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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-22</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>ЭНДОКРИНОЛОГИЯ</subject></subj-group></article-categories><title-group><article-title>Влияние гиполипидемической терапии на инсулинорезистентность у пациентов с метаболическим синдромом</article-title><trans-title-group xml:lang="en"><trans-title></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>Мычка</surname><given-names>В. Б.</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>Чазова</surname><given-names>И. Е.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Институт клинической кардиологии им. А.Л.Мясникова РКНПК</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2004</year></pub-date><pub-date pub-type="epub"><day>23</day><month>12</month><year>2022</year></pub-date><issue>1</issue><fpage>16</fpage><lpage>18</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Мычка В.Б., Чазова И.Е., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Мычка В.Б., Чазова И.Е.</copyright-holder><copyright-holder xml:lang="en">Мычка В.Б., Чазова И.Е.</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/22">https://www.syst-hypertension.ru/jour/article/view/22</self-uri><abstract><p>Дислипидемия (ДЛП) является одним из основных признаков метаболического синдрома (МС) и факторов риска раннего развития атеросклероза.В настоящее время препаратами выбора первичной и вторичной профилактики сердечно-сосудистых заболеваний больных с МС являются статины. Их широкое применение при лечении дислипидемии у этих больных оправдано тем, что они обладают наиболее выраженным и мощным гипохолестеринемическим действием, имеют наименьшее число побочных эффектов и лучше переносятся больными. Они не влияют на показатели углеводного обмена и не взаимодействуют с гипогликемическими препаратами. Статины положительно зарекомендовали себя в качестве препаратов, позволяющих снизить риск осложнений от ИБС и смертность у пациентов с нарушенной толерантностью к глюкозе (НТГ).Согласно результатам нашего исследования терапия аторвастатином на протяжении 24 нед привела к достоверному снижению общего ХС на 28% и ХС ЛПНП на 37%. Целевого уровня ХС ЛПНП (ниже 2,6 ммоль/л) удалось достичь у 69% пациентов.Как показали результаты нашего исследования, терапия аторвастатином оказала благоприятное влияние и на показатели углеводного обмена.Таким образом, аторвастатин может являться препаратом выбора для лечения дислипидемии у больных СД типа 2 и у пациентов с МС, особенно при наличии у них ИР.</p></abstract><kwd-group xml:lang="ru"><kwd>метаболический синдром</kwd><kwd>дислипидемия</kwd><kwd>углеводный обмен</kwd><kwd>инсулинорезистентность</kwd><kwd>статины</kwd><kwd>аторвастатин</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">Goldschmidt M.G, Barret-Conner E, Edelstein S.L et al. Dyslipidaemia and ischaemic heart disease mortality among men and women with diabetes. Circulation 1994; 89: 991–7.</mixed-citation><mixed-citation xml:lang="en">Goldschmidt M.G, Barret-Conner E, Edelstein S.L et al. 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