Differences in the response to TNF inhibitors at distinct joint locations in patients with psoriatic arthritis: results from nine European registries
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, pozorovací studie, multicentrická studie
PubMed
39891200
PubMed Central
PMC11783721
DOI
10.1186/s13075-025-03488-w
PII: 10.1186/s13075-025-03488-w
Knihovny.cz E-zdroje
- MeSH
- antirevmatika * terapeutické užití MeSH
- dospělí MeSH
- inhibitory TNF terapeutické užití MeSH
- kohortové studie MeSH
- lidé středního věku MeSH
- lidé MeSH
- psoriatická artritida * farmakoterapie MeSH
- registrace * MeSH
- senioři MeSH
- TNF-alfa antagonisté a inhibitory MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- Geografické názvy
- Evropa epidemiologie MeSH
- Názvy látek
- antirevmatika * MeSH
- inhibitory TNF MeSH
- TNF-alfa MeSH
BACKGROUND: Efficacy of tumour necrosis factor inhibitors (TNFi) for peripheral arthritis in patients with psoriatic arthritis (PsA) has been established in randomized clinical trials that have used improvement in summated joint counts as an outcome. Whether joints at different anatomical locations might respond differentially to TNFi remains unknown. The aim of the study was to investigate potential variations in the responsiveness to a first tumour necrosis factor inhibitor (TNFi) among joints at distinct locations in patients with psoriatic arthritis (PsA) treated in routine clinical care. METHODS: Bionaive PsA patients from nine European countries were included in this observational cohort study if ≥ 1 joint was swollen at the initiation of a first TNFi as monotherapy or added to methotrexate. Only the 28-joint count was available without imaging data confirming the presence of synovitis. The primary outcome was time to first resolution of joint swelling at each joint level. Hazard ratios (HR) for resolution comparing different joint locations were estimated using interval-censored mixed-effects Cox proportional hazards models, including a random effect for country and patient, adjusted for age and sex. RESULTS: A total of 1729 patients with 8397 swollen joints at the start of TNFi were included. Considering the upper extremity, a higher rate of resolution of joint swelling (HR, 95% CI) was observed for the shoulder (1.65, 1.16-2.35) and elbow (1.90, 1.38-2.61), while a lower rate was found for the wrist (0.72, 0.62-0.83) compared to the joints of digit 3. Within fingers, and using the same reference, joint swelling resolved fastest in digit 4 (1.77, 1.49-2.11) and digit 5 (1.88, 1.53-2.31). A lower rate of resolution of joint swelling was found for the knee in comparison to the elbow, the corresponding joint on the upper limb (0.56, 0.40-0.78). CONCLUSION: The time to resolution of joint swelling upon treatment with TNFi in patients with PsA seems to depend on the localisation of the affected joints.
Aberdeen Centre for Arthritis and Musculoskeletal Health University of Aberdeen Aberdeen UK
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 Reykjavik Iceland
Centro de Estudos de Doenças Cronicas NOVA Medical School Lisbon Portugal
DANBIO Registry Rigshospitalet Glostrup Denmark
Department of Clinical Medicine Aarhus University Aarhus Denmark
Department of Clinical Medicine University of Copenhagen Copenhagen Denmark
Department of Rheumatology 1st Faculty of Medicine Charles University Prague Czech Republic
Department of Rheumatology Aarhus University Hospital Aarhus Denmark
Department of Rheumatology and Immunology Inselspital University Hospital Bern Switzerland
Department of Rheumatology Centro Hospitalar Do Médio Tejo Torres Novas Portugal
Department of Rheumatology Geneva University Hospital Geneva Switzerland
Department of Rheumatology Hospital General Universitario Gregorio Marañón Madrid Spain
Department of Rheumatology Radboud University Medical Center Nijmegen the Netherlands
Department of Rheumatology University Medical Centre Ljubljana Ljubljana Slovenia
Faculty of Medicine and Health Technology Tampere University Tampere Finland
Faculty of Medicine Complutense University of Madrid Madrid Spain
Faculty of Medicine University of Iceland Reykjavik Iceland
Faculty of Medicine University of Ljubljana Ljubljana Slovenia
Research Unit Sørlandet Hospital Kristiansand Norway
Rheumatology Unit University of Modena and Reggio Emilia Modena Italy
Swiss Ankylosing Spondylitis Association Zurich Switzerland
Swiss Tropical and Public Health Institute Allschwil Switzerland
Tampere University Hospital Centre for Rheumatic Diseases Tampere Finland
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