巴西系统性硬化症患者的大队伍中重叠综合征的特征:回顾性分析
Cipriano R Gama1, Andre S Franco2, Adriana B Bortoluzzo3
1C.R. Gama, MD, Division of Rheumatology, Hospital das Clinicas HCFMUSP, Faculdade de Medicina da Universidade de São Paulo, São Paulo.
The Journal of rheumatology
|February 15, 2025
概括
巴西的全身性硬化重叠综合征 (OS) 患者年轻,具有独特的临床特征,包括有限的SSc和瘤. 尽管治疗需求不同,这些患者的预后并没有变得更差.
科学领域:
- 类风湿病学 类风湿病学
- 内部医学 内部医学
- 自免疫性疾病 自免疫性疾病
背景情况:
- 系统性硬化症 (SSc) 可以与其他连接组织疾病同时发生,形成重叠综合征 (OS).
- 将SSc与OS进行表征对于理解疾病异质性和管理至关重要.
研究的目的:
- 为了比较SSc患者的临床和人口特征,有和没有OS.
- 确定与SSc患者OS发展相关的因素.
主要方法:
- 从电子医疗记录中对787名SSc患者的数据进行了追溯分析.
- 根据SSc和其他结缔组织疾病 (SLE,IIM,SjD,RA) 的既定标准对患者进行分类.
- 统计分析,包括单变量和多变量方法,以确定与OS相关的因素.
主要成果:
- 11.6%的SSc患者患有OS,最常见的是SLE,SjD,RA或IIM.
- 在发病和诊断时,OS患者的年龄较小,有限的SSc,肌肉骨和sicca症状以及瘤的患病率更高.
- OS与肺高血压和糖尿病和脂质失调等并发症的频率较低有关,以及特定的自身抗体概况 (抗Ro+,抗Scl70-).
- OS患者更频繁地接受葡萄糖皮质类药物,甲醇和莱夫卢诺米德;多变量分析将有限的SSc,瘤和特定治疗与OS联系起来.
- 在SSc患者和没有OS患者之间没有观察到预后的显著差异.
结论:
- 与没有OS的患者相比,巴西的SSc患者具有不同的临床和人口特征.
- 特定因素,如有限的SSc,瘤和某些治疗方法与SSc中的OS有关.
- 在SSc中存在OS似乎不会导致更糟糕的预后.
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