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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/DM8005</article-id><article-id custom-type="elpub" pub-id-type="custom">diaendo-8005</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>Диагностика, контроль, лечение</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Diagnosis, control, treatment</subject></subj-group></article-categories><title-group><article-title>Эмпаглифлозин: новая стратегия нефропротекции при сахарном диабете</article-title><trans-title-group xml:lang="en"><trans-title>Empagliflozin: a new strategy for nephroprotection in diabetes</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3502-5892</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Корбут</surname><given-names>Антон Иванович</given-names></name><name name-style="western" xml:lang="en"><surname>Korbut</surname><given-names>Anton Ivanovich</given-names></name></name-alternatives><bio xml:lang="ru"><p>Младший научный сотрудник лабораторим эндокринологии</p></bio><bio xml:lang="en"><p>MD, junior research associate laboratory of Endocrinology</p></bio><email xlink:type="simple">anton.korbut@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/0000-0002-5407-8722</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Климонтов</surname><given-names>Вадим Валерьевич</given-names></name><name name-style="western" xml:lang="en"><surname>Klimontov</surname><given-names>Vadim Valer'evich</given-names></name></name-alternatives><bio xml:lang="ru"><p>Доктор медицинских наук, профессор РАН, заведующий лабораторией эндокринологии, зам. директора по научной работе</p></bio><bio xml:lang="en"><p>MD, PhD, Professor, Head of the Laboratory of Endocrinology, Deputy Director for Science</p></bio><email xlink:type="simple">klimontov@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>&lt;p&gt;ФГБНУ Научно-исследовательский институт клинической и экспериментальной лимфологии&lt;/p&gt;</institution><country>Россия</country></aff><aff xml:lang="en"><institution>&lt;p&gt;Scientific Institute of Clinical and Experimental Lymphology&lt;/p&gt;</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>11</day><month>05</month><year>2017</year></pub-date><volume>20</volume><issue>1</issue><fpage>75</fpage><lpage>84</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Корбут А.И., Климонтов В.В., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Корбут А.И., Климонтов В.В.</copyright-holder><copyright-holder xml:lang="en">Korbut A.I., Klimontov V.V.</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/8005">https://www.dia-endojournals.ru/jour/article/view/8005</self-uri><abstract><p>Ингибитор глюкозо-натриевого симпортера 2 (SGLT2) эмпаглифлозин – представитель нового класса сахароснижающих препаратов с многочисленными плейотропными эффектами. В обзоре суммированы данные о влиянии эмпаглифлозина на структурные и функциональные изменения в почках в моделях сахарного диабета (СД) и у пациентов с СД. Поиск источников проведен в базах данных Medline/PubMed, Scopus, Web of Science, ClinicalTrials.gov, eLibrary. Результаты экспериментальных исследований свидетельствуют о снижении гликемии и АД, уменьшении клубочковой гиперфильтрации и гиперэкспрессии провоспалительных и фиброгенных факторов в почках под влиянием эмпаглифлозина. В большинстве клинических исследований показан антиальбуминурический эффект эмпаглифлозина у пациентов с СД2. В исследовании EMPA-REG OUTCOME выявлено замедление прогрессирования хронической болезни почек, снижение частоты новых случаев терминальной почечной недостаточности и смерти от почечных причин у больных СД2 на лечении эмпаглифлозином в сравнении с плацебо. Механизм нефропротективного действия эмпаглифлозина включает системные и почечные эффекты. Снижение гипергликемии, артериального давления, массы тела, устранение клубочковой гиперфильтрации, увеличение экскреции натрия, подавление воспалительных и фиброгенных сигнальных путей в почках могут способствовать замедлению развития диабетического поражения почек под влиянием эмпаглифлозина. Возможность экстраполяции доказанных для эмпаглифлозина свойств на другие ингибиторы SGLT2 нуждается в дальнейших исследованиях.</p></abstract><trans-abstract xml:lang="en"><p>Empagliflozin, an inhibitor of sodium–glucose symporter type 2 (SGLT2), is a new class of antidiabetic agents with numerous pleiotropic effects. The review summarises data on the influence of empagliflozin on the structural and functional changes in the kidneys of the models of diabetes mellitus (DM) and of patients with DM. A literature search was conducted using the databases of Medline/PubMed, Scopus, Web of Science, ClinicalTrials.gov and eLibrary. The experimental results showed a decrease in the blood glucose level, blood pressure, glomerular hyperfiltration and overexpression of proinflammatory and fibrogenic factors in the kidneys under the influence of empagliflozin. Most clinical studies have demonstrated the albuminuria-lowering effect of empagliflozin in patients with type 2 DM. The EMPA-REG OUTCOME study has demonstrated slowing of the chronic kidney disease progression, decrease in the incidence of end-stage renal failure and death from renal causes in patients with type 2 DM undergoing the empagliflozin treatment compared with those receiving placebo. The mechanisms of the nephroprotective effect of empagliflozin included systemic and renal effects. The decrease in hyperglycaemia, blood pressure and body weight; reduction in glomerular hyperfiltration; enhancement of sodium excretion and suppression of inflammatory and fibrogenic signalling pathways in the kidneys may help slow the development of diabetic kidney damage under the influence of empagliflozin. The possibility of extrapolating the confirmed properties of empagliflozin to other SGLT2 inhibitors needs further investigation.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сахарный диабет</kwd><kwd>диабетическая нефропатия</kwd><kwd>хроническая болезнь почек</kwd><kwd>ингибитор SGLT2</kwd><kwd>эмпаглифлозин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>diabetes</kwd><kwd>diabetic nephropathy</kwd><kwd>chronic kidney disease</kwd><kwd>SGLT2 inhibitors</kwd><kwd>empagliflozin</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">Farber SJ, Berger EY, Earle DP. 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