Comparing DAPSA, DAPSA28, and DAS28-CRP in Patients With Psoriatic Arthritis Initiating a First Tumor Necrosis Factor Inhibitor Across Nine European Countries.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
26 Jun 2024
Historique:
revised: 05 06 2024
received: 21 02 2024
accepted: 07 06 2024
pubmed: 27 6 2024
medline: 27 6 2024
entrez: 26 6 2024
Statut: aheadofprint

Résumé

Because 66/68 joint counts are not always performed in routine care, we aimed to determine which of the modified 28-joint disease activity index for psoriatic arthritis (DAPSA28) or 28-joint disease activity score with C-reactive protein (DAS28-CRP) should be preferred for monitoring disease activity in psoriatic arthritis (PsA) when the original DAPSA (66/68 joints) is not available. Prospectively collected real-world data of European bionaive patients with PsA initiating a first tumor necrosis factor inhibitor were pooled. Remission and response status were evaluated at 6 months by remission (DAPSA ≤ 4, DAPSA28 ≤ 4, and DAS28-CRP < 2.6), response (75% improvement for DAPSA and DAPSA28), and combined EULAR good/moderate responses for DAS28-CRP. Logistic regression analyses on multiple imputed data were used to identify baseline predictors. Remission and response cohorts included 3,159 and 1,866 patients, respectively. The 6-month proportions achieving remission/response were DAPSA (27%/44%), DAPSA28 (28%/44%), and DAS28-CRP (59%/80%). Of 14 possible baseline predictors, 11 predicted both DAPSA and DAPSA28 remission (8 of which also predicted their response, indicated by "*"): longer disease duration*, male sex*, and higher CRP* were positive, whereas older age*, higher body mass index*, patient fatigue*, and global, physician global, health assessment questionnaire score*, and tender and swollen* joint counts were negative predictors. Eight and five of these predicted DAS28-CRP remission and response, respectively. In patients with PsA, DAPSA28 should be preferred over DAS28-CRP as a substitute for DAPSA when 66/68 joint counts are not available because of the large overlap in remission and response status and in predictors between DAPSA and DAPSA28.

Identifiants

pubmed: 38926900
doi: 10.1002/acr.25396
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Novartis Pharma AG and IQVIA

Informations de copyright

© 2024 The Author(s). Arthritis Care & Research published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

Références

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Auteurs

Louise Linde (L)

Rigshospitalet, Glostrup, Denmark.

Stylianos Georgiadis (S)

Rigshospitalet, Glostrup, Denmark.

Lykke M Ørnbjerg (LM)

Rigshospitalet, Glostrup, Denmark.

Simon H Rasmussen (SH)

Rigshospitalet, Glostrup, Denmark.

Brigitte Michelsen (B)

Rigshospitalet, Glostrup, Denmark, Diakonhjemmet Hospital, Oslo, Norway, and Sørlandet Sykehus HF, Kristiansand, Norway.

Johan Askling (J)

Karolinksa Institutet, Stockholm, Sweden.

Daniela Di Giuseppe (D)

Karolinksa Institutet, Stockholm, Sweden.

Johan K Wallman (JK)

Skåne University Hospital, Lund, Sweden.

Jakub Závada (J)

Institute of Rheumatology and Charles University First Faculty of Medicine, Prague, the Czech Republic.

Karel Pavelka (K)

Institute of Rheumatology and Charles University First Faculty of Medicine, Prague, the Czech Republic.

Miguel Bernardes (M)

University of Porto and Centro Hospitalar Universitário de São João, Porto, Portugal.

Carolina O Matos (CO)

Hospital de Santa Maria and Centro Academico de Medicina de Lisboa, Lisbon, Portugal.

Bente Glintborg (B)

The DANBIO Registry, Glostrup, Denmark, and University of Copenhagen, Copenhagen, Denmark.

Anne Gitte Loft (AG)

Aarhus University Hospital and Aarhus Universitet, Aarhus, Denmark.

Dan Nordström (D)

Helsinki University Central Hospital, Helsinki, Finland.

Laura Kuusalo (L)

University of Turku and Turku University Hospital, Turku, Finland.

Burkhard Möller (B)

Inselspital University Hospital Bern, Bern, Switzerland.

Michael J Nissen (MJ)

Geneva University Hospitals, Geneva, Switzerland.

Catalin Codreanu (C)

University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

Corina Mogosan (C)

University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

Bjorn Gudbjornsson (B)

Landspitali National University Hospital of Iceland and University of Iceland, Reykjavik, Iceland.

Thorvardur Jon Love (TJ)

Landspitali National University Hospital of Iceland and University of Iceland, Reykjavik, Iceland.

Cansu Akleylek (C)

TC Demiroglu Bilim University, Istanbul, Turkey.

Florenzo Iannone (F)

University of Bari, Bari, Italy.

Tore K Kvien (TK)

Diakonhjemmet Hospital, Oslo, Norway.

Ziga Rotar (Z)

University Medical Centre Ljubljana and University of Ljubljana, Ljubljana, Slovenia.

Isabel Castrejon (I)

General University Hospital Gregorio Maranon and Complutense University of Madrid, Madrid, Spain.

Gary J Macfarlane (GJ)

University of Aberdeen, Aberdeen, Scotland.

Merete L Hetland (ML)

Rigshospitalet, Glostrup, Denmark, and University of Copenhagen, Copenhagen, Denmark.

Mikkel Østergaard (M)

Rigshospitalet, Glostrup, Denmark, and University of Copenhagen, Copenhagen, Denmark.

Classifications MeSH