Cardiorespiratory fitness in long-term juvenile dermatomyositis: a controlled, cross-sectional study of active/inactive disease.


Journal

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

Informations de publication

Date de publication:
01 03 2019
Historique:
received: 23 05 2018
accepted: 15 10 2018
pubmed: 7 12 2018
medline: 10 1 2020
entrez: 4 12 2018
Statut: ppublish

Résumé

To compare cardiorespiratory fitness (CRF) expressed as maximal oxygen uptake (VO2max) between patients with long-term JDM and controls and between patients with active and inactive disease, as well as to explore exercise limiting factors and associations between CRF and disease variables. JDM patients (n = 45) and age- and gender-matched controls (n = 45) performed a cardiopulmonary exercise test (CPET) on a treadmill until exhaustion. Physical activity was measured by accelerometers. Disease activity, damage and muscle strength/function were assessed by validated tools. Clinically inactive disease was defined according to PRINTO criteria. The mean disease duration was 20.8 (s.d. 11.9) years and 29/45 (64%) patients had inactive disease. A low VO2max was found in 27% of patients vs 4% of controls (P = 0.006). The mean VO2max and maximal ventilation (VEmax) were lower in patients with active and inactive disease compared with controls. Patients with active disease also had lower maximal voluntary ventilation (MVV) compared with controls and lower VEmax and MVV compared with those with inactive disease. Patients with inactive disease had lower physical activity levels compared with controls. VO2max correlated negatively with disease damage in patients with inactive disease and positively with muscle strength/function in patients with active disease. CRF was lower in JDM patients, both with active and inactive disease, compared with controls after a mean 20 years disease duration. Cardiopulmonary exercise test results suggested different limiting factors contributing to the reduced CRF according to disease activity, including deconditioning in inactive disease and reduced ventilatory capacity in active disease. Further research is needed to verify this.

Identifiants

pubmed: 30508195
pii: 5224787
doi: 10.1093/rheumatology/key342
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

492-501

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Kristin Schjander Berntsen (KS)

Department of Rheumatology, Oslo University Hospital, Rikshospitalet, Norway.

Elisabeth Edvardsen (E)

Department of Sports Medicine, Norwegian School of Sport Sciences, Oslo University Hospital, Ullevål, Norway.
Department of Pulmonary Medicine, Oslo University Hospital, Ullevål, Norway.

Bjørge Herman Hansen (BH)

Department of Sports Medicine, Norwegian School of Sport Sciences, Oslo University Hospital, Ullevål, Norway.

Berit Flatø (B)

Department of Rheumatology, Oslo University Hospital, Rikshospitalet, Norway.
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Norway.

Ivar Sjaastad (I)

Institute for Experimental Medical Research, Oslo University Hospital and University of Oslo, Norway.
Department of Cardiology, Oslo University Hospital, Ullevål, Norway.
K.G. Jebsen Center for Cardiac Research, University of Oslo, Oslo, Norway.

Helga Sanner (H)

Department of Rheumatology, Oslo University Hospital, Rikshospitalet, Norway.
Norwegian National Advisory Unit on Rheumatic Diseases in Children and Adolescents, Oslo University Hospital, Rikshospitalet, Norway.
Bjørknes University College, Oslo, Norway.

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