Simplified Ankylosing Spondylitis Disease Activity Score (SASDAS) Versus ASDAS: A Post Hoc Analysis of a Randomized Controlled Trial.


Journal

The Journal of rheumatology
ISSN: 0315-162X
Titre abrégé: J Rheumatol
Pays: Canada
ID NLM: 7501984

Informations de publication

Date de publication:
10 2022
Historique:
accepted: 11 04 2022
pubmed: 16 7 2022
medline: 26 10 2022
entrez: 15 7 2022
Statut: ppublish

Résumé

To compare the Simplified Ankylosing Spondylitis Disease Activity Score (SASDAS) against the Ankylosing Spondylitis Disease Activity Score (ASDAS) for measuring and categorizing disease activity using data from the EMBARK trial (ClinicalTrials.gov: NCT01258738), a randomized controlled trial of etanercept (ETN) for axial spondyloarthritis (axSpA). Patients with early active axSpA received ETN 50 mg once weekly (n = 106) or placebo (PBO; n = 109) for 12 weeks in a double-blind manner; they then received open-label ETN for 92 weeks. For this analysis, ASDAS-C-reactive protein (CRP) and SASDAS-CRP were calculated at baseline, week 12, and week 24. The SASDAS was calculated by the linear addition of the ASDAS components without adjustment. A very strong correlation, as determined by the Spearman correlation coefficient, was observed between the ASDAS and SASDAS for continuous variables at baseline and during treatment. For pooled categorical data at baseline, the SASDAS placed 69.9% of patients in the same disease categories as the ASDAS but overestimated for 17.8% of patients and underestimated for 12.2% of patients. A similar pattern was seen postbaseline. Cohen weighted [Formula: see text] statistics for all individual and pooled treatments and timepoints (0.54-0.73) reflected moderate to substantial agreement. The capacity to differentiate between treatments (ie, ETN and PBO/ETN) was higher with the ASDAS (effect size -0.74, 95% CI -1.03 to -0.46) compared with the SASDAS (effect size -0.51, 95% CI -0.79 to -0.23), but sensitivity to change was generally similar. A very strong correlation between the SASDAS and ASDAS was observed when considering continuous variables; however, moderate to substantial agreement was observed for categorical data, and the SASDAS classified a lower proportion of patients as being in the inactive and low disease activity categories.

Identifiants

pubmed: 35840157
pii: jrheum.211075
doi: 10.3899/jrheum.211075
doi:

Substances chimiques

Etanercept OP401G7OJC
C-Reactive Protein 9007-41-4

Banques de données

ClinicalTrials.gov
['NCT01258738']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1100-1108

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 by the Journal of Rheumatology.

Auteurs

Emilce E Schneeberger (EE)

E.E. Schneeberger, MD, G. Citera, MD, Department of Rheumatology, Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina; eschneeb@gmail.com.

Gustavo Citera (G)

E.E. Schneeberger, MD, G. Citera, MD, Department of Rheumatology, Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina.

Dario Ponce de Leon (DP)

D. Ponce de Leon, MD, Medical Affairs, Pfizer Inc., Lima, Peru.

Annette E Szumski (AE)

A.E. Szumski, MA, Biostatistics, Syneos Health, Princeton, NJ, USA.

Kenneth Kwok (K)

K. Kwok, MSc, Global Biostatistics and Data Management, Pfizer Inc., New York, NY, USA.

Mariel Cutri (M)

M. Cutri, MD, Immunology & Inflammation, Pfizer Inc., Buenos Aires, Argentina.

Maxime Dougados (M)

M. Dougados, MD, Department of Rheumatology, Paris Descartes University, Rheumatology Department, Hôpital Cochin, AP-HP, and INSERM (U1153): Clinical Epidemiology and Biostatistics, PRES Sorbonne Paris-Cité, Paris, France.

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Classifications MeSH