Remission in systemic lupus erythematosus: testing different definitions in a large multicentre cohort.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
07 2020
Historique:
received: 30 01 2020
revised: 13 03 2020
accepted: 01 04 2020
pubmed: 24 4 2020
medline: 10 7 2020
entrez: 24 4 2020
Statut: ppublish

Résumé

Remission in systemic lupus erythematosus (SLE) is defined through a combination of 'clinical SLE Disease Activity Index (cSLEDAI)=0', 'physician's global assessment (PGA) <0.5' and 'prednisone (PDN) ≤5 mg/day'. We investigated the performance of these items, alone or in combination, in defining remission and in predicting SLICC/ACR Damage Index. We tested seven potential definitions of remission in SLE patients followed-up for ≥5 years: PDN ≤5 mg/day; PGA <0.5; cSLEDAI=0; PGA <0.5 plus PDN ≤5 mg/day; cSLEDAI=0 plus PGA <0.5; cSLEDAI=0 plus PDN ≤5 mg/day; cSLEDAI=0 plus PDN ≤5 mg/day plus PGA <0.5. The effect of these definitions on damage was evaluated by Poisson regression analysis; the best performance was identified as the lowest Akaike and Bayesian information criterion (AIC and BIC). Positive and negative predictive values in identifying no damage increase were calculated. We included 646 patients (mean±SD disease duration 9.2±6.9 years). At multivariate analysis, ≥2 consecutive year remission according to all definitions protected against damage (OR, 95% CI: PGA <0.5 0.631, 0.444 to 0.896; cSLEDAI=0 0.531, 0.371 to 0.759; PGA <0.5 plus PDN ≤5 mg/day 0.554, 0.381 to 0.805; cSLEDAI=0 plus PGA <0.5 0.574, 0.400 to 0.826; cSLEDAI=0 plus PDN ≤5 mg/day 0.543, 0.376 to 0.785; cSLEDAI=0 plus PDN ≤5 mg/day plus PGA <0.5 0.532, 0.363 to 0.781, p<0.01 for all), except PDN ≤5 mg/day, which required four consecutive years (OR 0.534, 95% CI 0.325 to 0.877, p=0.013). Positive and negative predictive values were similar; however, cSLEDAI=0 showed the best performance (AIC 1082.90, BIC 1109.72, p<0.0001). Adding PGA <0.5 and/or PDN ≤5 mg/day to cSLEDAI=0 decreased remission duration (-1.8 and -1.5 year/patient, respectively) without increasing cSLEDAI=0 performance in predicting damage accrual. cSLEDAI=0 is the most attainable definition of remission, while displaying the best performance in predicting damage progression in the short-to-mid-term follow-up.

Identifiants

pubmed: 32321721
pii: annrheumdis-2020-217070
doi: 10.1136/annrheumdis-2020-217070
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Prednisone VB0R961HZT

Types de publication

Comparative Study Evaluation Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

943-950

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Francesca Saccon (F)

Department of Medicine, Division of Rheumatology, University of Padua, Padova, Italy.

Margherita Zen (M)

Department of Medicine, Division of Rheumatology, University of Padua, Padova, Italy.

Mariele Gatto (M)

Department of Medicine, Division of Rheumatology, University of Padua, Padova, Italy.

Domenico Paolo Emanuele Margiotta (DPE)

Unit of Allergology, Immunolgy, Rheumatology, Department of Medicine, Universita Campus Bio-Medico di Roma, Roma, Italy.

Antonella Afeltra (A)

Unit of Allergology, Immunolgy, Rheumatology, Department of Medicine, Universita Campus Bio-Medico di Roma, Roma, Italy.

Fulvia Ceccarelli (F)

Dipartimento di Medicina Interna e Specialità Mediche, Reumatologia, Sapienza University of Rome, Roma, Lazio, Italy.

Fabrizio Conti (F)

Department of Clinical, Internal, Anesthesiological and Cardiovascular Sciences, Rheumatology Unit, Sapienza University of Rome, Roma, Lazio, Italy.

Alessandra Bortoluzzi (A)

University Hospital Arcispedale Sant'Anna, Department of Medical Sciences, Division of Rheumatology, University of Ferrara, Ferrara, Emilia-Romagna, Italy.

Marcello Govoni (M)

University Hospital Arcispedale Sant'Anna, Department of Medical Sciences, Division of Rheumatology, University of Ferrara, Ferrara, Emilia-Romagna, Italy.

Giulia Frontini (G)

Nephrology Unit, La Fondazione IRCCS Ca' Granda Ospedale Maggiore di Milano Policlinico, Milano, Lombardia, Italy.

Gabriella Moroni (G)

Nephrology Unit, La Fondazione IRCCS Ca' Granda Ospedale Maggiore di Milano Policlinico, Milano, Lombardia, Italy.

Francesca Dall'Ara (F)

ASST-Spedali Civili, Rheumatology and Clinical Immunology, University of Brescia, Brescia, Lombardia, Italy.

Angela Tincani (A)

ASST-Spedali Civili, Rheumatology and Clinical Immunology, University of Brescia, Brescia, Lombardia, Italy.

Viola Signorini (V)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Toscana, Italy.

Marta Mosca (M)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Toscana, Italy.

Anna Chiara Frigo (AC)

Department of Cardiac-Thoracic-Vascular Sciences and Public Health, Biostatistics, Epidemiology and Public Health Unit, University of Padua, Padova, Veneto, Italy.

Luca Iaccarino (L)

Department of Medicine, Division of Rheumatology, University of Padua, Padova, Italy.

Andrea Doria (A)

Department of Medicine, Division of Rheumatology, University of Padua, Padova, Italy adoria@unipd.it.

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Classifications MeSH