Title
Changes in quality of life in the first 5 years of disease in a multicenter cohort of patients with systemic lupus erythematosus
Date Issued
01 September 2014
Access level
open access
Resource Type
journal article
Author(s)
Urowitz M.
Gladman D.D.
Ibañez D.
Sanchez-Guerrero J.
Bae S.C.
Gordon C.
Fortin P.R.
Clarke A.
Bernatsky S.
Hanly J.G.
Wallace D.J.
Isenberg D.
Rahman A.
Merrill J.
Ginzler E.
Fessler B.
Khamashta M.
Steinsson K.
Petri M.
Dooley M.
Bruce I.N.
Manzi S.
Sturfelt G.
Nived O.
Ramsey-Goldman R.
Zoma A.
Maddison P.
Kalunian K.
Van Vollenhoven R.
Aranow C.
Romero Diaz J.
Stoll T.
Systemic Lupus International Collaborating Clinics
Publisher(s)
John Wiley and Sons Inc
Abstract
Objective. The Medical Outcomes Study Short Form 36 (SF-36) is recommended to assess quality of life (QOL) in systemic lupus erythematosus (SLE). The aim of the current study was to assess QOL over time in the first 5 years of a multicenter inception cohort of patients with SLE. Methods. An inception SLE cohort was assembled according to a standardized protocol between 2000 and 2012. In addition to clinical and laboratory assessments, patients completed the SF-36 at yearly intervals. Only patients who had ≥5 completed QOL questionnaires were included in these analyses. Generalized estimating equation models were run separately for each of the 8 subscales and for the physical and mental component summary scores, adjusting for repeated measures by patients. Results. A total of 495 patients were included. The mean ± SD disease duration at the first visit was 5.3 ± 4.1 months. The mean ± SD age at enrollment was 35.8 ± 13.2 years. All 8 subscales and the 2 summary scores showed improvement in the first 2 years from enrollment. Between years 2 and 5, none of the subscales or summary scores showed any change. Minimum clinically important improvement was achieved by 35-56% of the patients and was influenced by demographic and disease factors. Conclusion. Unlike late-stage lupus, where QOL is stable over time, in patients with early disease, all subscales improve in early followup up to 2 years. Therefore, the SF-36 may be a sensitive outcome measure in early disease in patients with SLE. Copyright © 2014 by the American College of Rheumatology.
Start page
1374
End page
1379
Volume
66
Issue
9
Language
English
OCDE Knowledge area
Inmunología
Reumatología
Scopus EID
2-s2.0-84906703030
PubMed ID
Source
Arthritis Care and Research
ISSN of the container
2151464X
Sources of information:
Directorio de Producción Científica
Scopus