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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">ateroskleroz</journal-id><journal-title-group><journal-title xml:lang="ru">Атеросклероз</journal-title><trans-title-group xml:lang="en"><trans-title>Ateroscleroz</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2078-256X</issn><issn pub-type="epub">2949-3633</issn><publisher><publisher-name>НИИТПМ-филиал ИЦиГ СО РАН</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">ateroskleroz-44</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>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ МАРКЕРЫ НАРУШЕНИЙ ЛИПИДНОГО ОБМЕНА И ВНЕЗАПНАЯ СЕРДЕЧНАЯ СМЕРТЬ</article-title><trans-title-group xml:lang="en"><trans-title>MOLECULAR-GENETICAL MARKERS OF LIPID ABNORMALITIES AND SUDDEN CARDIAC DEATH</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>Иванова</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanova</surname><given-names>A. A.</given-names></name></name-alternatives><email xlink:type="simple">ivanova_a_a@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ НИИ терапии и профилактической медицины</institution></aff><aff xml:lang="en"><institution>Institute of Internal and Preventive Medicine</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>27</day><month>09</month><year>2019</year></pub-date><volume>13</volume><issue>2</issue><fpage>33</fpage><lpage>40</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Иванова А.А., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Иванова А.А.</copyright-holder><copyright-holder xml:lang="en">Ivanova A.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://ateroskleroz.elpub.ru/jour/article/view/44">https://ateroskleroz.elpub.ru/jour/article/view/44</self-uri><abstract><p>Внезапная сердечная смерть продолжает оставаться одной из нерешенных проблем современного здравоохранения. До 50 % летальных исходов вследствие сердечно-сосудистых заболеваний составляет внезапная сердечная смерть, при этом большинство умерших внезапно не имели ранее известного сердечно-сосудистого заболевания. С целью разработки качественной системы диагностики предрасположенности и профилактики развития внезапной сердечной смерти, в первую очередь у лиц без сердечной патологии в анамнезе, исследуются молекулярно-генетические маркеры внезапной сердечной смерти. Одним из факторов риска внезапной сердечной смерти является уровень липидов. В отношении ассоциации с внезапной сердечной смертью изучены однонуклеотидные полиморфизмы генов, ответственных за липидный обмен, таких как CETP, APOE, SREBF2, SCAP, LIPC, USF1, LDLR .</p></abstract><trans-abstract xml:lang="en"><p>Sudden cardiac death is one of main problem of modern medicine. Sudden cardiac death is about 50 % of all cardiac deaths. The main part of people who died of sudden cardiac death didn’t have any cardiac illnesses. In the world molecular genetic markers of sudden cardiac death are studied to create an effective system of diagnostic of predisposition and prophylactic of sudden deaths, especially to people without cardiac diseases. Lipid abnormalities are one of risk factor of sudden cardiac death. Single nucleotide polymorphisms of CETP, APOE, SREBF2, SCAP, LIPC, USF1, LDLR genes were studied as molecular genetic markers of sudden cardiac death.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>внезапная сердечная смерть</kwd><kwd>однонуклеотидный полиморфизм</kwd></kwd-group><kwd-group xml:lang="en"><kwd>APOE</kwd><kwd>LIPC</kwd><kwd>SREBF2</kwd><kwd>USF1</kwd><kwd>CETP</kwd><kwd>USF1</kwd><kwd>LDLR</kwd><kwd>sudden cardiac death</kwd><kwd>single nucleotide polymorphism</kwd><kwd>APOE</kwd><kwd>LIPC</kwd><kwd>SREBF2</kwd><kwd>USF1</kwd><kwd>CETP</kwd><kwd>USF1</kwd><kwd>LDLR</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">Priori S.G., Aliot E., Blømstrom-Lundqvist C. et al. The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC) // G. Ital. Cardiol. 2016. 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