What does this research mean for the field?

The Arg16 polymorphism of the beta2-adrenergic receptor is associated with enhanced agonist-mediated vascular desensitization, whereas the Glu27 polymorphism is associated with increased agonist-mediated responsiveness. Novelty: ClaimNovelty.NOVEL_FINDING. Consensus alignment: ConsensusAlignment.NEUTRAL.

October 4, 2001

The Effect of Common Polymorphisms of the β2-Adrenergic Receptor on Agonist-Mediated Vascular Desensitization

Structured PICO

Do common polymorphisms of the beta2-adrenergic receptor affect agonist-mediated vascular desensitization in healthy subjects?

Population

26 healthy subjects selected to represent three genotypes of the beta2-adrenergic receptor (7 homozygous for Arg16 and Gln27, 8 homozygous for Gly16 and Gln27, and 11 homozygous for Gly16 and Glu27)

Intervention

Isoproterenol infusion (dose-response curve 4 to 480 ng per minute, followed by a 2-hour continuous infusion to induce desensitization)

Comparator

Comparison between different beta2-adrenergic receptor genotypes (Arg16 vs. Gly16, and Glu27 vs. Gln27)

Outcome

Agonist-mediated vasodilatation and desensitization assessed by measuring changes in the diameter of a dorsal hand vein at 30, 60, 90, and 120 minutes after the start of the infusionsurrogate

The Arg16 polymorphism of the beta2-adrenergic receptor is associated with enhanced agonist-mediated vascular desensitization, while the Glu27 polymorphism is associated with increased responsiveness.

Abstract

BACKGROUND: With continuous exposure to beta2-adrenergic agonists, vascular tissue becomes desensitized to agonist-mediated vasodilatation. We studied the effects of two common polymorphisms of the beta2-adrenergic receptor, one at codon 16 and one at codon 27, on agonist-mediated vasodilatation and desensitization in the vascular bed. METHODS: We studied 26 healthy subjects who were selected to represent three genotypes: 7 were homozygous for the alleles encoding Arg16 and Gln27, 8 were homozygous for the alleles encoding Gly16 and Gln27, and 11 were homozygous for the alleles encoding Gly16 and Glu27. Vascular responses were assessed by measuring changes in the diameter of a dorsal hand vein. A dose-response curve of the effect of the beta2-adrenergic-receptor agonist isoproterenol was constructed (dose range, 4 to 480 ng per minute). Desensitization was then induced by a 2-hour continuous infusion of isoproterenol, and venodilatation was measured 30, 60, 90, and 120 minutes after the start of the infusion. RESULTS: Subjects who were homozygous for Arg16 had almost complete desensitization; venodilatation in response to isoproterenol in this group decreased from a mean (+/-SE) of 44+/-11 percent to 8+/-4 percent (P=0.006). In contrast, subjects who were homozygous for Gly16 did not have significant desensitization, irrespective of the amino acid encoded by codon 27. Subjects who were homozygous for Glu27 had higher maximal venodilatation in response to isoproterenol than those who were homozygous for Gln27 (86+/-13 percent vs. 54+/-8 percent, P=0.03). CONCLUSIONS: The Arg16 polymorphism of the beta2-adrenergic receptor is associated with enhanced agonist-mediated desensitization in the vasculature, and the Glu27 polymorphism is associated with increased agonist-mediated responsiveness. Therefore, polymorphisms of the beta2-adrenergic receptor are potentially important determinants of the vascular response to stress.

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