bioRxivPathologyPreprint
Characterization of Gait Kinematics and Muscle Function in Becker Muscular Dystrophy Pigs: a pilot study
Aaron B. MortoniD, Jacob A. KendraiD, Shadi GolpasandiiD, Macie L. Mackey, Haley Russell, Connor Hendrie, Kuanting CheniD, Zoë E KieferiD, Jennifer M. YentesiD, Jason W. RossiD, Joshua Taylor SelsbyiD, Nicolaas E.P. DeutziD, Peter P. NghiemiD
Abstract
Vertebrate animal models of Becker muscular dystrophy (BMD) have been developed. Here, we characterized the gait kinematics and muscle function of a naturally occurring BMD pig model of dystrophin insufficiency. BMD pigs tended to have alterations in hip range of motion (ROM): hip (67%, 95% CI -0.64 to 14.12 degrees). While parameters were unaltered in extensor muscles, the dystrophin levels in flexor tibiotarsal joint muscles correlated with fatigue index as well as reduced isometric force (48%, 95% CI -1.86 to -0.61 N-m), and a 33% increase in fatigue index (95% CI -36.25 to 96.71 percent); the extensor muscles had no observable reductions in muscle force, with a 48% increase in fatigue index (95% CI -232.6 to 472.6 percent). Histological analysis of muscle biopsies supported a BMD phenotype in the flexor muscles of BMD pigs, with a 75% (95% CI -55.14 to -15.66 percent) decrease in large and a 43% (95% CI 17.74 to 57.38 percent) increase in small muscle fiber cross-sectional area. Dystrophin protein abundance was 28% less in flexor muscles from BMD pigs (95% CI -49.63 to 11.41 arbitrary units). Together, our model may serve as a clinically relevant model of BMD to assess safety and efficacy of therapeutics.
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