疾病
全基因组关联研究
表观基因组
表观遗传学
遗传关联
生物信息学
医学
DNA甲基化
糖尿病
遗传学
单核苷酸多态性
生物
内科学
基因型
内分泌学
基因
基因表达
作者
Niina Sandholm,Emma H. Dahlström,Per‐Henrik Groop
标识
DOI:10.3389/fendo.2023.1163001
摘要
Diabetic kidney disease (DKD) is a severe diabetic complication that affects up to half of the individuals with diabetes. Elevated blood glucose levels are a key underlying cause of DKD, but DKD is a complex multifactorial disease, which takes years to develop. Family studies have shown that inherited factors also contribute to the risk of the disease. During the last decade, genome-wide association studies (GWASs) have emerged as a powerful tool to identify genetic risk factors for DKD. In recent years, the GWASs have acquired larger number of participants, leading to increased statistical power to detect more genetic risk factors. In addition, whole-exome and whole-genome sequencing studies are emerging, aiming to identify rare genetic risk factors for DKD, as well as epigenome-wide association studies, investigating DNA methylation in relation to DKD. This article aims to review the identified genetic and epigenetic risk factors for DKD.
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