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Evaluation of a Pharmacogenetic Test in Thailand for Abacavir Hyper-sensitivity Screening in Human Immunodeficiency Virus Infection

机译:在泰国对人免疫缺陷病毒感染的阿巴卡韦超敏筛选的药物遗传学测试的评价

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Abacavir hypersensitivity reaction (ABC-HSR) is associated with the presence of HLA-B* 57:01 allele. Alternative tests for ABC-HSR associated allele determination are needed where sequence-based HLA typing is not available, particularly in resource-limited settings or developing countries. This study focused on the development and evaluation of two HLA-B* 57:01 tagging SNPs (single nucleotide polymorphism) HCP5 (HLA complex P5) rs2395029 and TNF (tumor necrosis factor) rs3093726 genotyping assays. Two hundred and thirteen purified genomic DNA samples were used to evaluate the performance characteristics of a HLA-B~* 57:01 screening method based on allele-specific polymerase chain reaction (AS-PCR) with melting curve analysis. HCP5 rs2395029 and TNF rs3093726 were also genotyped using simple probe real-time PCR assay. All samples were successfully genotyped wherein AS-PCR genotyping provided 100% sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) when compared with specific HLA-B status by sequencing based assay. When comparing the AS-PCR screening method with the HCP5 rs2395029 and TNF rs3093726 genotyping method, the former had 100% sensitivity, 100% specificity, 100% PPV and 100% NPV using a simple probe; while the latter one had 95.24% sensitivity, 100% specificity, 100% PPV and 99.48% NPV, respectively. In conclusion, our study lends support on a molecular tool for pharmacogenetic screening in resource-limited settings. Thus, serious drug hypersensitivity associated with ABC may potentially be reduced in Thailand by further evaluation of the proposed assay in clinical practice.
机译:阿巴卡韦超敏反应(ABC-HSR)与HLA-B * 57:01等位基因的存在有关。在无法使用基于序列的HLA分型的情况下,尤其是在资源有限的国家或发展中国家,需要用于ABC-HSR相关等位基因测定的替代测试。这项研究的重点是两个HLA-B * 57:01标记SNP(单核苷酸多态性)HCP5(HLA复合物P5)rs2395029和TNF(肿瘤坏死因子)rs3093726基因分型分析的开发和评估。 213个纯化的基因组DNA样品用于评估基于等位基因特异性聚合酶链反应(AS-PCR)和熔解曲线分析的HLA-B〜* 57:01筛选方法的性能特征。还使用简单的探针实时PCR分析对HCP5 rs2395029和TNF rs3093726进行了基因分型。通过基于测序的检测与所有HLA-B状态相比,所有样品均成功进行了基因分型,其中AS-PCR基因分型提供了100%的敏感性,特异性,阳性预测值(PPV)和阴性预测值(NPV)。当将AS-PCR筛选方法与HCP5 rs2395029和TNF rs3093726基因分型方法进行比较时,使用简单的探针,前者具有100%的敏感性,100%的特异性,100%的PPV和100%的NPV。后者的敏感性分别为95.24%,特异性100%,PPV 100%和NPV 99.48%。总之,我们的研究为在资源有限的环境中进行药物遗传学筛选的分子工具提供了支持。因此,通过在临床实践中进一步评估拟议的测定方法,泰国可能会降低与ABC相关的严重药物超敏反应。

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