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Global Impacts of Western Diet and Its Effects on Metabolism and Health: A Narrative Review
Open accessAbstract
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irrelevant topics, not germane to the review’s primary focus; (ii) Ph.D. dissertations, proceedings of conferences, and unpublished studies.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.
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Cites
Siegel, R. L., Miller, K. D., & Jemal, A. (2019) · CA: A Cancer Journal for Clinicians · doi:10.3322/caac.21551 · Cited by 20,160
Diet rapidly and reproducibly alters the human gut microbiome
David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100
Heart disease and stroke statistics-2018 update: a report from the american heart association
Benjamin, E. J., Virani, S. S., Callaway, C. W., Chamberlain, A. M., Chang, A. R., Cheng, S., Chiuve, S. E., Cushman, M., Delling, F. N., Deo, R., et al. (2018) · Circulation · doi:10.1161/cir.0000000000000558 · Cited by 7,146
Free radicals, metals and antioxidants in oxidative stress-induced cancer
Valko, M., Rhodes, C. J., Moncol, J., Izakovic, M., & Mazur, M. (2006) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2005.12.009 · Cited by 6,680
Global aetiology and epidemiology of type 2 diabetes mellitus and its complications
Zheng, Y., Ley, S. H., & Hu, F. B. (2018) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2017.151 · Cited by 5,697
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286
Lloyd-Jones, D. M., Hong, Y., Labarthe, D., Mozaffarian, D., Appel, L. J., Van Horn, L., Greenlund, K., Daniels, S., Nichol, G., Tomaselli, G. F., et al. (2010) · Circulation · doi:10.1161/circulationaha.109.192703 · Cited by 4,750
Adipokines in inflammation and metabolic disease
Ouchi, N., Parker, J. L., Lugus, J. J., & Walsh, K. (2011) · Nature Reviews Immunology · doi:10.1038/nri2921 · Cited by 4,625
Sedentary Behavior Research Network (SBRN)—Terminology Consensus Project process and outcome
on behalf of SBRN Terminology Consensus Project Participants, Tremblay, M. S., Aubert, S., Barnes, J. D., Saunders, T. J., Carson, V., Latimer-Cheung, A. E., Chastin, S. F. M., Altenburg, T. M., & Chinapaw, M. J. M. (2017) · International Journal of Behavioral Nutrition and Physical Activity · doi:10.1186/s12966-017-0525-8 · Cited by 3,793
TLR4 links innate immunity and fatty acid-induced insulin resistance
Shi, H., Kokoeva, M. V., Inouye, K., Tzameli, I., Yin, H., & Flier, J. S. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28898 · Cited by 3,690
The Effect of Diet on the Human Gut Microbiome: A Metagenomic Analysis in Humanized Gnotobiotic Mice
Turnbaugh, P. J., Ridaura, V. K., Faith, J. J., Rey, F. E., Knight, R., & Gordon, J. I. (2009) · Science Translational Medicine · doi:10.1126/scitranslmed.3000322 · Cited by 3,058 · cited 1×
“The Western diet evokes structural and behavioral changes in the resident microbiome, which alters the representation of metabolic pathways in the microbiome and alters microbiome gene expression [35], as well as inducing epigenetic changes in monocytes that affect their inflammatory response and cytokine production […”
BackgroundUltra-processed foods: What they are and how to identify them
Monteiro, C. A., Cannon, G., Levy, R. B., Moubarac, J.-C., Louzada, M. L., Rauber, F., Khandpur, N., Cediel, G., Neri, D., Martinez-Steele, E., et al. (2019) · Public Health Nutrition · doi:10.1017/s1368980018003762 · Cited by 2,964
Influence of diet on the gut microbiome and implications for human health
Singh, R. K., Chang, H.-W., Yan, D., Lee, K. M., Ucmak, D., Wong, K., Abrouk, M., Farahnik, B., Nakamura, M., Zhu, T. H., et al. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-017-1175-y · Cited by 2,599
The Firmicutes/Bacteroidetes Ratio: A Relevant Marker of Gut Dysbiosis in Obese Patients?
Magne, F., Gotteland, M., Gauthier, L., Zazueta, A., Pesoa, S., Navarrete, P., & Balamurugan, R. (2020) · Nutrients · doi:10.3390/nu12051474 · Cited by 2,335
Mozaffarian, D. (2016) · Circulation · doi:10.1161/circulationaha.115.018585 · Cited by 2,216
Sies, H. (2017) · Redox Biology · doi:10.1016/j.redox.2016.12.035 · Cited by 2,148
de Souza, R. J., Mente, A., Maroleanu, A., Cozma, A. I., Ha, V., Kishibe, T., Uleryk, E., Budylowski, P., Schünemann, H., Beyene, J., et al. (2015) · BMJ · doi:10.1136/bmj.h3978 · Cited by 1,424
The local food environment and diet: a systematic review
Caspi, C. E., Sorensen, G., Subramanian, S. V., & Kawachi, I. (2012) · Health & Place · doi:10.1016/j.healthplace.2012.05.006 · Cited by 1,404
The Role of Polyphenols in Human Health and Food Systems: A Mini-Review
Cory, H., Passarelli, S., Szeto, J., Tamez, M., & Mattei, J. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00087 · Cited by 1,297
Yu, T., Robotham, J. L., & Yoon, Y. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0511154103 · Cited by 1,246
Carlsen, M. H., Halvorsen, B. L., Holte, K., Bøhn, S. K., Dragland, S., Sampson, L., Willey, C., Senoo, H., Umezono, Y., Sanada, C., et al. (2010) · Nutrition Journal · doi:10.1186/1475-2891-9-3 · Cited by 1,118
Dietary factors and low-grade inflammation in relation to overweight and obesity
Calder, P. C., Ahluwalia, N., Brouns, F., Buetler, T., Clement, K., Cunningham, K., Esposito, K., Jönsson, L. S., Kolb, H., Lansink, M., et al. (2011) · British Journal of Nutrition · doi:10.1017/s0007114511005460 · Cited by 1,098 · cited 6×
“Thus, trans fatty acids may have a negative effect on health due to their potentially pro-inflammatory activity, enhancing cytokine release from monocytes and macrophages, such as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and monocyte chemoattractant protein (MCP) [310,311].”
BackgroundInfluentialFiolet, T., Srour, B., Sellem, L., Kesse-Guyot, E., Allès, B., Méjean, C., Deschasaux, M., Fassier, P., Latino-Martel, P., Beslay, M., et al. (2018) · BMJ · doi:10.1136/bmj.k322 · Cited by 1,057
Nicholls, S. J., Lincoff, A. M., Garcia, M., Bash, D., Ballantyne, C. M., Barter, P. J., Davidson, M. H., Kastelein, J. J. P., Koenig, W., McGuire, D. K., et al. (2020) · JAMA · doi:10.1001/jama.2020.22258 · Cited by 1,028
Aune, D., Keum, N., Giovannucci, E., Fadnes, L. T., Boffetta, P., Greenwood, D. C., Tonstad, S., Vatten, L. J., Riboli, E., & Norat, T. (2016) · BMJ · doi:10.1136/bmj.i2716 · Cited by 1,013 · cited 1×
“[62] including cardiovascular disease, cancer, and neurodegenerative disorders [63,64].”
BackgroundThe Mediterranean Diet, its Components, and Cardiovascular Disease
Widmer, R. J., Flammer, A. J., Lerman, L. O., & Lerman, A. (2015) · The American Journal of Medicine · doi:10.1016/j.amjmed.2014.10.014 · Cited by 963
Artinian, N. T., Fletcher, G. F., Mozaffarian, D., Kris-Etherton, P., Van Horn, L., Lichtenstein, A. H., Kumanyika, S., Kraus, W. E., Fleg, J. L., Redeker, N. S., et al. (2010) · Circulation · doi:10.1161/cir.0b013e3181e8edf1 · Cited by 919
Western Diet and the Immune System: An Inflammatory Connection
Christ, A., Lauterbach, M., & Latz, E. (2019) · Immunity · doi:10.1016/j.immuni.2019.09.020 · Cited by 907
Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism
Bach, D., Pich, S., Soriano, F. X., Vega, N., Baumgartner, B., Oriola, J., Daugaard, J. R., Lloberas, J., Camps, M., Zierath, J. R., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212754200 · Cited by 832
Mayer, E. A., Nance, K., & Chen, S. (2022) · Annual Review of Medicine · doi:10.1146/annurev-med-042320-014032 · Cited by 813
The Western Diet–Microbiome-Host Interaction and Its Role in Metabolic Disease
Zinöcker, M. K., & Lindseth, I. A. (2018) · doi:10.20944/preprints201803.0064.v1 · Cited by 776
Sparks, L. M., Xie, H., Koza, R. A., Mynatt, R., Hulver, M. W., Bray, G. A., & Smith, S. R. (2005) · Diabetes · doi:10.2337/diabetes.54.7.1926 · Cited by 629
Bolte, L. A., Vich Vila, A., Imhann, F., Collij, V., Gacesa, R., Peters, V., Wijmenga, C., Kurilshikov, A., Campmans-Kuijpers, M. J. E., Fu, J., et al. (2021) · Gut · doi:10.1136/gutjnl-2020-322670 · Cited by 595
Components of a Cardioprotective Diet: New Insights
Mozaffarian, D., Appel, L. J., & Van Horn, L. (2011) · Circulation · doi:10.1161/circulationaha.110.968735 · Cited by 571 · cited 1×
“A study conducted in the United States found that individuals consuming a Western diet had a higher risk of heart disease, diabetes, and stroke than those consuming a healthy diet [65].”
BackgroundMetabolic syndrome in psychiatric patients: overview, mechanisms, and implications
Penninx, B. W. J. H., & Lange, S. M. M. (2018) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2018.20.1/bpenninx · Cited by 566
Martinez-Medina, M., Denizot, J., Dreux, N., Robin, F., Billard, E., Bonnet, R., Darfeuille-Michaud, A., & Barnich, N. (2014) · Gut · doi:10.1136/gutjnl-2012-304119 · Cited by 539
High-fat diets cause insulin resistance despite an increase in muscle mitochondria
Hancock, C. R., Han, D.-H., Chen, M., Terada, S., Yasuda, T., Wright, D. C., & Holloszy, J. O. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802057105 · Cited by 538
A calculated response: control of inflammation by the innate immune system
Barton, G. M. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34431 · Cited by 532
Anand, S. S., Hawkes, C., de Souza, R. J., Mente, A., Dehghan, M., Nugent, R., Zulyniak, M. A., Weis, T., Bernstein, A. M., Krauss, R. M., et al. (2015) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2015.07.050 · Cited by 507
Black, P. H. (2003) · Brain Behavior and Immunity · doi:10.1016/s0889-1591(03)00048-5 · Cited by 502
Tong, M., Saito, T., Zhai, P., Oka, S.-I., Mizushima, W., Nakamura, M., Ikeda, S., Shirakabe, A., & Sadoshima, J. (2019) · Circulation Research · doi:10.1161/circresaha.118.314607 · Cited by 498
Ghanim, H., Abuaysheh, S., Sia, C. L., Korzeniewski, K., Chaudhuri, A., Fernandez-Real, J. M., & Dandona, P. (2009) · Diabetes Care · doi:10.2337/dc09-0979 · Cited by 494
The role of adipokines in health and disease
Clemente-Suárez, V. J., Redondo-Flórez, L., Beltrán-Velasco, A. I., Martín-Rodríguez, A., Martínez-Guardado, I., Navarro-Jiménez, E., Laborde-Cárdenas, C. C., & Tornero-Aguilera, J. F. (2023) · Biomedicines · doi:10.3390/biomedicines11051290 · Cited by 463
Self-citationVery long-chain n -3 fatty acids and human health: fact, fiction and the future
Calder, P. C. (2018) · Proceedings of the Nutrition Society · doi:10.1017/s0029665117003950 · Cited by 419
Bertoia, M. L., Mukamal, K. J., Cahill, L. E., Hou, T., Ludwig, D. S., Mozaffarian, D., Willett, W. C., Hu, F. B., & Rimm, E. B. (2015) · PLOS Medicine · doi:10.1371/journal.pmed.1001878 · Cited by 397 · cited 1×
“One study found that increasing the consumption of fruits and vegetables, which are high in antioxidants, was associated with a lower risk of mortality from cardiovascular disease and cancer [70].”
BackgroundSchnabel, L., Kesse-Guyot, E., Allès, B., Touvier, M., Srour, B., Hercberg, S., Buscail, C., & Julia, C. (2019) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2018.7289 · Cited by 390
Rethinking the Warburg Effect with Myc Micromanaging Glutamine Metabolism
Dang, C. V. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-3556 · Cited by 379
Functional Foods and Lifestyle Approaches for Diabetes Prevention and Management
Alkhatib, A., Tsang, C., Tiss, A., Bahorun, T., Arefanian, H., Barake, R., Khadir, A., & Tuomilehto, J. (2017) · Nutrients · doi:10.3390/nu9121310 · Cited by 376
Diet and the human gut microbiome: An international review
Wilson, A. S., Koller, K. R., Ramaboli, M. C., Nesengani, L. T., Ocvirk, S., Chen, C., Flanagan, C. A., Sapp, F. R., Merritt, Z. T., Bhatti, F., et al. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06112-w · Cited by 369
Wright, N., Wilson, L., Smith, M., Duncan, B., & McHugh, P. (2017) · Nutrition & Diabetes · doi:10.1038/nutd.2017.3 · Cited by 340
Noble, E. E., Hsu, T. M., & Kanoski, S. E. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00009 · Cited by 333
Martín-Peláez, S., Fito, M., & Castaner, O. (2020) · Nutrients · doi:10.3390/nu12082236 · Cited by 330
Zhong, V. W., Van Horn, L., Cornelis, M. C., Wilkins, J. T., Ning, H., Carnethon, M. R., Greenland, P., Mentz, R. J., Tucker, K. L., Zhao, L., et al. (2019) · JAMA · doi:10.1001/jama.2019.1572 · Cited by 327
The neuroendocrinology of the microbiota-gut-brain axis: a behavioural perspective
Cussotto, S., Sandhu, K. V., Dinan, T. G., & Cryan, J. F. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.04.002 · Cited by 326
A Taxonomic Signature of Obesity in the Microbiome? Getting to the Guts of the Matter
Finucane, M. M., Sharpton, T. J., Laurent, T. J., & Pollard, K. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084689 · Cited by 321
Nani, A., Murtaza, B., Sayed Khan, A., Khan, N. A., & Hichami, A. (2021) · Molecules · doi:10.3390/molecules26040985 · Cited by 321
Mediterranean Diet as an Antioxidant: The Impact on Metabolic Health and Overall Wellbeing
Gantenbein, K. V., & Kanaka-Gantenbein, C. (2021) · Nutrients · doi:10.3390/nu13061951 · Cited by 288
De Filippo, C., Di Paola, M., Ramazzotti, M., Albanese, D., Pieraccini, G., Banci, E., Miglietta, F., Cavalieri, D., & Lionetti, P. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01979 · Cited by 270
Potato and french fry consumption and risk of type 2 diabetes in women
Halton, T. L., Willett, W. C., Liu, S., Manson, J. E., Stampfer, M. J., & Hu, F. B. (2006) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/83.2.284 · Cited by 257
Dietary protein intake and risk of type 2 diabetes in US men and women
Malik, V. S., Li, Y., Tobias, D. K., Pan, A., & Hu, F. B. (2016) · American Journal of Epidemiology · doi:10.1093/aje/kwv268 · Cited by 251
Cerdá, B., Pérez, M., Pérez-Santiago, J. D., Tornero-Aguilera, J. F., González-Soltero, R., & Larrosa, M. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00051 · Cited by 247
Self-citationBlood n-3 fatty acid levels and total and cause-specific mortality from 17 prospective studies
Harris, W. S., Tintle, N. L., Imamura, F., Qian, F., Korat, A. V. A., Marklund, M., Djoussé, L., Bassett, J. K., Carmichael, P.-H., Chen, Y.-Y., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22370-2 · Cited by 244
Microbiota and the gut–brain axis
Bienenstock, J., Kunze, W., & Forsythe, P. (2015) · Nutrition Reviews · doi:10.1093/nutrit/nuv019 · Cited by 234
Microbiota and Lifestyle: A Special Focus on Diet
Redondo-Useros, N., Nova, E., González-Zancada, N., Díaz, L. E., Gómez-Martínez, S., & Marcos, A. (2020) · Nutrients · doi:10.3390/nu12061776 · Cited by 189
Cordero, M. D., De Miguel, M., Moreno Fernández, A. M., Carmona López, I. M., Garrido Maraver, J., Cotán, D., Gómez Izquierdo, L., Bonal, P., Campa, F., Bullon, P., et al. (2010) · Arthritis Research & Therapy · doi:10.1186/ar2918 · Cited by 165
Microbial Reprogramming Inhibits Western Diet-Associated Obesity
Poutahidis, T., Kleinewietfeld, M., Smillie, C., Levkovich, T., Perrotta, A., Bhela, S., Varian, B. J., Ibrahim, Y. M., Lakritz, J. R., Kearney, S. M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068596 · Cited by 164
Frankenfeld, C. L., Sikaroodi, M., Lamb, E., Shoemaker, S., & Gillevet, P. M. (2015) · Annals of Epidemiology · doi:10.1016/j.annepidem.2015.06.083 · Cited by 123
Cooksey Stowers, K., Jiang, Q., Atoloye, A., Lucan, S., & Gans, K. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17197143 · Cited by 117
Jenkins, D. J. A., Wong, J. M. W., Kendall, C. W. C., Esfahani, A., Ng, V. W. Y., Leong, T. C. K., Faulkner, D. A., Vidgen, E., Paul, G., Mukherjea, R., et al. (2014) · BMJ Open · doi:10.1136/bmjopen-2013-003505 · Cited by 109
Khan, T. A., Tayyiba, M., Agarwal, A., Mejia, S. B., de Souza, R. J., Wolever, T. M. S., Leiter, L. A., Kendall, C. W. C., Jenkins, D. J. A., & Sievenpiper, J. L. (2019) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2019.05.034 · Cited by 93
Gut Microbiota and Type 1 Diabetes Mellitus: The Effect of Mediterranean Diet
Calabrese, C. M., Valentini, A., & Calabrese, G. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2020.612773 · Cited by 58
The relationship between obesity and other medical comorbidities
Afolabi, H. A., Zakariya, Z. B., Ahmed Shokri, A. B., Mohammad Hasim, M. N. B., Vinayak, R., Afolabi-Owolabi, O. T., & Elesho, R. F. (2020) · Obesity Medicine · doi:10.1016/j.obmed.2019.100164 · Cited by 54
Luu, N.-T., Madden, J., Calder, P. C., Grimble, R. F., Shearman, C. P., Chan, T., Dastur, N., Howell, W. M., Rainger, G. E., & Nash, G. B. (2007) · The Journal of Nutrition · doi:10.1093/jn/137.12.2769 · Cited by 41
Torrico, B., Shaw, A. D., Mosca, R., Vivó-Luque, N., Hervás, A., Fernàndez-Castillo, N., Aloy, P., Bayés, M., Fullerton, J. M., Cormand, B., et al. (2019) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.180184 · Cited by 34
Turner-McGrievy, G. M., Wilcox, S., Frongillo, E. A., Murphy, E. A., Hutto, B., Wilson, M., Davey, M., Bernhart, J. A., Okpara, N., Bailey, S., et al. (2023) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.50626 · Cited by 27
Research works printed but not linked: 307
- 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
- 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
- Kennedy, 2004, Globalization of food systems in developing countries: Impact on food security and nutrition, FAO Food Nutr. Pap., 83, 1
- 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
- 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
- Rakhra, 2020, Obesity and the Western Diet: How We Got Here, Mo. Med., 117, 536
- 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
- Mahfoud, 2022, Arterial hypertension—Clinical trials update 2021, Nutr. Metab. Cardiovasc. Dis., 32, 21, 10.1016/j.numecd.2021.09.007 · DOI
- Lindeberg, 2011, The western diet and lifestyle and diseases of civilization, Res. Rep. Clin. Cardiol., 2, 15
- 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
- Naude, 2022, Low-carbohydrate versus balanced-carbohydrate diets for reducing weight and cardiovascular risk, Cochrane Database Syst. Rev., 1, CD013334
- Hariharan, 2015, The Western Diet and Chronic Kidney Disease, Curr. Hypertens. Rep., 17, 16, 10.1007/s11906-014-0529-6 · DOI
- Arsene, 2021, Short review on the potential alternatives to antibiotics in the era of antibiotic resistance, J. Appl. Pharm. Sci., 12, 29
- 2018, Mediterranean Diet and Cardiovascular Disease Prevention: What Do We Know?, Prog. Cardiovasc. Dis., 61, 62, 10.1016/j.pcad.2018.04.006 · DOI
- Mariotti, 2019, Animal and Plant Protein Sources and Cardiometabolic Health, Adv. Nutr., 10, S351, 10.1093/advances/nmy110 · DOI
- 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
- 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
- Wolever, 2001, Carbohydrates and health—The FAO/WHO consultation, Aust. J. Nutr. Diet., 58, S3
- 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
- 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
- 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
- Park, 2016, Dietary patterns and colorectal cancer risk in a Korean population: A case-control study, Medicine, 95, e3759, 10.1097/MD.0000000000003759 · DOI
- 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
- 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
- Conejo, 2020, Western Diet: Implications for Brain Function and Behavior, Front. Psychol., 11, 564413, 10.3389/fpsyg.2020.564413 · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Lally, 2011, Social norms and diet in adolescents, Appetite, 57, 623, 10.1016/j.appet.2011.07.015 · DOI
- 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
- Cheeseman, 1993, An introduction to free radical biochemistry, Br. Med. Bull., 49, 481, 10.1093/oxfordjournals.bmb.a072625 · DOI · Paper page
- 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
- Halliwell, 1995, How to characterize an antioxidant: An update, Biochem. Soc. Symp., 61, 73, 10.1042/bss0610073 · DOI · Paper page
- 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
- Kunwar, 2011, Free radicals, oxidative stress and importance of antioxidants in human health, J. Med. Allied Sci., 1, 53
- 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
- Wu, 2004, Glutathione metabolism and its implications for health, J. Nutr., 134, 489, 10.1093/jn/134.3.489 · DOI · Paper page
- 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
- 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
- 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
- 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
- Packer, 1979, Direct observation of a free radical interaction between vitamin E and vitamin C, Nature, 278, 737, 10.1038/278737a0 · DOI · Paper page
- Slavin, 2012, Health benefits of fruits and vegetables, Adv. Nutr., 3, 506, 10.3945/an.112.002154 · DOI · Paper page
- Lobo, 2010, Free radicals, antioxidants and functional foods: Impact on human health, Pharmacogn. Rev., 4, 118, 10.4103/0973-7847.70902 · DOI · Paper page
- Mitchelson, 2020, Regulating metabolic inflammation by nutritional modulation, J. Allergy Clin. Immunol., 146, 706, 10.1016/j.jaci.2020.08.013 · DOI
- 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
- 2002, Effects of antioxidants on immune system ageing, Eur. J. Clin. Nutr., 56, S5, 10.1038/sj.ejcn.1601476 · DOI
- Carr, A.C., and Maggini, S. (2017). Vitamin C and Immune Function. Nutrients, 9. · DOI · Paper page
- 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
- Bautista, 2011, Inflammation, oxidative stress, and obesity, Int. J. Mol. Sci., 12, 3117, 10.3390/ijms12053117 · DOI · Paper page
- Zorov, 2014, Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release, Physiol. Rev., 94, 909, 10.1152/physrev.00026.2013 · DOI · Paper page
- 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
- 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
- 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
- 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
- Slavin, 2003, Why whole grains are protective: Biological mechanisms, Proc. Nutr. Soc., 62, 129, 10.1079/PNS2002221 · DOI · Paper page
- 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
- 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
- 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
- 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
- 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
- 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
- Multhoff, 2011, Chronic inflammation in cancer development, Front. Immunol., 2, 98
- 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
- Mittal, 2014, Reactive oxygen species in inflammation and tissue injury, Antioxid. Redox Signal., 20, 1126, 10.1089/ars.2012.5149 · DOI · Paper page
- 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
- 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
- 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
- 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
- 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
- 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
- Calder, 2020, Nutrition, immunity and COVID-19, BMJ Nutr. Prev. Health, 3, 74, 10.1136/bmjnph-2020-000085 · DOI · Paper page
- Takeda, 2004, TLR signaling pathways, Semin. Immunol., 16, 3, 10.1016/j.smim.2003.10.003 · DOI · Paper page
- 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
- 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
- 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
- Khalid, M., Petroianu, G., and Adem, A. (2022). Advanced Glycation End Products and Diabetes Mellitus: Mechanisms and Perspectives. Biomolecules, 12. · DOI · Paper page
- Stadler, R.H., and Theurillat, V. (2017). Chemical Contaminants and Residues in Food, Elsevier.
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Fu, 2014, Diet, the gut microbiome, and epigenetics, Cancer J., 20, 170, 10.1097/PPO.0000000000000053 · DOI
- 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
- Shi, Z. (2019). Gut Microbiota: An Important Link between Western Diet and Chronic Diseases. Nutrients, 11. · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- García-García, F.J., Monistrol-Mula, A., Cardellach, F., and Garrabou, G. (2020). Nutrition, Bioenergetics, and Metabolic Syndrome. Nutrients, 12. · DOI
- 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
- Yang, 2020, Adipocyte lipolysis: From molecular mechanisms of regulation to disease and therapeutics, Biochem. J., 477, 985, 10.1042/BCJ20190468 · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Abdelhamid, 2018, Omega-3 fatty acids for the primary and secondary prevention of cardiovascular disease, Cochrane Database Syst. Rev., 7, CD003177
- 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
- Hartley, 2013, Increased consumption of fruit and vegetables for the primary prevention of cardiovascular diseases, Cochrane Database Syst. Rev., 2013, CD009874
- 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
- 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
- Ghosh, 2022, Ghost mitochondria drive metastasis through adaptive GCN2/Akt therapeutic vulnerability, Proc. Natl. Acad. Sci. USA, 119, e2115624119, 10.1073/pnas.2115624119 · DOI
- Mozaffarian, 2010, Dietary guidelines in the 21st century--a time for food, JAMA, 304, 681, 10.1001/jama.2010.1116 · DOI · Paper page
- Bowen, 2018, Nutrition and cardiovascular disease—an update, Curr. Atheroscler. Rep., 20, 8, 10.1007/s11883-018-0704-3 · DOI
- 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
- 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
- Virmani, 2014, Recent highlights of ATVB: Calcification, Arterioscler. Thromb. Vasc. Biol., 34, 1329, 10.1161/ATVBAHA.114.304000 · DOI
- 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
- 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
- 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
- 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
- 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
- Oikonomou, 2018, Western Dietary Pattern Is Associated with Severe Coronary Artery Disease, Angiology, 69, 339, 10.1177/0003319717721603 · DOI
- Rees, 2019, Mediterranean-style diet for the primary and secondary prevention of cardiovascular disease, Cochrane Database Syst. Rev., 3, CD009825
- 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
- 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
- Casas, R., Castro-Barquero, S., Estruch, R., and Sacanella, E. (2018). Nutrition and Cardiovascular Health. Int. J. Mol. Sci., 19. · DOI · Paper page
- 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
- Paglia, 2019, The sweet danger of added sugars, Eur. J. Paediatr. Dent., 20, 89
- 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
- Andrade, 2018, Dietary Pattern and Macronutrients Profile on the Variation of Inflammatory Biomarkers: Scientific Update, Cardiol. Res. Pract., 2018, 4762575
- 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
- Zampelas, 2020, Dietary patterns and risk of cardiovascular diseases: A review of the evidence, Proc. Nutr. Soc., 79, 68, 10.1017/S0029665119000946 · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- Wang, 2016, Gut Microbiota-brain Axis, Chin. Med. J., 129, 2373, 10.4103/0366-6999.190667 · DOI · Paper page
- 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
- 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
- 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
- Durgan, 2019, Examining the Role of the Microbiota-Gut-Brain Axis in Stroke, Stroke, 50, 2270, 10.1161/STROKEAHA.119.025140 · DOI
- 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
- 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
- Rohleder, 2014, Stimulation of systemic low-grade inflammation by psychosocial stress, Psychosom. Med., 76, 181, 10.1097/PSY.0000000000000049 · DOI · Paper page
- Walker, W.A. (2017). The Microbiota in Gastrointestinal Pathophysiology, Elsevier.
- 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
- Shahda, 2010, Study of the prevalence of metabolic syndrome among psychiatric patients and its correlation with diagnosis and medications, Egypt. J. Psychiatry, 31, n2
- Mousa, 2017, Metabolic syndrome in psychiatric patients (comparative study), Egypt. J. Psychiatry, 38, 179, 10.4103/ejpsy.ejpsy_24_17 · DOI
- 2008, Metabolic Syndrome and Psychiatric Illness: Interactions, Pathophysiology, Assessment, and Treatment, Am. J. Psychiatry, 165, 1056, 10.1176/appi.ajp.2008.08030485 · DOI
- 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
- 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
- Lee, 2021, Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders, Biol. Psychiatry, 89, 20, 10.1016/j.biopsych.2020.09.026 · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- Walker, 1998, Diet and bacterial colonization: Role of probiotics and prebiotics, J. Nutr. Biochem., 9, 668, 10.1016/S0955-2863(98)00058-8 · DOI
- Douglas, 2008, Probiotics and prebiotics in dietetics practice, J. Am. Diet. Assoc., 108, 510, 10.1016/j.jada.2007.12.009 · DOI · Paper page
- 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
- 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
- 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
- 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
- Nanno, M., Matsumoto, S., and Shida, K. (2014). ECAB Health Impact of Probiotics: Vision & Opportunities-E-Book, Elsevier.
- 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
- 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
- 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
- Taverniti, 2012, Health-Promoting Properties of Lactobacillus helveticus, Front. Microbiol., 3, 392, 10.3389/fmicb.2012.00392 · DOI
- Benno, 1992, Impact of Bifidobacterium longum on human fecal microflora, Microbiol. Immunol., 36, 683, 10.1111/j.1348-0421.1992.tb02071.x · DOI
- Underwood, 2015, Bifidobacterium longum subspecies infantis: Champion colonizer of the infant gut, Pediatr. Res., 77, 229, 10.1038/pr.2014.156 · DOI · Paper page
- Abhari, 2018, Psychobiotics: Next Generation Treatment for Mental Disorders, J. Clin. Nutr. Diet, 4, 1, 10.4172/2472-1921.100063 · DOI
- 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
- 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
- Jain, 2015, Omega-3 fatty acids and cardiovascular disease, Eur. Rev. Med. Pharmacol. Sci., 19, 441
- 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
- Dreher, M.L. (2018). Whole Fruits and Fruit Fiber Emerging Health Effects. Nutrients, 10. · DOI · Paper page
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Ansari, P., Khan, J. T., Choudhary, S., Reberio, A. D., Kumar, S., Seidel, V., Abdel-Wahab, Y. H. A., & Flatt, P. R. (2024) · doi:10.20944/preprints202408.1739.v1 · Cited by 89
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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
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