Researchers in the Department of Human Nutrition, Foods, and Exercise in the Virginia Tech College of Agriculture and Life Sciences were awarded a nearly $130,000 grant from the venture philanthropy organization SOLVE FSHD to research potential therapeutic avenues for facioscapulohumeral muscular dystrophy.
Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic neuromuscular disorder that progressively weakens and atrophies muscles. It takes its name from the areas of the body it typically affects: the facial muscles (facio-), shoulder blades (scapulo-), and upper arms (humeral). Although it affects a relatively small number of individuals, with an estimated prevalence of 1 in 8,000, it can profoundly impact those who have it and their families.
Professor Robert Grange, assistant department head of human nutrition, foods, and exercise and director of the Metabolism Core at Virginia Tech, is one of the investigators on the project. His research will center on assessing skeletal muscle torque as a functional outcome measure in a specialized mouse model of facioscapulohumeral muscular dystrophy. By focusing on this mouse model, Grange aims to unravel critical insights into the underlying mechanisms of the disorder and develop innovative strategies for intervention and treatment.
Grange will partner with Scott Harper, a distinguished researcher from Nationwide Children’s Hospital who developed the facioscapulohumeral muscular dystrophy mouse model used in the funded study. Their combined expertise in muscle biology and genetic disorders ensures a comprehensive approach to tackling the challenges posed by the disorder.
This research project was selected as one of four initiatives to receive funding from Solve FSHD’s recent Collaborative Grant award. Solve FSHD, a leading organization dedicated to accelerating FSHD research, awarded a total of $1.4 million toward projects embracing collaboration between institutions to catalyze and enhance novel potential therapeutics for FSHD.
