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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">10.20996/1819-6446-2018-14-3-319-323</article-id><article-id custom-type="elpub" pub-id-type="custom">rpcardio-1683</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>ORIGINAL STUDIES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group></article-categories><title-group><article-title>CARDIOPROTECTIVE PROPERTIES OF LISINOPRIL: NEW POSSIBILITIES</article-title><trans-title-group xml:lang="ru"><trans-title>КАРДИОПРОТЕКТИВНЫЕ СВОЙСТВА ЛИЗИНОПРИЛА: НОВЫЕ ВОЗМОЖНОСТИ</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>Подзолков</surname><given-names>В. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Podzolkov</surname><given-names>V. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор, зав. кафедрой факультетской терапии №2,</p><p>119991, Москва, ул. Трубецкая, 8 стр. 2</p></bio><bio xml:lang="en"><p>MD, PhD, Professor, Head of Chair of Faculty Therapy №2,</p><p>Trubetskaya ul. 8-2, Moscow, 119991</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тарзиманова</surname><given-names>А. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Tarzimanova</surname><given-names>A. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.м.н., доцент, кафедра факультетской терапии №2, </p><p>119991, Москва, ул. Трубецкая, 8 стр. 2</p></bio><bio xml:lang="en"><p>MD, PhD, Associate Professor, Chair of Faculty Therapy №2, </p><p>Trubetskaya ul. 8-2, Moscow, 119991</p></bio><email xlink:type="simple">tarzimanova@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>Гатаулин</surname><given-names>Р. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Gataulin</surname><given-names>R. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>ординатор, кафедра факультетской терапии №2, </p><p>119991, Москва, ул. Трубецкая, 8 стр. 2</p></bio><bio xml:lang="en"><p>MD, Resident, Chair of Faculty Therapy №2,</p><p>Trubetskaya ul. 8-2, Moscow, 119991</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет им. И.М. Сеченова (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov First Moscow State Medical University (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>03</day><month>07</month><year>2018</year></pub-date><volume>14</volume><issue>3</issue><fpage>319</fpage><lpage>323</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Podzolkov V.I., Tarzimanova A.I., Gataulin R.G., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Подзолков В.И., Тарзиманова А.И., Гатаулин Р.Г.</copyright-holder><copyright-holder xml:lang="en">Podzolkov V.I., Tarzimanova A.I., Gataulin R.G.</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/1683">https://www.rpcardio.online/jour/article/view/1683</self-uri><abstract><sec><title>Aim</title><p>Aim. To study the changes in the stiffness of the arterial wall, vasomotor function of the endothelium, and appearance of new cases of atrial fibrillation (AF) in patients with arterial hypertension with long-term treatment with lisinopril.</p></sec><sec><title>Material and method</title><p>Material and method. 66 hypertensive patients with cardiac sinus rhythm at the age of 48-64 years (mean age 58.4±4.2 years) were included into the study. They were randomized into 2 groups: patients of group 1 (n=35) were prescribed lisinopril or a combination of lisinopril with hydrochlorothiazide over the 5-year follow-up; patients of group 2 (control) did not receive angiotensin converting enzyme inhibitors or angiotensin II receptor blockers. The follow-up duration was from September 2010 until June 2016. It included telephone calls once every 3 months and annual clinical, instrumental and laboratory examination. The new-onset AF was identified by the 24-hour Holter ECG monitoring results and by patient symptom diaries.</p></sec><sec><title>Results</title><p>Results. New-onset AF was registered in 2 patients (6%) in the lisinopril group and in 4 patients (13%) from the control group (p=0.001) over the 5-year follow-up. Lisinopril significantly reduced AF incidence in hypertensive patients. The patients on lisinopril were found to have no significant changes in the left ventricular mass index and left atrial size according to echocardiography done after the 5-year follow-up whereas in the patients of control group both parameters increased significantly. Lisinopril contributed to the maintenance of endothelial vasodilator function and prevented increase in arterial wall stiffness.</p></sec><sec><title>Conclusion</title><p>Conclusion. Long term lisinopril treatment was found to significantly reduce the AF incidence in hypertensive patients over the 5-year follow-up. Lisinopril demonstrated organoprotective properties throughout the cardiovascular disease continuum and can be recommended for primary prevention of arrhythmia in hypertensive patients. </p></sec></abstract><trans-abstract xml:lang="ru"><sec><title>Цель</title><p>Цель. Изучить изменения жесткости сосудистой стенки, сосудодвигательной функции эндотелия и появления новых случаев фибрилляции предсердий (ФП) у больных артериальной гипертензией (АГ) при длительном лечении лизиноприлом.</p></sec><sec><title>Материал и методы</title><p>Материал и методы. В исследование включено 66 больных АГ с синусовым ритмом в возрасте от 48 до 64 лет (средний возраст 58,4±4,2 лет). Пациенты были рандомизированы в две группы: 1 группу составили 35 больных АГ, которые на протяжении 5-летнего наблюдения получали терапию лизиноприлом или комбинацию лизионоприла с гидрохлоротиазидом, во 2 группу (группа сравнения) включены 31 пациент, которые не получали ингибиторы ангиотензинпревращающего фермента или блокаторы рецепторов ангиотензина II. Проспективное наблюдение за больными проводилось с сентября 2010 по июнь 2016 гг. и включало телефонные контакты с пациентами каждые 3 мес, ежегодное общеклиническое и лабораторно-инструментальное обследование. По результатам суточного мониторирования ЭКГ по Холтеру и данных дневников пациентов проводился мониторинг новых случаев ФП.</p></sec><sec><title>Результаты</title><p>Результаты. Появление новых случаев ФП за 5 лет наблюдений было отмечено у 2(6%) больных в группе принимавших лизиноприл, и у 4 (13%) пациентов в группе сравнения (р=0,001). Проводимая терапия лизиноприлом достоверно уменьшала появление новых случаев ФП. При проведении повторной эхокардиографии через 5 лет лечения было обнаружено, что у пациентов, принимавших лизиноприл, индекс массы миокарда левого желудочка (ИММ ЛЖ) и размер левого предсердия (ЛП) не имели достоверной динамики на протяжении 5-летнего наблюдения, в группе сравнения наблюдалось достоверное увеличение ИММ ЛЖ и размера ЛП. Назначение лизиноприла способствовало длительному сохранению сосудодвигательной функции эндотелия и предупреждало появление жесткости сосудистой стенки.</p></sec><sec><title>Заключение</title><p>Заключение. При 5-летнем наблюдении за пациентами было выявлено, что длительное назначение лизиноприла достоверно уменьшало развитие новых случаев ФП. Лизиноприл обеспечивает органопротекцию на различных этапах сердечно–сосудистого континуума, что позволяет рекомендовать его применение для первичной профилактики аритмии у больных АГ. </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>фибрилляция предсердий</kwd><kwd>лизиноприл</kwd><kwd>первичная профилактика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>atrial fibrillation</kwd><kwd>lisinopril</kwd><kwd>primary prevention</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">Lip G.Y., Tse H.F., Lane D.A. Atrial fibrillation. Lancet. 2012;379:648-61. doi: 10.1016/S0140- 6736(11)61514-6.</mixed-citation><mixed-citation xml:lang="en">Lip G.Y., Tse H.F., Lane D.A. Atrial fibrillation. 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