Understanding Dietary Intervention-Mediated Epigenetic Modifications in Metabolic Diseases

被引:38
作者
Asif, Shaza [1 ,2 ]
Morrow, Nadya M. [1 ,3 ]
Mulvihill, Erin E. [1 ,3 ]
Kim, Kyoung-Han [1 ,2 ]
机构
[1] Univ Ottawa Heart Inst, Ottawa, ON, Canada
[2] Univ Ottawa, Fac Med, Dept Cellular & Mol Med, Ottawa, ON, Canada
[3] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON, Canada
基金
加拿大健康研究院;
关键词
non-alcoholic fatty liver disease; type; 2; diabetes; obesity; dietary interventions; intermittent fasting; caloric restriction; DNA methylation; histone modification; FATTY LIVER-DISEASE; PANCREATIC BETA-CELLS; BROWN ADIPOSE-TISSUE; DIFFERENTIAL DNA METHYLATION; STIMULATED INSULIN-SECRETION; HEPATIC GLUCOSE-PRODUCTION; MORBIDLY OBESE-PATIENTS; C/EBP-ALPHA EXPRESSION; LOW-CALORIE DIET; GENE-EXPRESSION;
D O I
10.3389/fgene.2020.590369
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The global prevalence of metabolic disorders, such as obesity, diabetes and fatty liver disease, is dramatically increasing. Both genetic and environmental factors are well-known contributors to the development of these diseases and therefore, the study of epigenetics can provide additional mechanistic insight. Dietary interventions, including caloric restriction, intermittent fasting or time-restricted feeding, have shown promising improvements in patients' overall metabolic profiles (i.e., reduced body weight, improved glucose homeostasis), and an increasing number of studies have associated these beneficial effects with epigenetic alterations. In this article, we review epigenetic changes involved in both metabolic diseases and dietary interventions in primary metabolic tissues (i.e., adipose, liver, and pancreas) in hopes of elucidating potential biomarkers and therapeutic targets for disease prevention and treatment.
引用
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页数:32
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