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Title: | SMART-SLE: serology monitoring and repeat testing in systemic lupus erythematosus?an analysis of anti-double-stranded DNA monitoring |
Author: | Yeo, A. L. Kandane-Rathnayake, R. Koelmeyer, R. Golder, V. Louthrenoo, W. Chen, Y. H. Cho, J. Lateef, A. Hamijoyo, L. Luo, S. F. Wu, Y. J. J. Navarra, S. V. Zamora, L. Li, Z. An, Y. Sockalingam, S. Katsumata, Y. Harigai, M. Hao, Y. Zhang, Z. Basnayake, B. M. D. B. Chan, M. Kikuchi, J. Takeuchi, T. Bae, S. C. Oon, S. O?Neill, S. Goldblatt, F. Ng, K. P. L. Law, A. Tugnet, N. Kumar, S. Tee, C. Tee, M. Ohkubo, N. Tanaka, Y. Lau, C. S. Nikpour, M. Hoi, A. Leech, M. Morand, E. F. |
SWSLHD Author: | O'Neill, Sean |
Issue Date: | 2024 |
Journal: | Rheumatology (United Kingdom) |
Abstract: | Objective: Disease activity monitoring in 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. Methods: Data were analysed from patients in a multinational longitudinal cohort with known anti-dsDNA results from 2013 to 2021. Patients were categorized 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. Results: Data from 37 582 visits of 3484 patients were analysed. Of the patients 1029 (29.5%) had persistently positive anti-dsDNA and 1195 (34.3%) 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 [HR] 1.56; 95% CI: 1.30, 1.87; P < 0.001) and fluctuating cohort (adjusted HR 1.46; 95% CI: 1.28, 1.66), both for a ratio >3. Both increases and decreases in anti-dsDNA more than 2-fold compared with the previous visit were associated with increased risk of flare in the fluctuating cohort (adjusted HR 1.33; 95% CI: 1.08, 1.65; P = 0.008) and the persistently positive cohort (adjusted HR 1.36; 95% CI: 1.08, 1.71; P = 0.009). Conclusion: 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. © The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. |
ISSN: | 14620324 (ISSN) |
Digital object identifier: | 10.1093/rheumatology/kead231 |
URI: | https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12655 |
Department: | Liverpool Hospital, Department of Rheumatology |
Appears in Collections: | Liverpool Hospital |
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