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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">therapeutic</journal-id><journal-title-group><journal-title xml:lang="ru">Южно-Российский журнал терапевтической практики</journal-title><trans-title-group xml:lang="en"><trans-title>South Russian Journal of Therapeutic Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2712-8156</issn><issn pub-type="epub">3033-8344</issn><publisher><publisher-name>РостГМУ</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21886/2712-8156-2025-6-4-7-15</article-id><article-id custom-type="elpub" pub-id-type="custom">therapeutic-681</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>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Возможности оптимизации терапии хронической сердечной недостаточности с сохраненной фракцией выброса с помощью применения агонистов рецепторов глюкагоноподобного пептида-1</article-title><trans-title-group xml:lang="en"><trans-title>Possibilities of optimizing therapy of heart failure with preserved ejection fraction using glucagon-like peptide-1 receptor agonists</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8070-2234</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кужелева</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kuzheleva</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кужелева Елена Андреевна, к.м.н., старший научный сотрудник отделения патологии миокарда</p><p>Томск</p></bio><bio xml:lang="en"><p>Elena A. Kuzheleva, PhD, Senior Researcher, Department of Myocardial Pathology</p><p>Tomsk</p></bio><email xlink:type="simple">kea@cardio-tomsk.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/0000-0002-9488-6900</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гарганеева</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Garganeeva</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гарганеева Алла Анатольевна, д.м.н., профессор, заведующая отделением патологии миокарда</p><p>Томск</p></bio><bio xml:lang="en"><p>Alla A. Garganeeva, Dr. Sci (Med.), Professor, Head of the Department of Myocardial Pathology</p><p>Tomsk</p></bio><email xlink:type="simple">aag@cardio-tomsk.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/0009-0009-4372-4782</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сыромятникова</surname><given-names>Е. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Syromyatnikova</surname><given-names>E. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Сыромятникова Екатерина Егоровна, ординатор отделения патологии миокарда, лаборант-исследователь</p><p>Томск</p></bio><bio xml:lang="en"><p>Ekaterina E. Syromyatnikova, Resident, Departmeent of Myocardial Pathology</p><p>Tomsk</p></bio><email xlink:type="simple">katy00.syrr@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/0000-0002-7661-5808</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тукиш</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tukish</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тукиш Ольга Викторовна, к.м.н., научный сотрудник, отделение патологии  миокарда</p><p>Томск</p></bio><bio xml:lang="en"><p>Olga V. Tukish, PhD, Researcher, Departmeent of Myocardial Pathology</p><p>Tomsk</p></bio><email xlink:type="simple">olgatukish@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт кардиологии, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>23</day><month>12</month><year>2025</year></pub-date><volume>6</volume><issue>4</issue><fpage>7</fpage><lpage>15</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Кужелева Е.А., Гарганеева А.А., Сыромятникова Е.Е., Тукиш О.В., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Кужелева Е.А., Гарганеева А.А., Сыромятникова Е.Е., Тукиш О.В.</copyright-holder><copyright-holder xml:lang="en">Kuzheleva E.A., Garganeeva A.A., Syromyatnikova E.E., Tukish O.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.therapeutic-j.ru/jour/article/view/681">https://www.therapeutic-j.ru/jour/article/view/681</self-uri><abstract><p>В статье представлен систематический обзор литературы, посвящённый анализу эффективности и безопасности применения агонистов рецепторов глюкагоноподобного пептида-1 (арГПП-1) при хронической сердечной недостаточности (СН) с сохранённой фракцией выброса левого желудочка (ХСНсФВ). Вопрос исследования касался возможностей совместного приёма препаратов из групп ингибиторов натрий-глюкозного котранспортера 2 типа (иНГЛТ2) и арГПП-1. Поиск литературы осуществлялся в системе PubMed. В окончательный анализ вошли 11 исследований, соответствующих изучаемой теме. Согласно анализу, арГПП-1 являются эффективным средством для терапии пациентов с ХСНсФВ, приводя к уменьшению симптомов СН и улучшению качества жизни таких больных. Вопросы одновременного назначения арГПП-1 и иНГЛТ2 достаточно подробно изучены у пациентов с сахарным диабетом 2 типа: продемонстрированы эффективность и безопасность такой комбинации. При отсутствии СД у пациентов с ХСНсФВ оптимизация лечения с использованием класса арГПП-1 требует проведения дополнительных специально спланированных исследований.</p></abstract><trans-abstract xml:lang="en"><p>The article presents a systematic review of the literature devoted to the analysis of the efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1 RA) in chronic heart failure with preserved ejection fraction (HFpEF). The research question concerned the possibilities of co-administration of drugs from the groups of sodium-glucose cotransporter-2 inhibitors (iSGLT-2) and GLP-1 RA. The literature was searched in the PubMed system. The final analysis included 11 studies relevant to the topic under study. According to the analysis, GLP-1 RA is an effective treatment for patients with CHF, leading to a reduction in HF symptoms and an improvement in the quality of life of such patients. The issues of simultaneous administration of GLP-1 RA and iSGLT-2 have been studied in sufficient detail in patients with type 2 diabetes mellitus: the effectiveness and safety of such a combination have been demonstrated. In the absence of diabetes in patients with HF, optimization of treatment using the GLP-1 RA class requires additional specially planned studies. The article presents a systematic review of the literature devoted to the analysis of the efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1 RA) in chronic heart failure with preserved ejection fraction (HFpEF). The research question concerned the possibilities of co-administration of drugs from the groups of sodium-glucose cotransporter-2 inhibitors (iSGLT-2) and GLP-1 RA. The literature was searched in the PubMed system. The final analysis included 11 studies relevant to the topic under study. According to the analysis, GLP-1 RA is an effective treatment for patients with CHF, leading to a reduction in HF symptoms and an improvement in the quality of life of such patients. The issues of simultaneous administration of GLP-1 RA and iSGLT-2 have been studied in sufficient detail in patients with type 2 diabetes mellitus: the effectiveness and safety of such a combination have been demonstrated. In the absence of diabetes in patients with HF, optimization of treatment using the GLP-1 RA class requires additional specially planned studies.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Хроническая сердечная недостаточность</kwd><kwd>агонисты рецепторов глюкагоноподобного пептида-1</kwd><kwd>арГПП-1</kwd><kwd>ХСНсФВ</kwd><kwd>иНГЛТ2</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Chronic heart failure</kwd><kwd>glucagon-like peptide-1 receptor agonists</kwd><kwd>HFpEF</kwd><kwd>iSGLT-2</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">GBD 2017 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392(10159):1789-1858. 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