Abstract
AimsGenetic determinants of variability in response to β-blockers are poorly characterized. We defined changes in mRNA expression after a β-blocker to identify novel genes that could affect response and correlated these with inhibition of exercise-induced tachycardia, a measure of β-blocker sensitivity.MethodsNine subjects exercised before and after a single oral dose of 25mg atenolol and mRNA gene expression was measured using an Affymetrix GeneChip Human Gene 1.0 ST Array. The area under the heart rate-exercise intensity curve (AUC) was calculated for each subject; the difference between post- and pre-atenolol AUCs (Δ AUC), a measure of β-blocker response, was correlated with the fold-change in mRNA expression of the genes that changed more than 1.3-fold.ResultsFifty genes showed more than 1.3-fold increase in expression; 9 of these reached statistical significance (P < 0.05). Thirty-six genes had more than 1.3-fold decrease in expression after atenolol; 6 of these reached statistical significance (P < 0.05). Change in mRNA expression of FGFBP2 and Probeset ID 8118979 was significantly correlated with atenolol response (P = 0.03 and 0.02, respectively).ConclusionThe expression of several genes not previously identified as part of the adrenergic signaling pathway changed in response to a single oral dose of atenolol. Variation in these genes could contribute to unexplained differences in response to β-blockers.
Highlights
Beta-blockers are frequently prescribed to treat ischemic heart disease, heart failure, hypertension, and arrhythmias [1,2,3,4,5]
We studied the correlation between change in messenger RNA (mRNA) expression after atenolol administration and b-blocker sensitivity, assessed by attenuation of exercise-induced tachycardia [9]
There is no information about the effect of a b-blocker on mRNA expression, our finding that several genes are upregulated or downregulated are of interest
Summary
Beta-blockers are frequently prescribed to treat ischemic heart disease, heart failure, hypertension, and arrhythmias [1,2,3,4,5]. They block the effects of agonists acting on b-adrenergic receptors (ARs) and influence downstream signaling pathways. The relationship between variability in ADRB1 and other candidate genes and variability in response to b-blockers has been extensively evaluated [6,8], but much of the variability remains unexplained Another approach to identifying the mechanisms underlying interindividual variability in response would be to identify additional candidate.
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have