Literature DB >> 30347435

Association between muscle strength, histopathology, and magnetic resonance imaging in sporadic inclusion body myositis.

Kathe Dahlbom1, Mats Geijer2,3, Anders Oldfors4, Christopher Lindberg5.   

Abstract

OBJECTIVES: Inclusion body myositis is characterized by inflammatory and degenerative changes, but the temporal relation of these events is unknown.
MATERIALS AND METHODS: In nineteen patients with inclusion body myositis, muscle strength was correlated with inflammatory and degenerative findings on magnetic resonance imaging (MRI) and in muscle biopsies in three different muscles (tibialis anterior, vastus lateralis, and biceps brachii). Muscle strength, measured with a handheld dynamometer, was described as percentage of muscle strength in age- and sex-matched normal individuals. The muscles were categorized as the strongest, the intermediate, and the weakest muscle in each individual. T1-weighted sequences on MRI were used to evaluate the degree of fatty infiltration and muscle atrophy and STIR sequences to evaluate edematous changes.
RESULTS: The vastus lateralis, which in general was the weakest muscle, was significantly more atrophic compared to the other two muscles and also demonstrated most edema. The biceps brachii had in most cases an intermediate degree of weakness and atrophy but the most pronounced inflammatory cell infiltration on biopsy. Cytochrome c oxidase-negative muscle fibers were significantly more prevalent in the vastus lateralis and biceps brachii muscles than in the tibialis anterior and thus correlated with muscular atrophy, indicating that this is a secondary change. Inflammatory changes as assessed by MRI and muscle biopsy were seen in all muscles irrespective of atrophy and thus appear to be prevalent at all stages of the disease.
CONCLUSIONS: Our study could not provide an answer to the question which comes first, the inflammation or the degenerative changes.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  inclusion body myositis; magnetic resonance imaging; morphology; muscle biopsy; muscle function

Mesh:

Year:  2018        PMID: 30347435     DOI: 10.1111/ane.13040

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  1 in total

1.  Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing.

Authors:  Carola Hedberg-Oldfors; Ulrika Lindgren; Swaraj Basu; Kittichate Visuttijai; Christopher Lindberg; Maria Falkenberg; Erik Larsson Lekholm; Anders Oldfors
Journal:  Brain Pathol       Date:  2021-05       Impact factor: 6.508

  1 in total

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