Muscle contractility of leg muscles in patients with mitochondrial myopathies

Nanna Scharff Poulsen*, Julia Rebecka Dahlqvist, Gitte Hedermann, Nicoline Løkken, John Vissing

*Corresponding author for this work
2 Citations (Scopus)

Abstract

Background: The primary disease mechanism underlying mitochondrial myopathies (MM) is impaired energy generation to support muscle endurance. Little is known about muscle contractility before energy becomes deficient during muscle contractions. We investigated muscle contractility in MM to uncover potentially fixed weakness aspects of the disorders. Methods: Contractility of calf and thigh muscles was investigated by comparing strength with contractile cross-sectional area (CCSA) of the used muscles, as measured by stationary dynamometry and MRI, respectively. Results and discussion: Our findings suggest reduced contractile properties in thigh and calf muscles of patients with MM.

Original languageEnglish
JournalMitochondrion
Volume46
Pages (from-to)221-227
ISSN1567-7249
DOIs
Publication statusPublished - May 2019

Fingerprint

Dive into the research topics of 'Muscle contractility of leg muscles in patients with mitochondrial myopathies'. Together they form a unique fingerprint.

Cite this