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Использование пищевых продуктов на основе растительного белка для коррекции паттернов питания при алиментарно-зависимых заболеваниях: возможности и перспективы - Журнал Терапевтический архив №8 Вопросы лечения 2025
Использование пищевых продуктов на основе растительного белка для коррекции паттернов питания при алиментарно-зависимых заболеваниях: возможности и перспективы
Морозов С.В., Пилипенко В.И., Исаков В.А., Сасунова А.Н., Гончаров А.А., Кочеткова А.А. Использование пищевых продуктов на основе растительного белка для коррекции паттернов питания при алиментарно-зависимых заболеваниях: возможности и перспективы. Терапевтический архив. 2025;97(8):727–734. DOI: 10.26442/00403660.2025.08.203302
© ООО «КОНСИЛИУМ МЕДИКУМ», 2025 г.
© ООО «КОНСИЛИУМ МЕДИКУМ», 2025 г.
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Аннотация
Возможности использования пищевых продуктов на основе растительного белка для коррекции паттернов питания при алиментарно-зависимых заболеваниях (АЗЗ) органов пищеварения изучены недостаточно. Целью обзора является анализ данных литературных источников для определения возможностей использования продуктов на основе растительного белка с целью коррекции паттернов питания при наиболее распространенных АЗЗ органов пищеварения. Проведен поиск в базах данных PubMed/Medline, Embase, Google Scholar, CyberLeninka, Elibrary с ключевыми словами, соответствующими целям исследования. Выявлено 314 исследований, однако после исключения дублирующихся публикаций и анализа релевантных данных включены в исследование 66 работ. Результаты анализа показали возможную пользу от использования растительного белка, что может иметь клиническое значение при таких заболеваниях, как метаболически ассоциированная жировая болезнь печени, гастроэзофагеальная рефлюксная болезнь, синдром раздраженного кишечника. Приведены данные об адекватности рационов с включением растительного белка и возможные нежелательные явления при их применении. Затронуты технологические и экономические перспективы использования продуктов на основе растительных белков для коррекции паттернов питания у больных с АЗЗ органов пищеварения.
Ключевые слова: пищевые паттерны, растительный белок, метаболически ассоциированная жировая болезнь печени, гастроэзофагеальная рефлюксная болезнь, синдром раздраженного кишечника
Keywords: nutritional patterns, vegetable protein, metabolically associated fatty liver disease, gastroesophageal reflux disease, irritable bowel syndrome
Ключевые слова: пищевые паттерны, растительный белок, метаболически ассоциированная жировая болезнь печени, гастроэзофагеальная рефлюксная болезнь, синдром раздраженного кишечника
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Keywords: nutritional patterns, vegetable protein, metabolically associated fatty liver disease, gastroesophageal reflux disease, irritable bowel syndrome
Полный текст
Список литературы
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3. Riboli E, Hunt KJ, Slimani N, et al. European Prospective Investigation into Cancer and Nutrition (EPIC): study populations and data collection. Public Health Nutr. 2002;5(6B):1113-24. DOI:10.1079/PHN2002394
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5. Green A, Blattmann C, Chen C, Mathys A. The role of alternative proteins and future foods in sustainable and contextually-adapted flexitarian diets. Trends in Food Science & Technology. 2022;124:250-5. DOI:10.1016/j.tifs.2022.03.026
6. Curtain F, Grafenauer S. Plant-Based Meat Substitutes in the Flexitarian Age: An Audit of Products on Supermarket Shelves. Nutrients. 2019;11(11):2603. DOI:10.3390/nu11112603
7. Lichtenstein AH, Appel LJ, Vadiveloo M, et al. 2021 Dietary Guidance to Improve Cardiovascular Health: A Scientific Statement From the American Heart Association. Circulation. 2021;144(23):e472-47. DOI:10.1161/CIR.0000000000001031
8. Willett W, Rockström J, Loken B, et al. Food in the Anthropocene: the EAT-Lancet Commission on healthy diets from sustainable food systems. Lancet. 2019;393(10170):447-92. DOI:10.1016/S0140-6736(18)31788-4
9. European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD), European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). J Hepatol. 2024;81(3):492-542. DOI:10.1016/j.jhep.2024.04.031
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11. Alferink LJ, Kiefte-de Jong JC, Erler NS, et al. Association of dietary macronutrient composition and non-alcoholic fatty liver disease in an ageing population: the Rotterdam Study. Gut. 2019;68(6):1088-98. DOI:10.1136/gutjnl-2017-315940
12. Markova M, Pivovarova O, Hornemann S, et al. Isocaloric Diets High in Animal or Plant Protein Reduce Liver Fat and Inflammation in Individuals With Type 2 Diabetes. Gastroenterology. 2017;152(3):571-85.e8. DOI:10.1053/j.gastro.2016.10.007
13. Lang S, Martin A, Farowski F, et al. High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD. Hepatol Commun. 2020;4(5):681-95. DOI:10.1002/hep4.1509
14. Cocate PG, Natali AJ, de Oliveira A, et al. Red but not white meat consumption is associated with metabolic syndrome, insulin resistance and lipid peroxidation in Brazilian middle-aged men. Eur J Prev Cardiol. 2015;22(2):223-30. DOI:10.1177/2047487313507684
15. Zhang S, Cui Z, Zhang H, et al. Pea Albumin Extracted from Pea (Pisum sativum L.) Seeds Ameliorates High-Fat-Diet-Induced Non-Alcoholic Fatty Liver Disease by Regulating Lipogenesis and Lipolysis Pathways. Nutrients. 2024;16(14):2232. DOI:10.3390/nu16142232
16. Yang Z, Gong D, He X, et al. Association between daidzein intake and metabolic associated fatty liver disease: A cross-sectional study from NHANES 2017-2018. Front Nutr. 2023;10:1113789. DOI:10.3389/fnut.2023.1113789
17. Zhang S, Kumari S, Gu Y, et al. Soy Food Intake Is Inversely Associated with Newly Diagnosed Nonalcoholic Fatty Liver Disease in the TCLSIH Cohort Study. J Nutr. 2020;150(12):3280-27. DOI:10.1093/jn/nxaa297
18. McCarthy EM, Rinella ME. The role of diet and nutrient composition in nonalcoholic Fatty liver disease. J Acad Nutr Diet. 2012;112(3):401-9. DOI:10.1016/j.jada.2011.10.007
19. Amanat S, Eftekhari MH, Fararouei M, et al. Genistein supplementation improves insulin resistance and inflammatory state in non-alcoholic fatty liver patients: A randomized, controlled trial. Clin Nutr. 2018;37(4):1210-25. DOI:10.1016/j.clnu.2017.05.028
20. Li Y, Deng X, Guo X, et al. Preclinical and clinical evidence for the treatment of non-alcoholic fatty liver disease with soybean: A systematic review and meta-analysis. Front Pharmacol. 2023;14:1088614. DOI:10.3389/fphar.2023.1088614
21. Eslami O, Shidfar F, Maleki Z, et al. Effect of Soy Milk on Metabolic Status of Patients with Nonalcoholic Fatty Liver Disease: A Randomized Clinical Trial. J Am Coll Nutr. 2019;38(1):51-8. DOI:10.1080/07315724.2018.1479990
22. Liu N, Song Z, Jin W, et al. Pea albumin extracted from pea (Pisum sativum L.) seed protects mice from high fat diet-induced obesity by modulating lipid metabolism and gut microbiota. Journal of Functional Foods. 2022;97:105234. DOI:10.1016/j.jff.2022.105234
23. Liu B, Wang Z, Liang M, Yang L. Rice Protein Reduces Triglyceride Levels through Modulating CD36, MTP, FATP, and FABP Expression in Growing and Adult Rats. Foods. 2024;13(17):2704. DOI:10.3390/foods13172704
24. Kubota M, Watanabe R, Hosojima M, et al. Rice bran protein ameliorates diabetes, reduces fatty liver, and has renoprotective effects in Zucker Diabetic Fatty rats. Journal of Functional Foods. 2020;70:103981. DOI:10.1016/j.jff.2020.103981
25. Kadowaki M, Kubota M, Watanabe R. Physiological Multifunctions of Rice Proteins of Endosperm and Bran. J Nutr Sci Vitaminol (Tokyo). 2019;65(Suppl.):S42-4. DOI:10.3177/jnsv.65.S42
26. Alferink LJM, Erler NS, de Knegt RJ, et al. Adherence to a plant-based, high-fibre dietary pattern is related to regression of non-alcoholic fatty liver disease in an elderly population. Eur J Epidemiol. 2020;35(11):1069-85. DOI:10.1007/s10654-020-00627-2
27. Ivashkin VT, Maev IV, Trukhmanov AS, et al. Recommendations of the Russian Gastroenterological Association in Diagnosis and Treatment of Gastroesophageal Reflux Disease. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2020;30(4):70-97 (in Russian). DOI:10.22416/1382-4376-2020-30-4-70-97
28. Isakov VA, Morozov SV, Stavraki ES, Komarov RM. Heartburn prevalence analysis: national epidemiologic examination of adult urban population (ARIADNA). Experimental & Clinical Gastroenterology. 2008;1:20-30 (in Russian).
29. Kropochev VS, Morozov SV, Lantseva MA, et al. Food patterns in Russian patients with gastroesophageal reflux disease: the results of pilot comparative study. Terapevticheskii Arkhiv (Ter. Arkh.). 2020;92(8):66-72 (in Russian). DOI:10.26442/00403660.2020.08.000760
30. Borodina G, Morozov S. Children With Gastroesophageal Reflux Disease Consume More Calories and Fat Compared to Controls of Same Weight and Age. J Pediatr Gastroenterol Nutr. 2020;70(6):808-14. DOI:10.1097/MPG.0000000000002652
31. Morozov SV. Gastroesophageal reflux disease: the role of nutritional patterns in pathogenesis and treatment. Voprosy pitaniia. 2013;82(5):10-22 (in Russian).
32. Rizzo G, Baroni L, Bonetto C, et al. The Role of a Plant-Only (Vegan) Diet in Gastroesophageal Reflux Disease: Online Survey of the Italian General Population. Nutrients. 2023;15(22):4725. DOI:10.3390/nu15224725
33. Baroni L, Bonetto C, Solinas I, et al. Diets including Animal Food Are Associated with Gastroesophageal Reflux Disease. Eur J Investig Health Psychol Educ. 2023;13(12):2736-76. DOI:10.3390/ejihpe13120189
34. Bhatia SJ, Reddy DN, Ghoshal UC, et al. Epidemiology and symptom profile of gastroesophageal reflux in the Indian population: report of the Indian Society of Gastroenterology Task Force. Indian J Gastroenterol. 2011;30(3):118-27. DOI:10.1007/s12664-011-0112-x
35. Wenzl EM, Riedl R, Borenich A, et al. Low prevalence of gastroesophageal reflux symptoms in vegetarians. Indian J Gastroenterol. 2021;40(2):154-61. DOI:10.1007/s12664-021-01156-w
36. Jung JG, Kang HW, Hahn SJ, et al. Vegetarianism as a protective factor for reflux esophagitis: a retrospective, cross-sectional study between Buddhist priests and general population. Dig Dis Sci. 2013;58(8):2244-52. DOI:10.1007/s10620-013-2639-4
37. Morozov S, Isakov V, Konovalova M. Fiber-enriched diet helps to control symptoms and improves esophageal motility in patients with non-erosive gastroesophageal reflux disease. World J Gastroenterol. 2018;24(21):2291-29. DOI:10.3748/wjg.v24.i21.2291
38. Morozov S, Sentsova T. Local inflammatory response to gastroesophageal reflux: Association of gene expression of inflammatory cytokines with esophageal multichannel intraluminal impedance-pH data. World J Clin Cases. 2022;10(26):9254-23. DOI:10.12998/wjcc.v10.i26.9254
39. Martinucci I, Guidi G, Savarino EV, et al. Vegetal and Animal Food Proteins Have a Different Impact in the First Postprandial Hour of Impedance-pH Analysis in Patients with Heartburn. Gastroenterol Res Pract. 2018;2018:7572430. DOI:10.1155/2018/7572430
40. Greger M. Best foods for acid reflux (video transcript). NutritionFacts.org. 2019. Available at: https://nutritionfacts.org/blog/best-foods-for-acid-reflux/#:~:text=Based%20on%20a%20study%20of,prot.... Accessed: 27.04.2025.
41. Tan ESS, Zaman R, Memon MA, Tan CK. Effect of Fermented Soybean (FSB) Supplementation on Gastroesophageal Reflux Disease (GERD). Nutrients. 2024;16(16):2779. DOI:10.3390/nu16162779
42. Flashback Friday: Diet and GERD Acid Reflux Heartburn. Available at: https://nutritionfacts.org/video/flashback-friday-diet-gerd-acid-reflux-heartburn/#:~:text=Then%20in.... Accessed: 09.05.2025.
43. Zalvan CH, Hu S, Greenberg B, Geliebter J. A Comparison of Alkaline Water and Mediterranean Diet vs Proton Pump Inhibition for Treatment of Laryngopharyngeal Reflux. JAMA Otolaryngol Head Neck Surg. 2017;143(10):1023-9. DOI:10.1001/jamaoto.2017.1454
44. Hasani M, Mansour A, Asayesh H, et al. Effect of glutamine supplementation on cardiometabolic risk factors and inflammatory markers: a systematic review and meta-analysis. BMC Cardiovasc Disord. 2021;21(1):190. DOI:10.1186/s12872-021-01986-8
45. Mazzawi T, El-Salhy M. Effect of diet and individual dietary guidance on gastrointestinal endocrine cells in patients with irritable bowel syndrome (Review). Int J Mol Med. 2017;40(4):943-52. DOI:10.3892/ijmm.2017.3096
46. Rej A, Sanders DS. Gluten-Free Diet and Its 'Cousins' in Irritable Bowel Syndrome. Nutrients. 2018;10(11):1727. DOI:10.3390/nu10111727
47. Boettcher E, Crowe SE. Dietary proteins and functional gastrointestinal disorders. Am J Gastroenterol. 2013;108(5):728-36. DOI:10.1038/ajg.2013.97
48. Biesiekierski JR, Newnham ED, Irving PM, et al. Gluten causes gastrointestinal symptoms in subjects without celiac disease: a double-blind randomized placebo-controlled trial. Am J Gastroenterol. 2011;106(3):508-14. DOI:10.1038/ajg.2010.487
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9. European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD), European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines on the management of metabolic dysfunction-associated steatotic liver disease (MASLD). J Hepatol. 2024;81(3):492-542. DOI:10.1016/j.jhep.2024.04.031
10. Khazaei Y, Dehghanseresht N, Ebrahimi Mousavi S, et al. Association Between Protein Intake From Different Animal and Plant Origins and the Risk of Non-Alcoholic Fatty Liver Disease: A Case-Control Study. Clin Nutr Res. 2023;12(1):29-39. DOI:10.7762/cnr.2023.12.1.29
11. Alferink LJ, Kiefte-de Jong JC, Erler NS, et al. Association of dietary macronutrient composition and non-alcoholic fatty liver disease in an ageing population: the Rotterdam Study. Gut. 2019;68(6):1088-98. DOI:10.1136/gutjnl-2017-315940
12. Markova M, Pivovarova O, Hornemann S, et al. Isocaloric Diets High in Animal or Plant Protein Reduce Liver Fat and Inflammation in Individuals With Type 2 Diabetes. Gastroenterology. 2017;152(3):571-85.e8. DOI:10.1053/j.gastro.2016.10.007
13. Lang S, Martin A, Farowski F, et al. High Protein Intake Is Associated With Histological Disease Activity in Patients With NAFLD. Hepatol Commun. 2020;4(5):681-95. DOI:10.1002/hep4.1509
14. Cocate PG, Natali AJ, de Oliveira A, et al. Red but not white meat consumption is associated with metabolic syndrome, insulin resistance and lipid peroxidation in Brazilian middle-aged men. Eur J Prev Cardiol. 2015;22(2):223-30. DOI:10.1177/2047487313507684
15. Zhang S, Cui Z, Zhang H, et al. Pea Albumin Extracted from Pea (Pisum sativum L.) Seeds Ameliorates High-Fat-Diet-Induced Non-Alcoholic Fatty Liver Disease by Regulating Lipogenesis and Lipolysis Pathways. Nutrients. 2024;16(14):2232. DOI:10.3390/nu16142232
16. Yang Z, Gong D, He X, et al. Association between daidzein intake and metabolic associated fatty liver disease: A cross-sectional study from NHANES 2017-2018. Front Nutr. 2023;10:1113789. DOI:10.3389/fnut.2023.1113789
17. Zhang S, Kumari S, Gu Y, et al. Soy Food Intake Is Inversely Associated with Newly Diagnosed Nonalcoholic Fatty Liver Disease in the TCLSIH Cohort Study. J Nutr. 2020;150(12):3280-27. DOI:10.1093/jn/nxaa297
18. McCarthy EM, Rinella ME. The role of diet and nutrient composition in nonalcoholic Fatty liver disease. J Acad Nutr Diet. 2012;112(3):401-9. DOI:10.1016/j.jada.2011.10.007
19. Amanat S, Eftekhari MH, Fararouei M, et al. Genistein supplementation improves insulin resistance and inflammatory state in non-alcoholic fatty liver patients: A randomized, controlled trial. Clin Nutr. 2018;37(4):1210-25. DOI:10.1016/j.clnu.2017.05.028
20. Li Y, Deng X, Guo X, et al. Preclinical and clinical evidence for the treatment of non-alcoholic fatty liver disease with soybean: A systematic review and meta-analysis. Front Pharmacol. 2023;14:1088614. DOI:10.3389/fphar.2023.1088614
21. Eslami O, Shidfar F, Maleki Z, et al. Effect of Soy Milk on Metabolic Status of Patients with Nonalcoholic Fatty Liver Disease: A Randomized Clinical Trial. J Am Coll Nutr. 2019;38(1):51-8. DOI:10.1080/07315724.2018.1479990
22. Liu N, Song Z, Jin W, et al. Pea albumin extracted from pea (Pisum sativum L.) seed protects mice from high fat diet-induced obesity by modulating lipid metabolism and gut microbiota. Journal of Functional Foods. 2022;97:105234. DOI:10.1016/j.jff.2022.105234
23. Liu B, Wang Z, Liang M, Yang L. Rice Protein Reduces Triglyceride Levels through Modulating CD36, MTP, FATP, and FABP Expression in Growing and Adult Rats. Foods. 2024;13(17):2704. DOI:10.3390/foods13172704
24. Kubota M, Watanabe R, Hosojima M, et al. Rice bran protein ameliorates diabetes, reduces fatty liver, and has renoprotective effects in Zucker Diabetic Fatty rats. Journal of Functional Foods. 2020;70:103981. DOI:10.1016/j.jff.2020.103981
25. Kadowaki M, Kubota M, Watanabe R. Physiological Multifunctions of Rice Proteins of Endosperm and Bran. J Nutr Sci Vitaminol (Tokyo). 2019;65(Suppl.):S42-4. DOI:10.3177/jnsv.65.S42
26. Alferink LJM, Erler NS, de Knegt RJ, et al. Adherence to a plant-based, high-fibre dietary pattern is related to regression of non-alcoholic fatty liver disease in an elderly population. Eur J Epidemiol. 2020;35(11):1069-85. DOI:10.1007/s10654-020-00627-2
27. Ивашкин В.Т., Маев И.В., Трухманов А.С., и др. Рекомендации Российской гастроэнтерологической ассоциации по диагностике и лечению гастроэзофагеальной рефлюксной болезни. Российский журнал гастроэнтерологии, гепатологии, колопроктологии. 2020;30(4):70-97 [Ivashkin VT, Maev IV, Trukhmanov AS, et al. Recommendations of the Russian Gastroenterological Association in Diagnosis and Treatment of Gastroesophageal Reflux Disease. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2020;30(4):70-97 (in Russian)]. DOI:10.22416/1382-4376-2020-30-4-70-97
28. Исаков В.А., Морозов С.В., Ставраки Е.С., Комаров Р.М. Анализ распространенности изжоги: национальное эпидемиологическое исследование взрослого городского населения (АРИАДНА). Экспериментальная и клиническая гастроэнтерология. 2008;1:20-30 [Isakov VA, Morozov SV, Stavraki ES, Komarov RM. Heartburn prevalence analysis: national epidemiologic examination of adult urban population (ARIADNA). Experimental & Clinical Gastroenterology. 2008;1:20-30 (in Russian)].
29. Кропочев В.С., Морозов С.В., Ланцева М.А., и др. Анализ особенностей питания у больных гастроэзофагеальной рефлюксной болезнью: результаты пилотного исследования. Терапевтический архив. 2020;92(8):66-72 [Kropochev VS, Morozov SV, Lantseva MA, et al. Food patterns in Russian patients with gastroesophageal reflux disease: the results of pilot comparative study. Terapevticheskii Arkhiv (Ter. Arkh.). 2020;92(8):66-72 (in Russian)]. DOI:10.26442/00403660.2020.08.000760
30. Borodina G, Morozov S. Children With Gastroesophageal Reflux Disease Consume More Calories and Fat Compared to Controls of Same Weight and Age. J Pediatr Gastroenterol Nutr. 2020;70(6):808-14. DOI:10.1097/MPG.0000000000002652
31. Морозов С.В. Гастроэзофагеальная рефлюксная болезнь: роль факторов питания в патогенезе и лечении. Вопросы питания. 2013;82(5):10-22 [Morozov SV. Gastroesophageal reflux disease: the role of nutritional patterns in pathogenesis and treatment. Voprosy pitaniia. 2013;82(5):10-22 (in Russian)].
32. Rizzo G, Baroni L, Bonetto C, et al. The Role of a Plant-Only (Vegan) Diet in Gastroesophageal Reflux Disease: Online Survey of the Italian General Population. Nutrients. 2023;15(22):4725. DOI:10.3390/nu15224725
33. Baroni L, Bonetto C, Solinas I, et al. Diets including Animal Food Are Associated with Gastroesophageal Reflux Disease. Eur J Investig Health Psychol Educ. 2023;13(12):2736-76. DOI:10.3390/ejihpe13120189
34. Bhatia SJ, Reddy DN, Ghoshal UC, et al. Epidemiology and symptom profile of gastroesophageal reflux in the Indian population: report of the Indian Society of Gastroenterology Task Force. Indian J Gastroenterol. 2011;30(3):118-27. DOI:10.1007/s12664-011-0112-x
35. Wenzl EM, Riedl R, Borenich A, et al. Low prevalence of gastroesophageal reflux symptoms in vegetarians. Indian J Gastroenterol. 2021;40(2):154-61. DOI:10.1007/s12664-021-01156-w
36. Jung JG, Kang HW, Hahn SJ, et al. Vegetarianism as a protective factor for reflux esophagitis: a retrospective, cross-sectional study between Buddhist priests and general population. Dig Dis Sci. 2013;58(8):2244-52. DOI:10.1007/s10620-013-2639-4
37. Morozov S, Isakov V, Konovalova M. Fiber-enriched diet helps to control symptoms and improves esophageal motility in patients with non-erosive gastroesophageal reflux disease. World J Gastroenterol. 2018;24(21):2291-29. DOI:10.3748/wjg.v24.i21.2291
38. Morozov S, Sentsova T. Local inflammatory response to gastroesophageal reflux: Association of gene expression of inflammatory cytokines with esophageal multichannel intraluminal impedance-pH data. World J Clin Cases. 2022;10(26):9254-23. DOI:10.12998/wjcc.v10.i26.9254
39. Martinucci I, Guidi G, Savarino EV, et al. Vegetal and Animal Food Proteins Have a Different Impact in the First Postprandial Hour of Impedance-pH Analysis in Patients with Heartburn. Gastroenterol Res Pract. 2018;2018:7572430. DOI:10.1155/2018/7572430
40. Greger M. Best foods for acid reflux (video transcript). NutritionFacts.org. 2019. Available at: https://nutritionfacts.org/blog/best-foods-for-acid-reflux/#:~:text=Based%20on%20a%20study%20of,prot.... Accessed: 27.04.2025.
41. Tan ESS, Zaman R, Memon MA, Tan CK. Effect of Fermented Soybean (FSB) Supplementation on Gastroesophageal Reflux Disease (GERD). Nutrients. 2024;16(16):2779. DOI:10.3390/nu16162779
42. Flashback Friday: Diet and GERD Acid Reflux Heartburn. Available at: https://nutritionfacts.org/video/flashback-friday-diet-gerd-acid-reflux-heartburn/#:~:text=Then%20in.... Accessed: 09.05.2025.
43. Zalvan CH, Hu S, Greenberg B, Geliebter J. A Comparison of Alkaline Water and Mediterranean Diet vs Proton Pump Inhibition for Treatment of Laryngopharyngeal Reflux. JAMA Otolaryngol Head Neck Surg. 2017;143(10):1023-9. DOI:10.1001/jamaoto.2017.1454
44. Hasani M, Mansour A, Asayesh H, et al. Effect of glutamine supplementation on cardiometabolic risk factors and inflammatory markers: a systematic review and meta-analysis. BMC Cardiovasc Disord. 2021;21(1):190. DOI:10.1186/s12872-021-01986-8
45. Mazzawi T, El-Salhy M. Effect of diet and individual dietary guidance on gastrointestinal endocrine cells in patients with irritable bowel syndrome (Review). Int J Mol Med. 2017;40(4):943-52. DOI:10.3892/ijmm.2017.3096
46. Rej A, Sanders DS. Gluten-Free Diet and Its 'Cousins' in Irritable Bowel Syndrome. Nutrients. 2018;10(11):1727. DOI:10.3390/nu10111727
47. Boettcher E, Crowe SE. Dietary proteins and functional gastrointestinal disorders. Am J Gastroenterol. 2013;108(5):728-36. DOI:10.1038/ajg.2013.97
48. Biesiekierski JR, Newnham ED, Irving PM, et al. Gluten causes gastrointestinal symptoms in subjects without celiac disease: a double-blind randomized placebo-controlled trial. Am J Gastroenterol. 2011;106(3):508-14. DOI:10.1038/ajg.2010.487
49. Biesiekierski JR, Peters SL, Newnham ED, et al. No effects of gluten in patients with self-reported non-celiac gluten sensitivity after dietary reduction of fermentable, poorly absorbed, short-chain carbohydrates. Gastroenterology. 2013;145(2):320-8.e1-3. DOI:10.1053/j.gastro.2013.04.051
50. Buscail C, Sabate JM, Bouchoucha M, et al. Association between self-reported vegetarian diet and the irritable bowel syndrome in the French NutriNet cohort. PLoS One. 2017;12(8):e0183039. DOI:10.1371/journal.pone.0183039
51. Pilipenko V, Lanceva M, Isakov V, Vlasova A. Does a Decrease in Food Diversity Predispose to SIBO? Current Developments in Nutrition. 2021;5:443. DOI:10.1093/cdn/nzab038_055
52. Michel F, Hartmann C, Siegrist M. Consumers’ associations, perceptions and acceptance of meat and plant-based meat alternatives. Food Quality and Preference. 2020;87:104063. DOI:10.1016/j.foodqual.2020.104063
53. Farsi DN, Uthumange D, Munoz Munoz J, Commane DM. The nutritional impact of replacing dietary meat with meat alternatives in the UK: a modelling analysis using nationally representative data. Br J Nutr. 2022;127(11):1731-71. DOI:10.1017/S0007114521002750
54. Kaartinen NE, Tapanainen H, Maukonen M, et al. Partial replacement of red and processed meat with legumes: a modelling study of the impact on nutrient intakes and nutrient adequacy on the population level. Public Health Nutr. 2023;26(2):303-14. DOI:10.1017/S1368980022002440
55. Lawrence AS, Huang H, Johnson BJ, Wycherley TP. Impact of a Switch to Plant-Based Foods That Visually and Functionally Mimic Animal-Source Meat and Dairy Milk for the Australian Population – A Dietary Modelling Study. Nutrients. 2023;15(8):1825. DOI:10.3390/nu15081825
56. Schweiggert-Weisz U, Etzbach L, Gola S, et al. Opinion Piece: New Plant-Based Food Products Between Technology and Physiology. Mol Nutr Food Res. 2024;68(20):e2400376. DOI:10.1002/mnfr.202400376
57. Estévez M, Arjona A, Sánchez-Terrón G, et al. Ultra-processed vegan foods: Healthy alternatives to animal-source foods or avoidable junk? J Food Sci. 2024;89(11):7008-01. DOI:10.1111/1750-3841.17407
58. Salomé M, Huneau JF, Le Baron C, et al. Substituting Meat or Dairy Products with Plant-Based Substitutes Has Small and Heterogeneous Effects on Diet Quality and Nutrient Security: A Simulation Study in French Adults (INCA3). J Nutr. 2021;151(8):2435-45. DOI:10.1093/jn/nxab146
59. Marchese LE, McNaughton SA, Hendrie GA, et al. Modeling the Impact of Substituting Meat and Dairy Products with Plant-Based Alternatives on Nutrient Adequacy and Diet Quality. J Nutr. 2024;154(8):2411-41. DOI:10.1016/j.tjnut.2024.05.029
60. Mayer Labba IC, Steinhausen H, Almius L, et al. Nutritional Composition and Estimated Iron and Zinc Bioavailability of Meat Substitutes Available on the Swedish Market. Nutrients. 2022;14(19):3903. DOI:10.3390/nu14193903
61. Kumar M, Tomar M, Potkule J, et al. Advances in the plant protein extraction: Mechanism and recommendations. Food Hydrocolloids. 2021;115:106595. DOI:10.1016/j.foodhyd.2021.106595
62. Siegrist A, Green A, Michel F, Mathys A. Comparing the nutritional value and prices of meat and milk substitutes with their animal-based benchmarks across six European countries. Food Res Int. 2024;197(Pt 1):115213. DOI:10.1016/j.foodres.2024.115213
63. Hunt JR. Bioavailability of iron, zinc, and other trace minerals from vegetarian diets. Am J Clin Nutr. 2003;78(Suppl. 3):633S-3S. DOI:10.1093/ajcn/78.3.633S
64. Gibson RS, Raboy V, King JC. Implications of phytate in plant-based foods for iron and zinc bioavailability, setting dietary requirements, and formulating programs and policies. Nutr Rev. 2018;76(11):793-804. DOI:10.1093/nutrit/nuy028
65. Samad A, Kim SH, Kim CJ, et al. From Farms to Labs: The New Trend of Sustainable Meat Alternatives. Food Sci Anim Resour. 2025;45(1):13-30. DOI:10.5851/kosfa.2024.e105
66. Reese I, Schäfer C, Ballmer-Weber B, et al. Vegan diets from an allergy point of view – Position paper of the DGAKI working group on food allergy. Allergol Select. 2023;7:57-83. DOI:10.5414/ALX02400E
67. Elhalis H, See XY, Osen R, et al. Significance of Fermentation in Plant-Based Meat Analogs: A Critical Review of Nutrition, and Safety-Related Aspects. Foods. 2023;12(17):3222. DOI:10.3390/foods12173222
68. Augustin Mihalache O, Dellafiora L, Dall'Asta C. A systematic review of natural toxins occurrence in plant commodities used for plant-based meat alternatives production. Food Res Int. 2022;158:111490. DOI:10.1016/j.foodres.2022.111490
69. Kołodziejczak K, Onopiuk A, Szpicer A, Poltorak A. Meat Analogues in the Perspective of Recent Scientific Research: A Review. Foods. 2021;11(1):105. DOI:10.3390/foods11010105
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48. Biesiekierski JR, Newnham ED, Irving PM, et al. Gluten causes gastrointestinal symptoms in subjects without celiac disease: a double-blind randomized placebo-controlled trial. Am J Gastroenterol. 2011;106(3):508-14. DOI:10.1038/ajg.2010.487
49. Biesiekierski JR, Peters SL, Newnham ED, et al. No effects of gluten in patients with self-reported non-celiac gluten sensitivity after dietary reduction of fermentable, poorly absorbed, short-chain carbohydrates. Gastroenterology. 2013;145(2):320-8.e1-3. DOI:10.1053/j.gastro.2013.04.051
50. Buscail C, Sabate JM, Bouchoucha M, et al. Association between self-reported vegetarian diet and the irritable bowel syndrome in the French NutriNet cohort. PLoS One. 2017;12(8):e0183039. DOI:10.1371/journal.pone.0183039
51. Pilipenko V, Lanceva M, Isakov V, Vlasova A. Does a Decrease in Food Diversity Predispose to SIBO? Current Developments in Nutrition. 2021;5:443. DOI:10.1093/cdn/nzab038_055
52. Michel F, Hartmann C, Siegrist M. Consumers’ associations, perceptions and acceptance of meat and plant-based meat alternatives. Food Quality and Preference. 2020;87:104063. DOI:10.1016/j.foodqual.2020.104063
53. Farsi DN, Uthumange D, Munoz Munoz J, Commane DM. The nutritional impact of replacing dietary meat with meat alternatives in the UK: a modelling analysis using nationally representative data. Br J Nutr. 2022;127(11):1731-71. DOI:10.1017/S0007114521002750
54. Kaartinen NE, Tapanainen H, Maukonen M, et al. Partial replacement of red and processed meat with legumes: a modelling study of the impact on nutrient intakes and nutrient adequacy on the population level. Public Health Nutr. 2023;26(2):303-14. DOI:10.1017/S1368980022002440
55. Lawrence AS, Huang H, Johnson BJ, Wycherley TP. Impact of a Switch to Plant-Based Foods That Visually and Functionally Mimic Animal-Source Meat and Dairy Milk for the Australian Population – A Dietary Modelling Study. Nutrients. 2023;15(8):1825. DOI:10.3390/nu15081825
56. Schweiggert-Weisz U, Etzbach L, Gola S, et al. Opinion Piece: New Plant-Based Food Products Between Technology and Physiology. Mol Nutr Food Res. 2024;68(20):e2400376. DOI:10.1002/mnfr.202400376
57. Estévez M, Arjona A, Sánchez-Terrón G, et al. Ultra-processed vegan foods: Healthy alternatives to animal-source foods or avoidable junk? J Food Sci. 2024;89(11):7008-01. DOI:10.1111/1750-3841.17407
58. Salomé M, Huneau JF, Le Baron C, et al. Substituting Meat or Dairy Products with Plant-Based Substitutes Has Small and Heterogeneous Effects on Diet Quality and Nutrient Security: A Simulation Study in French Adults (INCA3). J Nutr. 2021;151(8):2435-45. DOI:10.1093/jn/nxab146
59. Marchese LE, McNaughton SA, Hendrie GA, et al. Modeling the Impact of Substituting Meat and Dairy Products with Plant-Based Alternatives on Nutrient Adequacy and Diet Quality. J Nutr. 2024;154(8):2411-41. DOI:10.1016/j.tjnut.2024.05.029
60. Mayer Labba IC, Steinhausen H, Almius L, et al. Nutritional Composition and Estimated Iron and Zinc Bioavailability of Meat Substitutes Available on the Swedish Market. Nutrients. 2022;14(19):3903. DOI:10.3390/nu14193903
61. Kumar M, Tomar M, Potkule J, et al. Advances in the plant protein extraction: Mechanism and recommendations. Food Hydrocolloids. 2021;115:106595. DOI:10.1016/j.foodhyd.2021.106595
62. Siegrist A, Green A, Michel F, Mathys A. Comparing the nutritional value and prices of meat and milk substitutes with their animal-based benchmarks across six European countries. Food Res Int. 2024;197(Pt 1):115213. DOI:10.1016/j.foodres.2024.115213
63. Hunt JR. Bioavailability of iron, zinc, and other trace minerals from vegetarian diets. Am J Clin Nutr. 2003;78(Suppl. 3):633S-3S. DOI:10.1093/ajcn/78.3.633S
64. Gibson RS, Raboy V, King JC. Implications of phytate in plant-based foods for iron and zinc bioavailability, setting dietary requirements, and formulating programs and policies. Nutr Rev. 2018;76(11):793-804. DOI:10.1093/nutrit/nuy028
65. Samad A, Kim SH, Kim CJ, et al. From Farms to Labs: The New Trend of Sustainable Meat Alternatives. Food Sci Anim Resour. 2025;45(1):13-30. DOI:10.5851/kosfa.2024.e105
66. Reese I, Schäfer C, Ballmer-Weber B, et al. Vegan diets from an allergy point of view – Position paper of the DGAKI working group on food allergy. Allergol Select. 2023;7:57-83. DOI:10.5414/ALX02400E
67. Elhalis H, See XY, Osen R, et al. Significance of Fermentation in Plant-Based Meat Analogs: A Critical Review of Nutrition, and Safety-Related Aspects. Foods. 2023;12(17):3222. DOI:10.3390/foods12173222
68. Augustin Mihalache O, Dellafiora L, Dall'Asta C. A systematic review of natural toxins occurrence in plant commodities used for plant-based meat alternatives production. Food Res Int. 2022;158:111490. DOI:10.1016/j.foodres.2022.111490
69. Kołodziejczak K, Onopiuk A, Szpicer A, Poltorak A. Meat Analogues in the Perspective of Recent Scientific Research: A Review. Foods. 2021;11(1):105. DOI:10.3390/foods11010105
Авторы
С.В. Морозов*1,2, В.И. Пилипенко1, В.А. Исаков1, А.Н. Сасунова1, А.А. Гончаров1, А.А. Кочеткова1
1ФГБУН «Федеральный исследовательский центр питания, биотехнологии и безопасности пищи», Москва, Россия;
2ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России, Москва, Россия
*morosoffsv@mail.ru
1Federal Research Centre of Nutrition, Biotechnology and Food Safety, Moscow, Russia;
2Russian Medical Academy of Continuous Professional Education, Moscow, Russia
*morosoffsv@mail.ru
1ФГБУН «Федеральный исследовательский центр питания, биотехнологии и безопасности пищи», Москва, Россия;
2ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России, Москва, Россия
*morosoffsv@mail.ru
________________________________________________
1Federal Research Centre of Nutrition, Biotechnology and Food Safety, Moscow, Russia;
2Russian Medical Academy of Continuous Professional Education, Moscow, Russia
*morosoffsv@mail.ru
Цель портала OmniDoctor – предоставление профессиональной информации врачам, провизорам и фармацевтам.
