Section of Rheumatology, Department of Clinical Sciences , Lund University , Lund , Sweden.
Department of Biochemistry , Institute of Medical Biology , University of Tromsø , Tromsø , Norway.
Lupus Sci Med. 2014 Apr 1;1(1):e000007. doi: 10.1136/lupus-2013-000007. eCollection 2014.
Despite anti-dsDNA antibodies constitute a wide range of specificities, they are considered as the hallmark for systemic lupus erythematosus (SLE).
To identify clinical phenotypes associated with anti-dsDNA antibodies, independently of any clinical diagnoses.
Patients with recent onset of any rheumatic symptoms were screened for antinuclear antibodies (ANA). All ANA-positive and matching ANA-negative patients were examined, and their clinical phenotypes were registered, using a systematic chart formulated after consensus between the participating centres. All patients were tested for different anti-dsDNA antibody specificities with assays habitually used in each participating laboratory. Crithidia Luciliae Immuno Fluorescence Test (CLIFT) was performed three times (with two different commercial kits); solid and solution phase ELISA were performed four times. Associations between clinical phenotypes and results of anti-dsDNA assays were evaluated by linear regression analysis (LRA) and principal component analysis (PCA).
Totally, 292 ANA-positive and 292 matching ANA-negative patients were included in the study. A full dataset for statistical analysis was obtained in 547 patients. Anti-dsDNA antibodies were most frequently detected by ELISA. LRA showed that overall positivity of anti-dsDNA antibodies was associated with proteinuria and pleuritis. Alopecia was significantly associated only with CLIFT-positivity. Besides confirming the same findings, PCA showed that combined positivity of CLIFT and ELISA was also associated with lymphopenia.
Our results show that different anti-dsDNA antibody specificities are associated with nephropathy, pleuritis, alopecia and lymphopenia, regardless of the diagnosis. It may challenge the importance of anti-dsDNA antibodies as a diagnostic hallmark for SLE.
确定与抗 dsDNA 抗体相关的临床表型,而不依赖于任何临床诊断。
筛选近期出现任何风湿症状的患者的抗核抗体 (ANA)。对所有 ANA 阳性和匹配的 ANA 阴性患者进行检查,并使用参与中心之间达成共识后制定的系统图表记录其临床表型。所有患者均使用每个参与实验室惯用的不同抗 dsDNA 抗体特异性检测方法进行检测。使用两种不同的商业试剂盒进行三次克劳氏丽蝇免疫荧光试验 (CLIFT);进行四次固相和液相 ELISA。通过线性回归分析 (LRA) 和主成分分析 (PCA) 评估临床表型与抗 dsDNA 检测结果之间的关系。
共纳入 292 例 ANA 阳性和 292 例匹配的 ANA 阴性患者进行研究。在 547 例患者中获得了完整的统计分析数据集。ELISA 最常检测到抗 dsDNA 抗体。LRA 显示,抗 dsDNA 抗体的总体阳性与蛋白尿和胸膜炎有关。脱发仅与 CLIFT 阳性显著相关。除了证实相同的发现外,PCA 还表明 CLIFT 和 ELISA 的联合阳性也与淋巴细胞减少症有关。
我们的结果表明,不同的抗 dsDNA 抗体特异性与肾病、胸膜炎、脱发和淋巴细胞减少症相关,而与诊断无关。这可能挑战了抗 dsDNA 抗体作为系统性红斑狼疮诊断标志的重要性。