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Rheumatoid Arthritis

Muscle stiffness in rheumatoid arthritis is not altered or associated with muscle weakness: A shear wave elastography study

ORCID Icon, , , &
Pages 617-625 | Received 15 May 2019, Accepted 12 Jul 2019, Published online: 01 Aug 2019
 

Abstract

Objectives: To investigate muscle stiffness and strength in rheumatoid arthritis patients compared to healthy controls.

Methods: A sample of 80 RA patients from three discrete groups: 1 – newly diagnosed treatment-naïve RA (n = 29), 2 – active RA for at least 1 year (n = 18) and 3 – in remission RA for at least 1 year (n = 33), was compared to 40 healthy controls. Shear wave velocity (SWV) was measured using shear wave elastography as a surrogate for tissue stiffness in multiple muscles. All participants performed isometric grip strength, timed get-up-and-go test, 30-s chair stand test and isokinetic knee extension/flexion (60°/s). The difference in SWV amongst the groups was tested using one-way ANOVA, and the correlation between SWV and muscle strength results were calculated using Pearson’s coefficients.

Results: The mean age ± SD was 61.2 ± 12.8 for RA patients and 61.5 ± 10.5 years for controls. SWV was not significantly different amongst the groups on all muscles (p > .05). In comparison to controls, the new and active RA groups showed a significantly lower isokinetic strength by –29% (p = .013) and –28% (p = .040), fewer chair stands by –28% (p = .001) and –44% (p < .001), longer walking times by –25% (p = .025) and –30% (p = .001), respectively, and weaker grip strength by –45% for both (p < .001). The muscle strength in the remission RA groups was not significantly lower, except in the isokinetic knee strength (–21%; p = .027). The correlations between SWE and the muscle assessment results were weak and insignificant (r < 0.30; p > .05).

Conclusion: Significant muscle weakness was demonstrated in patients with RA disease. However, muscle stiffness was normal and not associated with muscle strength.

Conflict of interest

None.

Additional information

Funding

The research is supported by the National Institute for Health Research (NIHR) Leeds Biomedical Research Centre.

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