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三种全身性红斑狼疮分类标准的比较和回顾,用于区分狼疮疾病谱中全身性红斑狼疮与单纯黏膜皮肤表现。

A comparison and review of three sets of classification criteria for systemic lupus erythematosus for distinguishing systemic lupus erythematosus from pure mucocutaneous manifestations in the lupus disease spectrum.

机构信息

Department of Dermatology, Hunan Key Laboratory of Medical Epigenomics, The Second Xiangya Hospital, Central South University, Changsha, China.

Research Unit of Key Technologies of Immune-Related Skin Diseases Diagnosis and Treatment, Chinese Academy of Medical Sciences (2019RU027), Changsha, China.

出版信息

Lupus. 2020 Dec;29(14):1854-1865. doi: 10.1177/0961203320959716. Epub 2020 Oct 7.

Abstract

Although the original purpose of the systemic lupus erythematosus (SLE) classification criteria was to distinguish SLE from other mimic diseases, and to facilitate sample selection in scientific research, they have become widely used as diagnostic criteria in clinical situations. It is not known yet if regarding classification criteria as diagnostic criteria, what problems might be encountered? This is the first study comparing the three sets of classification criteria for SLE, the 1997 American College of Rheumatology (ACR'97), 2012 Systemic Lupus International Collaborating Clinics (SLICC'12) and 2019 European League Against Rheumatism/American College of Rheumatology (EULAR/ACR'19), for their ability to distinguish patients with SLE from patients with pure mucocutaneous manifestations (isolated cutaneous lupus erythematosus without internal disease, i-CLE) in the lupus disease spectrum. 1,865 patients with SLE and 232 patients with i-CLE were recruited from a multicenter study. We found that, due to low specificity, none of the three criteria are adept at distinguishing patients with SLE from patients with i-CLE. SLICC'12 performed best among the original three criteria, but if a positive ANA was removed as an entry criterion, EULAR/ACR'19 would performed better. A review of previous studies that compared the three sets of criteria was presented in this work.

摘要

虽然系统性红斑狼疮 (SLE) 分类标准的最初目的是将 SLE 与其他模拟疾病区分开来,并为科学研究中的样本选择提供便利,但它们已广泛应用于临床诊断标准。目前尚不清楚将分类标准视为诊断标准会遇到哪些问题?这是第一项比较三组 SLE 分类标准(1997 年美国风湿病学会 (ACR'97)、2012 年系统性红斑狼疮国际合作临床组 (SLICC'12) 和 2019 年欧洲抗风湿病联盟/美国风湿病学会 (EULAR/ACR'19))的研究,旨在评估它们在狼疮疾病谱中区分 SLE 患者和仅有粘膜皮肤表现的患者(无内脏疾病的单纯皮肤红斑狼疮,i-CLE)的能力。这项多中心研究共纳入了 1865 例 SLE 患者和 232 例 i-CLE 患者。我们发现,由于特异性较低,这三组标准都不能很好地将 SLE 患者与 i-CLE 患者区分开来。在原始的三个标准中,SLICC'12 的表现最佳,但如果将阳性 ANA 作为纳入标准,EULAR/ACR'19 的表现会更好。本文还对以前比较这三组标准的研究进行了综述。

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