首页> 外文期刊>Arthritis & rheumatology. >Brief Report: How Do Patients With Newly Diagnosed Systemic Lupus Erythematosus Present? A Multicenter Cohort of Early Systemic Lupus Erythematosus to Inform the Development of New Classification Criteria
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Brief Report: How Do Patients With Newly Diagnosed Systemic Lupus Erythematosus Present? A Multicenter Cohort of Early Systemic Lupus Erythematosus to Inform the Development of New Classification Criteria

机译:简要介绍:新诊断患者患有新诊断的全身性红斑狼疮的患者如何存在? 早期系统性狼疮红斑狼疮的多中心队列,以告知新分类标准的发展

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Objective Systemic lupus erythematosus (SLE) presents with nonspecific signs and symptoms that are also found in other conditions. This study aimed to evaluate manifestations at disease onset and to compare early SLE manifestations to those of diseases mimicking SLE. Methods Academic lupus centers in Asia, Europe, North America, and South America collected baseline data on patients who were referred to them during the previous 3 years for possible SLE and who had a symptom duration of SLE and those diagnosed as having SLE-mimicking conditions. Diagnostic performance of the 1997 American College of Rheumatology (ACR) SLE classification criteria and the 2012 Systemic Lupus International Collaborating Clinics (SLICC) SLE classification criteria was tested. Results Data were collected on 389 patients with early SLE and 227 patients with SLE-mimicking conditions. Unexplained fever was more common in early SLE than in SLE-mimicking conditions (34.5% versus 13.7%, respectively; P 0.001). Features less common in early SLE included Raynaud's phenomenon (22.1% versus 48.5%; P 0.001), sicca symptoms (4.4% versus 34.4%; P 0.001), dysphagia (0.3% versus 6.2%; P 0.001), and fatigue (28.3% versus 37.0%; P = 0.024). Anti-double-stranded DNA, anti-beta(2)-glycoprotein I antibodies, positive Coombs' test results, autoimmune hemolytic anemia, hypocomplementemia, and leukopenia were more common in early SLE than in SLE-mimicking conditions. Symptoms detailed in the ACR and SLICC classification criteria were significantly more frequent among those with early SLE. Fewer patients with early SLE were not identified as having early SLE with use of the SLICC criteria compared to the ACR criteria (16.5% versus 33.9%), but the ACR criteria demonstrated higher specificity than the SLICC criteria (91.6% versus 82.4%). Conclusion In this multicenter cohort, clinical manifestations that could help to distinguish early SLE from SLE-mimicking conditions were identified. These findings may aid in earlier SLE diagnosis and provide information for ongoing initiatives to revise SLE classification criteria.
机译:目标Systemic Lupus红斑狼疮(SLE)呈现出在其他条件下发现的非特异性迹象和症状。本研究旨在评估疾病发作的表现,并将早期SLE表现与模仿SLE模仿的疾病。方法采用亚洲,欧洲,北美和南美洲的学术卢布中心收集了在前3年内提到的患者的基线数据,可能是SLE的症状持续时间和被诊断为具有SLE模仿条件的人。测试了1997年美国风湿病学院(ACR)SLE分类标准和2012年系统狼疮国际合作诊所(SLICC)SLE分类标准的诊断表现。结果数据在389例早期SLE和227名患者中收集了SLE模拟条件的患者。未解释的发热在早期的SLE中比在SL模拟条件下更常见(34.5%,分别为13.7%; P <0.001)。在早期SLE中不太常见的特点包括Raynaud的现象(22.1%,P <0.001),SICCA症状(4.4%与34.4%; P <0.001),吞咽困难(0.3%对6.2%; P <0.001)和疲劳(28.3%对37.0%; p = 0.024)。抗双链DNA,抗β(2) - 糖蛋白I抗体,阳性Coombs的试验结果,自身免疫溶血性贫血,低次血症和白细胞减少症在早期SLE比在SLE模仿条件下更常见。 ACR和SLICC分类标准中详述的症状在早期SLE的那些中明显更频繁。与ACR标准相比,利用SLICC标准(16.5%对33.9%)而言,未经早期SLE鉴定为早期SLE的患者未鉴定为早期SLE,但ACR标准比SLICC标准表现出更高的特异性(91.6%,而82.4%)。结论在这种多中心队列中,确定了可以有助于区分早期SLE与SLIMICING病症的临床表现。这些发现可能有助于早期的SLE诊断,并提供持续举措来修订SLE分类标准的信息。

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