Abstract
Objective. We previously described the multiplex autoantibody SLE-key Rule-Out test, which detects a signature of autoantibody reactivity that distinguishes healthy subjects from SLE patients with 94% sensitivity, 75% specificity and 93% negative predictive value; thus, an individual manifesting a positive Rule-Out test score is unlikely to have SLE (e.g. lupus is excluded). The objective of this current study was to evaluate the stability of the lupus-associated signature over time. Methods. We used banked serum samples from healthy subjects (n = 51) and lupus patients (n = 50 individual samples and n = 181 paired samples, for a total of n = 412 serum samples). The samples were drawn at different times after diagnosis to analyse the impact on the SLE-key Rule-Out test of time elapsed since diagnosis and any changes in disease activity (as reflected by the SLEDAI score). Results. The SLE signature remains stable for the first 10 years after diagnosis; in this time frame, <10% of patients manifested a positive Rule-Out score and the SLE-key Rule-Out score was independent of the underlying disease activity as reflected by the SLEDAI score. After 510 years, 30% of lupus subjects scored as SLE Ruled-Out; the proportion of patients manifesting this status was even greater in the subset of individuals with a SLEDAI score of 0. Conclusion. These findings raise the possibility that a significant number of SLE patients manifest a change in their serological signature over time, and that such a signature change may signify an evolution in the immunological features of their disease relevant to patient management.
Original language | English |
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Pages (from-to) | 1632-1640 |
Number of pages | 9 |
Journal | Rheumatology |
Volume | 57 |
Issue number | 9 |
DOIs | |
State | Published - 1 Sep 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2018 The Author(s).
Funding
The authors wish to acknowledge the invaluable contributions of Yakov Blumenstein, Ilana Gilkaite, Miriam Lerner, Ornit Cohen-Gindi, Olga Tarnapolski, Adrian Javaherian, Annmarie Goldstein, Vanessa Cabra-Hodge, Justin Pitts, Maggie Barton and Emileigh Wong The Hopkins Lupus Cohort is supported by the National Institute of Arthritis and Musculoskeletal Diseases at the National Institutes of Health [grant numbers R01 AR 43727 and 69572]. The MUSC cohort and authors were funded by the National Center for Research Resources at the National Institutes of Health [grant number UL1 RR029882], MUSC General and Clinical Research Center [grant number M01 RR001070], South Carolina Clinical & Translational Research Institute [grant number UL1 RR029882], the Multidisciplinary Clinical Research Center at MUSC [grant number P60 AR062755] and the Core Center for Clinical Research [grant number P30 AR072582]. Funding: This study was funded by ImmunArray.
Funders | Funder number |
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Core Center for Clinical Research | P30 AR072582 |
ImmunArray | |
MUSC General and Clinical Research Center | M01 RR001070 |
Multidisciplinary Clinical Research Center | P60 AR062755 |
South Carolina Clinical & Translational Research Institute | |
National Institutes of Health | R01 AR 43727, 69572 |
National Institute of Arthritis and Musculoskeletal and Skin Diseases | P30AR072582 |
National Center for Research Resources | UL1 RR029882 |
Keywords
- Autoantibodies
- Diagnosis
- Microarray
- Multivariate classifier
- Natural history
- SLE-key
- Systemic lupus erythematosus
- iCHIP