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Single nucleotide polymorphisms sensitively predicting adverse drug reactions (adr) and drug efficacy

机译:单核苷酸多态性可以灵敏地预测药物不良反应(adr)和药物疗效

摘要

Single Nucleotide Polymorphisms sensitively predicting Advserse Drug Reactions (ADR) and Drug Efficacy Abs tract. The invention provides diagnostic methods and kits including oligo and/or polynucleotides or derivatives, including as well antibodies determining whether a human subject is at risk of getting adverse drug reaction after statin therapy or whether the human subject is a high or low responder or a good a or bad metabolizer of statins. The invention provides further diagnostic methods and kits including antibodies determining whether a human subject is at risk for a cardiovascular disease. Still further the invention provides polymorphic sequences and other genes. The present invention further relates to isolated polynucleotides encoding a phenotype associated (PA) gene polypeptide useful in methods to identify therapeutic agents and useful for preparation of a medicament to treat cardiovascular disease or influence drug response, the polynucleotide is selected from the group comprising: SEQ ID 1-168 with allelic variation as indicated in the sequences section contained in a functional surrounding like full length cDNA for PA gene polypeptide and with or without the PA gene promoter sequence.
机译:单核苷酸多态性可以灵敏地预测Advserse药物反应(ADR)和药物功效的摘要。本发明提供了包括寡核苷酸和/或多核苷酸或衍生物的诊断方法和试剂盒,以及包括确定人类受试者在他汀类药物治疗后是否有发生不良药物反应风险或人类受试者是高反应还是低反应或良好反应的抗体的抗体。他汀类药物的代谢不良或代谢不良。本发明提供了进一步的诊断方法和试剂盒,包括确定人类受试者是否有心血管疾病风险的抗体。另外,本发明提供了多态性序列和其他基因。本发明进一步涉及编码表型相关(PA)基因多肽的分离的多核苷酸,其可用于鉴定治疗剂的方法和可用于制备治疗心血管疾病或影响药物反应的药物,所述多核苷酸选自:SEQ ID 1-168,如序列部分所示,具有等位基因变异,包含在PA基因多肽功能性全长全长cDNA中,带有或不带有PA基因启动子序列。

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