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Short-term outcome of neuropsychiatric events in systemic lupus erythematosus upon enrollment into an international inception cohort study

Authors
Hanly, J. G.Urowitz, M. B.Su, L.Sanchez-Guerrero, J.Bae, Sang CheolGordon, C.Wallace, D. J.Isenberg, D.Alarcon, G. S.Merrill, J. T.Clarke, A.Bernatsky, S.Dooley, M. A.Fortin, P. R.Gladman, D.Steinsson, K.Petri, M.Bruce, I. N.Manzi, S.Khamashta, M.Zoma, A.Font, J.Van Vollenhoven, R.Aranow, C.Ginzler, E.Nived, O.Sturfelt, G.Ramsey-Goldman, R.Kalunian, K.Douglas, J.Qi, K. QiufenThompson, K.Farewell, V.
Issue Date
May-2008
Publisher
John Wiley & Sons Inc.
Citation
Arthritis and Rheumatism, v.59, no.5, pp 721 - 729
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
Arthritis and Rheumatism
Volume
59
Number
5
Start Page
721
End Page
729
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/172077
DOI
10.1002/art.23566
ISSN
0004-3591
1529-0131
Abstract
Objective. To determine the short-term outcome of neuropsychiatric (NP) events upon enrollment into an international inception cohort of patients with systemic lupus erythematosus (SLE). Methods. The study was performed by the Systemic Lupus International Collaborating Clinics. Patients were enrolled within 15 months of SLE diagnosis and NP events were characterized using the American College of Rheumatology case definitions. Decision rules were derived to identify NP events attributable to SLE. Physician outcome scores of NP events and patient-derived mental component summary (MCS) and physical component summary (PCS) scores of the Short Form 36 were recorded. Results. There were 890 patients (88.7% female) with a mean +/- SD age of 33.8 +/- 13.4 years and mean disease duration of 5.3 +/- 4.2 months. Within the enrollment window, 271 (33.5%) of 890 patients had at least 1 NP event encompassing 15 NP syndromes. NP events attributed to SLE varied from 16.5% to 33.9% using alternate attribution models and occurred in 6.0-11.5% of patients. Outcome scores for NP events attributed to SLE were significantly better than for NP events due to non-SLE causes. Higher global disease activity was associated with worse outcomes. MCS scores were lower in patients with NP events, regardless of attribution, and were also lower in patients with diffuse and central NP events. There was a significant association between physician outcome scores and patient MCS scores only for NP events attributed to SLE. Conclusion. In SLE patients, the short-term outcome of NP events is determined by both the characteristics and attribution of the events.
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