Sjögren's疾病和系统性红斑狼疮重叠综合征作为两种自身免疫性疾病十字路口的独特实体:来自两个意大利参考中心的两种疾病的临床特征。

IF 3.4 4区 医学 Q2 RHEUMATOLOGY
Ginevra De Marchi, Alessia Nano, Giovanni Fulvio, Valeria Manfrè, Inmaculada Conception Navarro Garcia, Alen Zabotti, Elena Treppo, Chiara Baldini, Luca Quartuccio, Salvatore De Vita
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引用次数: 0

摘要

目的描述斯约戈伦病(SjD)与系统性红斑狼疮(SLE)重叠综合征的特征:方法:根据 SjD 和系统性红斑狼疮的分类标准,对意大利两家风湿病学中心的临床定义为 SjD 和系统性红斑狼疮重叠综合征(SjD-SLE)的连续患者进行分类。临床、功能、超声波和组织学数据与仅患有SjD或系统性红斑狼疮的患者进行了比较:结果:与 SjD 对照组相比,SjD-系统性红斑狼疮患者发病时更年轻(p 结论:我们的数据进一步凸显了 SjD 和系统性红斑狼疮分类的局限性:我们的数据进一步凸显了目前重叠综合征分类标准应用的局限性,因为这些标准主要基于临床表现和常见的自身抗体。分子特征可以解释系统性自身免疫性疾病的临床相似性和差异性,尤其有助于重叠综合征的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sjögren's disease and systemic lupus erythematosus overlap syndrome as distinct entity at crossroads of two autoimmune disorders: clinical characterisation from two Italian reference centres for both the diseases.

Objectives: To characterise the overlap syndrome between Sjögren's disease (SjD) and systemic lupus erythematosus (SLE).

Methods: Consecutive patients clinically defined as affected by SjD and SLE overlap syndrome (SjD-SLE), belonging to two Italian rheumatology centres were classified following the application of both the SjD and SLE classification criteria. Clinical, functional, ultrasound and histological data were compared with patients suffering from only SjD or SLE.

Results: Compared to SjD controls, SjD-SLE patients were younger at onset (p<0.0001). Schirmer's test and parotid swelling were comparable between the two groups, while unstimulated sialometry was more impaired in the SjD controls (p=0.0001). SjD-SLE cases showed increased joint (p=0.009), mucocutaneous (p<0.0001), renal (p=0.001) involvement, and serositis (p<0.0001). Ultrasound changes in the major salivary glands were prevalent in SjD controls, while the histological findings of the minor salivary glands were similar. Furthermore, SjD-SLE cases presented a higher prevalence of anti-SSA (p<0.0001) and lower presence of rheumatoid factor (p=0.008) and serum cryoglobulins (p=0.035). Compared to SLE controls, SjD-SLE were older (p=0.044). The frequency of extra-glandular manifestations of SjD-SLE was similar compared to SLE, including renal involvement. SjD-SLE patients showed higher prevalence of anti-SSA and anti-SSB (p<0.0001), C4 reduction (p=0.011), and leukopenia (p=0.025).

Conclusions: Our data further highlight the limitations of the application of the current classification criteria in overlap syndrome, since they are primarily based on clinical manifestations and common autoantibodies. Molecular signatures may explain clinical similarities and differences among systemic autoimmune diseases, and they may be particularly helpful in overlap syndromes.

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来源期刊
CiteScore
6.10
自引率
18.90%
发文量
377
审稿时长
3-6 weeks
期刊介绍: Clinical and Experimental Rheumatology is a bi-monthly international peer-reviewed journal which has been covering all clinical, experimental and translational aspects of musculoskeletal, arthritic and connective tissue diseases since 1983.
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