Impact of the β1-adrenoceptor Arg389Gly polymorphism on heart-rate responses to bisoprolol and carvedilol in heart-failure patients.

Link:
Autor/in:
Erscheinungsjahr:
2012
Medientyp:
Text
Schlagworte:
  • Humans
  • Male
  • Aged
  • Female
  • Treatment Outcome
  • Double-Blind Method
  • Polymorphism, Single Nucleotide
  • Dose-Response Relationship, Drug
  • Adrenergic beta-1 Receptor Antagonists/administration & dosage/pharmacokinetics
  • *Atrial Fibrillation/complications/drug therapy/genetics
  • *Bisoprolol/administration & dosage/pharmacokinetics
  • *Carbazoles/administration & dosage/pharmacokinetics
  • *Heart Failure/complications/drug therapy/genetics
  • *Heart Rate/drug effects/genetics
  • *Propanolamines/administration & dosage/pharmacokinetics
  • Receptors, Adrenergic, beta-1/*genetics
  • Humans
  • Male
  • Aged
  • Female
  • Treatment Outcome
  • Double-Blind Method
  • Polymorphism, Single Nucleotide
  • Dose-Response Relationship, Drug
  • Adrenergic beta-1 Receptor Antagonists/administration & dosage/pharmacokinetics
  • *Atrial Fibrillation/complications/drug therapy/genetics
  • *Bisoprolol/administration & dosage/pharmacokinetics
  • *Carbazoles/administration & dosage/pharmacokinetics
  • *Heart Failure/complications/drug therapy/genetics
  • *Heart Rate/drug effects/genetics
  • *Propanolamines/administration & dosage/pharmacokinetics
  • Receptors, Adrenergic, beta-1/*genetics
Beschreibung:
  • This pharmacogenetic substudy of the prospective, double-blind, randomized CIBIS-ELD trial determined the impact of the ?1-adrenoceptor Arg189Gly polymorphism on heart-rate responses to bisoprolol or carvedilol in elderly patients with heart failure (421 with sinus rhythm, 107 with atrial fibrillation). Patients were randomized 1:1 to bisoprolol or carvedilol with a fortnightly dose-doubling scheme and guideline target doses. Patients with sinus rhythm responded essentially identically to bisoprolol and carvedilol, independent of genotype. Atrial fibrillation patients homozygous for Arg389 had a much smaller response to carvedilol than carriers of at least one Gly389 allele (mean difference 12 bpm, P < 0.00001). Carvedilol up to 2 × 12.5 mg did not reduce heart rate in Arg389Arg homozygotes at all. Interestingly, the immediate response to carvedilol did not differ between genotypes. The Arg389Gly polymorphism has a major impact on the heart-rate response to carvedilol (but not bisoprolol) in patients with heart failure plus atrial fibrillation.
  • This pharmacogenetic substudy of the prospective, double-blind, randomized CIBIS-ELD trial determined the impact of the ?1-adrenoceptor Arg189Gly polymorphism on heart-rate responses to bisoprolol or carvedilol in elderly patients with heart failure (421 with sinus rhythm, 107 with atrial fibrillation). Patients were randomized 1:1 to bisoprolol or carvedilol with a fortnightly dose-doubling scheme and guideline target doses. Patients with sinus rhythm responded essentially identically to bisoprolol and carvedilol, independent of genotype. Atrial fibrillation patients homozygous for Arg389 had a much smaller response to carvedilol than carriers of at least one Gly389 allele (mean difference 12 bpm, P < 0.00001). Carvedilol up to 2 × 12.5 mg did not reduce heart rate in Arg389Arg homozygotes at all. Interestingly, the immediate response to carvedilol did not differ between genotypes. The Arg389Gly polymorphism has a major impact on the heart-rate response to carvedilol (but not bisoprolol) in patients with heart failure plus atrial fibrillation.
Lizenz:
  • info:eu-repo/semantics/restrictedAccess
Quellsystem:
Forschungsinformationssystem des UKE

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