The longitudinal study of muscle changes with ultrasound: Differential changes in idiopathic inflammatory myopathy subgroups.

Myositis idiopathic inflammatory myopathies muscle power Doppler shear wave elastography ultrasound

Journal

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

Informations de publication

Date de publication:
24 May 2023
Historique:
received: 23 02 2023
revised: 21 04 2023
accepted: 13 05 2023
medline: 25 5 2023
pubmed: 25 5 2023
entrez: 24 5 2023
Statut: aheadofprint

Résumé

We investigated shear wave elastography (SWE), B mode ultrasound (US) and power Doppler (PD) as imaging biomarkers for longitudinal follow-up in idiopathic inflammatory myopathy (IIM), with a particular focus on immune-mediated necrotising myopathy (IMNM) and dermatomyositis (DM). Participants had serial SWE, US and PD on the deltoid (D) and vastus lateralis (VL) muscles on four occasions at intervals of 3-6 months. Clinical assessments included manual muscle testing, and patient and physician reported outcome scales. Thirty three participants were included: IMNM= 17, DM = 12, overlap myositis= 3, polymyositis =1. Twenty were in a prevalent clinic group, and 13 were recently treated cases in an incident group. Differential changes in SWS and US domains occurred with time in both the prevalent and incident groups. In VL-prevalent, echogenicity increased over time (p = 0.040), while in incident cases there was a trend of reduction to normal over time (p = 0.097) with treatment. Muscle bulk reduced in D-prevalent group (p = 0.096) over time, suggesting atrophy. SWS also reduced in the VL-incident (p = 0.096) group over time, suggesting a trend towards improvement in muscle stiffness with treatment. SWE and US appear promising as imaging biomarkers for patient follow-up in IIM and indicate changes over time, especially with echogenicity, muscle bulk and SWS in the VL. Due to the limitations of participant numbers, additional studies with a larger cohort will help to evaluate these US domains further and outline specific characteristics within the IIM subgroups.

Identifiants

pubmed: 37225404
pii: 7177985
doi: 10.1093/rheumatology/kead239
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. 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

Shereen Paramalingam (S)

University of Notre Dame Australia, Fremantle, Western Australia, Australia.
Department of Rheumatology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Merrilee Needham (M)

University of Notre Dame Australia, Fremantle, Western Australia, Australia.
Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia.
Department of Neurology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Max Bulsara (M)

Institute for Health Research, Notre Dame Australia, Fremantle, Western Australia, Australia.

Frank L Mastaglia (FL)

Perron Institute for Neurological and Translational Science, University of Western Australia, Australia.

Helen I Keen (HI)

Department of Rheumatology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
School of Medicine, University of Western Australia, Australia.

Classifications MeSH