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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">kpccz</journal-id><journal-title-group><journal-title xml:lang="ru">Комплексные проблемы сердечно-сосудистых заболеваний</journal-title><trans-title-group xml:lang="en"><trans-title>Complex Issues of Cardiovascular Diseases</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2306-1278</issn><issn pub-type="epub">2587-9537</issn><publisher><publisher-name>Federal State Budgetary Institution “Research Institute for Complex Issues of Cardiovascular Diseases”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17802/2306-1278-2018-7-1-94-101</article-id><article-id custom-type="elpub" pub-id-type="custom">kpccz-399</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>АНАЛИТИЧЕСКИЙ ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ANALYTICAL REVIEW</subject></subj-group></article-categories><title-group><article-title>НОВЫЕ МАРКЕРЫ СЕРДЕЧНОЙ НЕДОСТАТОЧНОСТИ: ЗНАЧЕНИЕ ДЛЯ ДИАГНОСТИКИ И ПРОГНОЗИРОВАНИЯ NT-proBNP И ИНТЕРЛЕЙКИНОВЫХ РЕЦЕПТОРОВ – ЧЛЕНОВ СЕМЕЙСТВА ST2</article-title><trans-title-group xml:lang="en"><trans-title>NEW BIOMARKERS OF HEART FAILURE: DIAGNOSTIC AND PROGNOSTIC VALUE OF NT-proBNP AND INTERLEUKIN RECEPTOR FAMILY MEMBER ST2</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Копьева</surname><given-names>К. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kopeva</surname><given-names>K. V.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гракова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Grakova</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Для корреспонденции: Гракова Елена Викторовна, адрес: 634012, г. Томск, ул. Киевская, 111а</p></bio><bio xml:lang="en"/><email xlink:type="simple">vgelen1970@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тепляков</surname><given-names>А. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Teplyakov</surname><given-names>A. T.</given-names></name></name-alternatives><bio xml:lang="ru"/><bio xml:lang="en"/><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Федеральное государственное бюджетное научное учреждение «Томский национальный исследовательский медицинский центр Российской академии наук» «Научно-исследовательский институт кардиологии»<country>Россия</country></aff><aff xml:lang="en">Federal State Budgetary Institution «Tomsk National Research Medical Centre, Russian Academy of Sciences» «Cardiology Research Institute»<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>27</day><month>03</month><year>2018</year></pub-date><volume>7</volume><issue>1</issue><fpage>94</fpage><lpage>101</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Копьева К.В., Гракова Е.В., Тепляков А.Т., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Копьева К.В., Гракова Е.В., Тепляков А.Т.</copyright-holder><copyright-holder xml:lang="en">Kopeva K.V., Grakova E.V., Teplyakov A.T.</copyright-holder><license 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.nii-kpssz.com/jour/article/view/399">https://www.nii-kpssz.com/jour/article/view/399</self-uri><abstract><p>Статья посвящена перспективе использования новых биомаркеров для оценки тяжести течения и прогноза хронической сердечной недостаточности (ХСН). В последние десятилетия для оптимизации диагностики, прогнозирования и повышения эффективности терапии ХСН активно изучаются перспективные возможности применения биомаркерной стратегии ранней персонифицированной диагностики кардиоваскулярной патологии. Современные биомаркеры являются высокочувствительными медиаторами для оценки патогенетических механизмов развития и прогрессирования ХСН. Особый интерес представляют данные по плазменной концентрации нового биомаркера, экспрессируемого кардиомиоцитами, фибробластами и эндотелиальными клетками, члена семейства рецепторов интерлейкина-1 (IL1) – растворимой изоформы ST2 (sST2), лигандом которого является цитокин IL-33. Персонификация риска с помощью определения биомаркеров NT-proBNP и ST2 позволит выявить наиболее уязвимых пациентов, в отношении которых наиболее оправдана тактика мониторинга и интенсификации терапевтических вмешательств.</p></abstract><trans-abstract xml:lang="en"><p>The article discusses the use of new biomarkers for assessing the severity of the clinical course and the prognosis of chronic heart failure. In recent decades, prospective possibilities for using biomarkers as the part of early personalized diagnosis of cardiovascular disease have been actively studied to optimize the diagnosis process, patients’ prognosis and increase the effectiveness of therapy for chronic heart failure. New biomarkers are highly sensitive mediators for evaluation of pathogenetic mechanisms of the development and progression of chronic heart failure. Plasma levels of a new biomarker expressed by cardiomyocytes, fibroblasts and endothelial cells, a member of the IL-1 family of soluble isoform ST2 (sST2), which ligand is IL-33 cytokine, is of particular interest. Risk personification using NT-proBNP and ST2 biomarkers allows identifying themostvulnerablepatients for further monitoringand intensification of therapeutic interventions.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хроническая сердечная недостаточность</kwd><kwd>растворимый ST2</kwd><kwd>NT-proBNP</kwd><kwd>биомаркеры диагностика</kwd><kwd>прогнозирование</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic heart failure</kwd><kwd>soluble ST2</kwd><kwd>NT-proBNP</kwd><kwd>biomarkers</kwd><kwd>diagnostics</kwd><kwd>prediction</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">Агеев Ф.Т., Даниелян М.О., Мареев В.Ю., Беленков Ю.Н. 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