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METHODS AND COMPOSITIONS FOR SCD, CRT, CRT-D, OR SCA THERAPY IDENTIFICATION AND/OR SELECTION

机译:SCD,CRT,CRT-D或SCA治疗识别和/或选择的方法和成分

摘要

Compositions, polynucleotides, probes, kits, methods, computer systems, treatment methods and genetic markers useful for assessing the risk of Sudden Cardiac Death (SCD), Sudden Cardiac Arrest (SCA), Ventricular Arrhythmia (VA), or Heart Failure (HF) are provided herein. The compositions, polynucleotides, probes, kits, methods, computer systems, treatment methods and genetic markers of the invention can provide patients selection for those that can be treated with an ICD or CRT-D based on assessing the presence of one or more Single Nucleotide Polymorphisms (SNPs) associated with any one of Sudden Cardiac Death (SCD), Sudden Cardiac Arrest (SCA), Ventricular Arrhythmia (VA), or Heart Failure (HF), and can indicate treatment with certain drugs such as beta-blockers.
机译:可用于评估心脏猝死(SCD),心脏骤停(SCA),室性心律不齐(VA)或心力衰竭(HF)风险的组合物,多核苷酸,探针,试剂盒,方法,计算机系统,治疗方法和遗传标记本文提供。本发明的组合物,多核苷酸,探针,试剂盒,方法,计算机系统,治疗方法和遗传标记物可以基于评估一种或多种单核苷酸的存在为患者提供可以用ICD或CRT-D治疗的患者的选择。与心脏猝死(SCD),心脏骤停(SCA),室性心律不齐(VA)或心力衰竭(HF)中的任何一种相关的多态性(SNP),并且可以指示使用某些药物(例如β-受体阻滞剂)进行治疗。

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