Pharmacoepigenetics in type 2 diabetes: is it clinically relevant?

被引:3
|
作者
Ling, Charlotte [1 ]
机构
[1] Lund Univ, Scania Univ Hosp, Lund Univ Diabet Ctr, Dept Clin Sci,Epigenet & Diabet Unit, Malmo, Sweden
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
Adipose tissue; Beta cells; Blood; Blood-based epigenetic biomarkers; DNA methylation; Drug targets; Epigenetic enzymes; Epigenetics; Histone modification; Inhibitors; Liver; Non-coding RNA; Pancreatic islets; Pharmacogenetics; Precision medicine; Skeletal muscle; ALTERED DNA METHYLATION; CATION TRANSPORTER 1; GLYCEMIC RESPONSE; PANCREATIC-ISLETS; ADIPOSE-TISSUE; METFORMIN; EXPRESSION; GENES; SULFONYLUREAS; ASSOCIATION;
D O I
10.1007/s00125-022-05681-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Data generated over nearly two decades clearly demonstrate the importance of epigenetic modifications and mechanisms in the pathogenesis of type 2 diabetes. However, the role of pharmacoepigenetics in type 2 diabetes is less well established. The field of pharmacoepigenetics covers epigenetic biomarkers that predict response to therapy, therapy-induced epigenetic alterations as well as epigenetic therapies including inhibitors of epigenetic enzymes. Not all individuals with type 2 diabetes respond to glucose-lowering therapies in the same way, and there is therefore a need for clinically useful biomarkers that discriminate responders from non-responders. Blood-based epigenetic biomarkers may be useful for this purpose. There is also a need for a better understanding of whether existing glucose-lowering therapies exert their function partly through therapy-induced epigenetic alterations. Finally, epigenetic enzymes may be drug targets for type 2 diabetes. Here, I discuss whether pharmacoepigenetics is clinically relevant for type 2 diabetes based on studies addressing this topic.
引用
收藏
页码:1849 / 1853
页数:5
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