Key result
In nonischemic cardiomyopathy patients on carvedilol, the Arg389Arg-beta1 receptor phenotype was associated with greater LVEF improvement than Gly389 carriers (18.8% vs 9.4% and 6.0%; P<0.001).
Why the study?
Does the Arg389Arg-beta1-adrenergic receptor polymorphism determine greater improvement in LVEF in patients with nonischemic cardiomyopathy treated with carvedilol?
Cohort (n=135)
Does the Arg389Arg-beta1-adrenergic receptor polymorphism determine greater improvement in LVEF in patients with nonischemic cardiomyopathy treated with carvedilol?
p-value: p=<0.001
The Arg389Arg-beta1-adrenergic receptor polymorphism is associated with a significantly greater improvement in LVEF in patients with nonischemic cardiomyopathy treated with carvedilol.
May support pharmacogenetic stratification for carvedilol response; leaves open prospective validation before clinical adoption.
OBJECTIVE: Administration of the beta-adrenergic receptor blocker carvedilol to patients with chronic heart failure leads to clinically significant benefits, including improvement in left ventricular systolic function in some, but not all, patients. We sought to determine the basis of the variable effect obtained with carvedilol in patients with heart failure. Carvedilol blocks both beta1-adrenergic and beta2-adrenergic receptors, and both receptors exist as polymorphisms. We aimed to determine whether these polymorphisms contribute to variability in response to carvedilol in patients with chronic heart failure. METHODS: We retrospectively and prospectively investigated 135 patients with nonischemic cardiomyopathy and chronic stable heart failure (New York Heart Association class II, III) treated with carvedilol. Baseline echocardiography was obtained before introduction of carvedilol and repeated after stabilization of a maximally tolerated dose of carvedilol (50-100 mg/day) for at least 1 year. Polymerase chain reaction and restriction fragment length polymorphism analysis were used to genotype beta1-adrenergic and beta2-adrenergic receptor polymorphisms. RESULTS: When grouped according to receptor polymorphisms patients were well matched for severity of heart failure, comorbidity and treatment. No significant difference was observed in baseline left ventricular ejection fraction (LVEF) between groups (P>0.05). After 1.5 years of treatment with carvedilol patients with Arg389Arg-beta1-adrenergic receptors had a significantly greater improvement in LVEF compared with Gly389 carriers (Arg389Arg 18.8%; Arg389Gly 9.4%; Gly389Gly 6.0%; P<0.001) whereas there were no differences attributable to other beta1-adrenergic and beta2-adrenergic receptor polymorphisms (P>0.05). CONCLUSION: In patients with nonischemic dilated cardiomyopathy, carvedilol leads to a significantly greater improvement in LVEF in patients with the Arg389Arg-beta1 adrenergic receptor phenotype.
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Meyers et al. (2007) conducted a cohort in nonischemic cardiomyopathy and chronic stable heart failure (n=135). Arg389Arg-beta1-adrenergic receptor phenotype vs. Gly389 carriers (Arg389Gly and Gly389Gly) was evaluated on improvement in left ventricular ejection fraction (LVEF) (p=<0.001). In nonischemic cardiomyopathy patients on carvedilol, the Arg389Arg-beta1 receptor phenotype was associated with greater LVEF improvement than Gly389 carriers (18.8% vs 9.4% and 6.0%; P<0.001).
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