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Ultra-processed diet, systemic oxidative stress, and breach of immunologic tolerance
Abstract
In recent years, consumption of ultra-processed food around the world has been increasing. The nutritional profile of an ultra-processed diet is associated with the development of cellular alterations that lead to oxidative stress. The chronic prooxidative state leads to an environment that influences the proliferation, apoptosis, and signaling pathways of immune cells. Likewise, the decrease in the transcription factor NRF2, owing to exacerbated production of reactive oxygen species, leads to changes in immune function and response to infections. This review aims to analyze the connection between an ultra-processed diet, systemic oxidative stress, and immune tolerance, as a contribution to the scientific evidence on the impact of oxidative stress on health and the possible risk of infections-an important consideration in the association of eating pattern and the immune response.
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“Such nutrient-poor dietary profiles have been implicated in the prevalence and incidence of chronic diseases through various pathways, including inflammatory mechanisms.”
From Ultra-processed food exposure and adverse health outcomes: umbrella review of epidemiological meta-analyses (2024) · cites this paper as [14]
In the citing paper
“they suggest that higher consumption of ultra-processed foods within broader dietary patterns may have synergistic or compounded consequences compared with lower intakes”
From Ultra-processed food exposure and adverse health outcomes: umbrella review of epidemiological meta-analyses (2024) · cites this paper as [14]
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Cites
Chang, P. V., Hao, L., Offermanns, S., & Medzhitov, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322269111 · Cited by 2,175
The microbiome and innate immunity
Thaiss, C. A., Zmora, N., Levy, M., & Elinav, E. (2016) · Nature · doi:10.1038/nature18847 · Cited by 2,012
Hall, K. D., Ayuketah, A., Brychta, R., Cai, H., Cassimatis, T., Chen, K. Y., Chung, S. T., Costa, E., Courville, A., Darcey, V., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.05.008 · Cited by 1,971
Moodie, R., Stuckler, D., Monteiro, C., Sheron, N., Neal, B., Thamarangsi, T., Lincoln, P., & Casswell, S. (2013) · The Lancet · doi:10.1016/s0140-6736(12)62089-3 · Cited by 1,663
Johnson, R. K., Appel, L. J., Brands, M., Howard, B. V., Lefevre, M., Lustig, R. H., Sacks, F., Steffen, L. M., & Wylie-Rosett, J. (2009) · Circulation · doi:10.1161/circulationaha.109.192627 · Cited by 1,207
Microbes, Metabolites, and the Gut-Lung Axis
Dang, A. T., & Marsland, B. J. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0160-6 · Cited by 1,028
Consumption of ultra-processed foods and obesity in Brazilian adolescents and adults
Louzada, M. L. D. C., Baraldi, L. G., Steele, E. M., Martins, A. P. B., Canella, D. S., Moubarac, J.-C., Levy, R. B., Cannon, G., Afshin, A., Imamura, F., et al. (2015) · Preventive Medicine · doi:10.1016/j.ypmed.2015.07.018 · Cited by 656
Rauber, F., Da Costa Louzada, M. L., Steele, E., Millett, C., Monteiro, C. A., & Levy, R. B. (2018) · Nutrients · doi:10.3390/nu10050587 · Cited by 628
Martínez Steele, E., Popkin, B. M., Swinburn, B., & Monteiro, C. A. (2017) · Population Health Metrics · doi:10.1186/s12963-017-0119-3 · Cited by 585
Probiotics for preventing acute upper respiratory tract infections
Hao, Q., Dong, B. R., & Wu, T. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006895.pub3 · Cited by 569
Flagged first, then by citations
Research works printed but not linked: 99
- Monteiro, 2010, Increasing consumption of ultra-processed foods and likely impact on human health: evidence from Brazil, Public Health Nutr, 14, 5, 10.1017/S1368980010003241 · DOI · Paper page
- Pagliai, 2021, Consumption of ultra-processed foods and health status: a systematic review and meta-analysis, Br J Nutr, 125, 308, 10.1017/S0007114520002688 · DOI · Paper page
- Askari, 2020, Ultra-processed food and the risk of overweight and obesity: a systematic review and meta-analysis of observational studies, Int J Obes (Lond), 44, 2080, 10.1038/s41366-020-00650-z · DOI
- Zheng, 2020, A taxonomic note on the genus Lactobacillus: Description of 23 novel genera, emended description of the genus Lactobacillus Beijerinck 1901, and union of Lactobacikllaceae and Leuconostocaceae, Int J Syst Evol Microbiol, 70, 2782, 10.1099/ijsem.0.004107 · DOI · Paper page
- Gutteridge, 2018, Mini-review: oxidative stress, redox stress or redox success?, Biochem Biophys Res Commun, 502, 183, 10.1016/j.bbrc.2018.05.045 · DOI
- Song, 2020, The adipocyte and adaptive immunity, Front Immunol, 11, 10.3389/fimmu.2020.593058 · DOI
- Wesley, 2021, Mendonça Oliveira L de, Calvielli Castelo Branco AC, Zanete Pereira N, Notomi Sato M. Obesity as a risk factor for COVID-19: an overview, Crit Rev Food Sci Nutr, 61, 2262, 10.1080/10408398.2020.1775546 · DOI
- Nardocci, 2019, Consumption of ultra-processed foods and obesity in Canada, Can J Public Health, 110, 4, 10.17269/s41997-018-0130-x · DOI
- Ludwig, 2018, Dietary carbohydrates: role of quality and quantity in chronic disease, BMJ, 361, k2340, 10.1136/bmj.k2340 · DOI
- Makarem, 2018, Consumption of sugars, sugary foods, and sugary beverages in relation to cancer risk: a systematic review of longitudinal studies, Annu Rev Nutr, 38, 17, 10.1146/annurev-nutr-082117-051805 · DOI
- Tappy, 2010, Fructose and metabolic diseases: new findings, new questions, Nutrition, 26, 1044, 10.1016/j.nut.2010.02.014 · DOI
- Liu, 2020, Glucose-induced oxidative stress and accelerated aging in endothelial cells are mediated by the depletion of mitochondrial SIRTs, Physiol Rep, 8, e14331, 10.14814/phy2.14331 · DOI
- Prentice, 2003, Fast foods, energy density and obesity: a possible mechanistic link, Obes Rev, 4, 187, 10.1046/j.1467-789X.2003.00117.x · DOI
- Juul, 2021, Ultra-processed foods and cardiovascular diseases: potential mechanisms of action, Adv Nutr, 10.1093/advances/nmab049 · DOI · Paper page
- Srour, 2019, Ultra-processed food intake and risk of cardiovascular disease: prospective cohort study (NutriNet-Santé), BMJ, 365, l1451, 10.1136/bmj.l1451 · DOI · Paper page
- Benson, 2010, Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors, Proc Natl Acad Sci U S A, 107, 18933, 10.1073/pnas.1007028107 · DOI · Paper page
- Cuevas-Sierra, 2019, Diet, gut microbiota, and obesity: links with host genetics and epigenetics and potential applications, Adv Nutr, 10, S17, 10.1093/advances/nmy078 · DOI · Paper page
- Ranjbar, 2015, Urinary biomarkers of polycyclic aromatic hydrocarbons are associated with cardiometabolic health risk, PLoS One, 10, 10.1371/journal.pone.0137536 · DOI
- Farzan, 2016, Urinary polycyclic aromatic hydrocarbons and measures of oxidative stress, inflammation and renal function in adolescents: NHANES 2003–2008, Environ Res, 144, 149, 10.1016/j.envres.2015.11.012 · DOI
- Rauber, 2021, Ultra-processed food consumption and risk of obesity: a prospective cohort study of UK Biobank, Eur J Nutr, 60, 2169, 10.1007/s00394-020-02367-1 · DOI
- Levy, 2021, Ultra-processed food consumption and type 2 diabetes incidence: a prospective cohort study, Clin Nutr, 40, 3608, 10.1016/j.clnu.2020.12.018 · DOI
- Nardocci, 2021, Consumption of ultra-processed foods is associated with obesity, diabetes and hypertension in Canadian adults, Can J Public Health, 112, 421, 10.17269/s41997-020-00429-9 · DOI
- Beslay, 2020, Ultra-processed food intake in association with BMI change and risk of overweight and obesity: a prospective analysis of the French NutriNet-Santé cohort, PLoS Med, 17, 10.1371/journal.pmed.1003256 · DOI
- Pereira Machado, 2020, Ultra-processed food consumption and obesity in the Australian adult population, Nutr Diabetes, 10, 39, 10.1038/s41387-020-00141-0 · DOI
- Sandoval-Insausti, 2020, Ultra-processed food consumption is associated with abdominal obesity: a prospective cohort study in older adults, Nutrients, 12, 2368, 10.3390/nu12082368 · DOI
- Canhada, 2020, Ultra-processed foods, incident overweight and obesity, and longitudinal changes in weight and waist circumference: the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil), Public Health Nutr, 23, 1076, 10.1017/S1368980019002854 · DOI
- Smaira, 2020, Ultra-processed food consumption associates with higher cardiovascular risk in rheumatoid arthritis, Clin Rheumatol, 39, 1423, 10.1007/s10067-019-04916-4 · DOI
- Rauber, 2020, Ultra-processed food consumption and indicators of obesity in the United Kingdom population (2008-2016), PLoS One, 15, 10.1371/journal.pone.0232676 · DOI
- Mendonça, 2016, Ultraprocessed food consumption and risk of overweight and obesity: the University of Navarra Follow-Up (SUN) cohort study, Am J Clin Nutr, 104, 1433, 10.3945/ajcn.116.135004 · DOI · Paper page
- Collins, 2018, Obesity, metabolic syndrome, and musculoskeletal disease: common inflammatory pathways suggest a central role for loss of muscle integrity, Front Physiol, 9, 112, 10.3389/fphys.2018.00112 · DOI
- Geto, 2020, Mitochondrial dynamic dysfunction as a main triggering factor for inflammation associated chronic non-communicable diseases, J Inflamm Res, 13, 97, 10.2147/JIR.S232009 · DOI
- Hyatt, 2019, Mitochondrial dysfunction induces muscle atrophy during prolonged inactivity: a review of the causes and effects, Arch Biochem Biophys, 662, 49, 10.1016/j.abb.2018.11.005 · DOI
- Davis, 2012, Mitochondrial function and dysfunction: an update, J Pharmacol Exp Ther, 342, 598, 10.1124/jpet.112.192104 · DOI
- Li, 2018, Epigenetic activation of PERP transcription by MKL1 contributes to ROS-induced apoptosis in skeletal muscle cells, Biochim Biophys Acta Gene Regul Mech, 1861, 905, 10.1016/j.bbagrm.2018.07.011 · DOI
- Martínez Leo, 2019, Systemic oxidative stress: a key point in neurodegeneration—a review, J Nutr Health Aging, 23, 694, 10.1007/s12603-019-1240-8 · DOI
- Saha, 2017, Correlation between oxidative stress, nutrition, and cancer initiation, Int J Mol Sci, 18, 1544, 10.3390/ijms18071544 · DOI
- Tan, 2018, Nutrients and oxidative stress: friend or foe?, Oxid Med Cell Longev, 2018, 10.1155/2018/9719584 · DOI
- Araújo, 2017, Impact of high-fat diet on the intestinal microbiota and small intestinal physiology before and after the onset of obesity, Biochimie, 141, 97, 10.1016/j.biochi.2017.05.019 · DOI
- Endo, 2009, Isolation and characterization of fructophilic lactic acid bacteria from fructose-rich niches, Syst Appl Microbiol, 32, 593, 10.1016/j.syapm.2009.08.002 · DOI
- Vega-Magaña, 2020, Microbiome alterations are related to an imbalance of immune response and bacterial translocation in BDL-rats, Iran J Basic Med Sci, 23, 178
- Saiyasit, 2020, Gut dysbiosis develops before metabolic disturbance and cognitive decline in high-fat diet–induced obese condition, Nutrition, 69, 10.1016/j.nut.2019.110576 · DOI
- Muscogiuri, 2019, Gut microbiota: a new path to treat obesity, Int J Obes Suppl, 9, 10, 10.1038/s41367-019-0011-7 · DOI
- Levy, 2017, Dysbiosis and the immune system, Nat Rev Immunol, 17, 219, 10.1038/nri.2017.7 · DOI · Paper page
- Hayden, 2014, Regulation of NF-κB by TNF family cytokines, Semin Immunol, 26, 253, 10.1016/j.smim.2014.05.004 · DOI
- Boutagy, 2016, Metabolic endotoxemia with obesity: is it real and is it relevant?, Biochimie, 124, 11, 10.1016/j.biochi.2015.06.020 · DOI · Paper page
- Azain, 2004, Role of fatty acids in adipocyte growth and development, J Anim Sci, 82, 916, 10.2527/2004.823916x · DOI
- Kawasaki, 2012, Obesity-induced endoplasmic reticulum stress causes chronic inflammation in adipose tissue, Sci Rep, 2, 799, 10.1038/srep00799 · DOI
- Springer, 2019, Obesity-associated extracellular matrix remodeling promotes a macrophage phenotype similar to tumor-associated macrophages, Am J Pathol, 189, 2019, 10.1016/j.ajpath.2019.06.005 · DOI
- Mraz, 2014, The role of adipose tissue immune cells in obesity and low-grade inflammation, J Endocrinol, 222, R113, 10.1530/JOE-14-0283 · DOI · Paper page
- Sell, 2012, Adaptive immunity in obesity and insulin resistance, Nat Rev Endocrinol, 8, 709, 10.1038/nrendo.2012.114 · DOI · Paper page
- Kim, 2017, Pro-inflammatory hepatic macrophages generate ROS through NADPH oxidase 2 via endocytosis of monomeric TLR4–MD2 complex, Nat Commun, 8, 2247, 10.1038/s41467-017-02325-2 · DOI
- Vitale, 2013, Oxidative stress and the ageing endocrine system, Nat Rev Endocrinol, 9, 228, 10.1038/nrendo.2013.29 · DOI
- Saravia, 2020, Signaling networks in immunometabolism, Cell Res, 30, 328, 10.1038/s41422-020-0301-1 · DOI
- Ryan, 2020, Krebs cycle reborn in macrophage immunometabolism, Annu Rev Immunol, 38, 289, 10.1146/annurev-immunol-081619-104850 · DOI · Paper page
- Herbert, 1993, Stress and immunity in humans: a meta-analytic review, Psychosom Med, 55, 364, 10.1097/00006842-199307000-00004 · DOI
- Erdelyi, 2009, Western-style diets induce oxidative stress and dysregulate immune responses in the colon in a mouse model of sporadic colon cancer, J Nutr, 139, 2072, 10.3945/jn.108.104125 · DOI
- Hall, 2019, Ultra-processed diets cause excess calorie intake and weight gain: an inpatient randomized controlled trial of ad libitum food intake [published correction appears in Cell Metab 2019;30:226] [published correction appears in Cell Metab 2020;32:690], Cell Metab, 30, 67, 10.1016/j.cmet.2019.05.008 · DOI · Paper page
- De Rosa, 2017, Metabolic pressure and the breach of immunological self-tolerance, Nat Immunol, 18, 1190, 10.1038/ni.3851 · DOI
- Phan, 2017, Metabolic and epigenetic coordination of T cell and macrophage immunity, Immunity, 46, 714, 10.1016/j.immuni.2017.04.016 · DOI
- Liu, 2020, HIF1α regulates early metabolic changes due to activation of innate immunity in nuclear reprogramming, Stem Cell Reports, 14, 192, 10.1016/j.stemcr.2020.01.006 · DOI
- Ardeshna, 2000, The PI3 kinase, p38 SAP kinase, and NF-κB signal transduction pathways are involved in the survival and maturation of lipopolysaccharide-stimulated human monocyte–derived dendritic cells, Blood, 96, 1039, 10.1182/blood.V96.3.1039 · DOI
- Williams, 2008, Disruption of the transcription factor Nrf2 promotes pro-oxidative dendritic cells that stimulate Th2-like immunoresponsiveness upon activation by ambient particulate matter, J Immunol, 181, 4545, 10.4049/jimmunol.181.7.4545 · DOI
- Al-Huseini, 2013, Nuclear factor-erythroid 2 (NF-E2) p45-related factor-2 (Nrf2) modulates dendritic cell immune function through regulation of p38 MAPK-cAMP-responsive element binding protein/activating transcription factor 1 signaling, J Biol Chem, 288, 22281, 10.1074/jbc.M113.483420 · DOI
- Zha, 2014, Disulfiram targeting lymphoid malignant cell lines via ROS-JNK activation as well as Nrf2 and NF-kB pathway inhibition, J Transl Med, 12, 163, 10.1186/1479-5876-12-163 · DOI
- Moro-García, 2018, Influence of inflammation in the process of T lymphocyte differentiation: proliferative, metabolic, and oxidative changes, Front Immunol, 9, 339, 10.3389/fimmu.2018.00339 · DOI
- León-Cabrera, 2013, Hyperleptinemia is associated with parameters of low-grade systemic inflammation and metabolic dysfunction in obese human beings, Front Integr Neurosci, 7, 62, 10.3389/fnint.2013.00062 · DOI
- Matarese, 2010, La Cava A. Regulatory T cells in obesity: the leptin connection, Trends Mol Med, 16, 247, 10.1016/j.molmed.2010.04.002 · DOI
- Ohkura, 2013, Development and maintenance of regulatory T cells, Immunity, 38, 414, 10.1016/j.immuni.2013.03.002 · DOI
- Iuchi, 2007, Elevated oxidative stress in erythrocytes due to a SOD1 deficiency causes anaemia and triggers autoantibody production, Biochem J, 402, 219, 10.1042/BJ20061386 · DOI
- Arias-Bravo, 2020, Overnutrition in infants is associated with high level of leptin, viral coinfection and increased severity of respiratory infections: a cross-sectional study, Front Pediatr, 8, 44, 10.3389/fped.2020.00044 · DOI
- Al-Menhali, 2020, Lipid peroxidation is involved in calcium dependent upregulation of mitochondrial metabolism in skeletal muscle, Biochim Biophys Acta Gen Subj, 1864, 10.1016/j.bbagen.2019.129487 · DOI
- Grootjans, 2016, The unfolded protein response in immunity and inflammation, Nat Rev Immunol, 16, 469, 10.1038/nri.2016.62 · DOI
- King, 2006, Oxidative stress promotes polarization of human T cell differentiation toward a T helper 2 phenotype, J Immunol, 176, 2765, 10.4049/jimmunol.176.5.2765 · DOI
- Jena, 2019, Long-term Western diet intake leads to dysregulated bile acid signaling and dermatitis with Th2 and Th17 pathway features in mice, J Dermatol Sci, 95, 13, 10.1016/j.jdermsci.2019.05.007 · DOI
- Kimura, 2010, IL-6: regulator of Treg/Th17 balance, Eur J Immunol, 40, 1830, 10.1002/eji.201040391 · DOI
- Childs, 2019, Diet and immune function, Nutrients, 11, 1933, 10.3390/nu11081933 · DOI · Paper page
- Batatinha, 2019, Nutrients, immune system, and exercise: where will it take us?, Nutrition, 61, 151, 10.1016/j.nut.2018.09.019 · DOI
- Calder, 2020, Nutrition, immunity and COVID-19, BMJ Nutr Prev Health, 3, 74, 10.1136/bmjnph-2020-000085 · DOI
- Kazemi, 2020, Effect of probiotic and synbiotic supplementation on inflammatory markers in health and disease status: a systematic review and meta-analysis of clinical trials, Clin Nutr, 39, 789, 10.1016/j.clnu.2019.04.004 · DOI · Paper page
- Langlois, 2019, Vitamin C for the critically ill: is the evidence strong enough?, Nutrition, 60, 185, 10.1016/j.nut.2018.10.009 · DOI
- Carr, 2017, Vitamin C and immune function, Nutrients, 9, 1211, 10.3390/nu9111211 · DOI · Paper page
- Heuser, 1997, Enhancement of natural killer cell activity and T and B cell function by buffered vitamin C in patients exposed to toxic chemicals: the role of protein kinase-C, Immunopharmacol Immunotoxicol, 19, 291, 10.3109/08923979709046977 · DOI
- Bozonet, 2015, Enhanced human neutrophil vitamin C status, chemotaxis and oxidant generation following dietary supplementation with vitamin C-rich SunGold kiwifruit, Nutrients, 7, 2574, 10.3390/nu7042574 · DOI
- Hemilä, 2017, Vitamin C and infections, Nutrients, 9, 339, 10.3390/nu9040339 · DOI · Paper page
- Mah, 2011, Vitamin C status is related to proinflammatory responses and impaired vascular endothelial function in healthy, college-aged lean and obese men, J Am Diet Assoc, 111, 737, 10.1016/j.jada.2011.02.003 · DOI
- Langlois, 2019, Vitamin D in the ICU: more sun for critically ill adult patients?, Nutrition, 61, 173, 10.1016/j.nut.2018.11.001 · DOI
- Jolliffe, 2013, Vitamin D in the prevention of acute respiratory infection: systematic review of clinical studies, J Steroid Biochem Mol Biol, 136, 321, 10.1016/j.jsbmb.2012.11.017 · DOI
- Dickerson, 2019, Obesity attenuates serum 25-hydroxyvitamin D response to cholecalciferol therapy in critically ill patients, Nutrition, 63–64, 120, 10.1016/j.nut.2019.01.018 · DOI
- Urashima, 2010, Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren, Am J Clin Nutr, 91, 1255, 10.3945/ajcn.2009.29094 · DOI
- Zhou, 2018, Preventive effects of vitamin D on seasonal influenza A in infants: a multicenter, randomized, open, controlled clinical trial, Pediatr Infect Dis J, 37, 749, 10.1097/INF.0000000000001890 · DOI
- Arihiro, 2019, Randomized trial of vitamin D supplementation to prevent seasonal influenza and upper respiratory infection in patients with inflammatory bowel disease, Inflamm Bowel Dis, 25, 1088, 10.1093/ibd/izy346 · DOI
- Pludowski, 2018, Vitamin D supplementation guidelines, J Steroid Biochem Mol Biol, 175, 125, 10.1016/j.jsbmb.2017.01.021 · DOI
- Hill, 2014, The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic, Nat Rev Gastroenterol Hepatol, 11, 506, 10.1038/nrgastro.2014.66 · DOI
- Mak, 2020, Probiotics and COVID-19: one size does not fit all, Lancet Gastroenterol Hepatol, 5, 644, 10.1016/S2468-1253(20)30122-9 · DOI
- Sáez-Lara, 2016, Effects of probiotics and synbiotics on obesity, insulin resistance syndrome, type 2 diabetes and non-alcoholic fatty liver disease: a review of human clinical trials, Int J Mol Sci, 17, 928, 10.3390/ijms17060928 · DOI
- Borgeraas, 2018, Effects of probiotics on body weight, body mass index, fat mass and fat percentage in subjects with overweight or obesity: a systematic review and meta-analysis of randomized controlled trials, Obes Rev, 19, 219, 10.1111/obr.12626 · DOI · Paper page
- Pellegrini, 2020, Gut microbiota composition after diet and probiotics in overweight breast cancer survivors: a randomized open-label pilot intervention trial, Nutrition, 74, 10.1016/j.nut.2020.110749 · DOI
- Jayawardena, 2020, Enhancing immunity in viral infections, with special emphasis on COVID-19: a review, Diabetes Metab Syndr, 14, 367, 10.1016/j.dsx.2020.04.015 · DOI
- Lomax, 2009, Probiotics, immune function, infection and inflammation: a review of the evidence from studies conducted in humans, Curr Pharm Des, 15, 1428, 10.2174/138161209788168155 · DOI
Cited by
Sorted by citations
Lane, M. M., Gamage, E., Du, S., Ashtree, D. N., McGuinness, A. J., Gauci, S., Baker, P., Lawrence, M., Rebholz, C. M., Srour, B., et al. (2024) · BMJ · doi:10.1136/bmj-2023-077310 · Cited by 1,153
Metadata
- Authors
- Martínez Leo, E. E., Peñafiel, A. M., Hernández Escalante, V. M., & Cabrera Araujo, Z. M.
- Venue
- Nutrition
- Publisher
- Elsevier BV
- Published
- 2021-11
- Volume
- 91-92
- Pages
- 111419
- ISSN
- 0899-9007
- Cited by
- 49
- References
- 16
- Language
- en
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