析了来自加拿大硬皮病研究组注册表的数据,通过识别未生育妇女和在系统性硬化症诊断后怀孕大于或等于1的妇女。在登记时比较两组患者的特征。控制年龄、吸烟和自系统性硬化症诊断以来的时间,广义估计方程测试了怀孕对力量肺活量、肺一氧化碳弥散能力、右心室收缩压、肾小球滤过率、抗体状态、活动性数字溃疡、医生对活动性的总体评估和9年以上严重程度的影响。结果:在登记时,未分娩和系统性硬化症诊断组的妇女人数分别为153人和45人。6岁和9岁时分别为48和21岁,18和9岁。在系统性硬化症诊断后,抗拓扑异构酶阳性的患病率在未分娩时为18.3%,在妊娠时为12.5%。基线差异包括平均(标准差)诊断年龄(未产:38.8(14.0)岁,系统性硬化症诊断后妊娠:22.6(6.8)岁,p p p = 0.009)。随着时间的推移,两组之间的任何结果变化都没有显著差异。结论:结果表明,在系统性硬化症诊断后进行大于或等于1的妊娠似乎不会显著影响长期肾脏、呼吸或整体功能结果。虽然这为计划怀孕的系统性硬化症患者提供了一个充满希望的信息,但医生和患者应该对潜在的产后并发症保持警惕。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
31
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