Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12655
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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