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ORIGINAL RESEARCH article
Front. Physiol.
Sec. Striated Muscle Physiology
Volume 16 - 2025 | doi: 10.3389/fphys.2025.1575689
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Background: Skeletal muscle disease in patients with early-stage rheumatoid arthritis (RA) is understudied. The objective of this study was to identify if patients with early RA (symptoms < 6 months) have impaired skeletal muscle health.Methods: Participants with early RA (n=10) and age-, sex-, and BMI-matched healthy controls (n=10) underwent cross-sectional clinical, physiological, and muscle biomechanical property assessments. Upper and lower extremity muscles underwent in vivo passive biomechanical property -tone, stiffness, and elasticity -assessments via myotonometry (MyotonPro®). In vitro muscle force production and stiffness were assessed using 3D bioengineered myobundles derived from myoblasts obtained from vastus lateralis muscle biopsies.Results: Despite similar muscle mass and self-reported physical activity behaviors for early RA patients and healthy controls, early RA patients had poorer self-reported physical function, selfreported physical health, and right-handed grip strength (p < 0.05 for all). Early RA muscle tone and stiffness was less than controls (p < 0.05) and with an inverse association with prednisone use (rho=-0.72, p=0.02). While 3D bioengineered myobundle force production and passive stiffness were similar to controls, early RA myobundle stiffness correlated with swollen joint counts (rho=-0.67, p=0.04).In this exploratory study, as compared to controls with similar muscle mass and physical activity, patients with early RA exhibited multiple skeletal muscle deficits across clinical, physiologic, and biomechanical domains. Use of skeletal muscle biomechanical assessments -both in vivo and in vitro -may be useful to identify these deficits to better understand and improve RA muscle health.
Keywords: Rheumatoid arthritis, skeletal muscle, physical function, Biomechanical properties, grip strength Position: Horizontal: Left, Relative to: Column, Vertical: 0", Relative to: Paragraph
Received: 12 Feb 2025; Accepted: 13 Mar 2025.
Copyright: © 2025 Andonian, Patel, Xu, Sudnick, Johnson, Kraus, Truskey and Huffman. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Brian J Andonian, School of Medicine, Duke University, Durham, United States
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
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