J. Alroy et al., Inherited infantile dilated cardiomyopathy in dogs: Genetic, clinical, biochemical, and morphologic findings, AM J MED G, 95(1), 2000, pp. 57-66
Dilated cardiomyopathy, a lethal disease characterized by left ventricular
dilation and systolic dysfunction, is relatively common in humans and other
mammals. Idiopathic dilated cardiomyopathy (IDCM) is a primary myocardial
disease of unknown cause and can be a familial disorder. This report descri
bes autosomal recessive IDCM in dogs. It occurs in Portuguese Water Dog (PW
D) pups and is manifested by acute, vague clinical signs and sudden death.
Affected pups have progressive reduction of fractional shortening that can
be demonstrated by echocardiography prior to the development of clinical si
gns. Furthermore, these pups have low plasma taurine levels when consuming
certain diets. Affected pups had dilation of the left ventricle and alterat
ions in the sarcomere appearance, while immunohistochemical and biochemical
studies demonstrate an increase in desmin, a cytoskeleton protein. The cli
nical and morphologic findings of IDCM: in PWDs are distinct from those rep
orted in adult IDCM. Finally, the clinical and echocardiographic manifestat
ions were reversible in some pups following oral taurine supplementation fo
r 2 months. These results suggest that IDCM in PWDs is correlated with low
plasma taurine levels. (C) 2000 Wiley-Liss, Inc.