Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder affecting approximately 1 of 3,500newborn human males in which absence of the protein dystrophin causes progressive degeneration ofskeletal and cardiac muscle. Currently no treatment halts or reverses progression of DMD. Although cellularand gene therapies are promising, key questions must first be addressed in relevant animal models.Spontaneous forms of X-linked muscular dystrophy due to dystrophin deficiency have been identified inmice, multiple dog breeds, and cats. Unlike the dystrophin-deficient mdx mouse, which remains relativelynormal clinically, affected dogs develop progressive, fatal disease strikingly similar to the human condition.Accordingly, studies in the canine dystrophin deficient models, such as golden retriever muscular dystrophy(GRMD), are more likely than those in mdx mice to predict pathogenesis and outcome of treatment in DMD.Using FDA recommendations as a guiding principle, we have formulated a research initiative titled theNational Center for Canine Models of Duchenne Muscular Dystrophy (NCDMD). The overarching goal of theNCDMD is to develop and sustain dog models of DMD and expand country-wide collaborations withinvestigators pioneering translational research focused on the treatment of DMD. UNC is uniquely positionedto carry out this initiative having successfully developed a similar structure for the UNC hemophilic caninemodel. The emerging need for access to the GRMD and other DMD canine models is becoming imminent.Five therapeutic approaches detailed later in this summary are representative of the various approaches thathave shown promise in the mdx mouse and are now poised for further studies in canine models beforeentering clinical studies. Without the proposed NCDMD, it will be virtually impossible to meet the increasingdemand to utilize GRMD and other canine models of DMD in critical preclinical studies required for humanclinical trials. The NCDMD will also provide high quality facilities and services in compliance with GLPstandards to support pre-IND applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
1U24NS059696-01A1
Application #
7696322
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
2008-05-01
Project End
2013-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
1
Fiscal Year
2008
Total Cost
$991,633
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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Nghiem, Peter P; Hoffman, Eric P; Mittal, Priya et al. (2013) Sparing of the dystrophin-deficient cranial sartorius muscle is associated with classical and novel hypertrophy pathways in GRMD dogs. Am J Pathol 183:1411-24

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