儿童支气管扩张剂反应的药物基因组学最新分析。

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pharmacogenetics and genomics Pub Date : 2024-12-19 DOI:10.1097/FPC.0000000000000557
Jennifer Brailsford, Guillaume Labilloy, Nolan Menze, Morgan Henson, Jennifer Fishe
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引用次数: 0

摘要

这篇简短的交流是对先前发表的关于哮喘儿童支气管扩张剂反应(BDR)的初步研究结果的更新。我们将队列从54名扩大到165名因哮喘加重而寻求急诊科护理的儿科患者。我们使用儿科哮喘严重程度评分和收集的基因组DNA获得沙丁胺醇给药前后测量的BDR。在文献综述的基础上,我们分析了21个候选单核苷酸多态性(snp)是否与BDR相关。在我们的前期研究中最初报道的与BDR显著相关的三个snp (rs912142、rs7081864和rs7903366)中,我们证实rs7081864仍与次优BDR显著相关(优势比为0.47;置信区间0.24-0.92)。如果在更广泛的研究中得到外部验证,简单的门诊SNP变异检测可以帮助指导急性哮喘症状的药物治疗。
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Updated analysis of the pharmacogenomics of pediatric bronchodilator response.

This short communication serves as an update to previously published pilot study results on bronchodilator response (BDR) in children with asthma. We expanded our cohort from 54 to 165 pediatric patients seeking emergency department care for an asthma exacerbation. We obtained measured BDR before and after albuterol administration using the Pediatric Asthma Severity Score and collected genomic DNA. Based on a literature review, we analyzed whether 21 candidate single-nucleotide polymorphisms (SNPs) were associated with BDR. Among the three SNPs initially reported in our pilot study as significantly associated with BDR (rs912142, rs7081864, and rs7903366), we confirmed that rs7081864 was still significantly associated with suboptimal BDR (odds ratio, 0.47; confidence interval, 0.24-0.92). If externally validated in broader studies, simple outpatient testing for that SNP variant could help guide pharmacologic therapy for acute asthma symptoms.

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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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