Title
Flares after hydroxychloroquine reduction or discontinuation: results from the Systemic Lupus International Collaborating Clinics (SLICC) inception cohort
Date Issued
01 March 2022
Access level
open access
Resource Type
journal article
Author(s)
Almeida-Brasil C.C.
Hanly J.G.
Urowitz M.
Clarke A.E.
Ruiz-Irastorza G.
Gordon C.
Ramsey-Goldman R.
Petri M.
Ginzler E.M.
Wallace D.J.
Bae S.C.
Romero-Diaz J.
Dooley M.A.
Peschken C.
Isenberg D.
Rahman A.
Manzi S.
Jacobsen S.
Lim S.
van Vollenhoven R.F.
Nived O.
Jönsen A.
Kamen D.L.
Aranow C.
Sanchez-Guerrero J.
Gladman D.D.
Fortin P.R.
Merrill J.T.
Kalunian K.
Ramos-Casals M.
Steinsson K.
Zoma A.
Askanase A.
Khamashta M.A.
Bruce I.N.
Inanc M.
Abrahamowicz M.
Bernatsky S.
University of Alabama
Publisher(s)
BMJ Publishing Group
Abstract
OBJECTIVES: To evaluate systemic lupus erythematosus (SLE) flares following hydroxychloroquine (HCQ) reduction or discontinuation versus HCQ maintenance. METHODS: We analysed prospective data from the Systemic Lupus International Collaborating Clinics (SLICC) cohort, enrolled from 33 sites within 15 months of SLE diagnosis and followed annually (1999-2019). We evaluated person-time contributed while on the initial HCQ dose ('maintenance'), comparing this with person-time contributed after a first dose reduction, and after a first HCQ discontinuation. We estimated time to first flare, defined as either subsequent need for therapy augmentation, increase of ≥4 points in the SLE Disease Activity Index-2000, or hospitalisation for SLE. We estimated adjusted HRs (aHRs) with 95% CIs associated with reducing/discontinuing HCQ (vs maintenance). We also conducted separate multivariable hazard regressions in each HCQ subcohort to identify factors associated with flare. RESULTS: We studied 1460 (90% female) patients initiating HCQ. aHRs for first SLE flare were 1.20 (95% CI 1.04 to 1.38) and 1.56 (95% CI 1.31 to 1.86) for the HCQ reduction and discontinuation groups, respectively, versus HCQ maintenance. Patients with low educational level were at particular risk of flaring after HCQ discontinuation (aHR 1.43, 95% CI 1.09 to 1.87). Prednisone use at time-zero was associated with over 1.5-fold increase in flare risk in all HCQ subcohorts. CONCLUSIONS: SLE flare risk was higher after HCQ taper/discontinuation versus HCQ maintenance. Decisions to maintain, reduce or stop HCQ may affect specific subgroups differently, including those on prednisone and/or with low education. Further study of special groups (eg, seniors) may be helpful.
Start page
370
End page
378
Volume
81
Issue
3
Language
English
OCDE Knowledge area
Reumatología
Scopus EID
2-s2.0-85124635089
PubMed ID
Source
Annals of the rheumatic diseases
ISSN of the container
00034967
Source funding
Canadian Institutes of Health Research
Sponsor(s)
Core funding for this investigator-initiated study was provided to Dr SB by a Canadian Institutes of Health Research (CIHR) project grant (Fall 2017 competition). Dr CCA-B received postdoctoral salary awards from the Fonds de Recherche du Québec Santé (FRQS), the Research Institute of the McGill University Health Centre (RI-MUHC) and the CIHR Drug Safety and Effectiveness Cross-Disciplinary Training ProgramProgramme (DSECT). The Montreal General Hospital Lupus Clinic is partially supported by the Singer Family Fund for Lupus Research. Dr AEC holds The Arthritis Society Chair in Rheumatic Diseases at the University of Calgary. Dr CG is supported by Lupus UK, Sandwell and West Birmingham Hospitals NHS Trust and the National Institute for Health Research (NIHR)/ Wellcome Trust Birmingham Clinical Research Facility. Dr PRF is recipient of a tier 1 Canada Research Chair on Systemic Autoimmune Rheumatic Diseases. Dr S-CB’s work was supported in part by the Bio & Medical Technology Development Programme of the National Research Foundation of the Republic of Korea (grant NRF-2017M3A9B4050335). The Hopkins Lupus Cohort is supported by the NIH (grant AR43727 and AR69572). Dr IB is a National Institute for Health Research (NIHR) Senior Investigator and is supported by Arthritis Research UK, the NIHR Manchester Biomedical Centre and the NIHR/Wellcome Trust Manchester Clinical Research Facility. Dr SJ is supported by the Danish Rheumatism Association (A3865) and the Novo Nordisk Foundation (A05990). Dr RR-G’s work was supported by the NIH (grants 5UL1TR001422–02 (formerly 8UL1TR000150), UL-1RR-025741, K24-AR-02318 and P60AR064464 (formerly P60-AR-48098)). Dr MAD’s work was supported by the NIH grant RR00046. Dr GR-I is supported by the Department of Education, Universities and Research of the Basque Government. Dr SL’s work was supported, in part, by the Centers for Disease Control and Prevention grant U01DP005119. Dr DAI and Dr AR are supported by the National Institute for Health Research University College London Hospitals Biomedical Research Center. Preliminary results of this study were presented at the 2020 Meeting of the American College of Rheumatology (ACR Convergence 2020). Reference: Almeida-Brasil C, Hanly J, Urowitz M, et al. Outcomes After Hydroxychloroquine Reduction or Discontinuation in a Multinational Inception Cohort of Systemic Lupus [(abstract]). Arthritis Rheumatol. 2020; 72 (suppl 10). https://acrabstracts. org/abstract/outcomes-after-hydroxychloroquine-reduction-or-discontinuation-in-a-multinational-inception-cohort-of-systemic-lupus/.
Sources of information: Directorio de Producción Científica Scopus