Utkarsh Kohli MD, Britney L. Grayson BS, Thomas M. Aune PhD, Laxmi V. Ghimire MD, Daniel Kurnik MD, C. Michael Stein MD
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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.</p><p><b>Results. </b> Fifty genes showed more than 1.3-fold increase in expression; 9 of these reached statistical significance (<i>P</i> < 0.05). Thirty-six genes had more than 1.3-fold decrease in expression after atenolol; 6 of these reached statistical significance (<i>P</i> < 0.05). Change in mRNA expression of <i>FGFBP2</i> and Probeset ID 8118979 was significantly correlated with atenolol response (<i>P</i> = 0.03 and 0.02, respectively).</p><p><b>Conclusion. </b> The 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.</p>","PeriodicalId":8181,"journal":{"name":"Archives of Drug Information","volume":"2 3","pages":"41-50"},"PeriodicalIF":0.0000,"publicationDate":"2009-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1753-5174.2009.00020.x","citationCount":"3","resultStr":"{\"title\":\"Change in mRNA Expression after Atenolol, a Beta-adrenergic Receptor Antagonist and Association with Pharmacological Response\",\"authors\":\"Utkarsh Kohli MD, Britney L. Grayson BS, Thomas M. Aune PhD, Laxmi V. Ghimire MD, Daniel Kurnik MD, C. Michael Stein MD\",\"doi\":\"10.1111/j.1753-5174.2009.00020.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Aims. </b> Genetic determinants of variability in response to β-blockers are poorly characterized. 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引用次数: 3
摘要
目标对β-阻滞剂反应的可变性的遗传决定因素的特征很差。我们定义了β受体阻滞剂后mRNA表达的变化,以确定可能影响反应的新基因,并将这些基因与运动性心动过速的抑制(β受体阻滞剂敏感性的一种衡量指标)联系起来。9名受试者在单次口服阿替洛尔25mg之前和之后进行运动,使用Affymetrix基因芯片人类基因1.0 ST阵列测量mRNA基因表达。计算每个受试者的心率-运动强度曲线下面积(AUC);阿替洛尔治疗前后AUC的差异(Δ AUC)是衡量β受体阻滞剂反应的指标,与基因mRNA表达的翻倍变化相关,其变化超过1.3倍。50个基因表达量增加1.3倍以上;其中9例差异有统计学意义(P < 0.05)。36个基因在阿替洛尔治疗后表达量下降了1.3倍以上;其中6例差异有统计学意义(P < 0.05)。FGFBP2和Probeset ID 8118979 mRNA表达变化与阿替洛尔疗效显著相关(P值分别为0.03和0.02)。一些先前未被确定为肾上腺素能信号通路一部分的基因的表达在单次口服阿替洛尔后发生了变化。这些基因的变异可能导致对β受体阻滞剂的反应存在无法解释的差异。
Change in mRNA Expression after Atenolol, a Beta-adrenergic Receptor Antagonist and Association with Pharmacological Response
Aims. Genetic 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.
Methods. Nine 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.
Results. Fifty 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).
Conclusion. The 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.