Title
Factors associated with damage accrual in patients with systemic lupus erythematosus: Results from the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort
Date Issued
01 September 2015
Access level
open access
Resource Type
journal article
Author(s)
Bruce I.N.
O'Keeffe A.G.
Farewell V.
Hanly J.G.
Manzi S.
Su L.
Gladman D.D.
Bae S.C.
Sanchez-Guerrero J.
Romero-Diaz J.
Gordon C.
Wallace D.J.
Clarke A.E.
Bernatsky S.
Ginzler E.M.
Isenberg D.A.
Rahman A.
Merrill J.T.
Fessler B.J.
Fortin P.R.
Petri M.
Steinsson K.
Dooley M.A.
Khamashta M.A.
Ramsey-Goldman R.
Zoma A.A.
Sturfelt G.K.
Nived O.
Aranow C.
Mackay M.
Ramos-Casals M.
Van Vollenhoven R.F.
Kalunian K.C.
Ruiz-Irastorza G.
Lim S.
Kamen D.L.
Peschken C.A.
Inanc M.
Urowitz M.B.
University of Alabama
Publisher(s)
BMJ Publishing Group
Abstract
Background and aims: We studied damage accrual and factors determining development and progression of damage in an international cohort of systemic lupus erythematosus (SLE) patients. Methods: The Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort recruited patients within 15 months of developing four or more 1997 American College of Rheumatology (ACR) criteria for SLE; the SLICC/ACR damage index (SDI) was measured annually. We assessed relative rates of transition using maximum likelihood estimation in a multistate model. The Kaplan-Meier method estimated the probabilities for time to first increase in SDI score and Cox regression analysis was used to assess mortality. Results: We recruited 1722 patients; mean (SD) age 35.0 (13.4) years at cohort entry. Patients with damage at enrolment were more likely to have further worsening of SDI (SDI 0 vs ≥1; p<0.001). Age, USA African race/ethnicity, SLEDAI-2K score, steroid use and hypertension were associated with transition from no damage to damage, and increase(s) in pre-existing damage. Male gender (relative transition rates (95% CI) 1.48 (1.06 to 2.08)) and USA Caucasian race/ethnicity (1.63 (1.08 to 2.47)) were associated with SDI 0 to ≥1 transitions; Asian race/ethnicity patients had lower rates of new damage (0.60 (0.39 to 0.93)). Antimalarial use was associated with lower rates of increases in pre-existing damage (0.63 (0.44 to 0.89)). Damage was associated with future mortality (HR (95% CI) 1.46 (1.18 to 1.81) per SDI point). Conclusions: Damage in SLE predicts future damage accrual and mortality. We identified several potentially modifiable risk factors for damage accrual; an integrated strategy to address these may improve long-term outcomes.
Start page
1706
End page
1713
Volume
74
Issue
9
Language
English
OCDE Knowledge area
Reumatología
Scopus EID
2-s2.0-84924190291
PubMed ID
Source
Annals of the Rheumatic Diseases
ISSN of the container
00034967
Sponsor(s)
Canadian Institutes of Health Research MOP-49529, MOP-86526
Medical Research Council U105261167
National Institutes of Health K24-AR-02318, P60 AR062755, P60-AR-48095, P60-AR-48098, UL 1RR 025741, UL1 RR029882
National Center for Research Resources M01RR000052
Sources of information:
Directorio de Producción Científica
Scopus