Key result
A protocol was developed to evaluate muscle strength, dynamics, and fatigue in dystrophic pigs to monitor disease progression and assess therapeutic efficacy.
Why the study?
Accurate in vivo muscle function assessment is essential for monitoring disease progression and evaluating therapeutic interventions in porcine models of muscular dystrophies.
This paper presents a protocol for evaluating in vivo muscle function in dystrophic pigs to monitor disease progression and assess therapeutic efficacy.
Porcine models carrying DMD mutations recapitulate Duchenne and Becker muscular dystrophy (DMD and BMD), inherited disorders leading to progressive muscle weakness, with DMD presenting a far more severe and rapidly progressive phenotype. Accurate in vivo muscle function assessment is essential for monitoring disease progression and as an efficacy readout for therapeutic intervention. We present a protocol to evaluate muscle strength, dynamics, and fatigue in dystrophic pigs, including design setup, anesthesia, measurement, and data analysis. For complete details on the use and execution of this protocol, please refer to Blasi et al. 1
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Christov et al. (2026) studied Duchenne and Becker muscular dystrophy. In vivo muscle function assessment protocol was evaluated. A protocol was developed to evaluate muscle strength, dynamics, and fatigue in dystrophic pigs to monitor disease progression and assess therapeutic efficacy.
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