Duchenne muscular dystrophy affects 1 in 3,500 boys, stealing their ability to walk by age 12 and typically killing them by their mid-20s. Doctors know what causes the muscle-wasting disease, but, frustratingly, experimental treatments consistently fail. University of Virginia researchers are out to change that, however, with the help of a $2.5 million grant from the National Institutes of Health.
Researchers at UVA’s School of Medicine and UVA’s School of Engineering and Applied Science will use the funding to build an astonishingly sophisticated computer model of the disease to unlock the mysteries that have undermined efforts to develop new treatments. The model will incorporate every aspect of the research process, from the lab mice in which experimental treatments often show promise to the children in which those treatments subsequently fail. By taking a holistic, “multi-scale” approach, the researchers intend to determine what’s going wrong and pave the way for breakthroughs that are both long-awaited and desperately needed.
Duchenne is caused by the lack of a key cellular protein, dystrophin. The UVA researchers suspect that the difference in response to treatments in mice and people is the result of differences in both biomechanics and inflammation.
By creating this new model, the researchers seek to:
- Better understand how muscle damage and inflammation drive the disease;
- Better understand the relationship between movement and inflammation;
- Explain why previous attempts at creating treatments have worked in mice but failed in people;
- Create better mouse models to replicate the disease; and
- Identify new drugs and treatments that will work in humans.
“This complex disease is absolutely devastating,” said researcher Silvia Blemker, PhD, a co-principal investigator of the effort. “We truly believe that multi-scale computer models can provide key insights that will unravel the complexities of this disease and ultimately lead to new treatments that will improve the quality of life for patients and families.”
The multi-year project will include everything from studying the effects of the disease at the microscopic level to using magnetic-resonance imaging (MRI) to examine the changes in muscle tissue over time. The researchers will start out by looking at the disease in mice, then create a computer simulation of that effect before simulating the effect of the disease in boys. Ultimately, they plan to conduct “virtual clinical trials” simulating the effect of Duchenne on human muscle tissue over the course of many years and examining the effects of potential new treatments.
The researchers plan to use open-source software for their model so they can make it available to scientists everywhere to speed development of new treatments and, hopefully, a cure.
A New Approach
While there have been tens of thousands of scientific papers published on Duchenne muscular dystrophy, very few have employed computational or mathematical modeling to get at the fundamental questions that remain unanswered. The researchers are optimistic that this new approach can shed light on the matter.
“This project is an exciting collaboration that uniquely merges computational modeling from very disparate domains,” said Shayn Peirce-Cottler, PhD, co-principal investigator. “Ultimately, the multi-scale modeling framework we will develop has broad applicability beyond muscular dystrophies to many other tissues and disease processes.”
The project goals are lofty, so the lead researchers have assembled a cross-disciplinary team of top scientists and doctors with expertise in everything from the disease itself to inflammation to biomechanical modeling and muscle physiology.