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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">problendo</journal-id><journal-title-group><journal-title xml:lang="ru">Проблемы Эндокринологии</journal-title><trans-title-group xml:lang="en"><trans-title>Problems of Endocrinology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0375-9660</issn><issn pub-type="epub">2308-1430</issn><publisher><publisher-name>Endocrinology Research Centre</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14341/probl201258161-66</article-id><article-id custom-type="elpub" pub-id-type="custom">problendo-4704</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>Ингибиторы дипептидилпептидазы-4: сравнительный анализ представителей группы</article-title><trans-title-group xml:lang="en"><trans-title>Dipeptidyl peptidase-4 inhibitors: Comparative analysis of members of the group</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Shestakova</surname><given-names>E A</given-names></name></name-alternatives><email xlink:type="simple">katiashestakova@mail.ru</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="western" xml:lang="en"><surname>Galstian</surname><given-names>G R</given-names></name></name-alternatives><email xlink:type="simple">-</email></contrib></contrib-group><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>15</day><month>02</month><year>2012</year></pub-date><volume>58</volume><issue>1</issue><issue-title>ТОМ 58, №1 (2012)</issue-title><fpage>61</fpage><lpage>66</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Shestakova E.A., Galstian G.R., 2012</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="ru">Shestakova E.A., Galstian G.R.</copyright-holder><copyright-holder xml:lang="en">Shestakova E.A., Galstian G.R.</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.probl-endojournals.ru/jour/article/view/4704">https://www.probl-endojournals.ru/jour/article/view/4704</self-uri><abstract><p>Ингибиторы дипептидилпептидазы-4 (ДПП-4) - новый класс сахарснижающих препаратов, разработанных с учетом появившихся в XXI веке знаний о физиологии инкретинов. В настоящий момент появилось пять представителей данного класса, три из которых доступны на российском рынке. Ингибиторы ДПП-4 оказывают сахарснижающее действие за счет снижения тощаковой и постпрандиальной гипергликемии, не вызывают увеличения массы тела и имеют благоприятный профиль побочных эффектов. Тем не менее ингибиторы ДПП-4 отличаются по своей фармакодинамике и фармакокинетике, что обусловливает различия в длительности их действия, лекарственных взаимодействиях, возможности применения у отдельных категорий пациентов. В статье представлена сравнительная характеристика трех ингибиторов ДПП-4: вилдаглиптина, ситаглиптина и саксаглиптина.</p></abstract><trans-abstract xml:lang="en"><p>Dipeptidyl peptidase-4 inhibitors (DPP-4) is a new class of hypoglycemic drugs developed based on the knowledge of incretin physiology acquired in the 21st century. Currently, five members of this group are in use three of which are available on the Russian market. The hypoglycemic effect of dipeptidyl peptidase-4 inhibitors is due to reduction of fasting and postprandial hyperglycemia without a rise in the body weight and acceptable profile of side effects. Dipeptidyl peptidase-4 inhibitors differ in terms of pharmacodynamics and pharmacokinetics which implies different indications and duration of their use in different groups of patients as well as different character of their drug interaction. This paper compares three dipeptidyl peptidase-4 inhibitors, viz. vildagliptin, sitagliptin, and saxagliptin.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>ингибитор ДПП-4</kwd><kwd>инкретин</kwd><kwd>вилдаглиптин</kwd><kwd>ситаглиптин</kwd><kwd>саксаглиптин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>dipeptidyl peptidase-4 inhibitor</kwd><kwd>incretin</kwd><kwd>vildagliptin</kwd><kwd>sitagliptin</kwd><kwd>saxagliptin</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">Deacon C.F. Therapeutic strategies based on glucagon-like peptide 1. Diabetes 2004; 53: 2181-2189.</mixed-citation><mixed-citation xml:lang="en">Deacon C.F. Therapeutic strategies based on glucagon-like peptide 1. 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