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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Almanac of Clinical Medicine</journal-id><journal-title-group><journal-title xml:lang="en">Almanac of Clinical Medicine</journal-title><trans-title-group xml:lang="ru"><trans-title>Альманах клинической медицины</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2072-0505</issn><issn publication-format="electronic">2587-9294</issn><publisher><publisher-name xml:lang="en">Moscow Regional Research and Clinical Institute (MONIKI)</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">17271</article-id><article-id pub-id-type="doi">10.18786/2072-0505-2024-52-040</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW ARTICLE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Common pathogenetic mechanisms of inflammatory bowel diseases and atherosclerosis: a focus on cytokines</article-title><trans-title-group xml:lang="ru"><trans-title>Общие патогенетические механизмы воспалительных заболеваний кишечника и атеросклероза: акцент на цитокинах</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8762-9914</contrib-id><name-alternatives><name xml:lang="en"><surname>Zhigula</surname><given-names>Zinaida M.</given-names></name><name xml:lang="ru"><surname>Жигула</surname><given-names>Зинаида Михайловна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, PhD, Associate Professor, Department of Therapy, Faculty of Additional Professional Education</p></bio><bio xml:lang="ru"><p>канд. мед. наук, доцент кафедры терапии факультета дополнительного профессионального образования</p></bio><email>pustotinazm@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4405-2975</contrib-id><name-alternatives><name xml:lang="en"><surname>Zhilina</surname><given-names>Albina A.</given-names></name><name xml:lang="ru"><surname>Жилина</surname><given-names>Альбина Александровна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, PhD, Vice-Rector for Academic Affairs, Educational Activities and Youth Policy, Professor, Department of Therapy, Faculty of Additional Professional Education</p></bio><bio xml:lang="ru"><p>д-р мед. наук, проректор по учебной работе, воспитательной деятельности и молодежной политике, профессор кафедры терапии факультета дополнительного профессионального образования</p></bio><email>albina1228@ya.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9498-9216</contrib-id><name-alternatives><name xml:lang="en"><surname>Lareva</surname><given-names>Natalia V.</given-names></name><name xml:lang="ru"><surname>Ларева</surname><given-names>Наталья Викторовна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, PhD, Professor, Vice-Rector for Research and International Cooperation, Head of Department of Therapy, Faculty of Additional Professional Education</p></bio><bio xml:lang="ru"><p>д-р мед. наук, профессор, проректор по научной и международной работе, зав. кафедрой терапии факультета дополнительного профессионального образования</p></bio><email>larevanv@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Chita State Medical Academy</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Читинская государственная медицинская академия» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2025-02-05" publication-format="electronic"><day>05</day><month>02</month><year>2025</year></pub-date><pub-date date-type="pub" iso-8601-date="2024-12-27" publication-format="electronic"><day>27</day><month>12</month><year>2024</year></pub-date><volume>52</volume><issue>8</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>405</fpage><lpage>416</lpage><history><date date-type="received" iso-8601-date="2024-05-29"><day>29</day><month>05</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2025-01-23"><day>23</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Zhigula Z.M., Zhilina A.A., Lareva N.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Жигула З.М., Жилина А.А., Ларева Н.В.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Zhigula Z.M., Zhilina A.A., Lareva N.V.</copyright-holder><copyright-holder xml:lang="ru">Жигула З.М., Жилина А.А., Ларева Н.В.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://almclinmed.ru/jour/article/view/17271">https://almclinmed.ru/jour/article/view/17271</self-uri><abstract xml:lang="en"><p><bold>Objective:</bold> To analyze literature data and compare the common pathways of inflammation in inflammatory bowel diseases (IBD) and atherosclerosis with focus on the effects of proinflammatory cytokines on both pathologies, as well as from the perspective of potential role of gene polymorphism of proinflammatory cytokines in the pathophysiology of atherosclerosis in IBD patients.</p> <p><bold>Main provisions: </bold>In IBD, a serum cytokine profile initiates and supports the chronic inflammation. The main immunological mechanisms in both IBD and atherosclerosis are mediated by hyperproduction of proinflammatory cytokines, such as tumor necrosis factor α (TNF-α), interleukins (IL) IL-1β, IL-6, IL-8, IL-12, IL-23, IL-17, and relative insufficiency of anti-inflammatory IL-4 and IL-10, with significant increase in pro-inflammatory cytokines. An association has been established between the polymorphisms of <italic>TNF-α</italic> (rs1800629), <italic>IL-8</italic> (rs117518778, rs8057084), <italic>IL-10</italic> (rs3024505, rs1800896), <italic>IL-12</italic> (rs6887695, rs10045431), <italic>IL-23</italic> (rs11209026A) candidate genes and the development of ulcerative colitis (UC). The polymorphisms of the <italic>TNF-α</italic> (rs1800629), <italic>IL-8</italic> (rs117518778, rs8057084), <italic>IL-1β</italic> (rs16944), <italic>IL-17A</italic> (rs2275913), <italic>IL-4</italic> (rs2243250), <italic>IL-23</italic> (rs6682925T/C) genes are associated with a high risk of atherosclerosis. Protein tyrosine phosphatase, receptor type, C (PTPRC) was identified as the hub crosstalk gene for the comorbidity of UC and atherosclerosis. The effects of cytokine genes polymorphisms as key targets of the pathogenetically oriented IBD therapy on the development of atherosclerosis in these patients remain a poorly investigated question.</p> <p><bold>Conclusion:</bold> IBD and atherosclerosis are mediated by the shared mechanisms of enhanced synthesis of proinflammatory cytokines, as well as polymorphisms of the candidate genes. Studies on the polymorphism of proinflammatory cytokines genes and small molecules in patients with UC, as well as the association of these polymorphisms with the development of atherosclerosis would open up new possibilities for prediction of cardiovascular diseases in these patients, development of preventive measures, and for repositioning of biological therapy for the prevention and treatment of atherosclerosis.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Цель</bold> – по данным литературы сравнить общность механизмов развития воспаления при воспалительных заболеваниях кишечника (ВЗК) и атеросклерозе с точки зрения влияния провоспалительных цитокинов на оба процесса, а также с позиций возможной роли полиморфизма генов провоспалительных цитокинов в патогенезе атеросклероза у пациентов с ВЗК.</p> <p><bold>Основные положения.</bold> При ВЗК в крови формируется цитокиновый профиль, инициирующий и поддерживающий хроническое воспаление. Основные иммунологические механизмы как при ВЗК, так и при атеросклерозе реализуются вследствие гиперпродукции провоспалительных цитокинов – фактора некроза опухоли α (англ. tumor necrosis factor α, TNF-α), интерлейкина (англ. interleukin, IL) 1β, IL-6, IL-8, IL-12, IL-23, IL-17 и относительной недостаточности противовоспалительных IL-4 и IL-10 на фоне более значимого повышения провоспалительных цитокинов. Установлена связь между полиморфизмами генов-кандидатов <italic>TNF-α</italic> (rs1800629), <italic>IL-10</italic> (rs3024505, rs1800896), <italic>IL-12</italic> (rs6887695, rs10045431), <italic>IL-23</italic> (rs11209026A) и развитием язвенного колита. Полиморфизмы генов <italic>TNF-α</italic> (rs1800629), <italic>IL-8</italic> (rs117518778, rs8057084), <italic>IL-1β </italic>(rs16944), <italic>IL-17А</italic> (rs2275913), <italic>IL-4</italic> (rs2243250),<italic> IL-23</italic> (rs6682925T/C) ассоциированы с высоким риском развития атеросклероза. Белок тирозиновая протеинфосфатаза C рецепторного типа идентифицирован как ключевой ген перекрестного взаимодействия при коморбидности язвенного колита и атеросклероза. Малоизученным остается вопрос о влиянии полиморфизмов генов цитокинов – ключевых мишеней патогенетически ориентированной терапии ВЗК – на развитие атеросклероза у данных больных.</p> <p><bold>Заключение.</bold> В основе ВЗК и атеросклероза лежат общие механизмы усиленного синтеза провоспалительных цитокинов, а также полиморфизмы генов-кандидатов. Изучение полиморфизма генов провоспалительных цитокинов и малых молекул у больных ВЗК, а также взаимосвязей этих полиморфизмов с развитием атеросклероза позволит открыть новые возможности прогнозирования сердечно-сосудистых заболеваний у таких больных, разработать меры профилактики, а также репозиционировать биологическую терапию для профилактики и лечения атеросклероза.</p></trans-abstract><kwd-group xml:lang="en"><kwd>inflammatory bowel diseases</kwd><kwd>ulcerative colitis</kwd><kwd>Crohn's disease</kwd><kwd>atherosclerosis</kwd><kwd>chronic inflammation</kwd><kwd>pro-inflammatory cytokines</kwd><kwd>gene polymorphism</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>воспалительные заболевания кишечника</kwd><kwd>язвенный колит</kwd><kwd>болезнь Крона</kwd><kwd>атеросклероз</kwd><kwd>хроническое воспаление</kwd><kwd>провоспалительные цитокины</kwd><kwd>полиморфизм генов</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Sun HH, Tian F. 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