Prolonged remission in SLE is possible by using reduced doses of prednisone: An observational study from the Lupus-Cruces and Lupus-Bordeaux inception cohorts.
Administration, Oral
Adult
Cohort Studies
Disease-Free Survival
Dose-Response Relationship, Drug
Drug Administration Schedule
Female
France
/ epidemiology
Glucocorticoids
/ administration & dosage
Humans
Hydroxychloroquine
/ administration & dosage
Immunosuppressive Agents
/ administration & dosage
Lupus Erythematosus, Systemic
/ diagnosis
Male
Methotrexate
/ administration & dosage
Methylprednisolone
/ administration & dosage
Middle Aged
Prednisone
/ administration & dosage
Remission Induction
Spain
/ epidemiology
Treatment Outcome
Young Adult
Activity
Antimalarials
Damage
Glucocorticoids
Prognosis
Journal
Autoimmunity reviews
ISSN: 1873-0183
Titre abrégé: Autoimmun Rev
Pays: Netherlands
ID NLM: 101128967
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
15
02
2019
accepted:
20
02
2019
pubmed:
20
7
2019
medline:
24
10
2019
entrez:
20
7
2019
Statut:
ppublish
Résumé
The aim of this study is to compare the frequency of remission, according to DORIS definitions, of inception patients from two European SLE cohorts, with a special focus on the differences between the therapeutic schemes of both Units. Inception patients enrolled after 2000 from the longitudinal Cruces Lupus Cohort (CC) and Bordeaux Lupus Cohort (BC) were included. The main endpoint was the achievement of clinical remission on treatment (ClinROnT). ClinROnT was assessed yearly from the 1st until the 5th year following the diagnosis of SLE. 173 patients, 92 CC and 81 BC, were studied. The clinical presentation of both cohorts was similar, with no significant differences in the mean SLEDAI score at diagnosis (6.6 vs. 8.1, p = 0.06). Patients from CC were treated more frequently with hydroxychloroquine (mean 57 vs. 43 months), methotrexate (24% vs. 11%) and pulse methyl-prednisolone (42% vs. 26%), and received lower doses of oral prednisone (average dose during the follow up 2.3 vs. 7.2 mg/d, p < 0.001). Patients in CC were more likely to achieve ClinROnT at year one, 84% vs. 43% (p < 0.001). Prolonged ClinROnT during the 5 years of follow up was more frequent in CC: 70% vs. 28%, p < 0.001. Patients in CC were also more likely to achieve ClinROnT after controlling for baseline SLEDAI (adjusted HR 1.69, 95%CI 1.21-2.35) and for the presenting clinical manifestations (adjusted HR 1.72, 95% CI 1.2-2.4). Prolonged ClinROnT was achievable by using a therapeutic regime consisting of lower doses of oral prednisone and maximizing the use of hydroxychloroquine, pulse methyl-prednisolone and methotrexate.
Identifiants
pubmed: 31323362
pii: S1568-9972(19)30159-4
doi: 10.1016/j.autrev.2019.102359
pii:
doi:
Substances chimiques
Glucocorticoids
0
Immunosuppressive Agents
0
Hydroxychloroquine
4QWG6N8QKH
Prednisone
VB0R961HZT
Methylprednisolone
X4W7ZR7023
Methotrexate
YL5FZ2Y5U1
Types de publication
Journal Article
Multicenter Study
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
102359Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.