Clinical and preclinical pulmonary disease in newly diagnosed rheumatoid arthritis: a two-year follow-up study.


Journal

Scandinavian journal of rheumatology
ISSN: 1502-7732
Titre abrégé: Scand J Rheumatol
Pays: England
ID NLM: 0321213

Informations de publication

Date de publication:
11 2023
Historique:
medline: 17 11 2023
pubmed: 18 4 2023
entrez: 17 4 2023
Statut: ppublish

Résumé

Pulmonary disease is a major cause of excess mortality among patients with rheumatoid arthritis (RA). Interstitial lung disease (ILD) is a feared complication, but the benefit of screening is unknown. The aim of this study was to assess the frequency of pulmonary disease, including ILD, in early RA. Patients with newly diagnosed RA were recruited prospectively at a single centre and underwent systematic pulmonary function tests (PFTs) and computed tomography (CT) scans at inclusion and after two years. The study included 150 patients (mean age 57 years, 63% female; 59% current or former smokers). Of these, 136 underwent baseline PFTs and 137 CT. Mean forced expiratory volume in one second was 99% predicted and forced vital capacity 106%. Mean diffusing capacity of the lungs for carbon monoxide (DL Emphysema and bronchiectasis were common, but most patients had mild disease with preserved lung function. Preclinical or clinical ILD was seen in a minority in this early phase of RA. These findings suggest symptom-based screening and primary intervention focusing on smoking cessation rather than screening for ILD at the time of RA diagnosis.

Identifiants

pubmed: 37066633
doi: 10.1080/03009742.2023.2194105
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

601-608

Auteurs

C Hyldgaard (C)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.

S Harders (S)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.
Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

J Blegvad (J)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.

M Herly (M)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.
Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

D Masic (D)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.
Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

B K Sofíudóttir (BK)

Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

G Urbonaviciene (G)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.

F D Andersen (FD)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.

C Isaksen (C)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.

B Løgstrup (B)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.
Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

T Ellingsen (T)

Diagnostic Center, Silkeborg Regional Hospital, University Clinic for Innovative Patient Pathways, Aarhus University, Silkeborg, Denmark.
Rheumatology Research Unit, Odense University Hospital and University of Southern Denmark, Odense, Denmark.

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Classifications MeSH