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<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">diaendo</journal-id><journal-title-group><journal-title xml:lang="ru">Сахарный диабет</journal-title><trans-title-group xml:lang="en"><trans-title>Diabetes mellitus</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2072-0351</issn><issn pub-type="epub">2072-0378</issn><publisher><publisher-name>Endocrinology research centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/DM11493</article-id><article-id custom-type="elpub" pub-id-type="custom">diaendo-11493</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>Обзоры</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Review</subject></subj-group></article-categories><title-group><article-title>Роль терапии на основе инкретинов в лечении сахарного диабета 2 типа: прошлое, настоящее и будущее</article-title><trans-title-group xml:lang="en"><trans-title>The role of incretin-based therapies in the management of type 2 diabetes mellitus: perspectives on the past, present and 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/0000-0002-5835-8019</contrib-id><name-alternatives><name name-style="western" xml:lang="en"><surname>Meier</surname><given-names>Juris J.</given-names></name></name-alternatives><email xlink:type="simple">juris.meier@rub.de</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Диабетический центр Бохум-Хаттинген, больница Святого Иосифа, Рурский университет</institution><country>Германия</country></aff><aff xml:lang="en"><institution>Diabetes Center Bochum-Hattingen, St. Josef-Hospital, Ruhr-University Bochum</institution><country>Germany</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>17</day><month>01</month><year>2020</year></pub-date><volume>22</volume><issue>5</issue><fpage>461</fpage><lpage>466</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Meier J., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Meier J.</copyright-holder><copyright-holder xml:lang="en">Meier J.</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.dia-endojournals.ru/jour/article/view/11493">https://www.dia-endojournals.ru/jour/article/view/11493</self-uri><abstract><p>Постоянно увеличивающаяся распространенность сахарного диабета 2 типа (СД2) во всем мире привела к появлению нескольких противодиабетических лекарственных препаратов с различными механизмами действия. Инкретиновые гормоны и их влияние на метаболизм глюкозы и патогенез СД2 стали знаковым открытием в лечении этого все более распространенного нарушения обмена веществ. Агонисты рецептора глюкагоноподобного пептида-1 (ГПП-1) и ингибиторы дипептидилпептидазы-4 (ДПП-4) представляют собой два основных класса препаратов для лечения на основе инкретинов, которые различными способами регулируют механизм усвоения глюкозы, при этом снижают массу тела (агонисты рецептора ГПП-1) или не влияют на массу тела (ингибиторы ДПП-4) и связаны с низким риском гипогликемии и других нежелательных явлений. Кроме того, данные указывают на их возможный терапевтический потенциал при лечении других клинических состояний, таких как ожирение, сердечно-сосудистые заболевания и заболевания печени. В этом обзоре рассматриваются имеющиеся на сегодняшний день агонисты рецептора ГПП-1 и ингибиторы ДПП-4 и их использование в возможных стратегиях лечения СД2, а также их будущее в контексте лечения диабета и других заболеваний.</p></abstract><trans-abstract xml:lang="en"><p>The ever-increasing burden of type 2 diabetes mellitus (T2DM) worldwide, has led to the emergence of several antidiabetes drugs with different modes of action. Incretin hormones and their effect on glucose metabolism and pathogenesis of T2DM has been a landmark discovery in the management of this increasingly prevalent metabolic disorder. Glucagon like peptide-1 (GLP-1) receptor agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors are the two major classes of incretin-based therapies that regulate glucose mechanism through multiple pathways, demonstrate weight loss (GLP-1 receptor agonists) or a weight-neutral effect (DPP-4 inhibitors), and are associated with a low risk of hypoglycaemia and other adverse events. In addition, evidence reflects their possible therapeutic potential in the treatment of other clinical conditions such as obesity, cardiovascular disease and liver disorders. This review explores the availability and the impact of GLP-1 receptor agonists and DPP-4 inhibitors as potential therapeutic strategies for T2DM along with their future in the landscape of diabetes management and other clinical conditions.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сердечно-сосудистая система</kwd><kwd>ингибиторы дипептидилпептидазы-4</kwd><kwd>глюкозозависимый инсулинотропный полипептид</kwd><kwd>глюкагоноподобный пептид-1</kwd><kwd>агонисты рецептора ГПП-1</kwd><kwd>терапия на основе инкретинов</kwd><kwd>сахарный диабет 2 типа</kwd></kwd-group><kwd-group xml:lang="en"><kwd>cardiovascular</kwd><kwd>dipeptidyl peptidase-4 inhibitors</kwd><kwd>glucose-dependent insulinotropic polypeptide</kwd><kwd>glucagon like peptide -1</kwd><kwd>GLP-1 receptor agonists</kwd><kwd>incretin-based therapies</kwd><kwd>type 2 diabetes mellitus</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">International Diabetes Federation. 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