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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">cardiovascular</journal-id><journal-title-group><journal-title xml:lang="ru">Кардиоваскулярная терапия и профилактика</journal-title><trans-title-group xml:lang="en"><trans-title>Cardiovascular Therapy and Prevention</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1728-8800</issn><issn pub-type="epub">2619-0125</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15829/1728-8800-2011-6-24-29</article-id><article-id custom-type="elpub" pub-id-type="custom">cardiovascular-1958</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>АРТЕРИАЛЬНАЯ ГИПЕРТОНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ARTERIAL HYPERTENSION</subject></subj-group></article-categories><title-group><article-title>Возможности коррекции гиперурикемии лозартаном при метаболическом синдроме и артериальной гипертензии</article-title><trans-title-group xml:lang="en"><trans-title>Losartan therapy and hyperuricemia correction in patients with metabolic syndrome and arterial hypertension</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>Недогода</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Nedogoda</surname><given-names>S. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д. м. н., профессор, зав. кафедрой терапии и эндокринологии</p><p>Волгоград, Тел.: 8- 902-364-32-26 </p></bio><bio xml:lang="en"><p>Volgograd</p></bio><email xlink:type="simple">nedogodasv@ranbler.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>Чумачок</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Chumachok</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант кафедры</p><p>Волгоград</p></bio><bio xml:lang="en"><p>Volgograd</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>Ледяева</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ledyaeva</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>аспирант кафедры</p><p>Волгоград</p></bio><bio xml:lang="en"><p>Volgograd</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>Цома</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsoma</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>ассистент кафедры</p><p>Волгоград</p></bio><bio xml:lang="en"><p>Volgograd</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Волгоградский государственный медицинский университет</institution></aff><aff xml:lang="en"><institution>Volgograd State Medical University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2011</year></pub-date><pub-date pub-type="epub"><day>20</day><month>12</month><year>2011</year></pub-date><volume>10</volume><issue>6</issue><fpage>24</fpage><lpage>29</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Недогода С.В., Чумачок Е.В., Ледяева А.А., Цома В.В., 2011</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="ru">Недогода С.В., Чумачок Е.В., Ледяева А.А., Цома В.В.</copyright-holder><copyright-holder xml:lang="en">Nedogoda S.V., Chumachok E.V., Ledyaeva A.A., Tsoma V.V.</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://cardiovascular.elpub.ru/jour/article/view/1958">https://cardiovascular.elpub.ru/jour/article/view/1958</self-uri><abstract><p>Цель. Оценить возможности коррекции гиперурикемии (ГУ) у пациентов с артериальной гипертензией (АГ) и метаболическим синдромом (МС) при назначении блокатора рецепторов ангиотензина II лозартана. Материалы и методы. В открытое, рандомизируемое, контролируемое, сравнительное исследование в параллельных группах (лозартан vs традиционной терапии на протяжении 12 нед.) были включены 60 больных АГ с МС и ГУ. Результаты. Общей закономерностью, выявленной на всех сроках лечения, оказалось то, что достоверных различий между группами лозартана и традиционной терапии по антигипертензивной активности выявлено не было. В группе лозартана было отмечено значительно большее снижение уровня мочевой кислоты (МК) — 34,7 % vs 7,8 % в группе традиционной терапии (р &lt; 0,05); также имело место достоверное улучшение эластичности сосудов мышечного и эластического типов, что проявилось снижением СПВ на соответствующих режимах терапии: каротидно-феморальный — на 27,8 % vs 8,1 % (р &lt; 0,05) и каротидно-радиальной — на 30,2 % и 12,6 % (р &lt; 0,05). Заключение. Большее снижение уровня МК у пациентов с АГ, МС и ГУ, что приводит к достоверно большему улучшению эластичности сосудов.</p></abstract><trans-abstract xml:lang="en"><p>Aim. To assess the potential of the angiotensin II receptor antagonist losartan for the correction of hyperuricemia (HU) in patients with arterial hypertension (AH) and metabolic syndrome (MS). Material and methods. This open, randomised, controlled comparative study in parallel groups included 60 AH patients with MS and HU. The patients received losartan or standard therapy for 12 weeks. Results. Throughout the follow-up period, no significant difference in antihypertensive effect was observed between the losartan and standard therapy groups. Losartan group patients demonstrated a more pronounced decrease in uric acid levels (-34,7 % vs. -7,8 % in the standard therapy group; p&lt;0,05). In addition, losartan therapy, compared to the standard treatment, was associated with improved vascular elasticity, as manifested by the pulse wave velocity decrease (-27,8 % vs. -8,1 % for carotid-femoral index, and -30,2 % vs. -12,6 % for carotidradial index, respectively; both p&lt;0,05).</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гиперурикемия</kwd><kwd>артериальная гипертензия</kwd><kwd>скорость пульсовой волны</kwd><kwd>лозартан</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Hyperuricemia</kwd><kwd>arterial hypertension</kwd><kwd>pulse wave velocity</kwd><kwd>losartan</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">Alderman M, Aiyer KJ. Uric acid: role in cardiovascular disease and effects of losartan. Curr Med Res Opin 2004; 20: 3: 369-79.</mixed-citation><mixed-citation xml:lang="en">Alderman M, Aiyer KJ. 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