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28/04/2023
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Views PDF(English): 190
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LE NV, NGUYEN HN, NGUYEN TMN. AN OVERVIEW OF THE RELATIONSHIP BETWEEN DIETARY BEHAVIOR AND LIFESTYLE TO HEALTH AT MOLECULAR BIOLOGY MECHANISM. Tạp chí Dinh dưỡng và Thực phẩm. 2023;19(3E):1-15. doi:10.56283/1859-0381/420
AN OVERVIEW OF THE RELATIONSHIP BETWEEN DIETARY BEHAVIOR AND LIFESTYLE TO HEALTH AT MOLECULAR BIOLOGY MECHANISM
Main Article Content
Abstract
Following the green revolutions, the industrial revolution, and the fourth industrial wave, the quantity of food, goods, and products that serve human life has reached unprecedented levels. Advancements in agriculture productivity, production, and processing technologies, as well as smart supply chain control, have contributed to the "surplus crisis" of food in most countries, including Vietnam. The majority of the world's population consumes diets with excessive levels of fat, sugar, salt, and a lack of fiber. These unhealthy eating habits are known to be the main causes of chronic diseases, acting as silent killers of the health and lifespan of contemporary human society. Fortunately, a new trend of nutritious diets rich in fiber, positive thinking habits, exercise, and a harmonious lifestyle has been discovered as a "reform pill" for humans.
This article presents a synthesis and update of relevant research achievements, with the ambition to positively adjust unscientific eating habits and change negative thinking and behavior to improve the health and lifespan of human society.
Article Details
Keywords
Behavioral science, disease, eating behaviors, exercise, epigenetic, nutrigenomics, metabolism
References
1. Trovato GM. Behavior, nutrition and lifestyle in a comprehensive health and disease paradigm: skills and knowledge for a predictive, preventive and personalized medicine. EPMA Journal. 2012;3(1):8.
2. Hummel E, Hoffmann I. Complexity of nutritional behavior: Capturing and depicting its interrelated factors in a cause-effect model. Ecology of Food and Nutrition. 2016;55(3):241-257.
3. World Health Organization. WHO remains firmly committed to the principles set out in the preamble to the Constitution. Accessed Dec 7, 2022. https://www.who.int/about/governance/constitution
4. Nguyen TT, Hoang MV. Non-communicable diseases, food and nutrition in Vietnam from 1975 to 2015: the burden and national response. Asia Pacific journal of clinical nutrition. 2018;27(1):19-28.
5. Harris J, Nguyen PH, Tran LM, Huynh PN. Nutrition transition in Vietnam: Changing food supply, food prices, household expenditure, diet and nutrition outcomes. Food Security. 2020;12:1141-1155.
6. Embree JF. A bibliography of the physical anthropology of Indo‐China, 1938–1947. American Journal of Physical Anthropology. 1949;7(1):39-52.
7. Khan NC, Tue HH, Le BM, Le GV, Khoi HH. Secular trends in growth and nutritional status of Vietnamese adults in rural Red river delta after 30 years (1976-2006). Asia Pacific journal of clinical nutrition. 2010;19(3):412-416.
8. The World Bank. Cause of death, by non-communicable diseases (% of total) - Least developed countries: UN classification. Accessed Dec 7, 2022. https://data.worldbank.org/indicator/SH.DTH.NCOM.ZS?end=2019&locations=XL&start=2019&view=map&year=2019
9. Budreviciute A, Damiati S, Sabir DK, et al. Management and Prevention Strategies for Non-communicable Diseases (NCDs) and Their Risk Factors. Review. Frontiers in Public Health. 2020;8:788.
10. Habib SH, Saha S. Burden of non-communicable disease: Global overview. Diabetes & Metabolic Syndrome: Clinical Research & Reviews. 2010;4(1):41-47.
11. Villota-Salazar NA, Mendoza-Mendoza A, González-Prieto JM. Epigenetics: from the past to the present. Frontiers in Life Science. 2016;9(4):347-370.
12. Carson C, Lawson HA. Epigenetics of metabolic syndrome. Physiological genomics. 2018;50(11):947-955.
13. Roberti A, Valdes AF, Torrecillas R, Fraga MF, Fernandez AF. Epigenetics in cancer therapy and nanomedicine. Clinical epigenetics. 2019;11(1):1-18.
14. Peral-Sanchez I, Hojeij B, Ojeda DA, Steegers-Theunissen RP, Willaime-Morawek S. Epigenetics in the uterine environment: how maternal diet and ART may influence the epigenome in the offspring with long-term health consequences. Genes. 2021;13(1):31.
15. Gillespie SL, Hardy LR, Anderson CM. Patterns of DNA methylation as an indicator of biological aging: State of the science and future directions in precision health promotion. Nursing outlook. 2019;67(4):337-344.
16. Fiorino E, Giudici M, Ferrari A, et al. The sirtuin class of histone deacetylases: regulation and roles in lipid metabolism. IUBMB life. 2014;66(2):89-99.
17. Townsend LK, Wright DC. Looking on the “brite” side exercise-induced browning of white adipose tissue. Pflügers Archiv - European Journal of Physiology. 2019;471(3):455-465.
18. Krämer AI, Handschin C. How Epigenetic Modifications Drive the Expression and Mediate the Action of PGC-1α in the Regulation of Metabolism. International Journal of Molecular Sciences. 2019;20(21):5449.
19. Dimauro I, Paronetto MP, Caporossi D. Chapter 18 - Epigenomic adaptations of exercise in the control of metabolic disease and cancer. In: Ferguson BS, ed. Nutritional Epigenomics. Academic Press; 2019:289-316.
20. Jacobsen SC, Brøns C, Bork-Jensen J, et al. Effects of short-term high-fat overfeeding on genome-wide DNA methylation in the skeletal muscle of healthy young men. Diabetologia. 2012;55(12):3341-3349.
21. Motta VF, Bargut TL, Souza-Mello V, Aguila MB, Mandarim-de-Lacerda CA. Browning is activated in the subcutaneous white adipose tissue of mice metabolically challenged with a high-fructose diet submitted to high-intensity interval training. The Journal of Nutritional Biochemistry. 2019;70:164-173.
22. Min S-w, Sohn P, Cho S-h, Swanson R, Gan L. Sirtuins in neurodegenerative diseases: an update on potential mechanisms. Review. Frontiers in Aging Neuroscience. 2013;5:53.
23. Yamaguchi S, Yoshino J. Adipose tissue NAD+ biology in obesity and insulin resistance: From mechanism to therapy. BioEssays. 2017;39(5):1600227.
24. Hwang J-W, Sundar IK, Yao H, Rahman I. Chapter 15 - SIRT1 and Inflammaging in Chronic Obstructive Pulmonary Disease. In: Rahman I, Bagchi D, eds. Inflammation, Advancing Age and Nutrition. Academic Press; 2014:183-191.
25. Li J, Sha J, Sun L, Zhu D, Meng C. Contribution of Regulatory T Cell Methylation Modifications to the Pathogenesis of Allergic Airway Diseases. Journal of Immunology Research. 2021;2021:5590217.
26. Cho H, Kim C, Kim HJ, et al. Impact of smoking on neurodegeneration and cerebrovascular disease markers in cognitively normal men. European Journal of Neurology. 2016;23(1):110-119.
27. Wang T, Yan H, Lu Y, et al. Anti-obesity effect of Lactobacillus rhamnosus LS-8 and Lactobacillus crustorum MN047 on high-fat and high-fructose diet mice base on inflammatory response alleviation and gut microbiota regulation. European Journal of Nutrition. 2020;59(6):2709-2728.
28. Hedrick SM, Michelini RH, Doedens AL, Goldrath AW, Stone EL. FOXO transcription factors throughout T cell biology. Nature Reviews Immunology. 2012;12(9):649-661.
29. Qi J, Yu X-J, Shi X-L, et al. NF-κB Blockade in Hypothalamic Paraventricular Nucleus Inhibits High-Salt-Induced Hypertension Through NLRP3 and Caspase-1. Cardiovascular Toxicology. 2016;16(4):345-354.
30. Huang Y, Liu W, Liu J, et al. Association of Urinary Sodium Excretion and Diabetic Kidney Disease in Patients With Type 2 Diabetes Mellitus: A Cross-Sectional Study. Frontiers in Endocrinology. 2021;12:772073.
31. Marusawa H, Chiba T. Helicobacter pylori-induced activation-induced cytidine deaminase expression and carcinogenesis. Current Opinion in Immunology. 2010;22(4):442-447.
32. Wang B, Smyl C, Chen C-Y, et al. Suppression of Postprandial Blood Glucose Fluctuations by a Low-Carbohydrate, High-Protein, and High-Omega-3 Diet via Inhibition of Gluconeogenesis. International Journal of Molecular Sciences. 2018;19(7):1823.
33. Wang Y, He W. Improving the Dysregulation of FoxO1 Activity Is a Potential Therapy for Alleviating Diabetic Kidney Disease. Mini Review. Frontiers in Pharmacology. 2021;12:630617.
34. Balan Y, Packirisamy RM, P S M. High dietary salt intake activates inflammatory cascades via Th17 immune cells: impact on health and diseases. Arch Med Sci. 2022;18(2):459-465.
35. Luo Y, Yang Y, Liu M, et al. Oncogenic KRAS Reduces Expression of FGF21 in Acinar Cells to Promote Pancreatic Tumorigenesis in Mice on a High-Fat Diet. Gastroenterology. 2019;157(5):1413-1428.e11.
36. Costantino S, Mohammed SA, Ambrosini S, Paneni F. The vascular epigenome in patients with obesity and type 2 diabetes: opportunities for personalized therapies. Vascular Biology. 2020;2(1):H19-H28.
37. Opoku YK, Liu Z, Afrifa J, Khoso MH, Ren G, Li D. Therapeutic Role of Fibroblast Growth Factor 21 (FGF21) in the Amelioration of Chronic Diseases. International Journal of Peptide Research and Therapeutics. 2020;26(1):107-119.
38. Tang Y, Zhou J, Hooi SC, Jiang YM, Lu GD. Fatty acid activation in carcinogenesis and cancer development: Essential roles of long‑chain acyl‑CoA synthetases (Review). Oncol Lett. 2018;16(2):1390-1396.
39. Hagihara Y, Yoshimatsu Y, Mikami Y, Takada Y, Mizuno S, Kanai T. Epigenetic regulation of T helper cells and intestinal pathogenicity. Seminars in Immunopathology. 2019;41(3):379-399.
40. Hai R, He L, Shu G, Yin G. Characterization of Histone Deacetylase Mechanisms in Cancer Development. Review. Frontiers in Oncology. 2021;11:700947.
41. Erickson A, Moreau R. The regulation of FGF21 gene expression by metabolic factors and nutrients. Hormone Molecular Biology and Clinical Investigation. 2017;30(1):20160016.
42. Diamond JM, Ordunio D. Guns, germs, and steel. W. W. Norton & Company, 2020.
43. Lance C. Dalleck, Len Kravitz. The History of Fitness. Accessed Jan 07, 2022. https://www.unm.edu/~lkravitz/Article%20folder/history.html
44. Lindinger MI. A century of exercise physiology: key concepts in muscle cell volume regulation. European Journal of Applied Physiology. 2022;122(3):541-559.
45. Hansen JS, Pedersen BK, Xu G, Lehmann R, Weigert C, Plomgaard P. Exercise-Induced Secretion of FGF21 and Follistatin Are Blocked by Pancreatic Clamp and Impaired in Type 2 Diabetes. The Journal of Clinical Endocrinology & Metabolism. 2016;101(7):2816-2825.
46. Salminen A, Kauppinen A, Kaarniranta K. FGF21 activates AMPK signaling: impact on metabolic regulation and the aging process. Journal of Molecular Medicine. 2017;95(2):123-131.
47. Grijalva J, Hicks S, Zhao X, et al. Exercise training enhanced myocardial endothelial nitric oxide synthase (eNOS) function in diabetic Goto-Kakizaki (GK) rats. Cardiovascular Diabetology. 2008;7(1):34.
48. Kitada M, Ogura Y, Koya D. The protective role of Sirt1 in vascular tissue: its relationship to vascular aging and atherosclerosis. Aging. 2016;8(10):2290-2307.
2. Hummel E, Hoffmann I. Complexity of nutritional behavior: Capturing and depicting its interrelated factors in a cause-effect model. Ecology of Food and Nutrition. 2016;55(3):241-257.
3. World Health Organization. WHO remains firmly committed to the principles set out in the preamble to the Constitution. Accessed Dec 7, 2022. https://www.who.int/about/governance/constitution
4. Nguyen TT, Hoang MV. Non-communicable diseases, food and nutrition in Vietnam from 1975 to 2015: the burden and national response. Asia Pacific journal of clinical nutrition. 2018;27(1):19-28.
5. Harris J, Nguyen PH, Tran LM, Huynh PN. Nutrition transition in Vietnam: Changing food supply, food prices, household expenditure, diet and nutrition outcomes. Food Security. 2020;12:1141-1155.
6. Embree JF. A bibliography of the physical anthropology of Indo‐China, 1938–1947. American Journal of Physical Anthropology. 1949;7(1):39-52.
7. Khan NC, Tue HH, Le BM, Le GV, Khoi HH. Secular trends in growth and nutritional status of Vietnamese adults in rural Red river delta after 30 years (1976-2006). Asia Pacific journal of clinical nutrition. 2010;19(3):412-416.
8. The World Bank. Cause of death, by non-communicable diseases (% of total) - Least developed countries: UN classification. Accessed Dec 7, 2022. https://data.worldbank.org/indicator/SH.DTH.NCOM.ZS?end=2019&locations=XL&start=2019&view=map&year=2019
9. Budreviciute A, Damiati S, Sabir DK, et al. Management and Prevention Strategies for Non-communicable Diseases (NCDs) and Their Risk Factors. Review. Frontiers in Public Health. 2020;8:788.
10. Habib SH, Saha S. Burden of non-communicable disease: Global overview. Diabetes & Metabolic Syndrome: Clinical Research & Reviews. 2010;4(1):41-47.
11. Villota-Salazar NA, Mendoza-Mendoza A, González-Prieto JM. Epigenetics: from the past to the present. Frontiers in Life Science. 2016;9(4):347-370.
12. Carson C, Lawson HA. Epigenetics of metabolic syndrome. Physiological genomics. 2018;50(11):947-955.
13. Roberti A, Valdes AF, Torrecillas R, Fraga MF, Fernandez AF. Epigenetics in cancer therapy and nanomedicine. Clinical epigenetics. 2019;11(1):1-18.
14. Peral-Sanchez I, Hojeij B, Ojeda DA, Steegers-Theunissen RP, Willaime-Morawek S. Epigenetics in the uterine environment: how maternal diet and ART may influence the epigenome in the offspring with long-term health consequences. Genes. 2021;13(1):31.
15. Gillespie SL, Hardy LR, Anderson CM. Patterns of DNA methylation as an indicator of biological aging: State of the science and future directions in precision health promotion. Nursing outlook. 2019;67(4):337-344.
16. Fiorino E, Giudici M, Ferrari A, et al. The sirtuin class of histone deacetylases: regulation and roles in lipid metabolism. IUBMB life. 2014;66(2):89-99.
17. Townsend LK, Wright DC. Looking on the “brite” side exercise-induced browning of white adipose tissue. Pflügers Archiv - European Journal of Physiology. 2019;471(3):455-465.
18. Krämer AI, Handschin C. How Epigenetic Modifications Drive the Expression and Mediate the Action of PGC-1α in the Regulation of Metabolism. International Journal of Molecular Sciences. 2019;20(21):5449.
19. Dimauro I, Paronetto MP, Caporossi D. Chapter 18 - Epigenomic adaptations of exercise in the control of metabolic disease and cancer. In: Ferguson BS, ed. Nutritional Epigenomics. Academic Press; 2019:289-316.
20. Jacobsen SC, Brøns C, Bork-Jensen J, et al. Effects of short-term high-fat overfeeding on genome-wide DNA methylation in the skeletal muscle of healthy young men. Diabetologia. 2012;55(12):3341-3349.
21. Motta VF, Bargut TL, Souza-Mello V, Aguila MB, Mandarim-de-Lacerda CA. Browning is activated in the subcutaneous white adipose tissue of mice metabolically challenged with a high-fructose diet submitted to high-intensity interval training. The Journal of Nutritional Biochemistry. 2019;70:164-173.
22. Min S-w, Sohn P, Cho S-h, Swanson R, Gan L. Sirtuins in neurodegenerative diseases: an update on potential mechanisms. Review. Frontiers in Aging Neuroscience. 2013;5:53.
23. Yamaguchi S, Yoshino J. Adipose tissue NAD+ biology in obesity and insulin resistance: From mechanism to therapy. BioEssays. 2017;39(5):1600227.
24. Hwang J-W, Sundar IK, Yao H, Rahman I. Chapter 15 - SIRT1 and Inflammaging in Chronic Obstructive Pulmonary Disease. In: Rahman I, Bagchi D, eds. Inflammation, Advancing Age and Nutrition. Academic Press; 2014:183-191.
25. Li J, Sha J, Sun L, Zhu D, Meng C. Contribution of Regulatory T Cell Methylation Modifications to the Pathogenesis of Allergic Airway Diseases. Journal of Immunology Research. 2021;2021:5590217.
26. Cho H, Kim C, Kim HJ, et al. Impact of smoking on neurodegeneration and cerebrovascular disease markers in cognitively normal men. European Journal of Neurology. 2016;23(1):110-119.
27. Wang T, Yan H, Lu Y, et al. Anti-obesity effect of Lactobacillus rhamnosus LS-8 and Lactobacillus crustorum MN047 on high-fat and high-fructose diet mice base on inflammatory response alleviation and gut microbiota regulation. European Journal of Nutrition. 2020;59(6):2709-2728.
28. Hedrick SM, Michelini RH, Doedens AL, Goldrath AW, Stone EL. FOXO transcription factors throughout T cell biology. Nature Reviews Immunology. 2012;12(9):649-661.
29. Qi J, Yu X-J, Shi X-L, et al. NF-κB Blockade in Hypothalamic Paraventricular Nucleus Inhibits High-Salt-Induced Hypertension Through NLRP3 and Caspase-1. Cardiovascular Toxicology. 2016;16(4):345-354.
30. Huang Y, Liu W, Liu J, et al. Association of Urinary Sodium Excretion and Diabetic Kidney Disease in Patients With Type 2 Diabetes Mellitus: A Cross-Sectional Study. Frontiers in Endocrinology. 2021;12:772073.
31. Marusawa H, Chiba T. Helicobacter pylori-induced activation-induced cytidine deaminase expression and carcinogenesis. Current Opinion in Immunology. 2010;22(4):442-447.
32. Wang B, Smyl C, Chen C-Y, et al. Suppression of Postprandial Blood Glucose Fluctuations by a Low-Carbohydrate, High-Protein, and High-Omega-3 Diet via Inhibition of Gluconeogenesis. International Journal of Molecular Sciences. 2018;19(7):1823.
33. Wang Y, He W. Improving the Dysregulation of FoxO1 Activity Is a Potential Therapy for Alleviating Diabetic Kidney Disease. Mini Review. Frontiers in Pharmacology. 2021;12:630617.
34. Balan Y, Packirisamy RM, P S M. High dietary salt intake activates inflammatory cascades via Th17 immune cells: impact on health and diseases. Arch Med Sci. 2022;18(2):459-465.
35. Luo Y, Yang Y, Liu M, et al. Oncogenic KRAS Reduces Expression of FGF21 in Acinar Cells to Promote Pancreatic Tumorigenesis in Mice on a High-Fat Diet. Gastroenterology. 2019;157(5):1413-1428.e11.
36. Costantino S, Mohammed SA, Ambrosini S, Paneni F. The vascular epigenome in patients with obesity and type 2 diabetes: opportunities for personalized therapies. Vascular Biology. 2020;2(1):H19-H28.
37. Opoku YK, Liu Z, Afrifa J, Khoso MH, Ren G, Li D. Therapeutic Role of Fibroblast Growth Factor 21 (FGF21) in the Amelioration of Chronic Diseases. International Journal of Peptide Research and Therapeutics. 2020;26(1):107-119.
38. Tang Y, Zhou J, Hooi SC, Jiang YM, Lu GD. Fatty acid activation in carcinogenesis and cancer development: Essential roles of long‑chain acyl‑CoA synthetases (Review). Oncol Lett. 2018;16(2):1390-1396.
39. Hagihara Y, Yoshimatsu Y, Mikami Y, Takada Y, Mizuno S, Kanai T. Epigenetic regulation of T helper cells and intestinal pathogenicity. Seminars in Immunopathology. 2019;41(3):379-399.
40. Hai R, He L, Shu G, Yin G. Characterization of Histone Deacetylase Mechanisms in Cancer Development. Review. Frontiers in Oncology. 2021;11:700947.
41. Erickson A, Moreau R. The regulation of FGF21 gene expression by metabolic factors and nutrients. Hormone Molecular Biology and Clinical Investigation. 2017;30(1):20160016.
42. Diamond JM, Ordunio D. Guns, germs, and steel. W. W. Norton & Company, 2020.
43. Lance C. Dalleck, Len Kravitz. The History of Fitness. Accessed Jan 07, 2022. https://www.unm.edu/~lkravitz/Article%20folder/history.html
44. Lindinger MI. A century of exercise physiology: key concepts in muscle cell volume regulation. European Journal of Applied Physiology. 2022;122(3):541-559.
45. Hansen JS, Pedersen BK, Xu G, Lehmann R, Weigert C, Plomgaard P. Exercise-Induced Secretion of FGF21 and Follistatin Are Blocked by Pancreatic Clamp and Impaired in Type 2 Diabetes. The Journal of Clinical Endocrinology & Metabolism. 2016;101(7):2816-2825.
46. Salminen A, Kauppinen A, Kaarniranta K. FGF21 activates AMPK signaling: impact on metabolic regulation and the aging process. Journal of Molecular Medicine. 2017;95(2):123-131.
47. Grijalva J, Hicks S, Zhao X, et al. Exercise training enhanced myocardial endothelial nitric oxide synthase (eNOS) function in diabetic Goto-Kakizaki (GK) rats. Cardiovascular Diabetology. 2008;7(1):34.
48. Kitada M, Ogura Y, Koya D. The protective role of Sirt1 in vascular tissue: its relationship to vascular aging and atherosclerosis. Aging. 2016;8(10):2290-2307.