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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/DM13441</article-id><article-id custom-type="elpub" pub-id-type="custom">diaendo-13453</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>Оригинальные исследования</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Original Studies</subject></subj-group></article-categories><title-group><article-title>Оценка эффективности семаглутида в обеспечении метаболического контроля и коррекции инсулинорезистентности у больных сахарным диабетом 2 типа в условиях реальной клинической практики</article-title><trans-title-group xml:lang="en"><trans-title>Evaluation of the effectiveness of semaglutide in providing metabolic control and correction of insulin resistance in patients with type 2 diabetes mellitus in real clinical practice</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3920-5914</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Анциферова</surname><given-names>Д. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Antsiferova</surname><given-names>D. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Анциферова Дарья Михайловна, аспирант </p><p>119034, г. Москва, ул. Пречистенка, д. 37 </p></bio><bio xml:lang="en"><p>Daria M. Antsiferova, MD, PhD student </p><p>37 Prechistenka street, 119034 Moscow </p></bio><email xlink:type="simple">cifrenda@yandex.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/0000-0002-7936-7619</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аметов</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Ametov</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Аметов Александр Сергеевич, д.м.н., профессор </p><p>Москва</p></bio><bio xml:lang="en"><p>Alexander S. Ametov, MD, PhD, Professor </p><p>Moscow </p></bio><email xlink:type="simple">alexander.ametov@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8428-4116</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Котешкова</surname><given-names>О. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Koteshkova</surname><given-names>O. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Котешкова Ольга Михайловна, к.м.н. </p><p>Москва</p></bio><bio xml:lang="en"><p>Olga M. Koteshkova, MD, PhD </p><p>Moscow </p></bio><email xlink:type="simple">koala58@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ромашкина</surname><given-names>Л. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Romashkina</surname><given-names>L. P.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ромашкина Лада Павловн </p></bio><bio xml:lang="en"><p>Lada P. Romashkina, MD </p><p>Moscow </p></bio><email xlink:type="simple">ladina09@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9944-2997</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Анциферов</surname><given-names>М. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Antsiferov</surname><given-names>M. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Анциферов Михаил Борисович, д.м.н., профессор </p><p>Москва</p></bio><bio xml:lang="en"><p>Mikhail B. Antsiferov, MD, PhD, Professor </p><p>Moscow </p></bio><email xlink:type="simple">antsiferov@rambler.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Эндокринологический диспансер ; Российская медицинская академия непрерывного профессионального образования</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Endocrinology Dispensary ; Russian Medical Academy of Continuous Professional Education</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Российская медицинская академия непрерывного профессионального образования</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Russian Medical Academy of Continuous Professional Education</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Эндокринологический диспансер</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Endocrinology Dispensary</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>11</day><month>02</month><year>2026</year></pub-date><volume>29</volume><issue>1</issue><fpage>40</fpage><lpage>49</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Анциферова Д.М., Аметов А.С., Котешкова О.М., Ромашкина Л.П., Анциферов М.Б., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Анциферова Д.М., Аметов А.С., Котешкова О.М., Ромашкина Л.П., Анциферов М.Б.</copyright-holder><copyright-holder xml:lang="en">Antsiferova D.M., Ametov A.S., Koteshkova O.M., Romashkina L.P., Antsiferov M.B.</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/13453">https://www.dia-endojournals.ru/jour/article/view/13453</self-uri><abstract><sec><title>АКТУАЛЬНОСТЬ</title><p>АКТУАЛЬНОСТЬ. Сахарный диабет 2 типа (СД2) тесно связан с ожирением и инсулинорезистентностью (ИР). Семаглутид, агонист рецепторов ГПП-1, проявляет выраженные эффекты в отношении гликемического контроля и массы тела, однако данные о его влиянии на различные суррогатные индексы ИР в условиях рутинной практики ограничены.</p></sec><sec><title>ЦЕЛЬ</title><p>ЦЕЛЬ. Оценить влияние семаглутида (Семавик®) на метаболический контроль и ИР у пациентов с СД2 и ожирением, не достигших целевых показателей углеводного обмена на монотерапии метформином.</p></sec><sec><title>МАТЕРИАЛЫ И МЕТОДЫ</title><p>МАТЕРИАЛЫ И МЕТОДЫ. В проспективное исследование включили 31 пациента 40–65 лет с СД2, ИМТ 30,0–39,9 кг/м² и HbA1c 7,0–9,0% на фоне метформина; 28 пациентов завершили 24-недельное наблюдение. Оценивали антропометрические показатели, биоимпедансный состав тела, HbA1c, гликемию натощак, инсулин, С-пептид, свободные жирные кислоты и рассчитывали индексы HOMA-IR, QUICKI, TyG, Adipo-IR и молярное соотношение С-пептид/инсулин.</p></sec><sec><title>РЕЗУЛЬТАТЫ</title><p>РЕЗУЛЬТАТЫ. Через 24 недели терапии семаглутидом отмечено достоверное снижение массы тела (медиана −8,2% или 8,58 кг), ИМТ, окружности талии и жировой массы, а также улучшение показателей углеводного обмена: HbA1c снизился с 7,63% до 6,25%. 85,7% пациентов достигли HbA1c&lt;7,0%. Выявлено значимое снижение HOMA-IR, TyG, Adipo-IR, повышение QUICKI и молярного соотношения С-пептид/инсулин, что указывает на уменьшение ИР на уровне печени, жировой и периферических тканей. Нежелательные явления наблюдались у небольшой части пациентов и носили в основном диспепсический временный характер.</p></sec><sec><title>ВЫВОДЫ</title><p>ВЫВОДЫ. Семаглутид у пациентов с СД2  ожирением в реальной клинической практике обеспечивает клинически значимое уменьшение массы тела, улучшение гликемического контроля и многокомпонентное снижение ИР при благоприятном профиле безопасности.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>RELEVANCE</title><p>RELEVANCE. Type 2 diabetes mellitus (DM2) is closely related to obesity and insulin resistance (IR). Semaglutide, glucagon-like peptide-1 receptor agonist, exhibits pronounced effects on glycemic control and body weight. However, data on its effect on various surrogate IR indices in routine practice are limited.</p></sec><sec><title>AIM</title><p>AIM. To evaluate the effect of semaglutide (Semavic®) on metabolic control and IR in patients with DM2 and obesity who did not achieve the target values of carbohydrate metabolism on metformin monotherapy.</p></sec><sec><title>MATERIALS AND METHODS</title><p>MATERIALS AND METHODS. The prospective study included 31 patients aged 40–65 years with DM2, BMI 30.0–39.9 kg/m2 and HbA1c 7.0–9.0% on metformin treatment; 28 patients completed a 24-week follow-up. Anthropometric parameters, bioimpedance body composition, HbA1c, fasting glycemia, insulin, C-peptide, free fatty acids were evaluated. HOMA-IR, QUICKI, TyG, Adipo-IR indices, C peptide/insulin molar ratio were calculated.</p></sec><sec><title>RESULTS</title><p>RESULTS. After 24 weeks of semaglutide therapy, there was a significant decrease in body weight (median -8.2% or 8.58 kg), BMI, waist circumference and fat mass as well as an improvement in carbohydrate metabolism: HbA1c had decreased from 7.63% to 6.25%, 85.7% of patients reached HbA1c &lt;7.0%. There was a significant decrease of HOMA-IR, TyG, Adipo-IR indices, an increase of QUICKI and C peptide/insulin molar ratio indicating a decrease of IR in the liver, adipose and peripheral tissues. Adverse events were observed in a small proportion of patients and were mainly of a temporary dyspeptic nature.</p></sec><sec><title>CONCLUSIONS</title><p>CONCLUSIONS. Semaglutide in patients with DM2 and obesity in real clinical practice provides a significant reduction of body weight, improves glycemic control and leads to multicomponent reduction of IR with a favorable safety profile.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>сахарный диабет</kwd><kwd>ожирение</kwd><kwd>семаглутид</kwd><kwd>инсулинорезистентность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>diabetes mellitus</kwd><kwd>obesity</kwd><kwd>semaglutide</kwd><kwd>insulin resistance</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Спонсор исследования — ООО «Герофарм», Россия.</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">IDF Diabetes Atlas. 10th Edition. 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