<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-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">nogr</journal-id><journal-title-group><journal-title xml:lang="ru">Экспериментальная и клиническая гастроэнтерология</journal-title><trans-title-group xml:lang="en"><trans-title>Experimental and Clinical Gastroenterology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-8658</issn><publisher><publisher-name>«Global Media Technologies»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.31146/1682-8658-ecg-190-6-121-129</article-id><article-id custom-type="elpub" pub-id-type="custom">nogr-1685</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>ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Прецизионная медицина и воспалительные заболевания кишечника: концепция, стратегии, будущее</article-title><trans-title-group xml:lang="en"><trans-title>Precision medicine and inflammatory bowel diseases: concept, strategies, future</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9252-9152</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бикбавова</surname><given-names>Г. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Bikbavova</surname><given-names>G. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бикбавова Галия Равильевна, кафедра госпитальной терапии, эндокринологии, доцент, к. м. н.</p><p>Россия, 644099, г. Омск, ул. Ленина, д. 12</p></bio><bio xml:lang="en"><p>Galiya R. Bikbavova, Department of Hospital Therapy, Endocrinology, Associate Professor, PhD in Medical sciences</p><p>12 Lenina street, 644099 Omsk, Russia</p></bio><email xlink:type="simple">galiya1976@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/0000-0002-6581-7017</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ливзан</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Livzan</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ливзан Мария Анатольевна, ректор, заведующий кафедрой факультетской терапии и гастроэнтерологии, профессор, д. м. н.</p><p>Россия, 644099, г. Омск, ул. Ленина, д. 12</p></bio><bio xml:lang="en"><p>Mariya A. Livzan, Rector, Head of the Department of Faculty Therapy, Occupational Diseases, Professor, MD</p><p>12 Lenina street, 644099 Omsk, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4339-2222</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Новиков</surname><given-names>Д. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Novikov</surname><given-names>D. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Новиков Дмитрий Георгиевич, заведующий центральной научно- исследовательской лаборатории, доцент, к. м. н.</p><p>Россия, 644099, г. Омск, ул. Ленина, д. 12</p></bio><bio xml:lang="en"><p>Dmitry G. Novikov, Head of the Central Research Laboratory, Associate Professor, PhD in Medical sciences</p><p>12 Lenina street, 644099 Omsk, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бамбульская</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Bambulskaya</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бамбульская Евгения Александровна, студентка 6 курса лечебного факультета</p><p>Россия, 644099, г. Омск, ул. Ленина, д. 12</p></bio><bio xml:lang="en"><p>Evgeniya A. Bambulskaya, 6th year student of the Faculty of Medicine</p><p>12 Lenina street, 644099 Omsk, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБОУ ВО «Омский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Educational Establishment of Higher Education Omsk State Medical University of the Ministry of Health of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>31</day><month>08</month><year>2021</year></pub-date><volume>1</volume><issue>6</issue><fpage>121</fpage><lpage>129</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бикбавова Г.Р., Ливзан М.А., Новиков Д.Г., Бамбульская Е.А., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Бикбавова Г.Р., Ливзан М.А., Новиков Д.Г., Бамбульская Е.А.</copyright-holder><copyright-holder xml:lang="en">Bikbavova G.R., Livzan M.A., Novikov D.G., Bambulskaya E.A.</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://www.nogr.org/jour/article/view/1685">https://www.nogr.org/jour/article/view/1685</self-uri><abstract><sec><title>Цель обзора</title><p>Цель обзора: анализ и обобщение имеющейся на сегодняшний день информации и представление примеров применения современных подходов медицины в клинической практике на примере воспалительных заболеваний кишечника (ВЗК).</p></sec><sec><title>Основные положения</title><p>Основные положения. С появлением современных клеточных и геномных технологий мы стали участниками интеграции в практическое здравоохранение таких направлений как персонализированная, предиктивная, превентивная, партисипативная медицина обозначаемых как 4П-медицина и вместе с прецизионной медициной составляющих 5П-медицину. На смену классическим приемам диагностики и лечения заболеваний приходит медицина, которая дает возможность прогнозирования (предвидения) заболевания и персонального подхода к каждому пациенту с учетом его генетической, биохимической и физиологической уникальности. Прецизионная медицина стремится повысить качество медицинской помощи, открывая индивидуальный подход к пациенту и охватывает широкий круг областей, включая медикаментозную терапию, генетику, причинно- следственные связи для того, чтобы принимать верные решения на основе фактических данных. 5П-медицина объединяет в себе знания в области протеомики, метаболомики, геномики, биоинформатики с классическими подходами анатомии, терапии, лабораторной и инструментальной диагностики и общественного здоровья. Поиск литературы, содержащей информацию о соответствующих исследованиях проводился в системах PubMed и GoogleScholar по ключевым словам: прецизионная медицина, 4П-медицина, 5П-медицина, воспалительные заболевания кишечника.</p></sec><sec><title>Заключение</title><p>Заключение. Несмотря на значительный прогресс в медицине в целом, до реализации принципов прецизионной медицины в области ВЗК предстоит пройти еще долгий путь, так как многие клиницисты продолжают вести пациентов с ВЗК симптоматически. Однако, применение специфических биомаркеров и новых стратегий в лечении, описанных в обзоре, могут значительно ускорить этот путь и способствовать совершенствованию диагностических и терапевтических подходов.</p></sec></abstract><trans-abstract xml:lang="en"><p>With the advent of modern cellular and genomic technologies, we have become participants in the integration of such areas as personalized, predictive, preventive, and precision medicine (referred to as 4P-medicine), into practical healthcare. In replace of the classic methods of diagnosis and treatment of diseases comes medicine, which makes it possible to predict (anticipate) the disease, and a personalized approach to each patient, taking into account their genetic, biochemical and physiological uniqueness. Precision medicine aims to improve the quality of medical care by opening up an individual approach to the patient and covers a wide range of areas, including drug therapy, genetics, and cause-and-effect relationships in order to make the right decisions based on evidence. 4P-medicine combines knowledge in the field of proteomics, metabolomics, genomics, bioinformatics with classical approaches of anatomy, therapy, laboratory and instrumental diagnostics as well as public health. The purpose of this review is to analyze and summarize the information available to date and to present examples of the application of modern approaches of medicine into clinical practice by diving into the example of inflammatory bowel diseases (IBD). The search for literature containing scientific information about relevant studies was conducted in the PubMed and Google Scholar systems with the use of the following keywords: precision medicine, 4P medicine, inflammatory bowel diseases. Despite significant progress in medicine in general, there is still a long way to go before implementing the principles of precision medicine in the field of IBD, since many clinicians continue to treat patients with IBD symptomatically. However, the use of specific biomarkers and new treatment strategies as described in the review, can significantly accelerate this path and contribute to the improvement of diagnostic and therapeutic approaches.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>прецизионная медицина</kwd><kwd>4П-медицина</kwd><kwd>воспалительные заболевания кишечника</kwd></kwd-group><kwd-group xml:lang="en"><kwd>precision medicine</kwd><kwd>4P-medicine</kwd><kwd>inflammatory bowel diseases</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Публикация подготовлена ФГБОУ ВО «Омский государственный медицинский университет» Минздрава России за счет финансирования по Гранту Президента РФ для государственной поддержки ведущих научных школ (НШ-2558.2020.7) (соглашение № 075–15–2020–036 от 17 марта 2020 года) «Разработка технологии здоровьесбережения коморбидного больного гастроэнтерологического профиля на основе контроля приверженности».</funding-statement><funding-statement xml:lang="en">The publication was prepared by the Federal State Budgetary Educational Institution of Higher Education “Omsk State Medical University” of the Ministry of Health of Russia through funding under the Grant of the President of the Russian Federation for state support of leading scientifi c schools (NSh-2558.2020.7) (agreement No. 075–15–2020–036 of March 17, 2020) “Development of health preservation technologies of a comorbid gastroenterological patient on the basis of adherence control”.</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">Щербо С. Н., Щербо Д. С. Лабораторная диагностика как основа медицины 5П // Вестник РГМУ. – 2019. – № 1. – С. 5–14.</mixed-citation><mixed-citation xml:lang="en">Shcherbo, S. N. Shcherbo, D. S. (2019), “Laboratory diagnostics as a basis for 5P medicine”, Bulletin of RSMU, no. 1, p. 5–12. DOI: 10.24075/brsmu.2018.095</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Баранов В. С. Эволюция предиктивной медицины. Старые идеи, новые понятия // Медицинская гене- тика. – 2017. – Т. 16. – № 5. – С. 4–9.</mixed-citation><mixed-citation xml:lang="en">Baranov V. S. Evolution of predictive medicine. Old ideas and new entities. Medical Genetics. 2017; vol. 16, no. 5, pp. 4–9. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Grens K. FDA to 23 and Me: Stop marketing kits. The Scientist. November 26, 2013. https://www.the-scientist.com/the-nutshell/fda-to-23andme-stop-marketingkits-38354</mixed-citation><mixed-citation xml:lang="en">Grens K. FDA to 23 and Me: Stop marketing kits. The Scientist. November 26, 2013. https://www.the-scientist.com/the-nutshell/fda-to-23andme-stop-marketingkits-38354</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Усова Е. В., Попович М. В., Маньшина А. В., Драпкина О. М. Ответственность граждан за свое здоровье (исследование в фокус- группе) // Профилактическая медицина. – 2001. – Ч. 1. – Т. 24, № 1. – С. 35–43. Doi: 10.17116/profmed20212401135.</mixed-citation><mixed-citation xml:lang="en">Usova E.V., Popovich M. V., Manyshina A. V., Drakkin OM Responsibility of citizens Beginning health (research in the focus group). Profi lakticheskaya Meditsina. 2021, Vol. 24 Issue 1, p35–44. 10p. (in Russ.) Doi: 10.17116/profmed20212401135.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hood L., AuffraМухин В.Е.y C. Participatory medicine: a driving force for revolutionizing healthcare. Genome Med, 2013;5(12):110. doi:10.1186/gm514</mixed-citation><mixed-citation xml:lang="en">Hood L., AuffraМухин В.Е.y C. Participatory medicine: a driving force for revolutionizing healthcare. Genome Med, 2013;5(12):110. doi:10.1186/gm514</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Джайн К. К. Персонализированная медицина // Terra Medica. – 2009. – № 1. – С. 4–11.</mixed-citation><mixed-citation xml:lang="en">Jain K. K. Personalized Medicine. Terra Medica, 2009, no. 1, pp. 4–11 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Щербо С. Н., Щербо Д. С. Персонализированная медицина: монография в 7 т. – Т. 1 Биологические основы. – Москва: РУДН, 2016. – 224 с.; Т. 2 Лабораторные технологии. – Москва: РУДН, 2017. – 437 с.</mixed-citation><mixed-citation xml:lang="en">Shherbo S.N., Shherbo D. S. Personalizirovannaja medicina. [Personalized medicine]. Biological basis- Laboratory technologies. Moscow. RUDN Publ. 2016, Vol. 1–2, pp. 224–437 (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">U. S. Food and Drug Administration (FDA) Department of Health and Human Services. Paving the Way for Personalized Medicine FDA’s: Role in a New Era of Medical Product Development. 28 october 2013. Available from: https://www.fdanews.com/ext/resources/fi les/10/10–28–13-Personalized- Medicine.pdf</mixed-citation><mixed-citation xml:lang="en">U. S. Food and Drug Administration (FDA) Department of Health and Human Services. Paving the Way for Personalized Medicine FDA’s: Role in a New Era of Medical Product Development. 28 october 2013. Available from: https://www.fdanews.com/ext/resources/fi les/10/10–28–13-Personalized- Medicine.pdf</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">König I., Fuchs O., Hansen G., et. al. What is precision medicine? Europ Respir J, 2017, vol. 50, no. 4, pp. 1700391. doi:10.1183/13993003.00391–2017</mixed-citation><mixed-citation xml:lang="en">König I., Fuchs O., Hansen G., et. al. What is precision medicine? Europ Respir J, 2017, vol. 50, no. 4, pp. 1700391. doi:10.1183/13993003.00391–2017</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Kosorok M. R., Laber E. B. Precision Medicine. Ann Rev Start Appl, 2019, vol. 6, pp. 263–286. doi:10.1146/annurev- statistics-030718–105251</mixed-citation><mixed-citation xml:lang="en">Kosorok M. R., Laber E. B. Precision Medicine. Ann Rev Start Appl, 2019, vol. 6, pp. 263–286. doi:10.1146/annurev- statistics-030718–105251</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Пальцев М. А. Персонифицированная медицина // Наука в России. – 2011. – № 1. – С. 12–17. [</mixed-citation><mixed-citation xml:lang="en">Pal’cev M. A. Personifi cirovannaja medicina. [Personalized medicine]. Nauka v Rossii, 2011, vol. 1, pp. 12–17. (In Russ.) Available from: https://portalus.ru/modules/medecine/rus_readme.php?subaction=showfull&amp;id=1407769757&amp;archive=&amp;start_from=&amp;ucat=&amp;.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Алексеенко С. А., Багдасарян А. А., Бакулин И. Г., Брико Н. И., Вергазова Э. К., Гамбарян М. Г., и др. Краткие алгоритмы ведения пациентов на этапе оказания первичной медико-санитарной помощи: Пособие для врачей- терапевтов. – Москва: Видокс, 2019, 20 с.</mixed-citation><mixed-citation xml:lang="en">Aleekseenko S.A., Bagdasaryn A. A., Bakulin I. G., et. al. Brief algorithms of patient management at the stage of primary health. Moscow, Vidox, 2019. 20 p. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Jameson L., Longo J., Dan L. Precision Medicine – Personalized, Problematic, and Promising. N Engl J Med, 2015, vol. 70, no. 10, pp. 612–614. doi:10.1056/NEJMsb1503104.</mixed-citation><mixed-citation xml:lang="en">Jameson L., Longo J., Dan L. Precision Medicine – Personalized, Problematic, and Promising. N Engl J Med, 2015, vol. 70, no. 10, pp. 612–614. doi:10.1056/NEJMsb1503104.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Robinson P. N. Deep phenotyping for precision medicine. Hum Mutat, 2012, vol. 33, no. 5, pp. 777–780. doi:10.1002/ humu.22080.</mixed-citation><mixed-citation xml:lang="en">Robinson P. N. Deep phenotyping for precision medicine. Hum Mutat, 2012, vol. 33, no. 5, pp. 777–780. doi:10.1002/ humu.22080.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">McGrath S., Ghersi D. Building towards precision medicine: empowering medical professionals for the next revolution. BMC Med Genomics, 2016, vol. 9, no. 1, p. 23. doi:10.1186/s12920–016–0183–8.</mixed-citation><mixed-citation xml:lang="en">McGrath S., Ghersi D. Building towards precision medicine: empowering medical professionals for the next revolution. BMC Med Genomics, 2016, vol. 9, no. 1, p. 23. doi:10.1186/s12920–016–0183–8.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Borg- Bartolo S.P., Boyapati R. K., Satsangi J., Kalla R. Precision medicine in inflammatory bowel disease: concept, progress and challenges. F1000Res, 2020, vol. 9, F1000, FacultyRev-54. doi:10.12688/f1000research.20928.1</mixed-citation><mixed-citation xml:lang="en">Borg- Bartolo S.P., Boyapati R. K., Satsangi J., Kalla R. Precision medicine in inflammatory bowel disease: concept, progress and challenges. F1000Res, 2020, vol. 9, F1000, FacultyRev-54. doi:10.12688/f1000research.20928.1</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Prendes-Alvarez S., Nemeroff C. B. Personalized medicine: Prediction of disease vulnerability in mood disorders. Neurosci Lett, 2018; vol. 669, pp. 10–13. doi:10.1016/j.neulet.2016.09.049.</mixed-citation><mixed-citation xml:lang="en">Prendes-Alvarez S., Nemeroff C. B. Personalized medicine: Prediction of disease vulnerability in mood disorders. Neurosci Lett, 2018; vol. 669, pp. 10–13. doi:10.1016/j.neulet.2016.09.049.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mayeux R. Biomarkers: Potential uses and limitations. NeuroRx, 2004, vol. 1, no. 2, pp. 182–188. doi:10.1602/neurorx.1.2.182.</mixed-citation><mixed-citation xml:lang="en">Mayeux R. Biomarkers: Potential uses and limitations. NeuroRx, 2004, vol. 1, no. 2, pp. 182–188. doi:10.1602/neurorx.1.2.182.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Ливзан М. А., Макейкина М. А. Воспалительные заболевания кишечника: современные аспекты диагностики и лечения // Гастроэнтерология. Приложение к журналу CONSILIUM MEDICUM. – 2010. – № 2. – С. 60–65. [.</mixed-citation><mixed-citation xml:lang="en">Livzan M.A., Makeikina M. A. Inflammatory bowel diseases: modern aspects of diagnosis and treatment. Gastroenterology. Application to the journal CONSILIUM MEDICUM, 2010, no. 2, pp. 60–65. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Ungaro R., Mehandru S., Allen P. B., Peyrin- Biroulet L., Colombel J-F. Ulcerativecolitis. Lancet, 2017, vol. 389, no. 10080, pp. 1756–1770. doi:10.1016/S0140–6736(16)32126–2</mixed-citation><mixed-citation xml:lang="en">Ungaro R., Mehandru S., Allen P. B., Peyrin- Biroulet L., Colombel J-F. Ulcerativecolitis. Lancet, 2017, vol. 389, no. 10080, pp. 1756–1770. doi:10.1016/S0140–6736(16)32126–2</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Santos M. P.C., Gomes C., Torres J. Familial and Ethnic Risk in Inflammatory Bowel Disease. Ann Gastroenterol, 2018, vol. 31, no. 1, pp. 14–23. doi:10.20524/aog.2017.0208</mixed-citation><mixed-citation xml:lang="en">Santos M. P.C., Gomes C., Torres J. Familial and Ethnic Risk in Inflammatory Bowel Disease. Ann Gastroenterol, 2018, vol. 31, no. 1, pp. 14–23. doi:10.20524/aog.2017.0208</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Chen G., Lee S. H., Brion M. A., Montgomery G. W., et. al. Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data. Hum Mol Genet, 2014, vol. 23, no. 17, pp. 4710–4720. doi:10.1093/hmg/ddu174</mixed-citation><mixed-citation xml:lang="en">Chen G., Lee S. H., Brion M. A., Montgomery G. W., et. al. Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data. Hum Mol Genet, 2014, vol. 23, no. 17, pp. 4710–4720. doi:10.1093/hmg/ddu174</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Jostins L., Ripke S., Weersma R. K., et. al. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature, 2012, vol. 491, no. 7422, pp. 119–124. doi:10.1038/nature11582</mixed-citation><mixed-citation xml:lang="en">Jostins L., Ripke S., Weersma R. K., et. al. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature, 2012, vol. 491, no. 7422, pp. 119–124. doi:10.1038/nature11582</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J. Z., Sommeren SV., Huang H., Ng SC., Alberts R., Takahashi A., et. al. Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Nat Genet, 2015, vol. 47, no. 9, pp. 979–986. doi:10.1038/ng.3359</mixed-citation><mixed-citation xml:lang="en">Liu J. Z., Sommeren SV., Huang H., Ng SC., Alberts R., Takahashi A., et. al. Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Nat Genet, 2015, vol. 47, no. 9, pp. 979–986. doi:10.1038/ng.3359</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Luo Y., de Lange K. M., Jostins L., Moutsianas L., Randall J., Kennedy N. A. Exploring the genetic architecture of inflammatory bowel disease by whole- genome sequencing identifies association at ADCY7. Nat Genet, 2017, vol. 49, no. 2, pp.186–192. doi:10.1038/ng.3761</mixed-citation><mixed-citation xml:lang="en">Luo Y., de Lange K. M., Jostins L., Moutsianas L., Randall J., Kennedy N. A. Exploring the genetic architecture of inflammatory bowel disease by whole- genome sequencing identifies association at ADCY7. Nat Genet, 2017, vol. 49, no. 2, pp.186–192. doi:10.1038/ng.3761</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Huang H., Fang M., Jostins L., et. al. Fine-mapping inflammatory bowel disease loci to single- variant resolution. Nature, 2017, vol. 547, no. 7662, pp. 173–178. doi:10.1038/nature22969</mixed-citation><mixed-citation xml:lang="en">Huang H., Fang M., Jostins L., et. al. Fine-mapping inflammatory bowel disease loci to single- variant resolution. Nature, 2017, vol. 547, no. 7662, pp. 173–178. doi:10.1038/nature22969</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Макейкина М.А., Ливзан М. А. Генетические про- гностические факторы течения неспецифического язвенного колита // Практическая медицина. – 2012. – Т. 9. – № 65. – С. 133–136.</mixed-citation><mixed-citation xml:lang="en">Makeikina M. A., Livzan M. A. Genetic prognostic factors for the course of non-specific ulcerative colitis. Practical medicine, 2012, vol. 9, no. 65, pp. 133–136. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Cleynen I., Boucher G., Jostins L., et. al. Inherited determinants of Crohn’s disease and ulcerative colitis phenotypes: a genetic association study. Lancet, 2016, vol. 387, no. 10014, pp. 156–167. doi:10.1016/S0140–6736(15)00465–1.</mixed-citation><mixed-citation xml:lang="en">Cleynen I., Boucher G., Jostins L., et. al. Inherited determinants of Crohn’s disease and ulcerative colitis phenotypes: a genetic association study. Lancet, 2016, vol. 387, no. 10014, pp. 156–167. doi:10.1016/S0140–6736(15)00465–1.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Goyette P., Boucher G., Mallon D., et. al. High-density mapping of the MHC identifies a shared role for HLADRB1* 01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat Genet, 2015, vol. 47, no. 2, pp. 172–179. doi:10.1038/ng.3176</mixed-citation><mixed-citation xml:lang="en">Goyette P., Boucher G., Mallon D., et. al. High-density mapping of the MHC identifies a shared role for HLADRB1* 01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat Genet, 2015, vol. 47, no. 2, pp. 172–179. doi:10.1038/ng.3176</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Ventham N. T., Kennedy N. A., Nimmo E. R., Satsangi J. Beyond Gene Discovery in Inflammatory Bowel Disease: The Emerging Role of Epigenetics. Gastroenterology, 2013, vol. 145, no. 2, pp. 293–308. doi:10.1053/j.gastro.2013.05.050</mixed-citation><mixed-citation xml:lang="en">Ventham N. T., Kennedy N. A., Nimmo E. R., Satsangi J. Beyond Gene Discovery in Inflammatory Bowel Disease: The Emerging Role of Epigenetics. Gastroenterology, 2013, vol. 145, no. 2, pp. 293–308. doi:10.1053/j.gastro.2013.05.050</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Koizumi K., Alonso S., Miyaki Y., et. al. Array-based identifi cation of common DNA methylation alterations in ulcerative colitis. Int J Oncol, 2012, vol. 40, no. 4, pp. 983–994. doi:10.3892/ijo.2011.1283</mixed-citation><mixed-citation xml:lang="en">Koizumi K., Alonso S., Miyaki Y., et. al. Array-based identifi cation of common DNA methylation alterations in ulcerative colitis. Int J Oncol, 2012, vol. 40, no. 4, pp. 983–994. doi:10.3892/ijo.2011.1283</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Häsler R., Feng Z., Bäckdahl L., et. al. A functional methylome map of ulcerative colitis. Genome Res, 2012, vol. 22, no. 11, pp. 2130–2137. doi:10.1101/gr.138347.112</mixed-citation><mixed-citation xml:lang="en">Häsler R., Feng Z., Bäckdahl L., et. al. A functional methylome map of ulcerative colitis. Genome Res, 2012, vol. 22, no. 11, pp. 2130–2137. doi:10.1101/gr.138347.112</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Cooke J., Zhang H., Greger L., et. al. Mucosal Genomewide Methylation Changes in Inflammatory Bowel Disease. Inf lamm Bowel Dis, 2012, vol. 18, no. 11, pp. 2128–2137. doi:10.1002/ibd.22942</mixed-citation><mixed-citation xml:lang="en">Cooke J., Zhang H., Greger L., et. al. Mucosal Genomewide Methylation Changes in Inflammatory Bowel Disease. Inf lamm Bowel Dis, 2012, vol. 18, no. 11, pp. 2128–2137. doi:10.1002/ibd.22942</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Tahara T., Shibata T., Nakamura M., et. al. Effect of MDR1 gene promoter methylation in patients with ulcerative colitis. Int J Mol Med, 2009, vol. 23, no. 4, pp. 521–527. doi:10.3892/ijmm_00000160</mixed-citation><mixed-citation xml:lang="en">Tahara T., Shibata T., Nakamura M., et. al. Effect of MDR1 gene promoter methylation in patients with ulcerative colitis. Int J Mol Med, 2009, vol. 23, no. 4, pp. 521–527. doi:10.3892/ijmm_00000160</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Tahara T., Shibata T., Nakamura M., et. al. Promoter methylation of protease-activated receptor (PAR2) is associated with severe clinical phenotypes of ulcerative colitis (UC). Clin Exp Med, 2009, vol. 9, no. 2, pp. 125–130. doi:10.1007/s10238–008–0025-x</mixed-citation><mixed-citation xml:lang="en">Tahara T., Shibata T., Nakamura M., et. al. Promoter methylation of protease-activated receptor (PAR2) is associated with severe clinical phenotypes of ulcerative colitis (UC). Clin Exp Med, 2009, vol. 9, no. 2, pp. 125–130. doi:10.1007/s10238–008–0025-x</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Paramsothy S., Rosenstein A. K., Mehandru S., Colombel J. F. The current state of the art for biological therapies and new small molecules in inflammatory bowel disease. Mucosal Immuno, 2018, vol. 11, no. 6, 1558–1570. doi:10.1038/s41385–018–0050–3</mixed-citation><mixed-citation xml:lang="en">Paramsothy S., Rosenstein A. K., Mehandru S., Colombel J. F. The current state of the art for biological therapies and new small molecules in inflammatory bowel disease. Mucosal Immuno, 2018, vol. 11, no. 6, 1558–1570. doi:10.1038/s41385–018–0050–3</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Loukia G.T., Kazuhiro I., Jonathan J. P., Ian M. A., Neville P. Differential patterns of histone acetylation in inflammatory bowel diseases. J Inflamm (lond), 2011, vol. 8, no. 11, p. 1. doi:10.1186/1476–9255–8–1</mixed-citation><mixed-citation xml:lang="en">Loukia G.T., Kazuhiro I., Jonathan J. P., Ian M. A., Neville P. Differential patterns of histone acetylation in inflammatory bowel diseases. J Inflamm (lond), 2011, vol. 8, no. 11, p. 1. doi:10.1186/1476–9255–8–1</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Singh S., George J., Boland B. S., Casteele N. V., Sandborn W. J. Primary Non- Response to Tumor Necrosis Factor Antagonists is Associated with Inferior Response to Second-line Biologics in Patients with Inflammatory Bowel Diseases: A Systematic Review and Meta-analysis. J Crohns Colitis, 2018, vol. 12, no. 6, pp. 635–643. doi:10.1093/ecco-jcc/jjy004</mixed-citation><mixed-citation xml:lang="en">Singh S., George J., Boland B. S., Casteele N. V., Sandborn W. J. Primary Non- Response to Tumor Necrosis Factor Antagonists is Associated with Inferior Response to Second-line Biologics in Patients with Inflammatory Bowel Diseases: A Systematic Review and Meta-analysis. J Crohns Colitis, 2018, vol. 12, no. 6, pp. 635–643. doi:10.1093/ecco-jcc/jjy004</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Wu F., Zikusoka M., Trindade A., Themistocles D., Mary L. H., Bayless T. M., et al. MicroRNAs are differentially expressed in ulcerative colitis and alter expression of macrophage inflammatory peptide-2 alpha. Gastroenterology, 2008, vol. 135, no. 5, pp. 1624–1635. doi: 10.1053/j.gastro.2008.07.068</mixed-citation><mixed-citation xml:lang="en">Wu F., Zikusoka M., Trindade A., Themistocles D., Mary L. H., Bayless T. M., et al. MicroRNAs are differentially expressed in ulcerative colitis and alter expression of macrophage inflammatory peptide-2 alpha. Gastroenterology, 2008, vol. 135, no. 5, pp. 1624–1635. doi: 10.1053/j.gastro.2008.07.068</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Wu F., Zhang S., Dassopoulos T., et al. Identifi cation of microRNAs associated with ileal and colonic Crohn’s disease. Infl amm Bowel Dis, 2010, vol. 16, no. 10, pp.1729–1738. doi:10.1002/ibd.21267</mixed-citation><mixed-citation xml:lang="en">Wu F., Zhang S., Dassopoulos T., et al. Identifi cation of microRNAs associated with ileal and colonic Crohn’s disease. Infl amm Bowel Dis, 2010, vol. 16, no. 10, pp.1729–1738. doi:10.1002/ibd.21267</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Wu F., Guo N. J., Tian H., et al. Peripheral blood microRNAs distinguish active ulcerative colitis and Crohn’s disease. Inflamm Bowel Dis, 2012, vol. 17, no. 1, pp. 241–250. doi: 10.1002/ibd.21450</mixed-citation><mixed-citation xml:lang="en">Wu F., Guo N. J., Tian H., et al. Peripheral blood microRNAs distinguish active ulcerative colitis and Crohn’s disease. Inflamm Bowel Dis, 2012, vol. 17, no. 1, pp. 241–250. doi: 10.1002/ibd.21450</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Lee J. C. Predicting the course of IBD: light at the end of the tunnel? Dig Dis, 2012, vol. 30, no. 1, pp. 95–99. doi:10.1159/000341132</mixed-citation><mixed-citation xml:lang="en">Lee J. C. Predicting the course of IBD: light at the end of the tunnel? Dig Dis, 2012, vol. 30, no. 1, pp. 95–99. doi:10.1159/000341132</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Белоусова Е. А., Абдулганиева Д. И., Алексеева О. П., и др. Социально- демографическая характеристика, особенности течения и варианты лечения воспалительных заболеваний кишечника в России. Результаты двух многоцентровых исследований // Альманах клинической медицины. – 2018. – Т. 18. – № 5. – С. 445–463. [</mixed-citation><mixed-citation xml:lang="en">Belousova E. A., Abdulganieva D. I., Alexeeva O. P., et al. Social and demographic characteristics, features of disease course and treatment options of inflammatory bowel disease in Russia: results of two multicenter studies. Almanac of Clinical Medicine. 2018;46(5):445–463. (In Russ.) Doi:10.18786/2072–0505–2018–46–5–445–463</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Ивашкин В. Т., Шелыгин Ю. А., Халиф И. Л., и др. Клинические рекомендации Российской гастроэнтерологической ассоциации колопроктологов России по диагностике и лечению болезни Крона // Колопроктология. – 2017. – Т. 2, № 60. – С. 7–29.</mixed-citation><mixed-citation xml:lang="en">Ivashkin V. T., Shelygin Yu.A., Khalif I. L., et. al. Clinical guide of russian association of gastroenterology and russian association of coloproctology on diagnostics and treatment of crohn’’s disease. Koloproktologija, 2017, vol. 2, no. 60, pp. 7–29. (In Russ.) doi:10.33878/2073–7556–2017–0–2–7–29</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Travis S. P.L., Farrant J. M., Ricketts C., et al. Predicting outcome in severe ulcerative colitis. Gut, 1996, vol. 38, no. 6, pp. 905–910. doi:10.1136/gut.38.6.905</mixed-citation><mixed-citation xml:lang="en">Travis S. P.L., Farrant J. M., Ricketts C., et al. Predicting outcome in severe ulcerative colitis. Gut, 1996, vol. 38, no. 6, pp. 905–910. doi:10.1136/gut.38.6.905</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Colombel J-F., Panaccione R., Bossuyt P., et. al. Effect of tight control management on Crohn’s disease (CALM): a multicentre, randomised, controlled phase 3 trial. Lancet, 2017, vol. 390, no. 10114, pp. 2779–2789. doi:10.1016/S0140–6736(17)32641–7</mixed-citation><mixed-citation xml:lang="en">Colombel J-F., Panaccione R., Bossuyt P., et. al. Effect of tight control management on Crohn’s disease (CALM): a multicentre, randomised, controlled phase 3 trial. Lancet, 2017, vol. 390, no. 10114, pp. 2779–2789. doi:10.1016/S0140–6736(17)32641–7</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Heida A., Park K. T., Rheenen P. F. Clinical Utility of Fecal Calprotectin Monitoring in Asymptomatic Patients with Inflammatory Bowel Disease: A Systematic Review and Practical Guide. Inflam Bowel Dis, 2017, vol. 23, no. 6, pp. 894–902. doi:10.1097/MIB.0000000000001082</mixed-citation><mixed-citation xml:lang="en">Heida A., Park K. T., Rheenen P. F. Clinical Utility of Fecal Calprotectin Monitoring in Asymptomatic Patients with Inflammatory Bowel Disease: A Systematic Review and Practical Guide. Inflam Bowel Dis, 2017, vol. 23, no. 6, pp. 894–902. doi:10.1097/MIB.0000000000001082</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Florin T. H.J., Paterson E. W.J., Fowler E. V., Radford- Smith G. L. Clinically active Crohn’s disease in the presence of a low C-reactive protein. Scan J Gastroenterol, 2006, vol. 41, no. 3, pp. 306–11. doi:10.1080/00365520500217118</mixed-citation><mixed-citation xml:lang="en">Florin T. H.J., Paterson E. W.J., Fowler E. V., Radford- Smith G. L. Clinically active Crohn’s disease in the presence of a low C-reactive protein. Scan J Gastroenterol, 2006, vol. 41, no. 3, pp. 306–11. doi:10.1080/00365520500217118</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Осипенко М. Ф., Ливзан М. А., Скалинская М. И., Лялюкова Е. А. Концентрация фекального кальпроктектина в дифференциальной диагностике заболеваний кишечника // Терапевтический архив. – 2015. – Т. 87. – № 2. – С. 30–33.</mixed-citation><mixed-citation xml:lang="en">Osipenko M.F., Livzan M. A., Skalinskaia M. I., Lialiu ko va E. A. Fecal calprotectin concentration in the differential diagnosis of bowel diseases, 2015, vol. 87, no 2, pp. 30–33. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Ritchie S. C., Würtz P., Nath A. P., et. al. Th e biomarker GlycA is associated with chronic inflammation and predicts long-term risk of severe infection. Cell Syst, 2015, vol. 1, no. 4, pp. 1–9. doi:10.1016/j.cels.2015.09.007</mixed-citation><mixed-citation xml:lang="en">Ritchie S. C., Würtz P., Nath A. P., et. al. Th e biomarker GlycA is associated with chronic inflammation and predicts long-term risk of severe infection. Cell Syst, 2015, vol. 1, no. 4, pp. 1–9. doi:10.1016/j.cels.2015.09.007</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Dierckx T., Verstockt B., Vermeire S., Weyenbergh J. GlycA, a Nuclear Magnetic Resonance Spectroscopy Measure for Protein Glycosylation, is a Viable Biomarker for Disease Activity in IBD. J Crohns Colitis, 2019, vol. 13, no. 3, pp. 389–394. doi:10.1093/ecco-jcc/jjy162</mixed-citation><mixed-citation xml:lang="en">Dierckx T., Verstockt B., Vermeire S., Weyenbergh J. GlycA, a Nuclear Magnetic Resonance Spectroscopy Measure for Protein Glycosylation, is a Viable Biomarker for Disease Activity in IBD. J Crohns Colitis, 2019, vol. 13, no. 3, pp. 389–394. doi:10.1093/ecco-jcc/jjy162</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Kennedy N. A., Heap G. A., Green H. D., et. al. Predictors of anti- TNF treatment failure in anti- TNF-naive patients with active luminal Crohn’s disease: a prospective, multicentre, cohort study. Lancet Gastroenterol Hepatol, 2019, vol. 4, no. 5, pp. 341–353. doi:10.1016/S2468–1253(19)30012–3</mixed-citation><mixed-citation xml:lang="en">Kennedy N. A., Heap G. A., Green H. D., et. al. Predictors of anti- TNF treatment failure in anti- TNF-naive patients with active luminal Crohn’s disease: a prospective, multicentre, cohort study. Lancet Gastroenterol Hepatol, 2019, vol. 4, no. 5, pp. 341–353. doi:10.1016/S2468–1253(19)30012–3</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Mitrev N., Casteele N. V., Seow C. H., et. al. Review article: consensus statements on therapeutic drug monitoring of anti-tumour necrosis factor therapy in inflammatory bowel diseases. Aliment Pharmacol Ther, 2017, vol. 46, no. 11–12, pp. 1037–1053. doi:10.1111/apt.14368</mixed-citation><mixed-citation xml:lang="en">Mitrev N., Casteele N. V., Seow C. H., et. al. Review article: consensus statements on therapeutic drug monitoring of anti-tumour necrosis factor therapy in inflammatory bowel diseases. Aliment Pharmacol Ther, 2017, vol. 46, no. 11–12, pp. 1037–1053. doi:10.1111/apt.14368</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Ricciuto A., Dhaliwal J., Walters T. D., Griffiths A. M., Church P. C. Clinical Outcomes With Therapeutic Drug Monitoring in Inflammatory Bowel Disease: A Systematic Review With Meta- Analysis. J Crohns Colitis. 2018, vol. 12, no. 11, pp. 1302–1315. doi:10.1093/ecco-jcc/jjy109</mixed-citation><mixed-citation xml:lang="en">Ricciuto A., Dhaliwal J., Walters T. D., Griffiths A. M., Church P. C. Clinical Outcomes With Therapeutic Drug Monitoring in Inflammatory Bowel Disease: A Systematic Review With Meta- Analysis. J Crohns Colitis. 2018, vol. 12, no. 11, pp. 1302–1315. doi:10.1093/ecco-jcc/jjy109</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Dean L., Pratt V., McLeod H., Rubinstein W., Dean L., Kattman B., et. al. Azathioprine Th erapy and TPMT and NUDT15 Genotype. Medical Genetics Summaries. 2012, sep. 20. Available from: https://www.ncbi.nlm.nih.gov/books/NBK100661/</mixed-citation><mixed-citation xml:lang="en">Dean L., Pratt V., McLeod H., Rubinstein W., Dean L., Kattman B., et. al. Azathioprine Th erapy and TPMT and NUDT15 Genotype. Medical Genetics Summaries. 2012, sep. 20. Available from: https://www.ncbi.nlm.nih.gov/books/NBK100661/</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Boer N. K.H., Peyrin-Biroulet L., Jharap B., et. al. Thiopurines in Inflammatory Bowel Disease: New Findings and Perspectives. J Crohns Colitis, 2018, vol. 12, no. 5, pp. 610–620. Doi: 10.1093/ecco-jcc/jjx181</mixed-citation><mixed-citation xml:lang="en">Boer N. K.H., Peyrin-Biroulet L., Jharap B., et. al. Thiopurines in Inflammatory Bowel Disease: New Findings and Perspectives. J Crohns Colitis, 2018, vol. 12, no. 5, pp. 610–620. Doi: 10.1093/ecco-jcc/jjx181</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Pereira M. S., Maia L., Azevedo L. F., et. al. A [Glyco] biomarker that Predicts Failure to Standard Th erapy in Ulcerative Colitis Patients. J Crohns Colitis. 2019, vol. 13, no.1, pp. 39–49. doi:10.1093/ecco-jcc/jjy139</mixed-citation><mixed-citation xml:lang="en">Pereira M. S., Maia L., Azevedo L. F., et. al. A [Glyco] biomarker that Predicts Failure to Standard Th erapy in Ulcerative Colitis Patients. J Crohns Colitis. 2019, vol. 13, no.1, pp. 39–49. doi:10.1093/ecco-jcc/jjy139</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Chambrun G. P., PeyrinBiroulet L., Lémann M., Colombel J-F. Clinical implications of mucosal healing for the management of IBD. Nat Rev Gastroenterol Hepatol, 2010, vol. 7, no. 1, pp. 15–29. doi:10.1038/nrgastro.2009.203</mixed-citation><mixed-citation xml:lang="en">Chambrun G. P., PeyrinBiroulet L., Lémann M., Colombel J-F. Clinical implications of mucosal healing for the management of IBD. Nat Rev Gastroenterol Hepatol, 2010, vol. 7, no. 1, pp. 15–29. doi:10.1038/nrgastro.2009.203</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Fumery M., Singh S., Dulai P. S., Gower- Rousseau C., Peyrin- Biroulet L., Sandborn W. J. Natural history of adult ulcerative colitis in population- based cohorts: A systematic review. Clini Gastroenterol Hepatol, 2018, vol. 16, no. 3, pp. 343–356. doi:10.1016/j.cgh.2017.06.016</mixed-citation><mixed-citation xml:lang="en">Fumery M., Singh S., Dulai P. S., Gower- Rousseau C., Peyrin- Biroulet L., Sandborn W. J. Natural history of adult ulcerative colitis in population- based cohorts: A systematic review. Clini Gastroenterol Hepatol, 2018, vol. 16, no. 3, pp. 343–356. doi:10.1016/j.cgh.2017.06.016</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Turner D., Ricciuto A., LewisA., et. al. STRIDE-II: An Update on the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) Initiative of the International Organization for the Study of IBD (IOIBD): Determining Therapeutic Goals for Treat-to- Target strategies in IBD. Gastroenterology, 2021, vol. 161, no. 5, pp. 1570–1583. doi:10.1053/ j.gastro.2020.12.031</mixed-citation><mixed-citation xml:lang="en">Turner D., Ricciuto A., LewisA., et. al. STRIDE-II: An Update on the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) Initiative of the International Organization for the Study of IBD (IOIBD): Determining Therapeutic Goals for Treat-to- Target strategies in IBD. Gastroenterology, 2021, vol. 161, no. 5, pp. 1570–1583. doi:10.1053/ j.gastro.2020.12.031</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Peyrin-Biroulet L., Sandborn W., Sands B. E., Reinisch W., Bemelman W., Bryant R. V., et. al. Selecting Therapeutic targets in Inflammatory Bowel Disease (STRIDE): Determining Therapeutic Goals for Treat-to-Target. The Am J Gastroenterolog, 2015, vol. 110, no. 9, pp. 1324–1338. doi:10.1038/ajg.2015.233</mixed-citation><mixed-citation xml:lang="en">Peyrin-Biroulet L., Sandborn W., Sands B. E., Reinisch W., Bemelman W., Bryant R. V., et. al. Selecting Therapeutic targets in Inflammatory Bowel Disease (STRIDE): Determining Therapeutic Goals for Treat-to-Target. The Am J Gastroenterolog, 2015, vol. 110, no. 9, pp. 1324–1338. doi:10.1038/ajg.2015.233</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Arijs I., Hertogh G. D., Lemmens B., et. al. Effect of vedolizumab (anti-alpha4beta7-integrin) therapy on histological healing and mucosal gene expression in patients with UC. Gut. 2018, vol. 67, no. 1, pp. 43–52. doi:10.1136/gutjnl-2016–312293</mixed-citation><mixed-citation xml:lang="en">Arijs I., Hertogh G. D., Lemmens B., et. al. Effect of vedolizumab (anti-alpha4beta7-integrin) therapy on histological healing and mucosal gene expression in patients with UC. Gut. 2018, vol. 67, no. 1, pp. 43–52. doi:10.1136/gutjnl-2016–312293</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Yzet C., Ungaro R., Bossuyt P., et. al. OP35 Endoscopic and deep remission at 1 year prevents disease progression in early Crohn’s disease: Long-term data from CALM. Journal of Crohn’s and Colitis. 2019, vol. 13, S024–S025. doi:10.1093/ecco-jcc/jjy222.032</mixed-citation><mixed-citation xml:lang="en">Yzet C., Ungaro R., Bossuyt P., et. al. OP35 Endoscopic and deep remission at 1 year prevents disease progression in early Crohn’s disease: Long-term data from CALM. Journal of Crohn’s and Colitis. 2019, vol. 13, S024–S025. doi:10.1093/ecco-jcc/jjy222.032</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Bryant V. R., Costello P. S., Schoeman S., et. al. Limited uptake of ulcerative colitis “treat to target” recommendations in real-world practice. J Gastroenterol Hepatol. 2018, 33, no. 3, pp. 599–607. doi:10.1111/jgh.13923</mixed-citation><mixed-citation xml:lang="en">Bryant V. R., Costello P. S., Schoeman S., et. al. Limited uptake of ulcerative colitis “treat to target” recommendations in real-world practice. J Gastroenterol Hepatol. 2018, 33, no. 3, pp. 599–607. doi:10.1111/jgh.13923</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>
