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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">pulmo</journal-id><journal-title-group><journal-title xml:lang="ru">Пульмонология</journal-title><trans-title-group xml:lang="en"><trans-title>PULMONOLOGIYA</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0869-0189</issn><issn pub-type="epub">2541-9617</issn><publisher><publisher-name>Scientific and Practical Journal “PULMONOLOGIYA” LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18093/0869-0189-2024-34-6-887-895</article-id><article-id custom-type="elpub" pub-id-type="custom">pulmo-4326</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>Новые подходы в лечении легочной артериальной гипертензии</article-title><trans-title-group xml:lang="en"><trans-title>New approaches to the treatment of pulmonary arterial hypertension</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7606-6565</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хачатуров</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kchachaturov</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Хачатуров Михаил Викторович – студент VI курса Института клинической медицины имени Н.В. Склифосовского.</p><p>119991, Москва, ул. Трубецкая, 8, стр. 2; тел.: (495) 609-14-00</p></bio><bio xml:lang="en"><p>Michael V. Kchachaturov - 6th year student, N.V.Sklifosovsky Institute of Clinical Medicine.</p><p>Ul. Trubetskaya 8, build. 2, Moscow, 119991; tel.: (495) 609-14-00</p></bio><email xlink:type="simple">khachaturov.michael@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/0000-0001-9357-4924</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Царева</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsareva</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Царева Наталья Анатольевна – к. м. н., доцент кафедры пульмонологии Института клинической медицины имени Н.В. Склифосовского Первый МГМУ имени И.М. Сеченова; заведующая лабораторией интенсивной терапии и дыхательной недостаточности НИИП Федерального медико-биологического агентства.</p><p>119991, Москва, ул. Трубецкая, 8, стр. 2; тел.: (495) 609-14-00</p></bio><bio xml:lang="en"><p>Natalya A. Tsareva - Candidate of Medicine, Associate Professor, Department of Pulmonology, N.V. Sklifosovsky Institute of Clinical Medicine, Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov FMSMU; Head of the Laboratory of Intensive Care and Respiratory Failure, Pulmonology Scientific Research Institute.</p><p>Ul. Trubetskaya 8, build. 2, Moscow, 119991; (495) 609-14-00</p></bio><email xlink:type="simple">n_tsareva@mail.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/0000-0002-5999-2150</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Авдеев</surname><given-names>С. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Avdeev</surname><given-names>S. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>=</p><p>Авдеев Сергей Николаевич – д. м. н., профессор, академик Российской академии наук, проректор по научной и инновационной работе, заведующий кафедрой пульмонологии Института клинической медицины имени Н.В. Склифосовского Первый МГМУ имени И.М. Сеченова; директор Национального медицинского исследовательского центра по профилю «Пульмонология»; главный внештатный специалист-пульмонолог Министерства здравоохранения Российской Федерации.</p><p>119991, Москва, ул. Трубецкая, 8, стр. 2; тел.: (499) 246-75-18</p></bio><bio xml:lang="en"><p>Sergey N. Avdeev - Doctor of Medicine, Professor, Academician of Russian Academy of Sciences, Vice-Rector for Research and Innovation, Head of the Department of Pulmonology, N.V. Sklifosovsky Institute of Clinical Medicine, Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov FMSMU; Chief Freelance Pulmonologist of the Ministry of Health of the Russian Federation; Director of the NMRCP; Chief Freelance Pulmonologist of the MH RF.</p><p>Ul. Trubetskaya 8, build. 2, Moscow, 119991; tel.: (499) 246-75-18</p></bio><email xlink:type="simple">serg_avdeev@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное автономное образовательное учреждение высшего образования Первый Московский государственный медицинский университет имени И.М. Сеченова Министерства здравоохранения Российской Федерации (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>11</day><month>12</month><year>2024</year></pub-date><volume>34</volume><issue>6</issue><fpage>887</fpage><lpage>895</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Хачатуров М.В., Царева Н.А., Авдеев С.Н., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Хачатуров М.В., Царева Н.А., Авдеев С.Н.</copyright-holder><copyright-holder xml:lang="en">Kchachaturov M.V., Tsareva N.A., Avdeev S.N.</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://journal.pulmonology.ru/pulm/article/view/4326">https://journal.pulmonology.ru/pulm/article/view/4326</self-uri><abstract><p>Легочная гипертензия является полиэтиологическим заболеванием и характеризуется повышением среднего давления в легочной артерии &gt; 20 мм рт. ст. в покое. Наиболее изученной с точки зрения подбора оптимальной терапии является идиопатическая легочная артериальная гипертензия (ЛАГ), относящаяся к 1-й группе по классификации легочной гипертензии (2022). Это редкое и прогностически крайне неблагоприятное заболевание, которое возникает в результате ремоделирования сосудов дистальных отделов легочной артерии. В настоящее время лечение ЛАГ нацелено на 3 основных метаболических каскада: простациклиновый, эндотелиновый и путь оксида азота. Благодаря имеющимся методам терапии симптомы и качество жизни пациентов с ЛАГ улучшаются, но, к сожалению, ни один из них не влияет непосредственно на патогенез и не позволяет добиться полного контроля над заболеванием.</p><p>Целью обзора явился анализ литературных источников и демонстрация наиболее перспективных методов и потенциальных мишеней для лечения ЛАГ.</p><p>Заключение. В настоящий момент терапия ЛАГ является актуальной проблемой, при этом продолжаются активные исследования, направленные на поиск новых терапевтических мишеней и разработку потенциальных препаратов для них.</p></abstract><trans-abstract xml:lang="en"><p>Pulmonary hypertension (PH) is a polyetiological disease characterized by an increase in mean pulmonary artery pressure (MPP) by more than 20 mm Hg at rest. Idiopathic pulmonary arterial hypertension (PAH), which is assigned to the first group according to the 2018 PH classification, is the most studied in terms of optimal therapy selection. This is a rare but fatal disease that occurs as a result of vascular remodeling of the distal pulmonary arteries. Currently, PAH treatments target three major metabolic cascades: prostacyclin, endothelin, and nitric oxide. The available therapies improve the symptoms and quality of life of patients with PAH, but, unfortunately, none of them directly affect the pathogenesis or allow to achieve complete control of the disease.</p><p>The aim of the review was to analyze the literature and demonstrate of the most promising methods and potential targets for the treatment of PAH.</p><p>Conclusion. At the moment, PAH therapy is a serious clinical problem, and therefore, it is essential to study new therapeutic targets and develop the corresponding drugs.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>легочная артериальная гипертензия</kwd><kwd>костный морфогенетический белок</kwd><kwd>тромбоцитарный фактор роста</kwd><kwd>митохондриальная дисфункция</kwd><kwd>серотонин</kwd><kwd>эстроген</kwd><kwd>моноклональные антитела</kwd><kwd>тромбоксан</kwd></kwd-group><kwd-group xml:lang="en"><kwd>pulmonary arterial hypertension</kwd><kwd>bone morphogenetic protein</kwd><kwd>platelet growth factor</kwd><kwd>mitochondrial dysfunction</kwd><kwd>serotonin</kwd><kwd>estrogen</kwd><kwd>monoclonal antibodies</kwd><kwd>thromboxane</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Спонсорская поддержка отсутствовала</funding-statement><funding-statement xml:lang="en">The study was not sponsored</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">Humbert M., Kovacs G., Hoeper M.M. et al. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: Developed by the task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS). 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