An Overview of Epigenetics in Obesity: The Role of Lifestyle and Therapeutic Interventions

被引:106
作者
Mahmoud, Abeer M. [1 ]
机构
[1] Univ Illinois, Dept Med, Coll Med, Div Endocrinol Diabet & Metab, Chicago, IL 60612 USA
关键词
obesity; epigenetics; energy metabolism; lifestyle; DNA methylation; histone modifications; microRNAs; diet; physical activity; weight loss; GENOMIC DNA METHYLATION; HIGH-FAT; SKELETAL-MUSCLE; GENE-EXPRESSION; ENDURANCE EXERCISE; ADIPOSE-TISSUE; MOUSE MODEL; HISTONE ACETYLATION; METABOLIC SYNDROME; WEIGHT-LOSS;
D O I
10.3390/ijms23031341
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity has become a global epidemic that has a negative impact on population health and the economy of nations. Genetic predispositions have been demonstrated to have a substantial role in the unbalanced energy metabolism seen in obesity. However, these genetic variations cannot entirely explain the massive growth in obesity over the last few decades. Accumulating evidence suggests that modern lifestyle characteristics such as the intake of energy-dense foods, adopting sedentary behavior, or exposure to environmental factors such as industrial endocrine disruptors all contribute to the rising obesity epidemic. Recent advances in the study of DNA and its alterations have considerably increased our understanding of the function of epigenetics in regulating energy metabolism and expenditure in obesity and metabolic diseases. These epigenetic modifications influence how DNA is transcribed without altering its sequence. They are dynamic, reflecting the interplay between the body and its surroundings. Notably, these epigenetic changes are reversible, making them appealing targets for therapeutic and corrective interventions. In this review, I discuss how these epigenetic modifications contribute to the disordered energy metabolism in obesity and to what degree lifestyle and weight reduction strategies and pharmacological drugs can restore energy balance by restoring normal epigenetic profiles.
引用
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页数:21
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共 157 条
[1]   The role of DNA methylation in the pathogenesis of type 2 diabetes mellitus [J].
Ahmed, Sanabil Ali Hassan ;
Ansari, Suraiya Anjum ;
Mensah-Brown, Eric P. K. ;
Emerald, Bright Starling .
CLINICAL EPIGENETICS, 2020, 12 (01)
[2]   DNA Methylation Analysis in Nonalcoholic Fatty Liver Disease Suggests Distinct Disease-Specific and Remodeling Signatures after Bariatric Surgery [J].
Ahrens, Markus ;
Ammerpohl, Ole ;
von Schoenfels, Witigo ;
Kolarova, Julia ;
Bens, Susanne ;
Itzel, Timo ;
Teufel, Andreas ;
Herrmann, Alexander ;
Brosch, Mario ;
Hinrichsen, Holger ;
Erhart, Wiebke ;
Egberts, Jan ;
Sipos, Bence ;
Schreiber, Stefan ;
Haesler, Robert ;
Stickel, Felix ;
Becker, Thomas ;
Krawczak, Michael ;
Roecken, Christoph ;
Siebert, Reiner ;
Schafmayer, Clemens ;
Hampe, Jochen .
CELL METABOLISM, 2013, 18 (02) :296-302
[3]  
Al-Abri Mohammed A, 2016, Oman Med J, V31, P399, DOI 10.5001/omj.2016.81
[4]   Adipose Tissue Hypoxia Correlates with Adipokine Hypomethylation and Vascular Dysfunction [J].
Ali, Mohamed M. ;
Hassan, Chandra ;
Masrur, Mario ;
Bianco, Francesco M. ;
Naquiallah, Dina ;
Mirza, Imaduddin ;
Frederick, Patrice ;
Fernandes, Eduardo T. ;
Giulianotti, Cristoforo P. ;
Gangemi, Antonio ;
Phillips, Shane A. ;
Mahmoud, Abeer M. .
BIOMEDICINES, 2021, 9 (08)
[5]   DNA methylation profile of genes involved in inflammation and autoimmunity correlates with vascular function in morbidly obese adults [J].
Ali, Mohamed M. ;
Naquiallah, Dina ;
Qureshi, Maryam ;
Mirza, Mohammed Imaduddin ;
Hassan, Chandra ;
Masrur, Mario ;
Bianco, Francesco M. ;
Frederick, Patrice ;
Cristoforo, Giulianotti P. ;
Gangemi, Antonio ;
Phillips, Shane A. ;
Mahmoud, Abeer .
EPIGENETICS, 2022, 17 (01) :93-109
[6]  
Alkandari Abdullah, 2018, BMC Obes, V5, P20, DOI 10.1186/s40608-018-0199-z
[7]   Are epigenetic drugs for diabetes and obesity at our door step? [J].
Arguelles, Andrix O. ;
Meruvu, Sunitha ;
Bowman, John D. ;
Choudhury, Mahua .
DRUG DISCOVERY TODAY, 2016, 21 (03) :499-509
[8]   Valproic Acid Is a Novel Activator of AMP-Activated Protein Kinase and Decreases Liver Mass, Hepatic Fat Accumulation, and Serum Glucose in Obese Mice [J].
Avery, Lindsay B. ;
Bumpus, Namandje N. .
MOLECULAR PHARMACOLOGY, 2014, 85 (01) :1-10
[9]   HDAC11 suppresses the thermogenic program of adipose tissue via BRD2 [J].
Bagchi, Rushita A. ;
Ferguson, Bradley S. ;
Stratton, Matthew S. ;
Hu, Tianjing ;
Cavasin, Maria A. ;
Sun, Lei ;
Lin, Ying-Hsi ;
Liu, Dianxin ;
Londono, Pilar ;
Song, Kunhua ;
Pino, Maria F. ;
Sparks, Lauren M. ;
Smith, Steven R. ;
Scherer, Philipp E. ;
Collins, Sheila ;
Seto, Edward ;
McKinsey, Timothy A. .
JCI INSIGHT, 2018, 3 (15)
[10]   Chemical toxins: A hypothesis to explain the global obesity epidemic [J].
Baillie-Hamilton, PF .
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, 2002, 8 (02) :185-192