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<article article-type="review-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">arthyper</journal-id><journal-title-group><journal-title xml:lang="ru">Артериальная гипертензия</journal-title><trans-title-group xml:lang="en"><trans-title>"Arterial’naya Gipertenziya" ("Arterial Hypertension")</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1607-419X</issn><issn pub-type="epub">2411-8524</issn><publisher><publisher-name>Antihypertensive League</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18705/1607-419X-2023-29-5-442-455</article-id><article-id custom-type="edn" pub-id-type="custom">AQDQFT</article-id><article-id custom-type="elpub" pub-id-type="custom">arthyper-2362</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Articles</subject></subj-group></article-categories><title-group><article-title>Роль кишечной микробиоты в развитии сердечно-сосудистой патологии: фокус на метаболиты и маркеры повышенной кишечной проницаемости и воспаления кишечной стенки</article-title><trans-title-group xml:lang="en"><trans-title>Role of intestinal microbiota in the development of cardiovascular disease: focus on metabolites and markers of increased intestinal permeability and inflammation of the intestinal wall</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1073-3844</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Колесова</surname><given-names>Е. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolesova</surname><given-names>E. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Колесова Екатерина Павловна — кандидат медицинских наук, ведущий научный сотрудник научно-исследовательской лаборатории популяционной генетики научно-исследовательского отдела генетических рисков и персонифицированной профилактики Научного центра мирового уровня «Центр персонализированной медицины» </p><p>ул. Аккуратова, д. 2, Санкт-Петербург, 197341</p></bio><bio xml:lang="en"><p>Ekaterina P. Kolesova, Candidate of Medical Sciences, Leading Researcher at the Research Laboratory of Population Genetics of the Research Department of Genetic Risks and Personalized Prevention of the World-class Scientific Center “Center for Personalized Medicine”</p><p>2 Akkuratov street, St Petersburg, 197341 </p></bio><email xlink:type="simple">kolesova_ep@almazovcentre.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5601-0668</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бояринова</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Boyarinova</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бояринова Мария Анатольевна — научный сотрудник научно-исследовательской лаборатории популяционной генетики научно-исследовательского отдела генетических рисков и персонифицированной профилактики Научного центра мирового уровня «Центр персонализированной медицины» </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Maria A. Boyarinova, MD, Researcher at the Research Laboratory of Population Genetics of the Research Department of Genetic Risks and Personalized Prevention of the World-class Scientific Center “Center for Personalized Medicine”</p><p>St Petersburg</p></bio><email xlink:type="simple">essence_4@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2427-4148</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Маслянский</surname><given-names>А. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Maslyanskiy</surname><given-names>A. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Маслянский Алексей Леонидович — доктор медицинских наук, руководитель научно-исследовательской лаборатории ревматологии и иммунопатологии ФГБУ «НМИЦ им. В. А. Алмазова» Минздрава России, профессор Научно-клинического и образовательного центра гастроэнтерологии и гепатологии Санкт-Петербургского государственного университета</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Alexey L. Maslyanskiy, Doctor of Medical Sciences, Head of the Research Laboratory of Rheumatology and Immunopathology, Almazov National Medical Research Centre, Professor, Professor of the Scientific, Clinical and Educational Center of Gastroenterology and Hepatology of the St Petersburg University</p><p>St Petersburg</p></bio><email xlink:type="simple">esc_4@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9658-8712</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Малышкин</surname><given-names>К. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Malyshkin</surname><given-names>K. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Малышкин Константин Алексеевич — кандидат медицинских наук, доцент кафедры клинической лабораторной медицины </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Konstantin A. Malyshkin, Candidate of Medical Sciences, Associate Professor of the Department of Clinical Laboratory Medicine</p><p>St Petersburg</p></bio><email xlink:type="simple">malyshkin.konstantin@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3920-824X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кибкало</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kibkalo</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кибкало София Викторовна — клинический ординатор, лаборант-исследователь научно-исследовательской лаборатории эпидемиологии неинфекционных заболеваний Института сердца и сосудов </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Sofia V. Kibkalo, Clinical Resident, Laboratory Assistantresearcher of the Research Laboratory of Epidemiology of Noncommunicable Diseases of the Institute of Heart and Blood Vessels</p><p>St Petersburg</p></bio><email xlink:type="simple">sonia.kibkalo@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0029-0741</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Новикова</surname><given-names>Н. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Novikova</surname><given-names>N. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Новикова Надежда Сергеевна — младший научный сотрудник</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Nadezhda S. Novikova, Junior Researcher</p><p>St Petersburg</p></bio><email xlink:type="simple">nadezhda.lavrenova.vrn@gmail.com</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2569-6660</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ермоленко</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ermolenko</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ермоленко Елена Игоревна — доктор медицинских наук, заведующая лабораторией персонифицированной микробной терапии научно-образовательного центра «Молекулярные основы взаимодействия микроорганизмов и человека» Научного центра мирового уровня «Центр персонализированной медицины» </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Elena I. Ermolenko, Doctor of Medical Sciences, Head of the Laboratory of Personalized Microbial Therapy of the Scientific and Educational Center “Molecular Foundations of Interaction between microorganisms and Humans” of the World-class Scientific Center “Center for Personalized Medicine”</p><p>St Petersburg</p></bio><email xlink:type="simple">lermolenko1@yandex.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5282-8764</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Артемов</surname><given-names>Н. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Artomov</surname><given-names>N. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Артемов Никита Николаевич — кандидат химических наук, профессор педиатрии, руководитель научно-исследовательской лаборатории популяционной генетики научно-исследовательского отдела генетических рисков и персонифицированной профилактики Научного центра мирового уровня «Центр персонализированной медицины» ФГБУ «НМИЦ им. В. А. Алмазова» Минздрава России, доцент Института прикладных компьютерных наук ФГАОУ ВО НИУ ИТМО</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Nikita N. Artemov, Candidate of Chemical Sciences, Professor of Pediatrics, Head of the Research Laboratory of Population Genetics of the Research Department of Genetic Risks and Personalized Prevention of the World-class Scientific Center “Center for Personalized Medicine”, Almazov National Medical Research Centre, Associate Professor at the Institute of Applied Computer Sciences, ITMO University</p><p>St Petersburg</p></bio><email xlink:type="simple">artomov@broadinstitute.org</email><xref ref-type="aff" rid="aff-5"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5530-9772</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ротарь</surname><given-names>О. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Rotar</surname><given-names>O. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ротарь Оксана Петровна — доктор медицинских наук, главный научный сотрудник научно-исследовательской лаборатории эпидемиологии неинфекционных заболеваний Института сердца и сосудов, заведующая научно-исследовательской лабораторией популяционной генетики научно-исследовательского отдела генетических рисков и персонифицированной профилактики Научного центра мирового уровня «Центр персонализированной медицины» </p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Oksana P. Rotar, Doctor of Medical Sciences, Chief Researcher of the Research Laboratory of Epidemiology of Non-communicable Diseases of the Institute of Heart and Blood Vessels, Head of the Research Laboratory of Population Genetics of the Research Department of Genetic Risks and Personalized Prevention of the World-class Scientific Center “Center for Personalized Medicine”</p><p>St Petersburg</p></bio><email xlink:type="simple">rotar.oxana@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8169-7812</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Конради</surname><given-names>А. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Konradi</surname><given-names>A. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Конради Александра Олеговна — доктор медицинских наук, профессор, академик Российской академии наук, заведующая кафедрой организации, управления и экономики здравоохранения Института медицинского образования, заместитель генерального директора по научной работе ФГБУ «НМИЦ им. В. А. Алмазова» Минздрава России, руководитель международной лаборатории «Системы поддержки принятия решений в медицине», директор Института трансляционной медицины ФГАОУ ВО НИУ ИТМО</p><p>Санкт-Петербург</p></bio><bio xml:lang="en"><p>Aleksandra O. Konradi, Doctor of Medical Sciences, Professor, Academician of the Russian Academy of Sciences, Head of the Department of Organization, Management and Economics of Healthcare of the Institute of Medical Education, Deputy Director General for Scientific Work, Almazov National Medical Research Centre, Head of the International Laboratory “Decision Support Systems in Medicine”, Director of the Institute of Translational Medicine, ITMO University</p><p>St Petersburg</p></bio><email xlink:type="simple">konradi@almazovcentre.ru</email><xref ref-type="aff" rid="aff-5"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Национальный медицинский исследовательский центр им. В. А. Алмазова» Министерства Здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Almazov National Medical Research Centre</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Национальный медицинский исследовательский центр им. В. А. Алмазова» Министерства Здравоохранения Российской Федерации;&#13;
Научно-клинический и образовательный центр гастроэнтерологии и гепатологии Санкт-Петербургского государственного университета</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Almazov National Medical Research Centre;&#13;
Scientific, Clinical and Educational Centre of Gastroenterology and Hepatology of the St Petersburg University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное образовательное учреждение высшего образования «Первый Санкт-Петербургский государственный медицинский университет имени академика И. П. Павлова» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Pavlov State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное научное учреждение «Институт экспериментальной медицины»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Experimental Medicine</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-5"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Национальный медицинский исследовательский центр им. В. А. Алмазова» Министерства Здравоохранения Российской Федерации;&#13;
Федеральное государственное автономное образовательное учреждение высшего образования «Национальный исследовательский университет ИТМО»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Almazov National Medical Research Centre;&#13;
ITMO University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>27</day><month>09</month><year>2023</year></pub-date><volume>29</volume><issue>5</issue><fpage>442</fpage><lpage>455</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Колесова Е.П., Бояринова М.А., Маслянский А.Л., Малышкин К.А., Кибкало С.В., Новикова Н.С., Ермоленко Е.И., Артемов Н.Н., Ротарь О.П., Конради А.О., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Колесова Е.П., Бояринова М.А., Маслянский А.Л., Малышкин К.А., Кибкало С.В., Новикова Н.С., Ермоленко Е.И., Артемов Н.Н., Ротарь О.П., Конради А.О.</copyright-holder><copyright-holder xml:lang="en">Kolesova E.P., Boyarinova M.A., Maslyanskiy A.L., Malyshkin K.A., Kibkalo S.V., Novikova N.S., Ermolenko E.I., Artomov N.N., Rotar O.P., Konradi A.O.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://htn.almazovcentre.ru/jour/article/view/2362">https://htn.almazovcentre.ru/jour/article/view/2362</self-uri><abstract><p>В последние годы все больше исследований свидетельствуют о тесной взаимосвязи между составом и функцией микробиоты и здоровьем человека, в том числе с сердечно-сосудистыми заболеваниями (ССЗ). Повышенная проницаемость кишечника является одним из факторов, который может влиять на состояние микробиоты, а также привести к проникновению бактерий и их токсинов в кровоток, вызывая системное воспаление. Хроническое воспаление, в свою очередь, сопровождается повышенным уровнем цитокинов, которые могут вызвать повреждение эндотелия и привести к эндотелиальной дисфункции. Метаболиты некоторых бактерий могут снижать выработку молекул, регулирующих сосудистый тонус, таких как оксид азота, что может привести к вазоконстрикции и артериальной гипертензии. В обзоре уделяется внимание связи кальпротектина, зонулина, триметиламиноксида с риском возникновения ССЗ, а также освещаются возможные методы коррекции состава и функции микробиоты для профилактики ССЗ.</p></abstract><trans-abstract xml:lang="en"><p>In recent years, an increasing number of studies have shown a close relationship between the composition and function of the microbiota and human health, including cardiovascular diseases (CVD). Increased intestinal permeability is one of the factors that can influence the state of the microbiota and also lead to the penetration of bacteria and their toxins into the bloodstream, causing systemic inflammation. Chronic inflammation, in turn, is accompanied by increased levels of cytokines, which can cause endothelial damage and lead to endothelial dysfunction. Metabolites of some bacteria can reduce the production of molecules that regulate vascular tone, such as nitric oxide, which can lead to vasoconstriction and hypertension. The review focuses on the connection between calprotectin, zonulin, and trimethylamine oxide with the risk of CVD, and also highlights possible methods for correcting the composition and function of the microbiota for the prevention of CVD.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>микробиота кишечника</kwd><kwd>сердечно-сосудистые заболевания</kwd><kwd>эндотелиальная дисфункция</kwd><kwd>артериальная гипертензия</kwd><kwd>повышенная кишечная проницаемость</kwd><kwd>хроническое воспаление</kwd><kwd>метаболиты</kwd><kwd>зонулин</kwd><kwd>кальпротектин</kwd><kwd>триметиламиноксид</kwd></kwd-group><kwd-group xml:lang="en"><kwd>gut microbiota</kwd><kwd>cardiovascular diseases</kwd><kwd>endothelial dysfunction</kwd><kwd>arterial hypertension</kwd><kwd>increased intestinal permeability</kwd><kwd>chronic inflammation</kwd><kwd>metabolites</kwd><kwd>zonulin</kwd><kwd>calprotectin</kwd><kwd>trimethylamine oxide</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках государственного задания «Создание новой технологии таргетной коррекции микробиома кишечника и разработка персонифицированного подхода в проведении первичной профилактики и лечения атеросклероза при сердечно-сосудистых заболеваниях», регистрационный номер ЕГИСУ 121031100311-0</funding-statement><funding-statement xml:lang="en">The work was carried out within the framework of the state task “Creation of a new technology for targeted correction of the intestinal microbiome and the development of a personalized approach to the primary prevention and treatment of atherosclerosis in cardiovascular diseases”, registration number EGISU 121031100311-0</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Российский статистический ежегодник. 2021: Росстат. Стат. сб. Под ред. П.В. Малкова. М., 2021. 692 с.</mixed-citation><mixed-citation xml:lang="en">Russian statistical yearbook. 2021: Statistical collection/Rosstat. In Malkov PV editor. М., 2021. 692 p. In Russian.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Vernon ST, Coffey S, Bhindi R, Soo Hoo SY, Nelson GI, Ward MR et al. Increasing proportion of ST elevation myocardial infarction patients with coronary atherosclerosis poorly explained by standard modifiable risk factors. Eur J Prev Cardiol. 2017;24(17):1824–1830. doi:10.1177/2047487317720287</mixed-citation><mixed-citation xml:lang="en">Vernon ST, Coffey S, Bhindi R, Soo Hoo SY, Nelson GI, Ward MR et al. Increasing proportion of ST elevation myocardial infarction patients with coronary atherosclerosis poorly explained by standard modifiable risk factors. Eur J Prev Cardiol. 2017;24(17):1824–1830. doi:10.1177/2047487317720287</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Khot UN, Khot MB, Bajzer CT, Sapp SK, Ohman EM, Brener SJ et al. Prevalence of conventional risk factors in patients with coronary heart disease. JAMA. 2003;290(7):898–904. doi:10.1001/jama.290.7.898</mixed-citation><mixed-citation xml:lang="en">Khot UN, Khot MB, Bajzer CT, Sapp SK, Ohman EM, Brener SJ et al. Prevalence of conventional risk factors in patients with coronary heart disease. JAMA. 2003;290(7):898–904. doi:10.1001/jama.290.7.898</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Hijová E. Benefits of biotics for cardiovascular diseases. Int J Mol Sci. 2023;24(7):6292. doi:10.3390/ijms24076292</mixed-citation><mixed-citation xml:lang="en">Hijová E. Benefits of biotics for cardiovascular diseases. Int J Mol Sci. 2023;24(7):6292. doi:10.3390/ijms24076292</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">D’Argenio V, Salvatore F. The role of the gut microbiome in the healthy adult status. Clin Chim Acta. 2015;451(PtA):97–102. doi:10.1016/j.cca.2015.01.003</mixed-citation><mixed-citation xml:lang="en">D’Argenio V, Salvatore F. The role of the gut microbiome in the healthy adult status. Clin Chim Acta. 2015;451(PtA):97–102. doi:10.1016/j.cca.2015.01.003</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Gulshan K. Crosstalk between cholesterol, ABC transporters, and PIP2 in inflammation and atherosclerosis. Adv Exp Med Biol. 2023;1422:353–377. doi:10.1007/978-3-031-21547-613</mixed-citation><mixed-citation xml:lang="en">Gulshan K. Crosstalk between cholesterol, ABC transporters, and PIP2 in inflammation and atherosclerosis. Adv Exp Med Biol. 2023;1422:353–377. doi:10.1007/978-3-031-21547-613</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Sattar L, Memon RA, Ashfaq F, Hamdani SSQ, Rahim Vohra R, Ashraf J et al. Efficacy and safety of colchicine in prevention of secondary cardiovascular outcomes among patients with coronary vessel disease: a meta-analysis. Cureus. 2022;14(7): e26680. doi:10.7759/cureus.26680</mixed-citation><mixed-citation xml:lang="en">Sattar L, Memon RA, Ashfaq F, Hamdani SSQ, Rahim Vohra R, Ashraf J et al. Efficacy and safety of colchicine in prevention of secondary cardiovascular outcomes among patients with coronary vessel disease: a meta-analysis. Cureus. 2022;14(7): e26680. doi:10.7759/cureus.26680</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Маслянский А.Л., Пенин И.Н., Чешуина М.Д., Тришина И.Н., Новикова А.Н., Колесова Е.П. и др. Общие закономерности продукции цитокинов и хемокинов у больных диффузными заболеваниями соединительной ткани, воспалительными артропатиями и атеросклерозом. Цитокины и воспаление. 2014;13(3):9–21</mixed-citation><mixed-citation xml:lang="en">Maslyanskiy AL, Penin IN, Cheshuina MD, Trishina IN, Novikova AN, Kolesova EP et al. General patterns of cytokine and chemokine production in patients with diffuse connective tissue diseases, inflammatory arthropathy and atherosclerosis. Citokiny I Vospalenie = Cytokines And Inflammation. 2014;13(3):9–21. In Russian.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Aviña-Zubieta JA, Choi HK, Sadatsafavi M, Etminan M, Esdaile JM, Lacaille D. Risk of cardiovascular mortality in patients with rheumatoid arthritis: a meta-analysis of observational studies. Arthritis Rheum. 2008;59(12):1690–1697. doi:10.1002/art.24092</mixed-citation><mixed-citation xml:lang="en">Aviña-Zubieta JA, Choi HK, Sadatsafavi M, Etminan M, Esdaile JM, Lacaille D. Risk of cardiovascular mortality in patients with rheumatoid arthritis: a meta-analysis of observational studies. Arthritis Rheum. 2008;59(12):1690–1697. doi:10.1002/art.24092</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y, Kaplan MJ. Cardiovascular disease in systemic lupus erythematosus: an update. Curr Opin Rheumatol. 2018;30(5):441– 448. doi:10.1097/BOR.0000000000000528</mixed-citation><mixed-citation xml:lang="en">Liu Y, Kaplan MJ. Cardiovascular disease in systemic lupus erythematosus: an update. Curr Opin Rheumatol. 2018;30(5):441– 448. doi:10.1097/BOR.0000000000000528</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Sun HH, Tian F. Inflammatory bowel disease and cardiovascular disease incidence and mortality: a meta-analysis. Eur J Prev Cardiol. 2018;25(15):1623–1631. doi:10.1177/2047487318792952</mixed-citation><mixed-citation xml:lang="en">Sun HH, Tian F. Inflammatory bowel disease and cardiovascular disease incidence and mortality: a meta-analysis. Eur J Prev Cardiol. 2018;25(15):1623–1631. doi:10.1177/2047487318792952</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Mistry P, Reitz CJ, Khatua TN, Rasouli M, Oliphant K, Young ME et al. Circadian influence on the microbiome improves heart failure outcomes. J Mol Cell Cardiol. 2020;149:54–72. doi:10.1016/j.yjmcc.2020.09.006</mixed-citation><mixed-citation xml:lang="en">Mistry P, Reitz CJ, Khatua TN, Rasouli M, Oliphant K, Young ME et al. Circadian influence on the microbiome improves heart failure outcomes. J Mol Cell Cardiol. 2020;149:54–72. doi:10.1016/j.yjmcc.2020.09.006</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Mansuri NM, Mann NK, Rizwan S, Mohamed AE, Elshafey AE, Khadka A et al. Role of gut microbiome in cardiovascular events: a systematic review. Cureus. 2022;14(12):e32465. doi:10.7759/cureus.32465</mixed-citation><mixed-citation xml:lang="en">Mansuri NM, Mann NK, Rizwan S, Mohamed AE, Elshafey AE, Khadka A et al. Role of gut microbiome in cardiovascular events: a systematic review. Cureus. 2022;14(12):e32465. doi:10.7759/cureus.32465</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Kumarapperuma H, Wang R, Little PJ, Kamato D. Mechanistic insight: linking cardiovascular complications of inflammatory bowel disease [published online ahead of print, 2023 Jan 24]. Trends Cardiovasc Med. 2023; S1050–1738(23)00004-X. doi:10.1016/j.tcm.2023.01.002</mixed-citation><mixed-citation xml:lang="en">Kumarapperuma H, Wang R, Little PJ, Kamato D. Mechanistic insight: linking cardiovascular complications of inflammatory bowel disease [published online ahead of print, 2023 Jan 24]. Trends Cardiovasc Med. 2023; S1050–1738(23)00004-X. doi:10.1016/j.tcm.2023.01.002</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Kamperidis N, Kamperidis V, Zegkos T, Kostourou I, Nikolaidou O, Arebi N et al. Atherosclerosis and inflammatory bowel disease-shared pathogenesis and implications for treatment. Angiology. 2021;72(4):303–314. doi:10.1177/0003319720974552</mixed-citation><mixed-citation xml:lang="en">Kamperidis N, Kamperidis V, Zegkos T, Kostourou I, Nikolaidou O, Arebi N et al. Atherosclerosis and inflammatory bowel disease-shared pathogenesis and implications for treatment. Angiology. 2021;72(4):303–314. doi:10.1177/0003319720974552</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Violi F, Cammisotto V, Bartimoccia S, Pignatelli P, Carnevale R, Nocella C. Gut derived low-grade endotoxaemia, atherothrombosis and cardiovascular disease. Nat Rev Cardiol. 2023;20(1):24–37. doi:10.1038/s41569-022-00737-2</mixed-citation><mixed-citation xml:lang="en">Violi F, Cammisotto V, Bartimoccia S, Pignatelli P, Carnevale R, Nocella C. Gut derived low-grade endotoxaemia, atherothrombosis and cardiovascular disease. Nat Rev Cardiol. 2023;20(1):24–37. doi:10.1038/s41569-022-00737-2</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn’s disease. Nature. 2001;411(6837):603–606. doi:10.1038/35079114</mixed-citation><mixed-citation xml:lang="en">Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn’s disease. Nature. 2001;411(6837):603–606. doi:10.1038/35079114</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Galluzzo S, Patti G, Dicuonzo G, Di Sciascio G, Tonini G, Ferraro E et al. Association between NOD2/CARD15 polymorphisms and coronary artery disease: a case-control study. Hum Immunol. 2011;72(8):636–40. doi:10.1016/j.humimm.2011.04.005</mixed-citation><mixed-citation xml:lang="en">Galluzzo S, Patti G, Dicuonzo G, Di Sciascio G, Tonini G, Ferraro E et al. Association between NOD2/CARD15 polymorphisms and coronary artery disease: a case-control study. Hum Immunol. 2011;72(8):636–40. doi:10.1016/j.humimm.2011.04.005</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Wu H, Liu P, Gong S, Liu X, Hill MA, Liu Z et al. Inflammatory bowel disease increases the levels of albuminuria and the risk of urolithiasis: a two-sample Mendelian randomization study. Eur J Med Res. 2023;28(1):167. doi:10.1186/s40001-023-01128-0</mixed-citation><mixed-citation xml:lang="en">Wu H, Liu P, Gong S, Liu X, Hill MA, Liu Z et al. Inflammatory bowel disease increases the levels of albuminuria and the risk of urolithiasis: a two-sample Mendelian randomization study. Eur J Med Res. 2023;28(1):167. doi:10.1186/s40001-023-01128-0</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Di Tommaso N, Gasbarrini A, Ponziani FR. Intestinal barrier in human health and disease. Int J Environ Res Public Health. 2021;18(23):12836. doi:10.3390/ijerph182312836</mixed-citation><mixed-citation xml:lang="en">Di Tommaso N, Gasbarrini A, Ponziani FR. Intestinal barrier in human health and disease. Int J Environ Res Public Health. 2021;18(23):12836. doi:10.3390/ijerph182312836</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Larabi A, Barnich N, Nguyen HTT. New insights into the interplay between autophagy, gut microbiota and inflammatory responses in IBD. Autophagy. 2020;16(1):38–51. doi:10.1080/15548627.2019.1635384</mixed-citation><mixed-citation xml:lang="en">Larabi A, Barnich N, Nguyen HTT. New insights into the interplay between autophagy, gut microbiota and inflammatory responses in IBD. Autophagy. 2020;16(1):38–51. doi:10.1080/15548627.2019.1635384</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Sircana A, De Michieli F, Parente R, Framarin L, Leone N, Berrutti M et al. Gut microbiota, hypertension and chronic kidney disease: recent advances. Pharmacol Res. 2019;144:390–408. doi:10.1016/j.phrs.2018.01.013</mixed-citation><mixed-citation xml:lang="en">Sircana A, De Michieli F, Parente R, Framarin L, Leone N, Berrutti M et al. Gut microbiota, hypertension and chronic kidney disease: recent advances. Pharmacol Res. 2019;144:390–408. doi:10.1016/j.phrs.2018.01.013</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Kim S, Goel R, Kumar A, Qi Y, Lobaton G, Hosaka K et al. Imbalance of gut microbiome and intestinal epithelial barrier dysfunction in patients with high blood pressure. Clin Sci (Lond). 2018;132(6):701–718. doi:10.1042/CS20180087</mixed-citation><mixed-citation xml:lang="en">Kim S, Goel R, Kumar A, Qi Y, Lobaton G, Hosaka K et al. Imbalance of gut microbiome and intestinal epithelial barrier dysfunction in patients with high blood pressure. Clin Sci (Lond). 2018;132(6):701–718. doi:10.1042/CS20180087</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Li C, Xiao P, Lin D, Zhong HJ, Zhang R, Zhao ZG et al. Risk factors for intestinal barrier impairment in patients with essential hypertension. Front Med (Lausanne). 2021;27(7):543698. doi:10.3389/fmed.2020.5436982019</mixed-citation><mixed-citation xml:lang="en">Li C, Xiao P, Lin D, Zhong HJ, Zhang R, Zhao ZG et al. Risk factors for intestinal barrier impairment in patients with essential hypertension. Front Med (Lausanne). 2021;27(7):543698. doi:10.3389/fmed.2020.5436982019</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Andersen K, Kesper MS, Marschner JA, Konrad L, Ryu M, Kumar S et al. Intestinal dysbiosis, barrier dysfunction, and bacterial translocation account for CKD-related systemic inflammation. J Am Soc Nephrol. 2017;28(1):76–83. doi:10.1681/ASN.2015111285</mixed-citation><mixed-citation xml:lang="en">Andersen K, Kesper MS, Marschner JA, Konrad L, Ryu M, Kumar S et al. Intestinal dysbiosis, barrier dysfunction, and bacterial translocation account for CKD-related systemic inflammation. J Am Soc Nephrol. 2017;28(1):76–83. doi:10.1681/ASN.2015111285</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Kim S, Goel R, Kumar A, Qi Y, Lobaton G, Hosaka K et al. Imbalance of gut microbiome and intestinal epithelial barrier dysfunction in patients with high blood pressure. Clin Sci Lond. 2018;132(6):701–718. doi:10.1042/CS20180087.17</mixed-citation><mixed-citation xml:lang="en">Kim S, Goel R, Kumar A, Qi Y, Lobaton G, Hosaka K et al. Imbalance of gut microbiome and intestinal epithelial barrier dysfunction in patients with high blood pressure. Clin Sci Lond. 2018;132(6):701–718. doi:10.1042/CS20180087.17</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Li C, Gao M, Zhang W, Chen C, Zhou F, Hu Z et al. Zonulin regulates intestinal permeability and facilitates enteric bacteria permeation in coronary artery disease. Sci Rep. 2016;29(6):29142. doi:10.1038/srep29142</mixed-citation><mixed-citation xml:lang="en">Li C, Gao M, Zhang W, Chen C, Zhou F, Hu Z et al. Zonulin regulates intestinal permeability and facilitates enteric bacteria permeation in coronary artery disease. Sci Rep. 2016;29(6):29142. doi:10.1038/srep29142</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Blöbaum L, Witkowski M, Wegner M, Lammel S, Schencke PA, Jakobs K et al. Intestinal barrier dysfunction and microbial translocation in patients with first-diagnosed atrial fibrillation. Biomedicines. 2023;11(1):176. doi:10.3390/biomedicines11010176</mixed-citation><mixed-citation xml:lang="en">Blöbaum L, Witkowski M, Wegner M, Lammel S, Schencke PA, Jakobs K et al. Intestinal barrier dysfunction and microbial translocation in patients with first-diagnosed atrial fibrillation. Biomedicines. 2023;11(1):176. doi:10.3390/biomedicines11010176</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Khaleghi S, Ju JM, Lamba A, Murray JA. The potential utility of tight junction regulation in celiac disease: focus on larazotide acetate. Therap Adv Gastroenterol. 2016;9(1):37–49. doi:10.1177/1756283X15616576</mixed-citation><mixed-citation xml:lang="en">Khaleghi S, Ju JM, Lamba A, Murray JA. The potential utility of tight junction regulation in celiac disease: focus on larazotide acetate. Therap Adv Gastroenterol. 2016;9(1):37–49. doi:10.1177/1756283X15616576</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Kruzliak P, Novák J, Novák M, Fodor GJ. Role of calprotectin in cardiometabolic diseases. Cytokine Growth Factor Rev. 2014;25(1):67–75. doi:10.1016/j.cytogfr.2014.01.005</mixed-citation><mixed-citation xml:lang="en">Kruzliak P, Novák J, Novák M, Fodor GJ. Role of calprotectin in cardiometabolic diseases. Cytokine Growth Factor Rev. 2014;25(1):67–75. doi:10.1016/j.cytogfr.2014.01.005</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Jensen LJ, Kistorp C, Bjerre M, Raymond I, Flyvbjerg A. Plasma calprotectin levels reflect disease severity in patients with chronic heart failure. Eur J Prev Cardiol. 2012;19(5):999–1004. doi:10.1177/1741826711421078</mixed-citation><mixed-citation xml:lang="en">Jensen LJ, Kistorp C, Bjerre M, Raymond I, Flyvbjerg A. Plasma calprotectin levels reflect disease severity in patients with chronic heart failure. Eur J Prev Cardiol. 2012;19(5):999–1004. doi:10.1177/1741826711421078</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Kunutsor SK, Flores-Guerrero JL, Kieneker LM, Nilsen T, Hidden C, Sundrehagen E et al. Plasma calprotectin and risk of cardiovascular disease: Findings from the PREVEND prospective cohort study. Atherosclerosis. 2018;275:205–213. doi:10.1016/j.atherosclerosis.2018.06.817</mixed-citation><mixed-citation xml:lang="en">Kunutsor SK, Flores-Guerrero JL, Kieneker LM, Nilsen T, Hidden C, Sundrehagen E et al. Plasma calprotectin and risk of cardiovascular disease: Findings from the PREVEND prospective cohort study. Atherosclerosis. 2018;275:205–213. doi:10.1016/j.atherosclerosis.2018.06.817</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Løfblad L, Hov GG, Åsberg A, Videm V. Calprotectin and CRP as biomarkers of cardiovascular disease risk in patients with chronic kidney disease: a follow-up study at 5 and 10 years. Scand J Clin Lab Invest. 2023;83(4):258–263. doi:10.1080/00365513.2023.2211779</mixed-citation><mixed-citation xml:lang="en">Løfblad L, Hov GG, Åsberg A, Videm V. Calprotectin and CRP as biomarkers of cardiovascular disease risk in patients with chronic kidney disease: a follow-up study at 5 and 10 years. Scand J Clin Lab Invest. 2023;83(4):258–263. doi:10.1080/00365513.2023.2211779</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Sreejit G, Abdel Latif A, Murphy AJ, Nagareddy PR. Emerging roles of neutrophil-borne S100A8/A9 in cardiovascular inflammation. Pharmacol Res. 2020;161:105212. doi:10.1016/j.phrs.2020.105212</mixed-citation><mixed-citation xml:lang="en">Sreejit G, Abdel Latif A, Murphy AJ, Nagareddy PR. Emerging roles of neutrophil-borne S100A8/A9 in cardiovascular inflammation. Pharmacol Res. 2020;161:105212. doi:10.1016/j.phrs.2020.105212</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Bai B, Cheng M, Jiang L, Xu J, Chen H, Xu Y. High neutrophil to lymphocyte ratio and its gene signatures correlate with diastolic dysfunction in heart failure with preserved ejection fraction. Front Cardiovasc Med. 2021;8:614757. doi:10.3389/fcvm.2021.614757</mixed-citation><mixed-citation xml:lang="en">Bai B, Cheng M, Jiang L, Xu J, Chen H, Xu Y. High neutrophil to lymphocyte ratio and its gene signatures correlate with diastolic dysfunction in heart failure with preserved ejection fraction. Front Cardiovasc Med. 2021;8:614757. doi:10.3389/fcvm.2021.614757</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Bai B, Xu Y, Chen H. Pathogenic roles of neutrophil-derived alarmins (S100A8/A9) in heart failure: from molecular mechanisms to therapeutic insights. Br J Pharmacol. 2023;180(5):573–588. doi:10.1111/bph.15998</mixed-citation><mixed-citation xml:lang="en">Bai B, Xu Y, Chen H. Pathogenic roles of neutrophil-derived alarmins (S100A8/A9) in heart failure: from molecular mechanisms to therapeutic insights. Br J Pharmacol. 2023;180(5):573–588. doi:10.1111/bph.15998</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Sanchez-Gimenez R, Ahmed-Khodja W, Molina Y, Peiró OM, Bonet G, Carrasquer A et al. Gut microbiota-derived metabolites and cardiovascular disease risk: a systematic review of prospective cohort studies. Nutrients. 2022;14(13):2654. doi:10.3390/nu14132654</mixed-citation><mixed-citation xml:lang="en">Sanchez-Gimenez R, Ahmed-Khodja W, Molina Y, Peiró OM, Bonet G, Carrasquer A et al. Gut microbiota-derived metabolites and cardiovascular disease risk: a systematic review of prospective cohort studies. Nutrients. 2022;14(13):2654. doi:10.3390/nu14132654</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Jing W, Huang S, Xiang P, Huang J, Yu H. Dietary precursors and cardiovascular disease: a Mendelian randomization study. Front Cardiovasc Med. 2023;10:1061119. doi:10.3389/fcvm.2023.1061119</mixed-citation><mixed-citation xml:lang="en">Jing W, Huang S, Xiang P, Huang J, Yu H. Dietary precursors and cardiovascular disease: a Mendelian randomization study. Front Cardiovasc Med. 2023;10:1061119. doi:10.3389/fcvm.2023.1061119</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Cho CE, Caudill MA. Trimethylamine-N-oxide: friend, foe, or simply caught in the cross-fire? Trends Endocrinol Metab. 2017;28(2):121–130. doi:10.1016/j.tem.2016.10.005</mixed-citation><mixed-citation xml:lang="en">Cho CE, Caudill MA. Trimethylamine-N-oxide: friend, foe, or simply caught in the cross-fire? Trends Endocrinol Metab. 2017;28(2):121–130. doi:10.1016/j.tem.2016.10.005</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Sumida K, Kovesdy CP. The gut-kidney-heart axis in chronic kidney disease. Physiol Int. 2019;106(3):195–206. doi:10.1556/2060.106.2019.19</mixed-citation><mixed-citation xml:lang="en">Sumida K, Kovesdy CP. The gut-kidney-heart axis in chronic kidney disease. Physiol Int. 2019;106(3):195–206. doi:10.1556/2060.106.2019.19</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Xu KY, Xia GH, Lu JQ, Chen MX, Zhen X, Wang S et al. Impaired renal function and dysbiosis of gut microbiota contribute to increased trimethylamine-N-oxide in chronic kidney disease patients. Sci Rep. 2017;7(1):1445. doi:10.1038/s41598-017-01387-y</mixed-citation><mixed-citation xml:lang="en">Xu KY, Xia GH, Lu JQ, Chen MX, Zhen X, Wang S et al. Impaired renal function and dysbiosis of gut microbiota contribute to increased trimethylamine-N-oxide in chronic kidney disease patients. Sci Rep. 2017;7(1):1445. doi:10.1038/s41598-017-01387-y</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao J, Ning X, Liu B, Dong R, Bai M, Sun S. Specific alterations in gut microbiota in patients with chronic kidney disease: an updated systematic review. Ren Fail. 2021;43(1):102–112. doi: 10.1080/0886022X.2020.1864404</mixed-citation><mixed-citation xml:lang="en">Zhao J, Ning X, Liu B, Dong R, Bai M, Sun S. Specific alterations in gut microbiota in patients with chronic kidney disease: an updated systematic review. Ren Fail. 2021;43(1):102–112. doi: 10.1080/0886022X.2020.1864404</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao J, Ning X, Liu B, Dong R, Bai M, Sun S. Gut microbiota-derived trimethylamine N-oxide is associated with the risk of all-cause and cardiovascular mortality in patients with chronic kidney disease: a systematic review and dose-response meta-analysis. Ann Med. 2023;55(1):2215542. doi:10.1080/07853890.2023.2215542</mixed-citation><mixed-citation xml:lang="en">Zhao J, Ning X, Liu B, Dong R, Bai M, Sun S. Gut microbiota-derived trimethylamine N-oxide is associated with the risk of all-cause and cardiovascular mortality in patients with chronic kidney disease: a systematic review and dose-response meta-analysis. Ann Med. 2023;55(1):2215542. doi:10.1080/07853890.2023.2215542</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang W, Miikeda A, Zuckerman J, Jia X, Charugundla S, Zhou Z et al. Inhibition of microbiota-dependent TMAO production attenuates chronic kidney disease in mice. Sci Rep. 2021;11(1):518. doi:10.1038/s41598-020-80063-0</mixed-citation><mixed-citation xml:lang="en">Zhang W, Miikeda A, Zuckerman J, Jia X, Charugundla S, Zhou Z et al. Inhibition of microbiota-dependent TMAO production attenuates chronic kidney disease in mice. Sci Rep. 2021;11(1):518. doi:10.1038/s41598-020-80063-0</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Canyelles M, Borràs C, Rotllan N, Tondo M, Escolà-Gil JC, Blanco-Vaca F. Gut microbiota-derived TMAO: a causal factor promoting atherosclerotic cardiovascular disease? Int J Mol Sci. 2023;24(3):1940. doi:10.3390/ijms24031940</mixed-citation><mixed-citation xml:lang="en">Canyelles M, Borràs C, Rotllan N, Tondo M, Escolà-Gil JC, Blanco-Vaca F. Gut microbiota-derived TMAO: a causal factor promoting atherosclerotic cardiovascular disease? Int J Mol Sci. 2023;24(3):1940. doi:10.3390/ijms24031940</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Z, Klipfell E, Bennett BJ, Koeth R, Levison BS, Dugar B et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature. 2011;472(7341):57–63. doi:10.1038/nature09922</mixed-citation><mixed-citation xml:lang="en">Wang Z, Klipfell E, Bennett BJ, Koeth R, Levison BS, Dugar B et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature. 2011;472(7341):57–63. doi:10.1038/nature09922</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Li XS, Obeid S, Klingenberg R, Gencer B, Mach F, Räber L et al. Gut microbiota-dependent trimethylamine N-oxide in acute coronary syndromes: a prognostic marker for incident cardiovascular events beyond traditional risk factors. Eur Heart J. 2017;38(11):814–824. doi:10.1093/eurheartj/ehw582</mixed-citation><mixed-citation xml:lang="en">Li XS, Obeid S, Klingenberg R, Gencer B, Mach F, Räber L et al. Gut microbiota-dependent trimethylamine N-oxide in acute coronary syndromes: a prognostic marker for incident cardiovascular events beyond traditional risk factors. Eur Heart J. 2017;38(11):814–824. doi:10.1093/eurheartj/ehw582</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Asgary S, Rastqar A, Keshvari M. Functional food and cardiovascular disease prevention and treatment: a review. J Am Coll Nutr. 2018;37(5):429–455. doi:10.1080/07315724.2017.1410867</mixed-citation><mixed-citation xml:lang="en">Asgary S, Rastqar A, Keshvari M. Functional food and cardiovascular disease prevention and treatment: a review. J Am Coll Nutr. 2018;37(5):429–455. doi:10.1080/07315724.2017.1410867</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Derkach A, Sampson J, Joseph J, Playdon MC, StolzenbergSolomon RZ. Effects of dietary sodium on metabolites: the dietary approaches to stop hypertension (DASH)—sodium feeding study. Am J Clin Nutr. 2017;106(4):1131–1141. doi:10.3945/ajcn.116.150136</mixed-citation><mixed-citation xml:lang="en">Derkach A, Sampson J, Joseph J, Playdon MC, StolzenbergSolomon RZ. Effects of dietary sodium on metabolites: the dietary approaches to stop hypertension (DASH)—sodium feeding study. Am J Clin Nutr. 2017;106(4):1131–1141. doi:10.3945/ajcn.116.150136</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Delgado-Lista J, Perez-Martinez P, Garcia-Rios A, Alcala-Diaz JF, Perez-Caballero AI, Gomez-Delgado F et al. CORonary Diet Intervention with Olive oil and cardiovascular PREVention study (the CORDIOPREV study): Rationale, methods, and baseline characteristics: A clinical trial comparing the efficacy of a Mediterranean diet rich in olive oil versus a lowfat diet on cardiovascular disease in coronary patients. Am Heart J. 2016;177:42–50. doi:10.1016/j.ahj.2016.04.011</mixed-citation><mixed-citation xml:lang="en">Delgado-Lista J, Perez-Martinez P, Garcia-Rios A, Alcala-Diaz JF, Perez-Caballero AI, Gomez-Delgado F et al. CORonary Diet Intervention with Olive oil and cardiovascular PREVention study (the CORDIOPREV study): Rationale, methods, and baseline characteristics: A clinical trial comparing the efficacy of a Mediterranean diet rich in olive oil versus a lowfat diet on cardiovascular disease in coronary patients. Am Heart J. 2016;177:42–50. doi:10.1016/j.ahj.2016.04.011</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Jovanovski E, Nguyen M, Kurahashi Y, Komishon A, Li D, Hoang Vi Thanh H et al. Are all fibres created equal with respect to lipid lowering? Comparing the effect of viscous dietary fibre to non-viscous fibre from cereal sources: a systematic review and metaanalysis of randomised controlled trials. Br J Nutr. 2022;5:1–13. doi:10.1017/S0007114522002355</mixed-citation><mixed-citation xml:lang="en">Jovanovski E, Nguyen M, Kurahashi Y, Komishon A, Li D, Hoang Vi Thanh H et al. Are all fibres created equal with respect to lipid lowering? Comparing the effect of viscous dietary fibre to non-viscous fibre from cereal sources: a systematic review and metaanalysis of randomised controlled trials. Br J Nutr. 2022;5:1–13. doi:10.1017/S0007114522002355</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Reynolds AN, Akerman A, Kumar S, Diep Pham HT, Coffey S, Mann J. Dietary fibre in hypertension and cardiovascular disease management: systematic review and meta-analyses. BMC Med. 2022;20(1):139. doi:10.1186/s12916-022-02328-x</mixed-citation><mixed-citation xml:lang="en">Reynolds AN, Akerman A, Kumar S, Diep Pham HT, Coffey S, Mann J. Dietary fibre in hypertension and cardiovascular disease management: systematic review and meta-analyses. BMC Med. 2022;20(1):139. doi:10.1186/s12916-022-02328-x</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Markowiak P, Slizewska K. Effects of probiotics, prebiotics, and synbiotics on human health. Nutrients. 2017;9(9):1021. doi:10.3390/nu9091021</mixed-citation><mixed-citation xml:lang="en">Markowiak P, Slizewska K. Effects of probiotics, prebiotics, and synbiotics on human health. Nutrients. 2017;9(9):1021. doi:10.3390/nu9091021</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Frei R, Akdis M, O’Mahony L. Prebiotics, probiotics, synbiotics, and the immune system. Curr Opin Gastroenterol. 2015;31(2):153–158. doi:10.1097/MOG.0000000000000151</mixed-citation><mixed-citation xml:lang="en">Frei R, Akdis M, O’Mahony L. Prebiotics, probiotics, synbiotics, and the immune system. Curr Opin Gastroenterol. 2015;31(2):153–158. doi:10.1097/MOG.0000000000000151</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Capuano E. The behavior of dietary fiber in the gastrointestinal tract determines its physiological effect. Crit Rev Food Sci Nutr.2017;57(16):3543–3564. doi:10.1080/10408398.2016.1180501</mixed-citation><mixed-citation xml:lang="en">Capuano E. The behavior of dietary fiber in the gastrointestinal tract determines its physiological effect. Crit Rev Food Sci Nutr.2017;57(16):3543–3564. doi:10.1080/10408398.2016.1180501</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao L, Zhang F, Ding X, Wu G, Lam YY, Wang X et al. Gut bacteria selectively promoted by dietary fibers alleviate type 2 diabetes. Science. 2018;359(6380):1151–1156. doi:10.1126/science.aao5774</mixed-citation><mixed-citation xml:lang="en">Zhao L, Zhang F, Ding X, Wu G, Lam YY, Wang X et al. Gut bacteria selectively promoted by dietary fibers alleviate type 2 diabetes. Science. 2018;359(6380):1151–1156. doi:10.1126/science.aao5774</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Holscher HD. Dietary fiber and prebiotics and the gastrointestinal microbiota. Gut Microbes. 2017;8(2):172–184. doi:10.1080/19490976.2017.1290756</mixed-citation><mixed-citation xml:lang="en">Holscher HD. Dietary fiber and prebiotics and the gastrointestinal microbiota. Gut Microbes. 2017;8(2):172–184. doi:10.1080/19490976.2017.1290756</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Lordan C, Thapa D, Ross RP, Cotter PD. Potential for enriching next-generation health-promoting gut bacteria through prebiotics and other dietary components. Gut Microbes. 2020;11(1):1–20. doi:10.1080/19490976.2019.1613124</mixed-citation><mixed-citation xml:lang="en">Lordan C, Thapa D, Ross RP, Cotter PD. Potential for enriching next-generation health-promoting gut bacteria through prebiotics and other dietary components. Gut Microbes. 2020;11(1):1–20. doi:10.1080/19490976.2019.1613124</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Medina-Vera I, Sanchez-Tapia M, Noriega-López L, Granados-Portillo O, Guevara-Cruz M, Flores-López A et al. A dietary intervention with functional foods reduces metabolic endotoxaemia and attenuates biochemical abnormalities by modifying faecal microbiota in people with type 2 diabetes. Diabetes Metab. 2019;45(2):122–131. doi:10.1016/j.diabet.2018.09.004</mixed-citation><mixed-citation xml:lang="en">Medina-Vera I, Sanchez-Tapia M, Noriega-López L, Granados-Portillo O, Guevara-Cruz M, Flores-López A et al. A dietary intervention with functional foods reduces metabolic endotoxaemia and attenuates biochemical abnormalities by modifying faecal microbiota in people with type 2 diabetes. Diabetes Metab. 2019;45(2):122–131. doi:10.1016/j.diabet.2018.09.004</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Javanshir N, Hosseini GNG, Sadeghi M, Esmaeili R, Satarikia F, Ahmadian G et al. Evaluation of the function of probiotics, emphasizing the role of their binding to the intestinal Epithelium in the stability and their effects on the immune system. Biol Proced Online. 2021;23(1):23. doi:10.1186/s12575-021-00160-w</mixed-citation><mixed-citation xml:lang="en">Javanshir N, Hosseini GNG, Sadeghi M, Esmaeili R, Satarikia F, Ahmadian G et al. Evaluation of the function of probiotics, emphasizing the role of their binding to the intestinal Epithelium in the stability and their effects on the immune system. Biol Proced Online. 2021;23(1):23. doi:10.1186/s12575-021-00160-w</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmadian F, Razmpoosh E, Ejtahed HS, Javadi M, Mirmiran P, Azizi F. Effects of probiotic supplementation on major cardiovascular-related parameters in patients with type 2 diabetes mellitus: a secondary-data analysis of a randomized doubleblind controlled trial. Diabetol Metab Syndr. 2022;14(1):52. doi:10.1186/s13098-022-00822-z</mixed-citation><mixed-citation xml:lang="en">Ahmadian F, Razmpoosh E, Ejtahed HS, Javadi M, Mirmiran P, Azizi F. Effects of probiotic supplementation on major cardiovascular-related parameters in patients with type 2 diabetes mellitus: a secondary-data analysis of a randomized doubleblind controlled trial. Diabetol Metab Syndr. 2022;14(1):52. doi:10.1186/s13098-022-00822-z</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Dixon A, Robertson K, Yung A, Que M, Randall H, Wellalagodage D et al. Efficacy of probiotics in patients of cardiovascular disease risk: a systematic review and meta-analysis. Curr Hypertens Rep. 2020;22(9):74. doi:10.1007/s11906-020-01080-y</mixed-citation><mixed-citation xml:lang="en">Dixon A, Robertson K, Yung A, Que M, Randall H, Wellalagodage D et al. Efficacy of probiotics in patients of cardiovascular disease risk: a systematic review and meta-analysis. Curr Hypertens Rep. 2020;22(9):74. doi:10.1007/s11906-020-01080-y</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Khalesi S, Sun J, Buys N, Jayasinghe R. Effect of probiotics on blood pressure a systematic review and meta-analysis of randomized, controlled trials. Hypertension. 2014;64(4):897–903. doi:10.1161/Hypertensionaha.114.03469</mixed-citation><mixed-citation xml:lang="en">Khalesi S, Sun J, Buys N, Jayasinghe R. Effect of probiotics on blood pressure a systematic review and meta-analysis of randomized, controlled trials. Hypertension. 2014;64(4):897–903. doi:10.1161/Hypertensionaha.114.03469</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Cicero AFG, Fogacci F, Bove M, Giovannini M, Borghi C. Impact of a short-term synbiotic supplementation on metabolic syndrome and systemic inflammation in elderly patients: a randomized placebo-controlled clinical trial. Eur J Nutr. 2021;60(2):655–663. doi:10.1007/s00394-020-02271-8</mixed-citation><mixed-citation xml:lang="en">Cicero AFG, Fogacci F, Bove M, Giovannini M, Borghi C. Impact of a short-term synbiotic supplementation on metabolic syndrome and systemic inflammation in elderly patients: a randomized placebo-controlled clinical trial. Eur J Nutr. 2021;60(2):655–663. doi:10.1007/s00394-020-02271-8</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Żółkiewicz J, Marzec A, Ruszczyński M, Feleszko W. Postbiotics — a step beyond pre- and probiotics. Nutrients. 2020;12(8):2189. doi:10.3390/nu12082189</mixed-citation><mixed-citation xml:lang="en">Żółkiewicz J, Marzec A, Ruszczyński M, Feleszko W. Postbiotics — a step beyond pre- and probiotics. Nutrients. 2020;12(8):2189. doi:10.3390/nu12082189</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Hernández MAG, Canfora EE, Jocken JWE, Blaak EE. The short-chain fatty acid acetate in body weight control and insulin sensitivity. Nutrients. 2019;11(8):1943. doi:10.3390/nu11081943</mixed-citation><mixed-citation xml:lang="en">Hernández MAG, Canfora EE, Jocken JWE, Blaak EE. The short-chain fatty acid acetate in body weight control and insulin sensitivity. Nutrients. 2019;11(8):1943. doi:10.3390/nu11081943</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Hamamah S, Gheorghita R, Lobiuc A, Sirbu IO, Covasa M. Fecal microbiota transplantation in non-communicable diseases: recent advances and protocols. Front Med. 2022;9:1060581. doi:10.3389/fmed.2022.1060581</mixed-citation><mixed-citation xml:lang="en">Hamamah S, Gheorghita R, Lobiuc A, Sirbu IO, Covasa M. Fecal microbiota transplantation in non-communicable diseases: recent advances and protocols. Front Med. 2022;9:1060581. doi:10.3389/fmed.2022.1060581</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Su L, Hong Z, Zhou T, Jian Y, Xu M, Zhang X et al. Health improvements of type 2 diabetic patients through diet and diet plus fecal microbiota transplantation. Sci Rep. 2022;12(1):1152. doi:10.1038/s41598-022-05127-9</mixed-citation><mixed-citation xml:lang="en">Su L, Hong Z, Zhou T, Jian Y, Xu M, Zhang X et al. Health improvements of type 2 diabetic patients through diet and diet plus fecal microbiota transplantation. Sci Rep. 2022;12(1):1152. doi:10.1038/s41598-022-05127-9</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Ng SC, Xu Z, Mak JWY, Yang K, Liu Q, Zuo T et al. Microbiota engraftment after faecal microbiota transplantation in obese subjects with type 2 diabetes: a 24-week, double-blind, randomised controlled trial. Gut. 2022;71(4):716–723. doi:10.1136/gutjnl2020-323617</mixed-citation><mixed-citation xml:lang="en">Ng SC, Xu Z, Mak JWY, Yang K, Liu Q, Zuo T et al. Microbiota engraftment after faecal microbiota transplantation in obese subjects with type 2 diabetes: a 24-week, double-blind, randomised controlled trial. Gut. 2022;71(4):716–723. doi:10.1136/gutjnl2020-323617</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Qiu B, Liang J, Li C. Effects of fecal microbiota transplantation in metabolic syndrome: a meta-analysis of randomized controlled trials. PLoS One. 2023;18(7):e0288718. doi:10.1371/journal.pone.0288718</mixed-citation><mixed-citation xml:lang="en">Qiu B, Liang J, Li C. Effects of fecal microbiota transplantation in metabolic syndrome: a meta-analysis of randomized controlled trials. PLoS One. 2023;18(7):e0288718. doi:10.1371/journal.pone.0288718</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Hu D, Zhao J, Zhang H, Wang G, Gu Z. Fecal microbiota transplantation for weight and glycemic control of obesity as well as the associated metabolic diseases: meta-analysis and comprehensive assessment. Life (Basel). 2023;13(7):1488. doi:10.3390/life13071488</mixed-citation><mixed-citation xml:lang="en">Hu D, Zhao J, Zhang H, Wang G, Gu Z. Fecal microbiota transplantation for weight and glycemic control of obesity as well as the associated metabolic diseases: meta-analysis and comprehensive assessment. Life (Basel). 2023;13(7):1488. doi:10.3390/life13071488</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Toral M, Robles-Vera I, de la Visitacion N, Romero M, Yang T, Sanchez M et al. Critical role of the interaction gut microbiota — sympathetic nervous system in the regulation of blood pressure. Front Physiol. 2019;10:231. doi:10.3389/fphys.2019.00231.96</mixed-citation><mixed-citation xml:lang="en">Toral M, Robles-Vera I, de la Visitacion N, Romero M, Yang T, Sanchez M et al. Critical role of the interaction gut microbiota — sympathetic nervous system in the regulation of blood pressure. Front Physiol. 2019;10:231. doi:10.3389/fphys.2019.00231.96</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Kim TT, Parajuli N, Sung MM, Bairwa SC, Levasseur J, Soltys CM et al. Fecal transplant from resveratrol-fed donors improves glycaemia and cardiovascular features of the metabolic syndrome in mice. Am J Physiol Endocrinol Metab. 2018;315(4): E511–E519. doi:10.1152/ajpendo.00471.2017.97</mixed-citation><mixed-citation xml:lang="en">Kim TT, Parajuli N, Sung MM, Bairwa SC, Levasseur J, Soltys CM et al. Fecal transplant from resveratrol-fed donors improves glycaemia and cardiovascular features of the metabolic syndrome in mice. Am J Physiol Endocrinol Metab. 2018;315(4): E511–E519. doi:10.1152/ajpendo.00471.2017.97</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
