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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">cardiotomsk</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский журнал клинической и экспериментальной медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Siberian Journal of Clinical and Experimental Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2713-2927</issn><issn pub-type="epub">2713-265X</issn><publisher><publisher-name>TSU publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29001/2073-8552-2017-32-1-31-35</article-id><article-id custom-type="elpub" pub-id-type="custom">cardiotomsk-264</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>КЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL STUDIES</subject></subj-group></article-categories><title-group><article-title>НЕБЛАГОПРИЯТНОЕ РЕМОДЕЛИРОВАНИЕ ЛЕВОГО ЖЕЛУДОЧКА И СЫВОРОТОЧНЫЙ УРОВЕНЬ МАТРИКСНЫХ МЕТАЛЛОПРОТЕИНАЗ, МАРКЕРОВ МИОКАРДИАЛЬНОЙ ДИСФУНКЦИИ И СУБКЛИНИЧЕСКОГО ВОСПАЛЕНИЯ У ПАЦИЕНТОВ С ОСТРЫМ ПЕРВИЧНЫМ ПЕРЕДНИМ ИНФАРКТОМ МИОКАРДА С ПОДЪЕМОМ СЕГМЕНТА ST</article-title><trans-title-group xml:lang="en"><trans-title>ADVERSE LEFT VENTRICULAR REMODELING AND THE SERUM LEVELS OF MATRIX METALLOPROTEINASES, BIOMARKERS OF MYOCARDIUM DYSFUNCTION AND INFLAMMATION IN PATIENTS WITH ACUTE PRIMARY ANTERIOR STEMI</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>Керчева</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kercheva</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант отделения неотложной кардиологии Научно-исследовательского института кардиологии, Томский национальный исследовательский медицинский центр Российской академии наук</p><p>Адрес: 634012, г. Томск, ул. Киевская, 111а</p></bio><email xlink:type="simple">tmkelka06@rambler.ru</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>Рябова</surname><given-names>Т. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Ryabova</surname><given-names>T. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, научный сотрудник отделения ультразвуковой и функциональной диагностики Научно-исследовательского института  кардиологии, Томский национальный исследовательский медицинский центр  Российской академии наук</p><p>Адрес: 634012, г. Томск, ул. Киевская, 111а</p></bio><email xlink:type="simple">rtrtom@mail.ru</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>Гусакова</surname><given-names>А. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Gusakova</surname><given-names>A. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. фарм. наук, научный сотрудник отделения функциональной и  лабораторной диагностики Научноисследовательского института кардиологии,  Томский национальный исследовательский медицинский центр Российской  академии наук</p><p>Адрес: 634012, г. Томск, ул. Киевская, 111а</p></bio><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>2017</year></pub-date><pub-date pub-type="epub"><day>04</day><month>10</month><year>2017</year></pub-date><volume>32</volume><issue>1</issue><fpage>31</fpage><lpage>35</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Керчева М.А., Рябова Т.Р., Гусакова А.М., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Керчева М.А., Рябова Т.Р., Гусакова А.М.</copyright-holder><copyright-holder xml:lang="en">Kercheva M.A., Ryabova T.R., Gusakova A.M.</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.sibjcem.ru/jour/article/view/264">https://www.sibjcem.ru/jour/article/view/264</self-uri><abstract><p>Цель работы: оценка динамики уровня матриксных металлопротеиназ (ММП-2, 3, 9), ST2, NTproBNP, IL1β, hCRP в сыворотке крови и ее влияния на структурно-функциональную  перестройку миокарда в ранние и отдаленные сроки у пациентов с острым первичным  передним инфарктом миокарда (ИМ) с подъемом сегмента ST (спST). В исследование  включен 21 пациент (средний возраст – 60,5±7,4 лет). Экстренная реперфузионная терапия  проведена у всех пациентов, у трети – в течение первых 3 ч. Эхокардиографию,  включая 2D speckle tracking режим (ste), проводили на 3-и (T2), 7-е (T3), 14-е сутки (T4) и  через 6 мес. после острого ИМ (Т5; “Vivid E9”, GE Healthcare). Содержание в сыворотке  крови ММП-2, 3, 9, ST2, IL1β, hCRP, NTproBNP методом количественного твердофазного иммуноферментного анализа определяли в те же временные точки, а также в  первые сутки (Т1). Затем пациентов поделили на 2 группы: с повышенной концентрацией  ST2 в Т1 (&gt;35 нг/мл) – ST2&gt;N и нормальной (&lt;35 нг/мл) – ST2 N.  Выявлено, что динамика всех маркеров имела разнонаправленный характер. Повышение  уровня ММП-3 к 7-м суткам, продолжающееся до 6-месячного периода наблюдения,  сопровождалось обратной динамикой ММП-9 в те же сроки. Значимой динамики показателя  ММП-2 не выявлено. Отмечено снижение показателя IL1β к 14-м суткам, а также ST2,  NTproBNP, hCRP уже к 7-м суткам. Наибольшей прогностической ценностью в отношении развития неблагоприятного ремоделирования левого желудочка обладал маркер  ST2. Его величина больше 35 нг/мл при поступлении была ассоциирована с наличием систолической дисфункции.</p></abstract><trans-abstract xml:lang="en"><p>The aim of this study was to assess the changes in serum levels of matrix metalloproteases (MMP-2, 3, 9), ST2, NTproBNP, IL1β, and hCRP and their impact on the adverse left ventricular remodeling (LVR) in patients with acute primary anterior STEMI. The study included 21 patients aged 60.5±7.4 years. All of them received urgent reperfusion therapy; one third of patients received the treatment during the first 3 h. Echocardiography with 2D speckle tracking imaging was performed at day 3 (T2), 7 (T3), and 14 (T4) after STEMI and after 6 months (T5) after AMI (Vivid E9, GE Healthcare). The concentrations of ММP-2, ММP-3, ММP-9, ST2, IL1β, hCRP, and NTproBNP were determined at the same time point and at a day of admission (T1) by the method of quantitative enzyme-linked immunosorbent assay. After that, patients were divided into 2 groups: group 1 comprised patients with the level of ST2 &gt; 35 ng/mL; group 2 comprised patients with ST2 &lt; 35 ng/mL at T1. The study showed that changes in the markers were multidirectional. The level of ММP-2 did not significantly change. The level of MМP-3 increased to T3 and continued to increase to T5; the changes in levels of ММP-9 were reverse over the same period. The level of IL1β decreased to T4 though this parameter as well as the levels of ST2, NTproBNP, and hCRP exceeded the normal range during the entire observation period. The levels of ST2, NTproBNP, and hCRP were changing to T3 and significantly decreased to T5. Marker ST2 demonstrated the best predictive value for the development of adverse left ventricular remodeling. ST2 level of more than 35 ng/mL at a time of admission was associated with the presence of systolic dysfunction, increased wall motion score index, increased end-systolic volume, increased 2D global longitudinal strain, and reduced ejection fraction in the early post-infarction period.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>матриксные металлопротеиназы</kwd><kwd>ST2</kwd><kwd>NTproBNP</kwd><kwd>IL1β</kwd><kwd>hCRP</kwd><kwd>инфаркт миокарда</kwd><kwd>неблагоприятное ремоделирование левого желудочка</kwd></kwd-group><kwd-group xml:lang="en"><kwd>MMP</kwd><kwd>ST2</kwd><kwd>NTproBNP</kwd><kwd>IL1β</kwd><kwd>hCRP</kwd><kwd>adverse left ventricular remodeling</kwd><kwd>acute myocardial infarction</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">Park J.P., Lee B.K. 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