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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">systhiper</journal-id><journal-title-group><journal-title xml:lang="ru">Системные гипертензии</journal-title><trans-title-group xml:lang="en"><trans-title>Systemic Hypertension</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2075-082X</issn><issn pub-type="epub">2542-2189</issn><publisher><publisher-name>LLC «ИнтерМедсервис»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">systhiper-514</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>СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ARTICLES</subject></subj-group></article-categories><title-group><article-title>Новый блокатор рецепторов ангиотензина II Эдарби® как часть патогенетического лечения артериальной гипертонии у больных с метаболическими нарушениями</article-title><trans-title-group xml:lang="en"><trans-title>The new angiotensin II receptor blocker Edarbi® as part of the pathogenetic treatment of arterial hypertension in patients with metabolic disorders</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>Чазова</surname><given-names>И. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Chazova</surname><given-names>I. Ye.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Жернакова</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhernakova</surname><given-names>Yu. V.</given-names></name></name-alternatives><email xlink:type="simple">*juli001@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Блинова</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Blinova</surname><given-names>N. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рогоза</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Rogoza</surname><given-names>A. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «НМИЦ кардиологии»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical Research Center of Cardiology of the Ministry of Health of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «НМИЦ кардиологии»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical Research Center of Cardiology of the Ministry of Health of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>23</day><month>12</month><year>2022</year></pub-date><volume>14</volume><issue>3</issue><fpage>28</fpage><lpage>35</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Чазова И.Е., Жернакова Ю.В., Блинова Н.В., Рогоза А.Н., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Чазова И.Е., Жернакова Ю.В., Блинова Н.В., Рогоза А.Н.</copyright-holder><copyright-holder xml:lang="en">Chazova I.Y., Zhernakova Y.V., Blinova N.V., Rogoza A.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://www.syst-hypertension.ru/jour/article/view/514">https://www.syst-hypertension.ru/jour/article/view/514</self-uri><abstract><p>Актуальность. В последнее время доля блокаторов рецепторов ангиотензина значительно возросла среди назначаемых антигипертензивных средств. Высокие органопротективные свойства, дополнительные метаболические эффекты и переносимость, сравнимая с плацебо, делают их препаратами выбора, особенно у пациентов с артериальной гипертонией (АГ) 1-2-й степени, имеющих низкую приверженность антигипертензивной терапии, но уже обремененных дополнительными метаболическими факторами риска. Цель исследования - изучение антигипертензивной эффективности блокатора рецепторов ангиотензина азилсартана медоксомила (Эдарби®), его влияния на кардиометаболические факторы риска и выраженность поражения органов-мишеней у больных АГ 1-2-й степени с метаболическим синдромом. Материалы и методы. В исследование включены 32 пациента (средний возраст 47,32±8,4 года), 19 мужчин и 13 женщин с АГ 1-2-й степени и метаболическим синдромом. Всем пациентам оценивалось клиническое артериальное давление (АД), определялся уровень общего холестерина, холестерина липопротеидов высокой плотности, холестерина липопротеидов низкой плотности, триглицерида, креатинина, уровень глюкозы в ходе теста толерантности к углеводам, проводилось суточное мониторирование АД, оценивались центральное систолическое давление в аорте, скорость пульсовой волны на каротидно-феморальном сегменте и определялась толщина комплекса интима-медиа исходно и через 6 мес терапии. Результаты. На фоне терапии Эдарби® 82% пациентов с АГ 1-2-й степени и метаболическим синдромом достигли целевого уровня АД, что сопровождалось значительным улучшением диастолической функции левого желудочка у 56% пациентов, уже в первые 6 мес лечения наблюдалось снижение жесткости магистральных артерий и улучшение метаболического контроля.</p></abstract><trans-abstract xml:lang="en"><p>Relevance. Recently, the proportion of angiotensin receptor blockers has significantly increased among prescribed antihypertensive drugs. High organoprotective properties, additional metabolic effects and tolerability comparable to placebo make them the drugs of choice, especially in patients with stage 1 and stage 2 hypertension having low adherence to antihypertensive therapy, but already burdened by additional metabolic risk factors. Purpose of the study - study of the antihypertensive efficacy of the angiotensin receptor blocker azilsartan medoxomil (Edarbi®), its effect on cardiometabolic risk factors and damage of target organs in patients with stage 2 hypertension. Materials and methods. The study included 32 patients (mean age 47.32±8.4 years), 19 men and 13 women with stage 2 hypertension. All patients were evaluated for clinical blood pressure (BP), total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglyceride, creatinine, glucose level in a carbohydrate tolerance test, 24-hour blood pressure monitoring, central aortic systolic pressure, сarotid-femoral pulse wave velocity and intima-media thickness was determined initially and after 6 months of therapy. Results. During taking Edarbi® 82% of patients with stage 1 and stage 2 hypertension and metabolic syndrome reached the target level of BP, which was accompanied by a significant improvement in diastolic function of the left ventricle in 56% of patients. Already in the first 6 months the treatment reduced arterial stiffness and improved metabolic control</p></trans-abstract><kwd-group xml:lang="ru"><kwd>артериальная гипертония</kwd><kwd>метаболический синдром</kwd><kwd>антигипертензивная терапия</kwd><kwd>органы-мишени</kwd></kwd-group><kwd-group xml:lang="en"><kwd>arterial hypertension</kwd><kwd>metabolic syndrome</kwd><kwd>antihypertensive therapy</kwd><kwd>target organs</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">Data from the National Health and Nutrition Examination Survey (NHANES). National Center for Health Statistics. Health, United States, 2013: With Special Feature on Prescription Drugs. Hyattsville, MD: 2014. Downloaded from http://www.cdc.gov/nchs/data/hus/hus13.pdf#064.</mixed-citation><mixed-citation xml:lang="en">Data from the National Health and Nutrition Examination Survey (NHANES). 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