Title: Sarcopenia assessed by DXA and hand-grip dynamometer: a potential marker of damage, disability and myokines imbalance in inflammatory myopathies.

antisynthetase syndrome body composition dermatomyositis inclusion body myositis inflammatory myopathies myokines myositis damage polymyositis sarcopenia scleromyositis

Journal

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

Informations de publication

Date de publication:
27 Mar 2024
Historique:
received: 04 08 2023
revised: 23 01 2024
accepted: 22 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: aheadofprint

Résumé

To assess the ability of dual-energy X-ray absorptiometry (DXA) and hand-grip dynamometer to measure damage in inflammatory myopathies (IM). . Forty adult IM patients with a disease duration ≥12 months, low or no disease activity for ≥6 months, were prospectively enrolled. Thirty healthy age and sex-matched volunteers were enrolled as controls. Whole-body DXA and hand-grip dynamometer were used to measure muscle mass, grip strength and diagnose sarcopenia (EWGSOP2 criteria). Relationships between the results of strength in 12 muscles, functional tests, patient-reported disability, IMACS damage score, and history of the disease were assessed. The serum levels of potential molecular actors of the damage were measured. DXA and grip strength measurements took ≤20 min. Both muscle mass and grip strength were decreased in IM patients vs volunteers (-10% and -30% respectively) with a dispersion that varied widely (IQR -24.3% to + 7.8% and -51.3% to -18.9% respectively). Muscle mass and grip strength were non-redundantly correlated (r up to 0.6, p= 0.0001) with strength in 14 muscles (manual muscle test and hand-held dynamometer), functions (of limbs, respiratory and deglutition muscles), patient-reported disability, damage (extension and severity in muscular and extra-muscular domains), and blood-levels of several myokines. Seven IM patients (17.5%) were sarcopenic. They had the worst damage, functions impairment, disability and history of severe myopathy. Decreased irisin and osteonectin levels were associated with sarcopenia (AUC 0.71 and 0.80, respectively). DXA and hand-grip dynamometer are useful tools to assess damage in IM. Irisin and osteonectin may play a role in IM damage pathogenesis.

Identifiants

pubmed: 38544289
pii: 7636484
doi: 10.1093/rheumatology/keae207
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. 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

Margherita Giannini (M)

Physiologie et explorations fonctionnelles musculaires, University hospital of Strasbourg, France.
UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.
Centre de Référence des Maladies Auto-immunes Systémiques Rares, University hospital of Strasbourg, France.

Anne-Laure Charles (AL)

UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.

Charles Evrard (C)

Physiologie et explorations fonctionnelles, University hospital of Strasbourg, France.

Julien Blaess (J)

Physiologie et explorations fonctionnelles musculaires, University hospital of Strasbourg, France.
Centre de Référence des Maladies Auto-immunes Systémiques Rares, University hospital of Strasbourg, France.

Maude Bouchard-Marmen (M)

Service de Rhumatologie, University hospital of Québec, University Laval, Québec, Canada.

Léa Debrut (L)

UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), University of Strasbourg, INSERM U1258, CNRS UMR 7104, Illkirch, 67404, France.

Simone Perniola (S)

Clinical Immunology Unit, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Roma, 00168, Italy.

Gilles Laverny (G)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), University of Strasbourg, INSERM U1258, CNRS UMR 7104, Illkirch, 67404, France.
Service de Rhumatologie, University hospital of Strasbourg, France.

Rose-Marie Javier (RM)

Centre de Référence des Maladies Auto-immunes Systémiques Rares, University hospital of Strasbourg, France.
Service de Rhumatologie, University hospital of Strasbourg, France.

Anne Charloux (A)

UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.
Physiologie et explorations fonctionnelles, University hospital of Strasbourg, France.

Bernard Geny (B)

UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.
Physiologie et explorations fonctionnelles, University hospital of Strasbourg, France.

Alain Meyer (A)

Physiologie et explorations fonctionnelles musculaires, University hospital of Strasbourg, France.
UR3072 "mitochondrie, stress oxydant et protection musculaire", Centre de Recherche en Biomédecine, University of Strasbourg, France.
Centre de Référence des Maladies Auto-immunes Systémiques Rares, University hospital of Strasbourg, France.
Service de Rhumatologie, University hospital of Strasbourg, France.

Classifications MeSH