Influence of β2-adrenergic receptor genotype on airway function during exercise in healthy adults

Eric M. Snyder, Kenneth C. Beck, Niki M. Dietz, Michael Joseph Joyner, Stephen T Turner, Bruce David Johnson

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Background: In humans, β2-adrenergic receptors (β2ARs) influence airway tone. There are known functional polymorphisms of the β2AR, such as substitution of glycine for arginine at codon 16. We sought to determine if this variation in genotype differentially influences airway function during exercise. Methods: Healthy subjects without asthma who were either homozygous for Arg16 (n = 16; mean age, 29 ± 2 years [± SD]; mean maximum oxygen uptake [Vo2], 32 ±2 mL/kg/min) or the Gly16 allele (n = 26; mean age, 30 ± 1 years; mean maximum Vo2, 33 ± 1 mL/kg/min) participated in the study. Baseline testing included spirometry and maximal symptom-limited exercise. On a separate day, an arterial cannula was placed to measure catecholamine levels. Subjects then performed exercise at two work levels (40% and 75% of peak work) for 9 min each and performed spirometry at 3-min intervals for assessment of airway function. Results: There were no statistically significant differences between groups in maximum Vo2 or baseline spirometry (p > 0.05). With both light and heavy exercise, the groups had similar increases in the forced expiratory flow at 50% of vital capacity (FEF50). FEF50 increased by 14 ± 4% and 15 ± 3% in arginine and glycine groups, respectively, by end exercise (p > 0.05). During recovery (5 min and 10 min after), the Gly16 homozygotes demonstrated persistent bronchodilation (10 min after FEF50 = + 7 ± 2% over pre-exercise) while the Arg16 subjects had a rapid return to baseline (10 min after FEF50 = -3 ± 3%, p = 0.007 between groups). No differences were observed in the catecholamine responses between genotypes, although the increase in epinephrine in the arginine group tended to be higher (p = 0.07). Conclusions: These data suggest that the Arg16Gly polymorphism of the β2AR does not influence airway function during short-duration low- and high-intensity exercise. However, during recovery, the Arg16 genotype is associated with a reduced bronchodilation, possibly due to increased catecholamine desensitization.

Original languageEnglish (US)
Pages (from-to)762-770
Number of pages9
JournalChest
Volume129
Issue number3
DOIs
StatePublished - Mar 2006

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Adrenergic Receptors
Genotype
Exercise
Spirometry
Catecholamines
Arginine
Glycine
Vital Capacity
Homozygote
Codon
Epinephrine
Healthy Volunteers
Asthma
Alleles
Oxygen
Light

Keywords

  • Bronchodilation
  • Catecholamines
  • Genetic

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Cite this

Influence of β2-adrenergic receptor genotype on airway function during exercise in healthy adults. / Snyder, Eric M.; Beck, Kenneth C.; Dietz, Niki M.; Joyner, Michael Joseph; Turner, Stephen T; Johnson, Bruce David.

In: Chest, Vol. 129, No. 3, 03.2006, p. 762-770.

Research output: Contribution to journalArticle

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abstract = "Background: In humans, β2-adrenergic receptors (β2ARs) influence airway tone. There are known functional polymorphisms of the β2AR, such as substitution of glycine for arginine at codon 16. We sought to determine if this variation in genotype differentially influences airway function during exercise. Methods: Healthy subjects without asthma who were either homozygous for Arg16 (n = 16; mean age, 29 ± 2 years [± SD]; mean maximum oxygen uptake [Vo2], 32 ±2 mL/kg/min) or the Gly16 allele (n = 26; mean age, 30 ± 1 years; mean maximum Vo2, 33 ± 1 mL/kg/min) participated in the study. Baseline testing included spirometry and maximal symptom-limited exercise. On a separate day, an arterial cannula was placed to measure catecholamine levels. Subjects then performed exercise at two work levels (40{\%} and 75{\%} of peak work) for 9 min each and performed spirometry at 3-min intervals for assessment of airway function. Results: There were no statistically significant differences between groups in maximum Vo2 or baseline spirometry (p > 0.05). With both light and heavy exercise, the groups had similar increases in the forced expiratory flow at 50{\%} of vital capacity (FEF50). FEF50 increased by 14 ± 4{\%} and 15 ± 3{\%} in arginine and glycine groups, respectively, by end exercise (p > 0.05). During recovery (5 min and 10 min after), the Gly16 homozygotes demonstrated persistent bronchodilation (10 min after FEF50 = + 7 ± 2{\%} over pre-exercise) while the Arg16 subjects had a rapid return to baseline (10 min after FEF50 = -3 ± 3{\%}, p = 0.007 between groups). No differences were observed in the catecholamine responses between genotypes, although the increase in epinephrine in the arginine group tended to be higher (p = 0.07). Conclusions: These data suggest that the Arg16Gly polymorphism of the β2AR does not influence airway function during short-duration low- and high-intensity exercise. However, during recovery, the Arg16 genotype is associated with a reduced bronchodilation, possibly due to increased catecholamine desensitization.",
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AU - Dietz, Niki M.

AU - Joyner, Michael Joseph

AU - Turner, Stephen T

AU - Johnson, Bruce David

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N2 - Background: In humans, β2-adrenergic receptors (β2ARs) influence airway tone. There are known functional polymorphisms of the β2AR, such as substitution of glycine for arginine at codon 16. We sought to determine if this variation in genotype differentially influences airway function during exercise. Methods: Healthy subjects without asthma who were either homozygous for Arg16 (n = 16; mean age, 29 ± 2 years [± SD]; mean maximum oxygen uptake [Vo2], 32 ±2 mL/kg/min) or the Gly16 allele (n = 26; mean age, 30 ± 1 years; mean maximum Vo2, 33 ± 1 mL/kg/min) participated in the study. Baseline testing included spirometry and maximal symptom-limited exercise. On a separate day, an arterial cannula was placed to measure catecholamine levels. Subjects then performed exercise at two work levels (40% and 75% of peak work) for 9 min each and performed spirometry at 3-min intervals for assessment of airway function. Results: There were no statistically significant differences between groups in maximum Vo2 or baseline spirometry (p > 0.05). With both light and heavy exercise, the groups had similar increases in the forced expiratory flow at 50% of vital capacity (FEF50). FEF50 increased by 14 ± 4% and 15 ± 3% in arginine and glycine groups, respectively, by end exercise (p > 0.05). During recovery (5 min and 10 min after), the Gly16 homozygotes demonstrated persistent bronchodilation (10 min after FEF50 = + 7 ± 2% over pre-exercise) while the Arg16 subjects had a rapid return to baseline (10 min after FEF50 = -3 ± 3%, p = 0.007 between groups). No differences were observed in the catecholamine responses between genotypes, although the increase in epinephrine in the arginine group tended to be higher (p = 0.07). Conclusions: These data suggest that the Arg16Gly polymorphism of the β2AR does not influence airway function during short-duration low- and high-intensity exercise. However, during recovery, the Arg16 genotype is associated with a reduced bronchodilation, possibly due to increased catecholamine desensitization.

AB - Background: In humans, β2-adrenergic receptors (β2ARs) influence airway tone. There are known functional polymorphisms of the β2AR, such as substitution of glycine for arginine at codon 16. We sought to determine if this variation in genotype differentially influences airway function during exercise. Methods: Healthy subjects without asthma who were either homozygous for Arg16 (n = 16; mean age, 29 ± 2 years [± SD]; mean maximum oxygen uptake [Vo2], 32 ±2 mL/kg/min) or the Gly16 allele (n = 26; mean age, 30 ± 1 years; mean maximum Vo2, 33 ± 1 mL/kg/min) participated in the study. Baseline testing included spirometry and maximal symptom-limited exercise. On a separate day, an arterial cannula was placed to measure catecholamine levels. Subjects then performed exercise at two work levels (40% and 75% of peak work) for 9 min each and performed spirometry at 3-min intervals for assessment of airway function. Results: There were no statistically significant differences between groups in maximum Vo2 or baseline spirometry (p > 0.05). With both light and heavy exercise, the groups had similar increases in the forced expiratory flow at 50% of vital capacity (FEF50). FEF50 increased by 14 ± 4% and 15 ± 3% in arginine and glycine groups, respectively, by end exercise (p > 0.05). During recovery (5 min and 10 min after), the Gly16 homozygotes demonstrated persistent bronchodilation (10 min after FEF50 = + 7 ± 2% over pre-exercise) while the Arg16 subjects had a rapid return to baseline (10 min after FEF50 = -3 ± 3%, p = 0.007 between groups). No differences were observed in the catecholamine responses between genotypes, although the increase in epinephrine in the arginine group tended to be higher (p = 0.07). Conclusions: These data suggest that the Arg16Gly polymorphism of the β2AR does not influence airway function during short-duration low- and high-intensity exercise. However, during recovery, the Arg16 genotype is associated with a reduced bronchodilation, possibly due to increased catecholamine desensitization.

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