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Pharmacogenetics of beta2 adrenergic receptor agonists in asthma management

机译:β2肾上腺素能受体激动剂在哮喘治疗中的药代动力学

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摘要

Beta2 (β2) adrenergic receptor agonists (beta agonists) are a commonly prescribed treatment for asthma despite the small increase in risk for life-threatening adverse responses associated with long-acting beta agonist (LABA). The concern for life-threatening adverse effects associated with LABA and the inter-individual variability of therapeutic responsiveness to LABA-containing combination therapies provide the rationale for pharmacogenetic studies of beta agonists. These studies primarily evaluated genes within the β2-adrenergic receptor and related pathways; however, recent genome-wide studies have identified novel loci for beta agonist response. Recent studies have identified a role for rare genetic variants in determining beta agonist response and, potentially, the risk for rare, adverse responses to LABA. Before genomics research can be applied to the development of genetic profiles for personalized medicine, it will be necessary to continue adapting to the analysis of an increasing volume of genetic data in larger cohorts with a combination of analytical methods and in vitro studies.
机译:Beta2(β2)肾上腺素能受体激动剂(β激动剂)是哮喘的常用处方疗法,尽管与长效β激动剂(LABA)相关的威胁生命的不良反应的风险增加很小。对与LABA相关的威胁生命的不良反应以及对含LABA的联合疗法的治疗反应的个体差异的担忧,为β激动剂的药物遗传学研究提供了理论依据。这些研究主要评估了β2-肾上腺素能受体内的基因和相关途径。但是,最近的全基因组研究已经确定了β激动剂反应的新基因座。最近的研究已经确定了罕见的遗传变异在确定β激动剂反应以及潜在的对LABA的不良反应风险中的作用。在将基因组学研究应用于个性化医学的遗传概况开发之前,有必要通过分析方法和体外研究相结合,继续适应较大人群中越来越多的遗传数据分析。

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