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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">rpcardio</journal-id><journal-title-group><journal-title xml:lang="en">Rational Pharmacotherapy in Cardiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Рациональная Фармакотерапия в Кардиологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1819-6446</issn><issn pub-type="epub">2225-3653</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20996/1819-6446-2022-10-01</article-id><article-id custom-type="elpub" pub-id-type="custom">rpcardio-2824</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="en"><subject>NOTES FROM PRACTICE</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КЛИНИЧЕСКИЙ ОПЫТ</subject></subj-group></article-categories><title-group><article-title>Insulin-like Growth Factor-1 and Myocardial Remodeling in Patients with Chronic Heart Failure of Ischemic Origin</article-title><trans-title-group xml:lang="ru"><trans-title>Инсулиноподобный фактор роста-1 и ремоделирование миокарда у мужчин с хронической сердечной недостаточностью ишемического генеза</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7886-2549</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Закирова</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Zakirova</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Закирова Аляра Нурмухаметовна</p><p>eLibrary SPIN 2224-2179</p><p> Уфа </p></bio><bio xml:lang="en"><p> Alyara N. Zakirova </p><p> Ufa </p></bio><email xlink:type="simple">zinfira.67@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/0000-0002-5462-4885</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Закирова</surname><given-names>Н. Э.</given-names></name><name name-style="western" xml:lang="en"><surname>Zakirova</surname><given-names>N. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Закирова Нэлли Эриковна</p><p>eLibrary SPIN 9132-7358</p><p> Уфа </p></bio><bio xml:lang="en"><p> Nelli E. Zakirova </p><p> Ufa </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4777-3281</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Низамова</surname><given-names>Д. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Nizamova</surname><given-names>D. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Низамова Динара Фаварисовна</p><p>eLibrary SPIN 3869-5492 </p><p> Уфа </p></bio><bio xml:lang="en"><p> Dinara F. Nizamova </p><p> Ufa </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>03</day><month>11</month><year>2022</year></pub-date><volume>18</volume><issue>5</issue><fpage>564</fpage><lpage>570</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Zakirova A.N., Zakirova N.E., Nizamova D.F., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Закирова А.Н., Закирова Н.Э., Низамова Д.Ф.</copyright-holder><copyright-holder xml:lang="en">Zakirova A.N., Zakirova N.E., Nizamova D.F.</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.rpcardio.online/jour/article/view/2824">https://www.rpcardio.online/jour/article/view/2824</self-uri><abstract><p>Aim. To study the presence and nature of correlations between the level of Insulin-like growth factor-1 (IGF-1) and structural and functional parameters of the heart in the development of myocardial remodeling and fibrosis in patients with chronic heart failure (CHF) of ischemic origin.Material and methods. The study included 120 men with class II-IV CHF who have history of myocardial infarction, which are divided into 3 groups depending on the CHF class. The control group included 25 healthy men. Assessment of left ventricular (LV) structural-functional state was carried out by echocardiography. Investigation of IGF-1 and N-terminal precursor indices of cerebral natriuretic peptide (NT-pro BNP) was performed by enzyme immunoassay.Results. Patients with class II CHF were hyperexpression of IGF-1, with class III CHF were registered low-normal level, with class IV CHF was established a deficiency of IGF-1. The most significant structural-geometric rearrangement of LV and significant deficit of IGF-1 recorded in patients with class IV CHF (95,6±7,02 ng/ml with class IV CHF versus 178,3±11,36 ng/ml and 124,3±9,14 ng/ml with class II and III CHF; р&lt;0,05). In patients of class III-IV CHF, correlation relationships between IGF-1 level and echocardiographic parameters (LV myocardial mass index are established: r=-0,59, p=0,05; end systolic volume index: r=-0,55, p=0,05; value of LV ejection fraction: r=0,61, p=0,05). Significant negative correlation are established in patients with class III-IV CHF between IGF-1 level and NT-pro BNP levels (r=-0,51; р=0,05).Conclusion. The intensity of myocardial remodeling and fibrosis processes in patients with a progressive course of CHF is related to deficit of IGF-1 and is associated with a high level of activity of natriuretic peptides.</p></abstract><trans-abstract xml:lang="ru"><p>Цель. Изучить наличие и характер корреляций между уровнем инсулиноподобного фактора роста (ИФР-1) и структурно-функциональными параметрами сердца при развитии процессов ремоделирования и фиброзирования миокарда у мужчин с хронической сердечной недостаточностью (ХСН) ишемического генеза.Материал и методы. В исследование включены 120 мужчин c ХСН II-IV функционального класса (ФК), перенесших инфаркт миокарда (ИМ), разделенных на 3 группы в зависимости от ФК. В контрольную группу вошли 25 здоровых мужчин. Оценка структурно-функционального состояния левого желудочка (ЛЖ) проведена методом эхокардиографии. Исследование показателей ИФР-1 и N-терминального предшественника мозгового натрийуретического пептида (NT-рrоBNP) выполнено методом иммуноферментного анализа.Результаты. У пациентов с ХСН II ФК выявлена гиперэкспрессия ИФР-1, при ХСН III ФК зарегистрирован низко-нормальный его уровень, при ХСН IV ФК – установлен дефицит активности ИФР-1. Наиболее существенная структурно-геометрическая перестройка ЛЖ и значимый дефицит ИФР-1 определены у пациентов с ХСН IV ФК (95,6±7,02 нг/мл при ХСН IV ФК против 178,3±11,36 и 124,3±9,14 нг/мл при ХСН II-III ФК; р&lt;0,05). У пациентов с ХСН III-IV ФК установлены ассоциации между уровнем ИФР-1 и эхокардиографическими параметрами (индексом массы миокарда ЛЖ: r=-0,59, p=0,05; конечным систолическим объемным индексом: r=-0,55, p=0,05; величиной фракции выброса ЛЖ: r=0,61, p=0,05). Значимые обратные корреляции определены у пациентов с ХСН III-IV ФК между концентрациями ИФР-1 и NT-рrоBNP (r=-0,51, р=0,05).Заключение. Интенсивность процессов ремоделирования и фиброзирования миокарда у пациентов с прогрессирующим течением ХСН взаимосвязана с дефицитом ИФР-1 и ассоциируется с высоким уровнем активности натрийуретических пептидов.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>хроническая сердечная недостаточность</kwd><kwd>инсулиноподобный фактор роста-1</kwd><kwd>N-терминальный предшественник мозгового натрийуретического пептида</kwd><kwd>ремоделирование</kwd><kwd>фиброзирование миокарда</kwd></kwd-group><kwd-group xml:lang="en"><kwd>chronic heart failure</kwd><kwd>Insulin-like growth factor-1</kwd><kwd>N-terminal precursor of cerebral natriuretic peptide</kwd><kwd>heart remodeling</kwd><kwd>myocardial fibrosis</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование проведено при поддержке Башкирского государственного медицинского университета.</funding-statement><funding-statement xml:lang="en">The study was performed with the support of the Bashkir State Medical University</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">Российское кардиологическое общество. 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