Assessing internal construct validity of DAPSA and DAPSA28 in psoriatic arthritis: a European observational study using confirmatory factor analysis and additional psychometric testing
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, pozorovací studie
PubMed
41436138
PubMed Central
PMC12730740
DOI
10.1136/rmdopen-2025-006104
PII: rmdopen-2025-006104
Knihovny.cz E-zdroje
- Klíčová slova
- Arthritis, Psoriatic, Epidemiology, Outcome Assessment, Health Care,
- MeSH
- dospělí MeSH
- faktorová analýza statistická MeSH
- lidé středního věku MeSH
- lidé MeSH
- psoriatická artritida * diagnóza epidemiologie psychologie MeSH
- psychometrie * metody MeSH
- reprodukovatelnost výsledků MeSH
- stupeň závažnosti nemoci MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- Geografické názvy
- Evropa epidemiologie MeSH
OBJECTIVES: The Disease Activity index for Psoriatic Arthritis (DAPSA) was developed to assess disease activity in patients with psoriatic arthritis (PsA). A modified version, DAPSA28, uses 28 joints instead of 66/68. This study evaluated key psychometric properties of DAPSA and DAPSA28. METHODS: Data from 1865 patients with PsA in the European Spondyloarthritis (EuroSpA) Research Collaboration Network, having DAPSA and DAPSA28 scores at baseline and follow-up, were analysed. Tests included assessment of internal construct validity by scree plots, confirmatory factor analysis (CFA) and structural equation modelling (SEM), supplemented by tests of differential item functioning (DIF) and evaluation of internal consistency reliability by Cronbach's α (CA). A subset of 625 patients was used for most analyses, except descriptive statistics, correlation matrix and CA. RESULTS: One-dimensional CFA models for DAPSA and DAPSA28 showed acceptable model fit at baseline (root mean square error of approximation, RMSEA: 0.020, 0.034). However, model fit at 6 months follow-up was poor (RMSEA: 0.057, 0.063). SEM combining baseline and follow-up data could not identify an acceptable model fit. DIF was found for sex and country. CA indicated acceptable internal consistency (DAPSA: 0.65; DAPSA28: 0.63). Heterogeneity across countries was observed. CONCLUSIONS: Overall, the model fit was acceptable across model fit statistics, supporting internal construct validity, but some evidence of misfit at country level was disclosed. Our findings support acceptable internal consistency reliability, but DIF was found for sex and country. Based on mixed results of model fit and DIF, further investigation of these and other PsA disease activity measures is warranted.
Center for Rheumatic Diseases University of Medicine and Pharmacy Bucharest Romania
Center for treatment of Rheumatic and Musculoskeletal Diseases Diakonhjemmet Hospital Oslo Norway
Centre for Rheumatology Research Landspitali University Hospital Reykjavík Iceland
DANBIO Rigshospitalet Glostrup Denmark
Department of Clinical Medicine Aarhus University Aarhus Denmark
Department of Clinical Medicine University of Copenhagen Copenhagen Denmark
Department of Internal Medicine University of Turku Turku Finland
Department of Public Health University of Copenhagen Copenhagen Denmark
Department of Rheumatology 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Rheumatology and DANBIO Aarhus University Hospital Aarhus Denmark
Department of Rheumatology Division of Medicine Turku University Central Hospital Turku Finland
Department of Rheumatology East Tallinn Central Hospital Tallinn Estonia
Department of Rheumatology Geneva University Hospitals Geneva Switzerland
Department of Rheumatology University Hospital Zurich University of Zurich Zürich Switzerland
Departments of Medicine and Rheumatology Helsinki University Central Hospital Helsinki Finland
Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark
Faculty of Medicine University of Iceland Reykjavík Iceland
Institute of Rheumatology Prague Czech Republic
Instituto Português de Reumatologia Lisbon Portugal
Landspitali University Hospital Reykjavík Iceland
Research Unit Sørlandet Sykehus HF Kristiansand Norway
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