The value of ultrasound-defined tenosynovitis and synovitis in the prediction of persistent arthritis.


Journal

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

Informations de publication

Date de publication:
01 03 2023
Historique:
received: 18 12 2021
revised: 21 03 2022
pubmed: 13 4 2022
medline: 4 3 2023
entrez: 12 4 2022
Statut: ppublish

Résumé

The value of US-defined tenosynovitis in predicting the persistence of inflammatory arthritis is not well described. In particular, the predictive utility of US-defined tenosynovitis of larger tendons is yet to be reported. We assessed the value of US-defined tenosynovitis alongside US-defined synovitis and clinical and serological variables in predicting persistent arthritis in an inception cohort of DMARD-naïve patients with early arthritis. One hundred and fifty DMARD-naïve patients with clinically apparent synovitis of one or more joints and a symptom duration of ≤3 months underwent baseline clinical, laboratory and US (of 19 bilateral joints and 16 bilateral tendon compartments) assessments. Outcomes were classified as persistent or resolving arthritis after 18 months' follow-up. The predictive value of US-defined tenosynovitis for persistent arthritis was compared with those of US-defined synovitis, and clinical and serological variables. At 18 months, 99 patients (66%) had developed persistent arthritis and 51 patients (34%) had resolving disease. Multivariate logistic regression analysis showed that US-detected digit flexor tenosynovitis [odds ratio (OR): 6.6, 95% CI: 2.0 , 22.1, P = 0.002] provided independent predictive data for persistence over and above the presence of US-detected joint synovitis and RF antibodies. In the RF/ACPA-negative subcohort, US-defined digit flexor tenosynovitis remained a significant predictive variable (OR: 4.7, 95% CI: 1.4, 15.8, P = 0.012), even after adjusting for US-defined joint synovitis. US-defined tenosynovitis provided independent predictive data for the development of persistent arthritis. The predictive role of US-defined digit flexor tenosynovitis should be further assessed; investigators should consider including this tendon site as a candidate variable when designing imaging-based predictive algorithms for persistent inflammatory arthritis development.

Identifiants

pubmed: 35412605
pii: 6567346
doi: 10.1093/rheumatology/keac199
pmc: PMC9977123
doi:

Substances chimiques

Antirheumatic Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1057-1068

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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Auteurs

Ilfita Sahbudin (I)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust.

Ruchir Singh (R)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
Department of Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust.

Paola De Pablo (P)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
Department of Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust.

Elizabeth Rankin (E)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Benjamin Rhodes (B)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Elizabeth Justice (E)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Emma Derrett-Smith (E)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Nicole Amft (N)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Nehal Narayan (N)

Rheumatology Department, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

Catherine McGrath (C)

Department of Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust.

Sangeetha Baskar (S)

Department of Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust.

Jeanette Trickey (J)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust.

Mark Maybury (M)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust.

Karim Raza (K)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
Department of Rheumatology, Sandwell and West Birmingham Hospitals NHS Trust.

Andrew Filer (A)

Rheumatology Research Group, Institute of Inflammation and Ageing.
Research into Inflammatory Arthritis Centre, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, University of Birmingham.
NIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust.

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