Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD).
Pradeep HarishAlberto MalerbaNgoc Lu-NguyenLeysa ForrestOrnella CappellariFanny RothCapucine TrolletLinda PopplewellGeorge DicksonPublished in: Journal of cachexia, sarcopenia and muscle (2019)
Our study supports the clinical translation of such antibody-mediated inhibition of myostatin as a treatment of OPMD. This strategy has implications to be used as adjuvant therapies with gene therapy based approaches, or to stabilize the muscle prior to myoblast transplantation.