Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 804

The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.

Global Impacts of Western Diet and Its Effects on Metabolism and Health: A Narrative Review

Open access
Clemente-Suárez, Vicente Javier, Beltrán-Velasco, Ana Isabel, Redondo-Flórez, Laura, Martín-Rodríguez, Alexandra, Tornero-Aguilera, José Francisco·2023·Nutrients

Abstract

The Western diet is a modern dietary pattern characterized by high intakes of pre-packaged foods, refined grains, red meat, processed meat, high-sugar drinks, candy, sweets, fried foods, conventionally raised animal products, high-fat dairy products, and high-fructose products. The present review aims to describe the effect of the Western pattern diet on the metabolism, inflammation, and antioxidant status; the impact on gut microbiota and mitochondrial fitness; the effect of on cardiovascular health, mental health, and cancer; and the sanitary cost of the Western diet. To achieve this goal, a consensus critical review was conducted using primary sources, such as scientific articles, and secondary sources, including bibliographic indexes, databases, and web pages. Scopus, Embase, Science Direct, Sports Discuss, ResearchGate, and the Web of Science were used to complete the assignment. MeSH-compliant keywords such “Western diet”, “inflammation”, “metabolic health”, “metabolic fitness”, “heart disease”, “cancer”, “oxidative stress”, “mental health”, and “metabolism” were used. The following exclusion criteria were applied: (i) studies with inappropriate or irrelevant topics, not germane to the review’s primary focus; (ii) Ph.D. dissertations, proceedings of conferences, and unpublished studies. This information will allow for a better comprehension of this nutritional behavior and its effect on an individual’s metabolism and health, as well as the impact on national sanitary systems. Finally, practical applications derived from this information are made.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/nu15122749

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 75 references

Research works printed but not linked: 307

  1. González Olmo, B.M., Butler, M.J., and Barrientos, R.M. (2021). Evolution of the Human Diet and Its Impact on Gut Microbiota, Immune Responses, and Brain Health. Nutrients, 13. · DOI
  2. Shively, 2019, Mediterranean versus Western Diet Effects on Caloric Intake, Obesity, Metabolism, and Hepatosteatosis in Nonhuman Primates, Obesity (Silver Spring Md.), 27, 777, 10.1002/oby.22436 · DOI
  3. Kennedy, 2004, Globalization of food systems in developing countries: Impact on food security and nutrition, FAO Food Nutr. Pap., 83, 1
  4. Bustamante-Sanchez, A., Villegas-Mora, B.E., Martínez-Guardado, I., Tornero-Aguilera, J.F., Ardigò, L.P., Nobari, H., and Clemente-Suárez, V.J. (2022). Physical Activity and Nutritional Pattern Related to Maturation and Development. Sustainability, 14. · DOI
  5. Kopp, 2019, How Western Diet and Lifestyle Drive The Pandemic Of Obesity And Civilization Diseases, Diabetes Metab. Syndr. Obes. Targets Ther., 12, 2221, 10.2147/DMSO.S216791 · DOI · Paper page
  6. Rakhra, 2020, Obesity and the Western Diet: How We Got Here, Mo. Med., 117, 536
  7. 2018, Dietary Fat and Risk for Type 2 Diabetes: A Review of Recent Research, Curr. Nutr. Rep., 7, 214, 10.1007/s13668-018-0244-z · DOI
  8. Mahfoud, 2022, Arterial hypertension—Clinical trials update 2021, Nutr. Metab. Cardiovasc. Dis., 32, 21, 10.1016/j.numecd.2021.09.007 · DOI
  9. Lindeberg, 2011, The western diet and lifestyle and diseases of civilization, Res. Rep. Clin. Cardiol., 2, 15
  10. Cordain, 2005, Origins and evolution of the Western diet: Health implications for the 21st century, Am. J. Clin. Nutr., 81, 341, 10.1093/ajcn.81.2.341 · DOI · Paper page
  11. Naude, 2022, Low-carbohydrate versus balanced-carbohydrate diets for reducing weight and cardiovascular risk, Cochrane Database Syst. Rev., 1, CD013334
  12. Hariharan, 2015, The Western Diet and Chronic Kidney Disease, Curr. Hypertens. Rep., 17, 16, 10.1007/s11906-014-0529-6 · DOI
  13. Arsene, 2021, Short review on the potential alternatives to antibiotics in the era of antibiotic resistance, J. Appl. Pharm. Sci., 12, 29
  14. 2018, Mediterranean Diet and Cardiovascular Disease Prevention: What Do We Know?, Prog. Cardiovasc. Dis., 61, 62, 10.1016/j.pcad.2018.04.006 · DOI
  15. Mariotti, 2019, Animal and Plant Protein Sources and Cardiometabolic Health, Adv. Nutr., 10, S351, 10.1093/advances/nmy110 · DOI
  16. Chun, 2015, Associations of colorectal cancer incidence with nutrient and food group intakes in korean adults: A case-control study, Clin. Nutr. Res., 4, 110, 10.7762/cnr.2015.4.2.110 · DOI
  17. Hunter, 2010, Cardiovascular disease risk of dietary stearic acid compared with trans, other saturated, and unsaturated fatty acids: A systematic review, Am. J. Clin. Nutr., 91, 46, 10.3945/ajcn.2009.27661 · DOI · Paper page
  18. Wolever, 2001, Carbohydrates and health—The FAO/WHO consultation, Aust. J. Nutr. Diet., 58, S3
  19. Mann, 2007, FAO/WHO Scientific Update on carbohydrates in human nutrition: Conclusions, Eur. J. Clin. Nutr., 61, S132, 10.1038/sj.ejcn.1602943 · DOI · Paper page
  20. Wu, 2015, Association between dietary whole grain intake and risk of mortality: Two large prospective studies in US men and women, JAMA Intern. Med., 175, 373, 10.1001/jamainternmed.2014.6283 · DOI · Paper page
  21. Ogden, 2020, Trends in Obesity Prevalence by Race and Hispanic Origin-1999-2000 to 2017-2018, JAMA, 324, 1208, 10.1001/jama.2020.14590 · DOI · Paper page
  22. Park, 2016, Dietary patterns and colorectal cancer risk in a Korean population: A case-control study, Medicine, 95, e3759, 10.1097/MD.0000000000003759 · DOI
  23. Lee, 2022, United States Dietary Trends Since 1800: Lack of Association Between Saturated Fatty Acid Consumption and Non-communicable Diseases, Front. Nutr., 8, 1267, 10.3389/fnut.2021.748847 · DOI
  24. Clemente-Suárez, V.J., Mielgo-Ayuso, J., Martín-Rodríguez, A., Ramos-Campo, D.J., Redondo-Flórez, L., and Tornero-Aguilera, J.F. (2022). The Burden of Carbohydrates in Health and Disease. Nutrients, 14. · DOI
  25. Conejo, 2020, Western Diet: Implications for Brain Function and Behavior, Front. Psychol., 11, 564413, 10.3389/fpsyg.2020.564413 · DOI
  26. Cinquina, 2020, Life-long epigenetic programming of cortical architecture by maternal ‘Western’ diet during pregnancy, Mol. Psychiatry, 25, 22, 10.1038/s41380-019-0580-4 · DOI
  27. Johnson, 2021, Contrasting effects of Western vs Mediterranean diets on monocyte inflammatory gene expression and social behavior in a primate model, eLife, 10, e68293, 10.7554/eLife.68293 · DOI
  28. Roberts, M.D., Mobley, C.B., Toedebush, R.G., Heese, A.J., Zhu, C., Krieger, A.E., Cruthirds, C.L., Lockwood, C.M., Hofheins, J.C., and Wiedmeyer, C.E. (2015). Western diet-induced hepatic steatosis and alterations in the liver transcriptome in adult Brown-Norway rats. BMC Gastroenterol., 15. · DOI
  29. Burrows, T.L., Whatnall, M.C., Patterson, A.J., and Hutchesson, M.J. (2017). Associations between Dietary Intake and Academic Achievement in College Students: A Systematic Review. Healthcare, 5. · DOI
  30. Yuan, M., Chen, W., Teng, B., and Fang, Y. (2016). Occupational Disparities in the Association between Self-Reported Salt-Eating Habit and Hypertension in Older Adults in Xiamen, China. Int. J. Environ. Res. Public Health, 13. · DOI
  31. Hu, 2004, Occupational, commuting, and leisure-time physical activity in relation to total and cardiovascular mortality among Finnish subjects with type 2 diabetes, Circulation, 110, 666, 10.1161/01.CIR.0000138102.23783.94 · DOI · Paper page
  32. Zhao, 2019, Beneficial associations of low and large doses of leisure time physical activity with all-cause, cardiovascular disease and cancer mortality: A national cohort study of 88,140 US adults, Br. J. Sport. Med., 53, 1405, 10.1136/bjsports-2018-099254 · DOI
  33. Salam, 2020, Update on the classification of higher ranks in the phylum Actinobacteria, Int. J. Syst. Evol. Microbiol., 70, 1331, 10.1099/ijsem.0.003920 · DOI
  34. Lally, 2011, Social norms and diet in adolescents, Appetite, 57, 623, 10.1016/j.appet.2011.07.015 · DOI
  35. Ballal, 2010, Obesogenic high fat western diet induces oxidative stress and apoptosis in rat heart, Mol. Cell. Biochem., 344, 221, 10.1007/s11010-010-0546-y · DOI
  36. Cheeseman, 1993, An introduction to free radical biochemistry, Br. Med. Bull., 49, 481, 10.1093/oxfordjournals.bmb.a072625 · DOI · Paper page
  37. McCord, 2000, The evolution of free radicals and oxidative stress, Am. J. Med., 108, 652, 10.1016/S0002-9343(00)00412-5 · DOI · Paper page
  38. Halliwell, 1995, How to characterize an antioxidant: An update, Biochem. Soc. Symp., 61, 73, 10.1042/bss0610073 · DOI · Paper page
  39. Shi, 1999, Comparative study on dynamics of antioxidative action of alpha-tocopheryl hydroquinone, ubiquinol, and alpha-tocopherol against lipid peroxidation, Free Radic. Biol. Med., 27, 334, 10.1016/S0891-5849(99)00053-2 · DOI
  40. Kunwar, 2011, Free radicals, oxidative stress and importance of antioxidants in human health, J. Med. Allied Sci., 1, 53
  41. Galli, 2009, Effects of fat and fatty acid intake on inflammatory and immune responses: A critical review, Ann. Nutr. Metab., 55, 123, 10.1159/000228999 · DOI · Paper page
  42. Wu, 2004, Glutathione metabolism and its implications for health, J. Nutr., 134, 489, 10.1093/jn/134.3.489 · DOI · Paper page
  43. Lu, W., Shi, Y., Wang, R., Su, D., Tang, M., Liu, Y., and Li, Z. (2021). Antioxidant Activity and Healthy Benefits of Natural Pigments in Fruits: A Review. Int. J. Mol. Sci., 22. · DOI
  44. Manzel, 2014, Role of ‘Western diet’ in inflammatory autoimmune diseases, Curr. Allergy Asthma. Rep., 14, 404, 10.1007/s11882-013-0404-6 · DOI · Paper page
  45. Blaner, 2021, Vitamin A and Vitamin E: Will the Real Antioxidant Please Stand Up?, Annu. Rev. Nutr., 41, 105, 10.1146/annurev-nutr-082018-124228 · DOI
  46. Hodge, 2007, Plasma phospholipid fatty acid composition as a biomarker of habitual dietary fat intake in an ethnically diverse cohort, Nutr. Metab. Cardiovasc. Dis. NMCD, 17, 415, 10.1016/j.numecd.2006.04.005 · DOI
  47. Packer, 1979, Direct observation of a free radical interaction between vitamin E and vitamin C, Nature, 278, 737, 10.1038/278737a0 · DOI · Paper page
  48. Slavin, 2012, Health benefits of fruits and vegetables, Adv. Nutr., 3, 506, 10.3945/an.112.002154 · DOI · Paper page
  49. Lobo, 2010, Free radicals, antioxidants and functional foods: Impact on human health, Pharmacogn. Rev., 4, 118, 10.4103/0973-7847.70902 · DOI · Paper page
  50. Mitchelson, 2020, Regulating metabolic inflammation by nutritional modulation, J. Allergy Clin. Immunol., 146, 706, 10.1016/j.jaci.2020.08.013 · DOI
  51. Gunnerud, U.J., Heinzle, C., Holst, J.J., Östman, E.M., and Björck IM, E. (2012). Effects of pre-meal drinks with protein and amino acids on glycemic and metabolic responses at a subsequent composite meal. PLoS ONE, 7. · DOI
  52. 2002, Effects of antioxidants on immune system ageing, Eur. J. Clin. Nutr., 56, S5, 10.1038/sj.ejcn.1601476 · DOI
  53. Carr, A.C., and Maggini, S. (2017). Vitamin C and Immune Function. Nutrients, 9. · DOI · Paper page
  54. Sesso, 2008, Vitamins E and C in the prevention of cardiovascular disease in men: The Physicians’ Health Study II randomized controlled trial, JAMA, 300, 2123, 10.1001/jama.2008.600 · DOI · Paper page
  55. Bautista, 2011, Inflammation, oxidative stress, and obesity, Int. J. Mol. Sci., 12, 3117, 10.3390/ijms12053117 · DOI · Paper page
  56. Zorov, 2014, Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release, Physiol. Rev., 94, 909, 10.1152/physrev.00026.2013 · DOI · Paper page
  57. Dato, 2013, Exploring the role of genetic variability and lifestyle in oxidative stress response for healthy aging and longevity, Int. J. Mol. Sci., 14, 16443, 10.3390/ijms140816443 · DOI
  58. Macho-González, A., Garcimartín, A., López-Oliva, M.E., Bastida, S., Benedí, J., Ros, G., Nieto, G., and Sánchez-Muniz, F.J. (2020). Can Meat and Meat-Products Induce Oxidative Stress?. Antioxidants, 9. · DOI
  59. Aune, 2009, Meat consumption and the risk of type 2 diabetes: A systematic review and meta-analysis of cohort studies, Diabetologia, 52, 2277, 10.1007/s00125-009-1481-x · DOI · Paper page
  60. Kaczmarczyk, 2012, The health benefits of dietary fiber: Beyond the usual suspects of type 2 diabetes mellitus, cardiovascular disease and colon cancer, Metab. Clin. Exp., 61, 1058, 10.1016/j.metabol.2012.01.017 · DOI · Paper page
  61. Slavin, 2003, Why whole grains are protective: Biological mechanisms, Proc. Nutr. Soc., 62, 129, 10.1079/PNS2002221 · DOI · Paper page
  62. Alzoubi, 2013, The combined effect of sleep deprivation and Western diet on spatial learning and memory: Role of BDNF and oxidative stress, J. Mol. Neurosci. MN, 50, 124, 10.1007/s12031-012-9881-7 · DOI
  63. Radak, 2013, Oxygen consumption and usage during physical exercise: The balance between oxidative stress and ROS-dependent adaptive signaling, Antioxid. Redox Signal., 18, 1208, 10.1089/ars.2011.4498 · DOI · Paper page
  64. Domenech, 2008, Oral administration of vitamin C decreases muscle mitochondrial biogenesis and hampers training-induced adaptations in endurance performance, Am. J. Clin. Nutr., 87, 142, 10.1093/ajcn/87.1.142 · DOI · Paper page
  65. Hecht, 2002, Cigarette smoking and lung cancer: Chemical mechanisms and approaches to prevention, Lancet Oncol., 3, 461, 10.1016/S1470-2045(02)00815-X · DOI · Paper page
  66. Olsen, 2006, Associations between GPX1 Pro198Leu polymorphism, erythrocyte GPX activity, alcohol consumption and breast cancer risk in a prospective cohort study, Carcinogenesis, 27, 820, 10.1093/carcin/bgi267 · DOI
  67. Hwang, 2008, Development of multiple complications in type 2 diabetes is associated with the increase of multiple markers of chronic inflammation, J. Clin. Lab. Anal., 22, 6, 10.1002/jcla.20207 · DOI
  68. Multhoff, 2011, Chronic inflammation in cancer development, Front. Immunol., 2, 98
  69. Esmaillzadeh, 2007, Dietary patterns, insulin resistance, and prevalence of the metabolic syndrome in women, Am. J. Clin. Nutr., 85, 910, 10.1093/ajcn/85.3.910 · DOI · Paper page
  70. Mittal, 2014, Reactive oxygen species in inflammation and tissue injury, Antioxid. Redox Signal., 20, 1126, 10.1089/ars.2012.5149 · DOI · Paper page
  71. Chen, 2021, Novel Sesquiterpene Glycoside from Loquat Leaf Alleviates Type 2 Diabetes Mellitus Combined with Nonalcoholic Fatty Liver Disease by Improving Insulin Resistance, Oxidative Stress, Inflammation, and Gut Microbiota Composition, J. Agric. Food Chem., 69, 14176, 10.1021/acs.jafc.1c05596 · DOI
  72. Sies, 2015, Oxidative stress: A concept in redox biology and medicine, Redox Biol., 4, 180, 10.1016/j.redox.2015.01.002 · DOI · Paper page
  73. Kim, 2013, Effects of turmeric (Curcuma longa L.) on antioxidative systems and oxidative damage in rats fed a high fat and cholesterol diet, J. Korean Soc. Food Sci. Nutr., 42, 570, 10.3746/jkfn.2013.42.4.570 · DOI
  74. Niki, 2005, Lipid peroxidation: Mechanisms, inhibition, and biological effects, Biochem. Biophys. Res. Commun., 338, 668, 10.1016/j.bbrc.2005.08.072 · DOI · Paper page
  75. Micha, 2010, Saturated fat and cardiometabolic risk factors, coronary heart disease, stroke, and diabetes: A fresh look at the evidence, Lipids, 45, 893, 10.1007/s11745-010-3393-4 · DOI · Paper page
  76. Djuricic, I., and Calder, P.C. (2021). Beneficial Outcomes of Omega-6 and Omega-3 Polyunsaturated Fatty Acids on Human Health: An Update for 2021. Nutrients, 13. · DOI · Paper page
  77. Calder, 2020, Nutrition, immunity and COVID-19, BMJ Nutr. Prev. Health, 3, 74, 10.1136/bmjnph-2020-000085 · DOI · Paper page
  78. Takeda, 2004, TLR signaling pathways, Semin. Immunol., 16, 3, 10.1016/j.smim.2003.10.003 · DOI · Paper page
  79. Vlassara, 2014, Advanced glycation end products (AGE) and diabetes: Cause, effect, or both?, Curr. Diabetes Rep., 14, 1, 10.1007/s11892-013-0453-1 · DOI · Paper page
  80. Saavedra, 2010, A diet based on high-heat-treated foods promotes risk factors for diabetes mellitus and cardiovascular diseases, Am. J. Clin. Nutr., 91, 1220, 10.3945/ajcn.2009.28737 · DOI
  81. Perrone, 2020, Advanced Glycation End Products (AGEs): Biochemistry, Signaling, Analytical Methods, and Epigenetic Effects, Oxid. Med. Cell Longev., 2020, 3818196, 10.1155/2020/3818196 · DOI · Paper page
  82. Khalid, M., Petroianu, G., and Adem, A. (2022). Advanced Glycation End Products and Diabetes Mellitus: Mechanisms and Perspectives. Biomolecules, 12. · DOI · Paper page
  83. Stadler, R.H., and Theurillat, V. (2017). Chemical Contaminants and Residues in Food, Elsevier.
  84. Uribarri, 2010, Advanced glycation end products in foods and a practical guide to their reduction in the diet, J. Am. Diet. Assoc., 110, 911, 10.1016/j.jada.2010.03.018 · DOI · Paper page
  85. Hills, R.D., Pontefract, B.A., Mishcon, H.R., Black, C.A., Sutton, S.C., and Theberge, C.R. (2019). Gut Microbiome: Profound Implications for Diet and Disease. Nutrients, 11. · DOI · Paper page
  86. Makki, 2018, The Impact of Dietary Fiber on Gut Microbiota in Host Health and Disease, Cell Host Microbe, 23, 705, 10.1016/j.chom.2018.05.012 · DOI · Paper page
  87. Cani, 2016, How gut microbes talk to organs: The role of endocrine and nervous routes, Mol. Metab., 5, 743, 10.1016/j.molmet.2016.05.011 · DOI · Paper page
  88. Narbad, 2011, The study on the impact of glycated pea proteins on human intestinal bacteria, Int. J. Food Microbiol., 145, 267, 10.1016/j.ijfoodmicro.2011.01.002 · DOI
  89. Butel, 2011, Intestinal microbiota in inflammation and insulin resistance: Relevance to humans, Curr. Opin. Clin. Nutr. Metab. Care, 14, 334, 10.1097/MCO.0b013e328347924a · DOI
  90. Kasai, C., Sugimoto, K., Moritani, I., Tanaka, J., Oya, Y., Inoue, H., Tameda, M., Shiraki, K., Ito, M., and Takei, Y. (2015). Comparison of the gut microbiota composition between obese and non-obese individuals in a Japanese population, as analyzed by terminal restriction fragment length polymorphism and next-generation sequencing. BMC Gastroenterol., 15. · DOI · Paper page
  91. Stojanov, S., Berlec, A., and Štrukelj, B. (2020). The Influence of Probiotics on the Firmicutes/Bacteroidetes Ratio in the Treatment of Obesity and Inflammatory Bowel disease. Microorganisms, 8. · DOI · Paper page
  92. Beam, A., Clinger, E., and Hao, L. (2021). Effect of Diet and Dietary Components on the Composition of the Gut Microbiota. Nutrients, 13. · DOI · Paper page
  93. Statovci, 2017, The Impact of Western Diet and Nutrients on the Microbiota and Immune Response at Mucosal Interfaces, Front. Immunol., 8, 838, 10.3389/fimmu.2017.00838 · DOI · Paper page
  94. Astudillo-López, C.C., Castro-Alarcón, N., Ariza, A.C., Muñoz-Valle, J.F., de la Cruz-Mosso, U., Flores-Alfaro, E., del Moral-Hernández, O., Moreno-Godínez, M.E., Ramírez-Vargas, M.A., and Matia-Garcia, I. (2021). Influence of Diet and Levels of Zonulin, Lipopolysaccharide and C-Reactive Protein on Cardiometabolic Risk Factors in Young Subjects. Nutrients, 13. · DOI
  95. Celiberto, 2018, Inflammatory bowel disease and immunonutrition: Novel therapeutic approaches through modulation of diet and the gut microbiome, Immunology, 155, 36, 10.1111/imm.12939 · DOI
  96. Tsigalou, C., Konstantinidis, T., Paraschaki, A., Stavropoulou, E., Voidarou, C., and Bezirtzoglou, E. (2020). Mediterranean Diet as a Tool to Combat Inflammation and Chronic Diseases. An Overview. Biomedicines, 8. · DOI · Paper page
  97. Illescas, O., Rodríguez-Sosa, M., and Gariboldi, M. (2021). Mediterranean Diet to Prevent the Development of Colon Diseases: A Meta-Analysis of Gut Microbiota Studies. Nutrients, 13. · DOI
  98. Bottero, V., and Potashkin, J.A. (2020). A Comparison of Gene Expression Changes in the Blood of Individuals Consuming Diets Supplemented with Olives, Nuts or Long-Chain Omega-3 Fatty Acids. Nutrients, 12. · DOI
  99. Clemente-Suárez, V.J., Ramos-Campo, D.J., Mielgo-Ayuso, J., Dalamitros, A.A., Nikolaidis, P.A., Hormeño-Holgado, A., and Tornero-Aguilera, J.F. (2021). Nutrition in the Actual COVID-19 Pandemic. A Narrative Review. Nutrients, 13. · DOI
  100. Fu, 2014, Diet, the gut microbiome, and epigenetics, Cancer J., 20, 170, 10.1097/PPO.0000000000000053 · DOI
  101. Huang, 2013, The role of diet in triggering human inflammatory disorders in the modern age, Microbes Infect., 15, 765, 10.1016/j.micinf.2013.07.004 · DOI
  102. Shi, Z. (2019). Gut Microbiota: An Important Link between Western Diet and Chronic Diseases. Nutrients, 11. · DOI
  103. Srour, 2022, Ultra-processed foods and human health: From epidemiological evidence to mechanistic insights, Lancet Gastroenterol. Hepatol., 7, 1128, 10.1016/S2468-1253(22)00169-8 · DOI · Paper page
  104. Machado, 2019, Ultra-processed foods and recommended intake levels of nutrients linked to non-communicable diseases in Australia: Evidence from a nationally representative cross-sectional study, BMJ Open, 9, e029544, 10.1136/bmjopen-2019-029544 · DOI · Paper page
  105. Li, 2015, Consumption of vegetables and fruit and the risk of inflammatory bowel disease: A meta-analysis, Eur. J. Gastroenterol. Hepatol., 27, 623, 10.1097/MEG.0000000000000330 · DOI
  106. Lane, M.M., Gamage, E., Travica, N., Dissanayaka, T., Ashtree, D.N., Gauci, S., Lotfaliany, M., O’Neil, A., Jacka, F.N., and Marx, W. (2022). Ultra-Processed Food Consumption and Mental Health: A Systematic Review and Meta-Analysis of Observational Studies. Nutrients, 14. · DOI · Paper page
  107. Rinninella, E., Cintoni, M., Raoul, P., Lopetuso, L.R., Scaldaferri, F., Pulcini, G., Miggiano, G.A.D., Gasbarrini, A., and Mele, M.C. (2019). Food Components and Dietary Habits: Keys for a Healthy Gut Microbiota Composition. Nutrients, 11. · DOI · Paper page
  108. Ketnawa, 2022, Changes in bioactive compounds and antioxidant activity of plant-based foods by gastrointestinal digestion: A review, Crit. Rev. Food Sci. Nutr., 62, 4684, 10.1080/10408398.2021.1878100 · DOI
  109. Ray, 2021, Evolving Interplay Between Dietary Polyphenols and Gut Microbiota—An Emerging Importance in Healthcare, Front. Nutr., 8, 634944, 10.3389/fnut.2021.634944 · DOI
  110. Wu, 2018, Aronia (Aronia melanocarpa) Polyphenols Modulate the Microbial Community in a Simulator of the Human Intestinal Microbial Ecosystem (SHIME) and Decrease Secretion of Proinflammatory Markers in a Caco-2/endothelial Cell Coculture Model, Mol. Nutr. Food Res., 62, e1800607, 10.1002/mnfr.201800607 · DOI
  111. Neufeld, 2011, Reduced anxiety-like behavior and central neurochemical change in germ-free mice, Neurogastroenterol. Motil. Off. J. Eur. Gastrointest. Motil. Soc., 23, 255, 10.1111/j.1365-2982.2010.01620.x · DOI · Paper page
  112. Martín-Rodríguez, A., Bustamante-Sánchez, Á, Martínez-Guardado, I., Navarro-Jiménez, E., Plata-SanJuan, E., Tornero-Aguilera, J.F., and Clemente-Suárez, V.J. (2022). Infancy Dietary Patterns, Development, and Health: An Extensive Narrative Review. Children, 9. · DOI
  113. Cena, H., and Calder, P.C. (2020). Defining a Healthy Diet: Evidence for The Role of Contemporary Dietary Patterns in Health and Disease. Nutrients, 12. · DOI · Paper page
  114. García-García, F.J., Monistrol-Mula, A., Cardellach, F., and Garrabou, G. (2020). Nutrition, Bioenergetics, and Metabolic Syndrome. Nutrients, 12. · DOI
  115. Burtscher, 2021, The central role of mitochondrial fitness on antiviral defenses: An advocacy for physical activity during the COVID-19 pandemic, Redox Biol., 43, 101976, 10.1016/j.redox.2021.101976 · DOI
  116. Yang, 2020, Adipocyte lipolysis: From molecular mechanisms of regulation to disease and therapeutics, Biochem. J., 477, 985, 10.1042/BCJ20190468 · DOI
  117. Chen, 2018, Resistin destroys mitochondrial biogenesis by inhibiting the PGC-1α/NRF1/TFAM signaling pathway, Biochem. Biophys. Res. Commun., 504, 13, 10.1016/j.bbrc.2018.08.027 · DOI
  118. Yamauchi, 2008, Physiological and pathophysiological roles of adiponectin and adiponectin receptors in the integrated regulation of metabolic and cardiovascular diseases, Int. J. Obes., 32, S13, 10.1038/ijo.2008.233 · DOI · Paper page
  119. Chen, 2018, A high-fat diet impairs mitochondrial biogenesis, mitochondrial dynamics, and the respiratory chain complex in rat myocardial tissues, J. Cell. Biochem., 119, 9602, 10.1002/jcb.27068 · DOI
  120. Lionetti, L., Mollica, M.P., Donizzetti, I., Gifuni, G., Sica, R., Pignalosa, A., Cavaliere, G., Gaita, M., De Filippo, C., and Zorzano, A. (2014). High-lard and high-fish-oil diets differ in their effects on function and dynamic behaviour of rat hepatic mitochondria. PLoS ONE, 9. · DOI
  121. Li, 2021, Effect of high-fat diet on respiratory function and diaphragm fibers in mice and its mitochondrial mechanism, Zhonghua Yi Xue Za Zhi, 101, 2893
  122. Jheng, 2012, Mitochondrial fission contributes to mitochondrial dysfunction and insulin resistance in skeletal muscle, Mol. Cell. Biol., 32, 309, 10.1128/MCB.05603-11 · DOI · Paper page
  123. Tarpey, 2017, Skeletal muscle autophagy and mitophagy in endurance-trained runners before and after a high-fat meal, Mol. Metab., 6, 1597, 10.1016/j.molmet.2017.10.006 · DOI
  124. Shao, 2020, Increasing Fatty Acid Oxidation Prevents High-Fat Diet-Induced Cardiomyopathy through Regulating Parkin-Mediated Mitophagy, Circulation, 142, 983, 10.1161/CIRCULATIONAHA.119.043319 · DOI
  125. Psaltopoulou, 2017, Socioeconomic status and risk factors for cardiovascular disease: Impact of dietary mediators, Hell. J. Cardiol. HJC Hell. Kardiol. Ep., 58, 32, 10.1016/j.hjc.2017.01.022 · DOI
  126. Droomers, 2013, The contribution of diet and lifestyle to socioeconomic inequalities in cardiovascular morbidity and mortality, Int. J. Cardiol., 168, 5190, 10.1016/j.ijcard.2013.07.188 · DOI
  127. Abdelhamid, 2018, Omega-3 fatty acids for the primary and secondary prevention of cardiovascular disease, Cochrane Database Syst. Rev., 7, CD003177
  128. Cho, 2013, Consumption of cereal fiber, mixtures of whole grains and bran, and whole grains and risk reduction in type 2 diabetes, obesity, and cardiovascular disease, Am. J. Clin. Nutr., 98, 594, 10.3945/ajcn.113.067629 · DOI · Paper page
  129. Hartley, 2013, Increased consumption of fruit and vegetables for the primary prevention of cardiovascular diseases, Cochrane Database Syst. Rev., 2013, CD009874
  130. Wallace, T.C., Murray, R., and Zelman, K.M. (2016). The Nutritional Value and Health Benefits of Chickpeas and Hummus. Nutrients, 8. · DOI · Paper page
  131. Salehin, S., Rasmussen, P., Mai, S., Mushtaq, M., Agarwal, M., Hasan, S.M., Salehin, S., Raja, M., Gilani, S., and Khalife, W.I. (2023). Plant Based Diet and Its Effect on Cardiovascular Disease. Int. J. Environ. Res. Public Health, 20. · DOI
  132. Ghosh, 2022, Ghost mitochondria drive metastasis through adaptive GCN2/Akt therapeutic vulnerability, Proc. Natl. Acad. Sci. USA, 119, e2115624119, 10.1073/pnas.2115624119 · DOI
  133. Mozaffarian, 2010, Dietary guidelines in the 21st century--a time for food, JAMA, 304, 681, 10.1001/jama.2010.1116 · DOI · Paper page
  134. Bowen, 2018, Nutrition and cardiovascular disease—an update, Curr. Atheroscler. Rep., 20, 8, 10.1007/s11883-018-0704-3 · DOI
  135. Libby, 2017, Interleukin-1 Beta as a Target for Atherosclerosis Therapy: Biological Basis of CANTOS and Beyond, J. Am. Coll. Cardiol., 70, 2278, 10.1016/j.jacc.2017.09.028 · DOI · Paper page
  136. Ley, 2017, ATVB Distinguished Scientist Award: How Costimulatory and Coinhibitory Pathways Shape Atherosclerosis, Arterioscler. Thromb. Vasc. Biol., 37, 764, 10.1161/ATVBAHA.117.308611 · DOI
  137. Virmani, 2014, Recent highlights of ATVB: Calcification, Arterioscler. Thromb. Vasc. Biol., 34, 1329, 10.1161/ATVBAHA.114.304000 · DOI
  138. Hess, 2016, Clinical Update: Cardiovascular Disease in Diabetes Mellitus: Atherosclerotic Cardiovascular Disease and Heart Failure in Type 2 Diabetes Mellitus—Mechanisms, Management, and Clinical Considerations, Circulation, 133, 2459, 10.1161/CIRCULATIONAHA.116.022194 · DOI · Paper page
  139. Yubero-Serrano, E.M., Fernandez-Gandara, C., Garcia-Rios, A., Rangel-Zuñiga, O.A., Gutierrez-Mariscal, F.M., Torres-Peña, J.D., Marin, C., Lopez-Moreno, J., Castaño, J.P., and Delgado-Lista, J. (2020). Mediterranean diet and endothelial function in patients with coronary heart disease: An analysis of the CORDIOPREV randomized controlled trial. PLoS Med., 17. · DOI
  140. Usui, 2012, Interleukin-17 deficiency reduced vascular inflammation and development of atherosclerosis in Western diet-induced apoE-deficient mice, Biochem. Biophys. Res. Commun., 420, 72, 10.1016/j.bbrc.2012.02.117 · DOI
  141. Tucker, 2016, Dietary Patterns Are Associated with Predicted Cardiovascular Disease Risk in an Urban Mexican Adult Population, J. Nutr., 146, 90, 10.3945/jn.115.217539 · DOI
  142. Atkins, 2016, Dietary patterns and the risk of CVD and all-cause mortality in older British men, Br. J. Nutr., 116, 1246, 10.1017/S0007114516003147 · DOI
  143. Oikonomou, 2018, Western Dietary Pattern Is Associated with Severe Coronary Artery Disease, Angiology, 69, 339, 10.1177/0003319717721603 · DOI
  144. Rees, 2019, Mediterranean-style diet for the primary and secondary prevention of cardiovascular disease, Cochrane Database Syst. Rev., 3, CD009825
  145. Viscogliosi, 2013, Mediterranean dietary pattern adherence: Associations with prediabetes, metabolic syndrome, and related microinflammation, Metab. Syndr. Relat. Disord., 11, 210, 10.1089/met.2012.0168 · DOI · Paper page
  146. Badimon, 2019, Diet and Cardiovascular Disease: Effects of Foods and Nutrients in Classical and Emerging Cardiovascular Risk Factors, Curr. Med. Chem., 26, 3639, 10.2174/0929867324666170428103206 · DOI
  147. Casas, R., Castro-Barquero, S., Estruch, R., and Sacanella, E. (2018). Nutrition and Cardiovascular Health. Int. J. Mol. Sci., 19. · DOI · Paper page
  148. Gao, M., Jebb, S.A., Aveyard, P., Ambrosini, G.L., Perez-Cornago, A., Carter, J., Sun, X., and Piernas, C. (2021). Associations between dietary patterns and the incidence of total and fatal cardiovascular disease and all-cause mortality in 116,806 individuals from the UK Biobank: A prospective cohort study. BMC Med., 19. · DOI
  149. Paglia, 2019, The sweet danger of added sugars, Eur. J. Paediatr. Dent., 20, 89
  150. Batista, 2021, Omega-3 mechanism of action in inflammation and endoplasmic reticulum stress in mononuclear cells from overweight non-alcoholic fatty liver disease participants: Study protocol for the ‘Brazilian Omega Study’ (BROS)-a randomized controlled trial, Trials, 22, 927, 10.1186/s13063-021-05702-x · DOI
  151. Andrade, 2018, Dietary Pattern and Macronutrients Profile on the Variation of Inflammatory Biomarkers: Scientific Update, Cardiol. Res. Pract., 2018, 4762575
  152. Dinu, 2017, Vegetarian, vegan diets and multiple health outcomes: A systematic review with meta-analysis of observational studies, Crit. Rev. Food Sci. Nutr., 57, 3640, 10.1080/10408398.2016.1138447 · DOI · Paper page
  153. Zampelas, 2020, Dietary patterns and risk of cardiovascular diseases: A review of the evidence, Proc. Nutr. Soc., 79, 68, 10.1017/S0029665119000946 · DOI
  154. Shah, 2018, Anti-Inflammatory Effects of a Vegan Diet Versus the American Heart Association-Recommended Diet in Coronary Artery Disease Trial, J. Am. Heart Assoc., 7, e011367, 10.1161/JAHA.118.011367 · DOI
  155. Djekic, 2020, Effects of a Vegetarian Diet on Cardiometabolic Risk Factors, Gut Microbiota, and Plasma Metabolome in Subjects with Ischemic Heart Disease: A Randomized, Crossover Study, J. Am. Heart Assoc., 9, e016518, 10.1161/JAHA.120.016518 · DOI
  156. Djekic, D., Shi, L., Calais, F., Carlsson, F., Landberg, R., Hyötyläinen, T., and Frøbert, O. (2020). Effects of a Lacto-Ovo-Vegetarian Diet on the Plasma Lipidome and Its Association with Atherosclerotic Burden in Patients with Coronary Artery Disease-A Randomized, Open-Label, Cross-over Study. Nutrients, 12. · DOI
  157. Mishra, 2013, A multicenter randomized controlled trial of a plant-based nutrition program to reduce body weight and cardiovascular risk in the corporate setting: The GEICO study, Eur. J. Clin. Nutr., 67, 718, 10.1038/ejcn.2013.92 · DOI
  158. Carson, 2020, Dietary cholesterol and cardiovascular risk: A science advisory from the American Heart Association, Circulation, 141, e39, 10.1161/CIR.0000000000000743 · DOI · Paper page
  159. Kuwahara, 2020, Microbiota-gut-brain axis: Enteroendocrine cells and the enteric nervous system form an interface between the microbiota and the central nervous system, Biomed. Res., 41, 199, 10.2220/biomedres.41.199 · DOI · Paper page
  160. Wang, 2016, Gut Microbiota-brain Axis, Chin. Med. J., 129, 2373, 10.4103/0366-6999.190667 · DOI · Paper page
  161. Dowling, 2022, Enteric nervous system and intestinal epithelial regulation of the gut-brain axis, J. Allergy Clin. Immunol., 150, 513, 10.1016/j.jaci.2022.07.015 · DOI
  162. Bonaz, 2018, The Vagus Nerve at the Interface of the Microbiota-Gut-Brain Axis, Front. Neurosci., 12, 49, 10.3389/fnins.2018.00049 · DOI · Paper page
  163. Barber, T.M., Valsamakis, G., Mastorakos, G., Hanson, P., Kyrou, I., Randeva, H.S., and Weickert, M.O. (2021). Dietary Influences on the Microbiota–Gut–Brain Axis. Int. J. Mol. Sci., 22. · DOI
  164. Durgan, 2019, Examining the Role of the Microbiota-Gut-Brain Axis in Stroke, Stroke, 50, 2270, 10.1161/STROKEAHA.119.025140 · DOI
  165. Hansson, 2019, The Importance and Control of Low-Grade Inflammation Due to Damage of Cellular Barrier Systems That May Lead to Systemic Inflammation, Front. Neurol., 10, 533, 10.3389/fneur.2019.00533 · DOI
  166. Minihane, 2015, Low-grade inflammation, diet composition and health: Current research evidence and its translation, Br. J. Nutr., 114, 999, 10.1017/S0007114515002093 · DOI · Paper page
  167. Rohleder, 2014, Stimulation of systemic low-grade inflammation by psychosocial stress, Psychosom. Med., 76, 181, 10.1097/PSY.0000000000000049 · DOI · Paper page
  168. Walker, W.A. (2017). The Microbiota in Gastrointestinal Pathophysiology, Elsevier.
  169. Stopińska, K., Radziwoń-Zaleska, M., and Domitrz, I. (2021). The Microbiota-Gut-Brain Axis as a Key to Neuropsychiatric Disorders: A Mini Review. J. Clin. Med., 10. · DOI
  170. Shahda, 2010, Study of the prevalence of metabolic syndrome among psychiatric patients and its correlation with diagnosis and medications, Egypt. J. Psychiatry, 31, n2
  171. Mousa, 2017, Metabolic syndrome in psychiatric patients (comparative study), Egypt. J. Psychiatry, 38, 179, 10.4103/ejpsy.ejpsy_24_17 · DOI
  172. 2008, Metabolic Syndrome and Psychiatric Illness: Interactions, Pathophysiology, Assessment, and Treatment, Am. J. Psychiatry, 165, 1056, 10.1176/appi.ajp.2008.08030485 · DOI
  173. Kim, 2010, The contribution of abdominal obesity and dyslipidemia to metabolic syndrome in psychiatric patients, Korean J. Intern. Med., 25, 168, 10.3904/kjim.2010.25.2.168 · DOI
  174. Fabbri, 2018, Pleiotropic genes in psychiatry: Calcium channels and the stress-related FKBP5 gene in antidepressant resistance, Prog. Neuro-Psychopharmacol. Biol. Psychiatry, 81, 203, 10.1016/j.pnpbp.2017.10.005 · DOI
  175. Lee, 2021, Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders, Biol. Psychiatry, 89, 20, 10.1016/j.biopsych.2020.09.026 · DOI
  176. Gorwood, 2004, Generalized anxiety disorder and major depressive disorder comorbidity: An example of genetic pleiotropy?, Eur. Psychiatry J. Assoc. Eur. Psychiatr., 19, 27, 10.1016/j.eurpsy.2003.10.002 · DOI
  177. Zheutlin, 2019, Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems, Am. J. Psychiatry, 176, 846, 10.1176/appi.ajp.2019.18091085 · DOI
  178. Zhu, F., Tu, H., and Chen, T. (2022). The Microbiota-Gut-Brain Axis in Depression: The Potential Pathophysiological Mechanisms and Microbiota Combined Antidepression Effect. Nutrients, 14. · DOI
  179. Hamamah, S., Aghazarian, A., Nazaryan, A., Hajnal, A., and Covasa, M. (2022). Role of Microbiota-Gut-Brain Axis in Regulating Dopaminergic Signaling. Biomedicines, 10. · DOI · Paper page
  180. Holzer, 2014, Neuropeptides and the microbiota-gut-brain axis, Adv. Exp. Med. Biol., 817, 195, 10.1007/978-1-4939-0897-4_9 · DOI · Paper page
  181. Xie, 2019, Specific Microbiota Dynamically Regulate the Bidirectional Gut-Brain Axis Communications in Mice Fed Meat Protein Diets, J. Agric. Food Chem., 67, 1003, 10.1021/acs.jafc.8b05654 · DOI
  182. Walker, 1998, Diet and bacterial colonization: Role of probiotics and prebiotics, J. Nutr. Biochem., 9, 668, 10.1016/S0955-2863(98)00058-8 · DOI
  183. Douglas, 2008, Probiotics and prebiotics in dietetics practice, J. Am. Diet. Assoc., 108, 510, 10.1016/j.jada.2007.12.009 · DOI · Paper page
  184. Green, M., Arora, K., and Prakash, S. (2020). Microbial Medicine: Prebiotic and Probiotic Functional Foods to Target Obesity and Metabolic Syndrome. Int. J. Mol. Sci., 21. · DOI · Paper page
  185. Muir, 1995, Resistant starch in the diet increases breath hydrogen and serum acetate in human subjects, Am. J. Clin. Nutr., 61, 792, 10.1093/ajcn/61.4.792 · DOI
  186. Popova, 2011, Effect of fibre-and starch-rich finishing diets on methanogenic Archaea diversity and activity in the rumen of feedlot bulls, Anim. Feed. Sci. Technol., 166, 113, 10.1016/j.anifeedsci.2011.04.060 · DOI
  187. Giacco, 2004, Effects of short-chain fructo-oligosaccharides on glucose and lipid metabolism in mild hypercholesterolaemic individuals, Clin. Nutr., 23, 331, 10.1016/j.clnu.2003.07.010 · DOI
  188. Nanno, M., Matsumoto, S., and Shida, K. (2014). ECAB Health Impact of Probiotics: Vision & Opportunities-E-Book, Elsevier.
  189. Weichselbaum, 2010, Potential benefits of probiotics--main findings of an in-depth review, Br. J. Community Nurs., 15, 110, 10.12968/bjcn.2010.15.3.46897 · DOI
  190. Pimentel, 2021, Health benefits and technological effects of Lacticaseibacillus casei-01: An overview of the scientific literature, Trends Food Sci. Technol., 114, 722, 10.1016/j.tifs.2021.06.030 · DOI
  191. Foster, 2011, A comprehensive post-market review of studies on a probiotic product containing Lactobacillus helveticus R0052 and Lactobacillus rhamnosus R0011, Benef. Microbes, 2, 319, 10.3920/BM2011.0032 · DOI
  192. Taverniti, 2012, Health-Promoting Properties of Lactobacillus helveticus, Front. Microbiol., 3, 392, 10.3389/fmicb.2012.00392 · DOI
  193. Benno, 1992, Impact of Bifidobacterium longum on human fecal microflora, Microbiol. Immunol., 36, 683, 10.1111/j.1348-0421.1992.tb02071.x · DOI
  194. Underwood, 2015, Bifidobacterium longum subspecies infantis: Champion colonizer of the infant gut, Pediatr. Res., 77, 229, 10.1038/pr.2014.156 · DOI · Paper page
  195. Abhari, 2018, Psychobiotics: Next Generation Treatment for Mental Disorders, J. Clin. Nutr. Diet, 4, 1, 10.4172/2472-1921.100063 · DOI
  196. Malesza, I.J., Malesza, M., Walkowiak, J., Mussin, N., Walkowiak, D., Aringazina, R., Bartkowiak-Wieczorek, J., and Mądry, E. (2021). High-Fat, Western-Style Diet, Systemic Inflammation, and Gut Microbiota: A Narrative Review. Cells, 10. · DOI · Paper page
  197. Shan, 2019, Trends in Dietary Carbohydrate, Protein, and Fat Intake and Diet Quality Among US Adults, 1999–2016, JAMA, 322, 1178, 10.1001/jama.2019.13771 · DOI · Paper page
  198. Jain, 2015, Omega-3 fatty acids and cardiovascular disease, Eur. Rev. Med. Pharmacol. Sci., 19, 441
  199. Shahidi, 2018, Omega-3 Polyunsaturated Fatty Acids and Their Health Benefits, Annu. Rev. Food Sci. Technol., 9, 345, 10.1146/annurev-food-111317-095850 · DOI · Paper page
  200. Dreher, M.L. (2018). Whole Fruits and Fruit Fiber Emerging Health Effects. Nutrients, 10. · DOI · Paper page

200 of 307 shown

Cited by

See all 804

Metadata

Authors
Clemente-Suárez, V. J., Beltrán-Velasco, A. I., Redondo-Flórez, L., Martín-Rodríguez, A., & Tornero-Aguilera, J. F.
Venue
Nutrients
Publisher
MDPI AG
Published
2023-06-14
Volume
15
Issue
12
Pages
2749
ISSN
2072-6643 (ISSN-L)
OpenAlex
W4380789025
Cited by
804
References
75
FWCI
51.49
Type
journal article
Language
en
Open access
gold

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Global Impacts of Western Diet and Its Effects on Metabolism and Health: A Narrative Review. https://app.cochat.ai/papers/10.3390/nu15122749
The paper
Clemente-Suárez, V. J., Beltrán-Velasco, A. I., Redondo-Flórez, L., Martín-Rodríguez, A., & Tornero-Aguilera, J. F. (2023). Global Impacts of Western Diet and Its Effects on Metabolism and Health: A Narrative Review. Nutrients. https://doi.org/10.3390/nu15122749

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.