External validation of the alternative Ankylosing Spondylitis Disease Activity Score in three randomized clinical trials of ixekizumab.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
01 06 2023
Historique:
received: 28 07 2022
accepted: 15 10 2022
medline: 5 6 2023
pubmed: 26 10 2022
entrez: 25 10 2022
Statut: ppublish

Résumé

The alternative ASDAS (altASDAS) is an index that can be used when patient global assessment is unavailable. Our aim was to test the truth and discrimination aspects according to OMERACT filter 2.0 of the altASDAS in an external cohort. Cohorts from the COAST trials of ixekizumab (COAST-V, -W, -X; 16-week primary endpoint) enrolling radiographic/non-radiographic axial SpA patients were pooled. The ASDAS [original formula with patient global assessment (PGA)] and altASDAS were calculated. Truth was assessed by agreement with the continuous ASDAS [intraclass correlation coefficients (ICCs)] and ASDAS disease activity (DA) states (weighted κ), Bland-Altman plots [mean difference (MD) and 95% limits of agreement (LoA)] and Pearson's correlations between altASDAS/ASDAS and other constructs. Discrimination was tested by the ability of altASDAS to distinguish high/low DA according to nocturnal pain >6/10 as an external anchor and agreement (κ) with ASDAS in major improvement (MI) and clinically important improvement (CII). A total of 958 patients were included. For truth, agreement with ASDAS was very good (ICC = 0.99, κ = 0.91), MD with ASDAS was 0.03 (95% LoA -0.31-0.24) and correlation coefficients of altASDAS with related constructs were within a prespecified 0.3-wide band around those between ASDAS and the same construct. For discrimination, the altASDAS discriminated between DA states and agreed with ASDAS response (κ MI = 0.91, CII = 0.93). The altASDAS was truthful and discriminative in an external cohort and as such has been fully validated to be used in cases when PGA is unavailable.

Identifiants

pubmed: 36282526
pii: 6772504
doi: 10.1093/rheumatology/keac618
doi:

Substances chimiques

ixekizumab BTY153760O
C-Reactive Protein 9007-41-4

Banques de données

ClinicalTrials.gov
['NCT02696785', 'NCT02696798', 'NCT02757352']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2257-2261

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Augusta Ortolan (A)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Rheumatology Unit, Department of Medicine, University of Padova, DIMED, Padova, Italy.

Sofia Ramiro (S)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Rheumatology, Zuyderland Medical Center, Heerlen, The Netherlands.

Roberta Ramonda (R)

Rheumatology Unit, Department of Medicine, University of Padova, DIMED, Padova, Italy.

Désirée van der Heijde (D)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

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Classifications MeSH