Key result
Duchenne's muscular dystrophy in dogs is linked to increased Q/R ratios and hyperechoic myocardial lesions.
Observational (n=24)
The canine model of Duchenne's muscular dystrophy exhibits specific ECG and echocardiographic abnormalities, establishing it as a valid model for Duchenne's cardiomyopathy and demonstrating cardiac involvement in carrier dogs.
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Supports canine DMD model for cardiomyopathy research; leaves open translation to human therapies.
Thirteen dogs affected with X-linked Duchenne's muscular dystrophy and 11 female carrier dogs were studied by electrocardiography (ECG) and echocardiography. Twelve of the affected dogs were studied as immature animals and followed at 1 to 6 month intervals until they were 7 to 46 months of age. Compared with control dogs, affected dogs had significantly increased (p less than 0.02) Q/R ratios in ECG leads II, III, aVF, CV6LL (V2) and CV6LU (V4). Carrier dogs had significantly increased (p less than 0.02) Q/R ratios in leads V2 and V4. The Q/R ratio increased in three of six dogs followed up from age 6 months to greater than 2 years. The PR intervals were significantly shorter (p less than 0.02) in affected dogs. Ventricular arrhythmias were identified in four of six mature affected dogs. Two-dimensional echocardiography revealed distinctive hyperechoic lesions in 12 of the 13 affected dogs and in 6 of the 11 carrier dogs. Hyperechoic lesions corresponded to calcified myocardium and surrounding dense connective tissue. This study establishes the dog affected with Duchenne's muscular dystrophy as an animal model of Duchenne's cardiomyopathy and demonstrates that the heart in carrier dogs is affected by the dystrophic process.
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Möise et al. (1991) conducted an observational in X-linked Duchenne's muscular dystrophy (n=24). X-linked Duchenne's muscular dystrophy vs. Control dogs was evaluated on Q/R ratios in ECG leads (p=<0.02). Dogs affected with Duchenne's muscular dystrophy and female carriers exhibited significantly increased Q/R ratios (p<0.02) and distinctive myocardial hyperechoic lesions compared to controls.
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