Prolonged remission in SLE is possible by using reduced doses of prednisone: An observational study from the Lupus-Cruces and Lupus-Bordeaux inception cohorts.


Journal

Autoimmunity reviews
ISSN: 1873-0183
Titre abrégé: Autoimmun Rev
Pays: Netherlands
ID NLM: 101128967

Informations de publication

Date de publication:
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

102359

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Guillermo Ruiz-Irastorza (G)

Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of The Basque Country, Bizkaia, The Basque Country, Spain. Electronic address: r.irastorza@outlook.es.

Beatriz Ruiz-Estevez (B)

Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of The Basque Country, Bizkaia, The Basque Country, Spain.

Estibaliz Lazaro (E)

Internal Medicine Department, Haut-Lévêque Hospital, Bordeaux, France; UMR CNRS5164, ImmunoconcEpT, Bordeaux University, Bordeaux, France; ACRONIM University Hospital Federation, Bordeaux, France.

Ioana Ruiz-Arruza (I)

Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of The Basque Country, Bizkaia, The Basque Country, Spain.

Pierre Duffau (P)

UMR CNRS5164, ImmunoconcEpT, Bordeaux University, Bordeaux, France; Internal Medicine Department, Saint-Andre Hospital, Bordeaux, France; ACRONIM University Hospital Federation, Bordeaux, France.

Miguel Martin-Cascon (M)

Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of The Basque Country, Bizkaia, The Basque Country, Spain.

Christophe Richez (C)

UMR CNRS5164, ImmunoconcEpT, Bordeaux University, Bordeaux, France; Rheumatology Department, Pellegrin Hospital, Bordeaux, France; ACRONIM University Hospital Federation, Bordeaux, France.

Amaia Ugarte (A)

Autoimmune Diseases Research Unit, Department of Internal Medicine, Biocruces Bizkaia Health Research Institute, Hospital Universitario Cruces, University of The Basque Country, Bizkaia, The Basque Country, Spain.

Patrick Blanco (P)

UMR CNRS5164, ImmunoconcEpT, Bordeaux University, Bordeaux, France; Immunology Department, Pellegrin Hospital, Bordeaux, France; ACRONIM University Hospital Federation, Bordeaux, France.

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Classifications MeSH