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GENES LINKING SEVERAL COMPLICATIONS OF TYPE-2 DIABETES (T2D)

机译:基因使2型糖尿病(T2D)的几种复杂情况联系在一起

摘要

The invention provides means and methods to predict, in subjects affected by type II diabetes (T2D), the probability of developing complications which include, but are not limited to, micro/macrovascular disorder, hypertension, neuropathy, atrial fibrillation, nephropathy and other major adverse cardiovascular events (MACE) that are associated with the disease, by detecting one or more genetic features. The genetic features that are useful in prediction include, but are not limited to, genes, single nucleotide polymorphisms (SNPs) and other genomic markers. The invention further involves characterizing individuals based on the probability of developing complications related to T2D, such as, micro/macrovascular disorder, hypertension, neuropathy, atrial fibrillation, nephropathy or MACE, based on the identification of one or more aforementioned genetic features. Also described are combinations and kits for carrying out the above-described methods.
机译:本发明提供了在患有II型糖尿病(T2D)的受试者中预测发生并发症的可能性的手段和方法,所述并发症包括但不限于微/微血管疾病,高血压,神经病,心房颤动,肾病和其他主要疾病通过检测一种或多种遗传特征,与疾病相关的不良心血管事件(MACE)。可用于预测的遗传特征包括但不限于基因,单核苷酸多态性(SNP)和其他基因组标记。本发明进一步涉及基于对一种或多种上述遗传特征的鉴定,基于发展与T2D相关的并发症(例如,微/微血管疾病,高血压,神经病,心房颤动,肾病或MACE)的可能性来表征个体。还描述了用于执行上述方法的组合和试剂盒。

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