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METHODS AND KITS FOR PREDICTING THE RISK OF DIABETES ASSOCIATED COMPLICATIONS USING GENETIC MARKERS AND ARRAYS

机译:利用遗传标记和阵列预测糖尿病相关并发症风险的方法和试剂盒

摘要

A method for diagnosing a genetic predisposition in a subject for diseases, disorders or conditions including a diabetic kidney complication such as kidney disease of type 2 diabetes or type 1 diabetes, end stage renal disease (ESRD) due to type 2 diabetes, ESRD due to hypertension in type 2 diabetes, ESRD due to type 1 diabetes; cardiovascular diseases due to type 2 diabetes or type 1 diabetes such as atherosclerotic peripheral vascular disease, hypertension, ischemic cardiomyopathy, and myocardial infarction due to type 2 diabetes or type 1 diabetes; and cerebrovascular accident due to type 2 diabetes. At least one polynucleotide is analyzed to detect a single nucleotide polymorphism (SNP), in which the presence of the single nucleotide polymorphism indicates that the subject is suffering from, at risk for, or suspected of suffering from the diseases, disorders or conditions. Also provided is an array or kit for diagnosing the genetic predisposition.
机译:一种用于诊断受试者的遗传易感性的疾病,病症或病状的方法,包括糖尿病性肾脏并发症,例如2型糖尿病或1型糖尿病的肾脏疾病,2型糖尿病引起的终末期肾病(ESRD), 2型糖尿病高血压,1型糖尿病引起的ESRD; 2型糖尿病或1型糖尿病引起的心血管疾病,例如动脉粥样硬化性外周血管疾病,高血压,缺血性心肌病和2型糖尿病或1型糖尿病引起的心肌梗塞;和2型糖尿病引起的脑血管意外。分析至少一种多核苷酸以检测单核苷酸多态性(SNP),其中单核苷酸多态性的存在表明受试者正在患疾病,处于危险中或被怀疑患有疾病,病症或病状。还提供了用于诊断遗传易感性的阵列或试剂盒。

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