SMART-SLE: serology monitoring and repeat testing in systemic lupus erythematosus—an analysis of anti-double-stranded DNA monitoring

医学 队列 内科学 危险系数 血清学 置信区间 队列研究 比例危险模型 系统性红斑狼疮 红斑狼疮 免疫学 胃肠病学 抗体 疾病
作者
Ai Li Yeo,Rangi Kandane‐Rathnayake,Rachel Koelmeyer,Vera Golder,Worawit Louthrenoo,Yi-Hsing Chen,Jiacai Cho,Aisha Lateef,Laniyati Hamijoyo,Shue‐Fen Luo,Yeong‐Jian Jan Wu,Sandra V. Navarra,Leonid Zamora,Zhanguo Li,Yuan An,Sargunan Sockalingam,Yasuhiro Katsumata,Masayoshi Harigai,Yanjie Hao,Zhuoli Zhang,B. M. D. B. Basnayake,Madelynn Chan,Jun Kikuchi,Tsutomu Takeuchi,Sang Cheol Bae,Shereen Oon,Sean O’Neill,Fiona Goldblatt,Kristine Ng,Annie Law,Nicola Tugnet,Sunil Kumar,Cherica A. Tee,Michael L. Tee,Yoshiya Tanaka,Yoshiya Tanaka,Chak Sing Lau,Mandana Nikpour,Alberta Hoi,Michelle Leech,Eric F Morand
出处
期刊:Rheumatology [Oxford University Press]
被引量:1
标识
DOI:10.1093/rheumatology/kead231
摘要

Disease activity monitoring in systemic lupus erythematosus (SLE) includes serial measurement of anti-double stranded-DNA (dsDNA) antibodies, but in patients who are persistently anti-dsDNA positive, the utility of repeated measurement is unclear. We investigated the usefulness of serial anti-dsDNA testing in predicting flare in SLE patients who are persistently anti-dsDNA positive.Data were analysed from patients in a multinational longitudinal cohort with known anti-dsDNA results from 2013 to 2021. Patients were categorised based on their anti-dsDNA results as persistently negative, fluctuating or persistently positive. Cox regression models were used to examine longitudinal associations of anti-dsDNA results with flare.Data from 37,582 visits of 3,484 patients were analysed. 1,029 (29.5%) of patients had persistently positive anti-dsDNA and 1,195 (34%) had fluctuating results. Anti-dsDNA expressed as a ratio to the normal cut-off was associated with the risk of subsequent flare, including in the persistently positive cohort (adjusted hazard ratio (95% confidence interval) 1.56 (1.30, 1.87) (p < 0.001) and fluctuating cohort (adjusted HR (95%CI) 1.46 (1.28, 1.66)), both for a ratio >3. Both increases and decreases in anti-dsDNA more than two-fold compared to the previous visit were associated with increased risk of flare in the the fluctuating cohort (adjusted HR(95%CI) 1.33(1.08, 1.65) p = 0.008) and the persistently positive cohort (adjusted HR (95%CI) 1.36 (1.08, 1.71) p = 0.009).Absolute value and change in anti-dsDNA titres predict flares, including in persistently anti-dsDNA positive patients. This indicates that repeat monitoring of dsDNA has value in routine testing.
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