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METHOD OF EPIGENETIC ANALYSIS FOR DETERMINING CLINICAL GENETIC RISK

机译:确定临床遗传风险的表观分析方法

摘要

The present invention provides a method for identifying a subject having or at risk of having a metabolic disease, such as diabetes or obesity. The invention is based on an approach to identify candidate genes involved in metabolic diseases, such as obesity and type 2 diabetes (T2D) through epigenetic mechanisms. The method includes identifying in the subject genetic markers correlating differentially methylated regions (DMRs) in the genome with genetic risk loci for the subject and comparing methylation patterns of the markers with a control sample from a subject not having the disease. In another embodiment, the invention also provides a method of treating a subject having or at risk of having a metabolic disease. In another embodiment, the invention provides a method of providing a prognostic evaluation of a subject having or at risk of having a metabolic disease.
机译:本发明提供了一种用于识别患有或处于患有代谢疾病例如糖尿病或肥胖症的对象的方法。本发明基于通过表观遗传机制鉴定与代谢性疾病例如肥胖症和2型糖尿病(T2D)有关的候选基因的方法。该方法包括在受试者中鉴定与该受试者的遗传风险基因座相关的基因组中的差异甲基化区域(DMR)相关的遗传标记,并将该标记的甲基化模式与来自没有该疾病的受试者的对照样品进行比较。在另一个实施方案中,本发明还提供了一种治疗患有代谢疾病或处于代谢疾病风险中的受试者的方法。在另一个实施方案中,本发明提供了一种对患有代谢疾病或处于代谢疾病风险中的受试者进行预后评估的方法。

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