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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 custom-type="elpub" pub-id-type="custom">cardiovascular-1530</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>ИШЕМИЧЕСКАЯ БОЛЕЗНЬ СЕРДЦА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CORONARY HEART DISEASE</subject></subj-group></article-categories><title-group><article-title>ID полиморфизм гена ангиотензин-превращающегофермента у больных с острым коронарным синдромом</article-title><trans-title-group xml:lang="en"><trans-title>ACE gene ID polymorphism in acute coronary syndrome patients</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>Сайгитов</surname><given-names>Р. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Saygitov</surname><given-names>R. T.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Глезер</surname><given-names>М. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Glezer</surname><given-names>M. G.</given-names></name></name-alternatives><email xlink:type="simple">glezermg@mtu7net.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>Семенцов</surname><given-names>Д. П.</given-names></name><name name-style="western" xml:lang="en"><surname>Sementsov</surname><given-names>D. P.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Малыгина</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Malygina</surname><given-names>N. A.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Российский научно-исследовательский институт геронтологии. Москва, Россия</institution></aff><aff xml:lang="en"><institution>Russian Research Institute of Gerontology. Moscow, Russia</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>НИЦ Московской медицинской академии им. И.М. Сеченова на базе городской клинической больницы №59. Москва</institution></aff><aff xml:lang="en"><institution>Research Center, I.M. Sechenov Moscow Medical Academy, City Clinical Hospital No 59. Moscow</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2006</year></pub-date><pub-date pub-type="epub"><day>01</day><month>01</month><year>1970</year></pub-date><volume>5</volume><issue>8</issue><fpage>34</fpage><lpage>41</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Сайгитов Р.Т., Глезер М.Г., Семенцов Д.П., Малыгина Н.А., 1970</copyright-statement><copyright-year>1970</copyright-year><copyright-holder xml:lang="ru">Сайгитов Р.Т., Глезер М.Г., Семенцов Д.П., Малыгина Н.А.</copyright-holder><copyright-holder xml:lang="en">Saygitov R.T., Glezer M.G., Sementsov D.P., Malygina N.A.</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/1530">https://cardiovascular.elpub.ru/jour/article/view/1530</self-uri><abstract><sec><title>Цель</title><p>Цель. Изучить ассоциацию ID полиморфизма гена ангиотензин-превращающего фермента (АПФ) с развитием и течением острого коронарного синдрома. Материал и методы. В проспективном исследовании анализировались госпитальные и постгоспитальные (в течение 1 года) исходы у больных (n=376) инфарктом миокарда (ИМ) и нестабильной стенокардией (НС) и их связь с ID полиморфизмом гена АПФ. Результаты. Риск развития ИМ с зубцом Q у больных с DD генотипом гена АПФ превыщал аналогичный у носителей ID и II генотипов в 2,1 и 2,5 раза соответственно. Напротив, эпизоды НС у таких больных регистрировались значительно реже - 24,8%, 45,8% и 52,3% больных с DD, ID и II генотипами (df=2; р&lt;0,001). Максимальная частота DD генотипа отмечена среди больных с уровнем креатинфосфокиназы и/или ее MB фракции (КФК/КФК-МВ) позитивным ИМ, особенно в возрастной группе &lt;65 лет. Напротив, при КФК/КФК-МВ негативном ИМ и при НС преобладали больные с ID и II генотипами. Генотипы ID и II гена АПФ ассоциировали с благоприятным прогнозом и после эпизода острой ищемии миокарда, но только в возрасте &lt; 75 лет. В старческом возрасте у таких больных отмечается резкое увеличение риска летального события, величина которого у носителей II генотипа более чем вдвое превыщает аналогичный риск у больных с DD генотипом. Заключение. Генотип DD гена АПФ ассоциирует с развитием крупноочагового ИМ, преимущественно в молодом возрасте. Генотипы ID и II являются протективными и отличаются относительно благоприятным прогнозом в возрасте &lt; 75 лет.</p></sec><sec><title> </title><p> </p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Aim</title><p>Aim. То investigate the association between ID polymorphism of ACE gene and acute coronary syndrome (ACS) development and progression. Material and metliods. This prospective study analyzed hospital and post-hospital (one-year) outcomes in 376 patients with myocardial infarction (MI) or unstable angina (UA), as well as outcome association with ACE gene ID polymorphism. Results. Q-wave IM risk in ACE gene DD genotype patients was 2,1 and 2,5 times higher than in participants with ID or II genotypes, respectively. On the contrary, UA episodes in these patients were significantly less frequent, being registered in 24,8%, 45,8%, and 52,3% of the subjects with DD, ID, and II genotypes, respectively (df=2; p&lt;0,001). Maximal DD genotype prevalence was observed in individuals with creatine kinase and/or its MB-fraction (CK/MB-CK) positive MI, especially in patients under 65. In CK/MB-CK negative MI, as well as in UA, ID and II genotype patients were more prevalent. ACE gene ID and II genotypes were associated with better outcomes after acute myocardial ischemia episodes, but only in those under 75. In the elderly, fatal event risk increased abruptly, being at least twice as high in II genotype individuals than in DD genotype patients. Conclusion. ACE gene DD genotype is associated with Q-wave MI, especially in younger individuals. ID and II genotypes are protective and associated with better outcomes in patients under 75.</p></sec><sec><title> </title><p> </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ангиотензин-превращающий фермент</kwd><kwd>полиморфизм гена</kwd><kwd>острый коронарный синдром</kwd><kwd>прогноз</kwd></kwd-group><kwd-group xml:lang="en"><kwd>angiotensin-converting enzyme</kwd><kwd>gene polymorphism</kwd><kwd>acute coronary syndrome</kwd><kwd>prognosis</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">Рекомендации ВНОК по лечению острого коронарного синдрома без стойкого подъема сегмента ST на ЭКГ. 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