Absence of Cardiac Benefit with Early Combination ACE Inhibitor and Beta Blocker Treatment in mdx Mice

A Blain, E Greally, SH Laval, AM Blamire… - Journal of …, 2015 - Springer
A Blain, E Greally, SH Laval, AM Blamire, GA MacGowan, VW Straub
Journal of cardiovascular translational research, 2015Springer
Most patients with Duchenne muscular dystrophy (DMD) will develop cardiomyopathy;
however, the evidence for prophylactic treatment of children with cardiac medications is
limited. We have used the mdx mouse model of DMD to assess if early combination
treatment with beta blocker (BB) and ACE inhibitor (AI) is superior to single treatment with
either one of these drugs. Mice were assessed with cardiac MRI (ventricular structure and
function, in vivo calcium influx (manganese-enhanced MRI)), pressure–volume loops, and …
Abstract
Most patients with Duchenne muscular dystrophy (DMD) will develop cardiomyopathy; however, the evidence for prophylactic treatment of children with cardiac medications is limited. We have used the mdx mouse model of DMD to assess if early combination treatment with beta blocker (BB) and ACE inhibitor (AI) is superior to single treatment with either one of these drugs. Mice were assessed with cardiac MRI (ventricular structure and function, in vivo calcium influx (manganese-enhanced MRI)), pressure–volume loops, and histopathology. Combination treatment did not show benefits over treatment with AI or BB alone. Indeed, some beneficial aspects of BB and AI were lost when used in combination. None of the treatments impacted RV function. Combination treatment had no significant effect on sarcolemmal damage or histopathology. The study suggests that combined BB and AI may not confer an advantage at an early stage in DMD cardiomyopathy. However, limitations of the mdx model should be considered.
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