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Udgivet

Neuropsychiatric Events in Systemic Lupus Erythematosus: Predictors of Occurrence and Resolution in a Longitudinal Analysis of an International Inception Cohort

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

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  • John G Hanly
  • Caroline Gordon
  • Sang-Cheol Bae
  • Juanita Romero-Diaz
  • Jorge Sanchez-Guerrero
  • Sasha Bernatsky
  • Ann E Clarke
  • Daniel J Wallace
  • David A Isenberg
  • Anisur Rahman
  • Joan T Merrill
  • Paul R Fortin
  • Dafna D Gladman
  • Murray B Urowitz
  • Ian N Bruce
  • Michelle Petri
  • Ellen M Ginzler
  • M A Dooley
  • Rosalind Ramsey-Goldman
  • Susan Manzi
  • Andreas Jonsen
  • Graciela S Alarcón
  • Ronald F van Vollenhoven
  • Cynthia Aranow
  • Meggan Mackay
  • Guillermo Ruiz-Irastorza
  • S Sam Lim
  • Murat Inanc
  • Kenneth C Kalunian
  • Soren Jacobsen
  • Christine A Peschken
  • Diane L Kamen
  • Anca Askanase
  • Vernon Farewell
Vis graf over relationer

OBJECTIVE: To determine predictors of change in neuropsychiatric (NP) event status in a large, prospective, international inception cohort of patients with systemic lupus erythematosus (SLE).

METHODS: Upon enrollment and annually thereafter, NP events attributed to SLE and non-SLE causes and physician-determined resolution were documented. Factors potentially associated with the onset and resolution of NP events were determined by time-to-event analysis using a multistate modeling structure.

RESULTS: NP events occurred in 955 (52.3%) of 1,827 patients, and 593 (31.0%) of 1,910 unique events were attributed to SLE. For SLE-associated NP (SLE NP) events, multivariate analysis revealed a positive association with male sex (P = 0.028), concurrent non-SLE NP events excluding headache (P < 0.001), active SLE (P = 0.012), and glucocorticoid use (P = 0.008). There was a negative association with Asian race (P = 0.002), postsecondary education (P = 0.001), and treatment with immunosuppressive drugs (P = 0.019) or antimalarial drugs (P = 0.056). For non-SLE NP events excluding headache, there was a positive association with concurrent SLE NP events (P < 0.001) and a negative association with African race (P = 0.012) and Asian race (P < 0.001). NP events attributed to SLE had a higher resolution rate than non-SLE NP events, with the exception of headache, which had comparable resolution rates. For SLE NP events, multivariate analysis revealed that resolution was more common in patients of Asian race (P = 0.006) and for central/focal NP events (P < 0.001). For non-SLE NP events, resolution was more common in patients of African race (P = 0.017) and less common in patients who were older at SLE diagnosis (P < 0.001).

CONCLUSION: In a large and long-term study of the occurrence and resolution of NP events in SLE, we identified subgroups with better and worse prognosis. The course of NP events differs greatly depending on their nature and attribution.

OriginalsprogEngelsk
TidsskriftArthritis and Rheumatology
Vol/bind73
Udgave nummer12
Sider (fra-til)2293-2302
Antal sider10
ISSN2326-5191
DOI
StatusUdgivet - dec. 2021

Bibliografisk note

© 2021, American College of Rheumatology.

ID: 73995308