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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">ymj</journal-id><journal-title-group><journal-title xml:lang="ru">Якутский медицинский журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Yakut Medical Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1813-1905</issn><issn pub-type="epub">2312-1017</issn><publisher><publisher-name>ЯНЦ КМП</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25789/YMJ.2018.64.31</article-id><article-id custom-type="elpub" pub-id-type="custom">ymj-1196</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>НАУЧНЫЕ ОБЗОРЫ И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SCIENTIFIC REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Необходимость проведения скрининга пациентов со стентированием по поводу острого коронарного синдрома по полиморфизму CYP2C19</article-title><trans-title-group xml:lang="en"><trans-title>Necessity of screening patients with stenting for acute coronary syndrome by CYP2C19 polymorphism</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>Терентьев</surname><given-names>И. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Terentiev</surname><given-names>I. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Терентьев Иван Титович – м.н.с., врач кардиолог Больницы </p></bio><bio xml:lang="en"><p>Terentiev Ivan Titovich - doctor cardiologist, junior researcher of the laboratory of heritable pathology </p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>+7 (924) 173 15 05 </p></bio><email xlink:type="simple">ivantit7313@mail.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>Варламова</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Varlamova</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Варламова Марина Алексеевна – н.с. </p></bio><bio xml:lang="en"><p>Varlamova Marina Alekseevna –researcher of the laboratory of heritable pathology </p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p> 8 (914) 298 87 60 </p></bio><email xlink:type="simple">varlamova.m@yandex.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>Павлова</surname><given-names>Н. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Pavlova</surname><given-names>N. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Павлова Надежда Ивановна – к.б.н., вр.и.о. в.н.с.-руковод. лаб. </p></bio><bio xml:lang="en"><p>Pavlova Nadezhda Ivanovna – cbs, temporary acting chief scientific officer - head of the laboratory of heritable pathology</p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>+7 (914) 289 39 36 </p></bio><email xlink:type="simple">solnishko_84@inbox.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>Дьяконова</surname><given-names>А. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>D’yakonova</surname><given-names>A. T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дьяконова Александра Тимофеевна – м.н.с. </p></bio><bio xml:lang="en"><p>D’yakonova Aleksandra Timofeevna – Junior researcher of the laboratory of heritable pathology</p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>8 (914) 238 68 93 </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>Соловьева</surname><given-names>Н. А,</given-names></name><name name-style="western" xml:lang="en"><surname>Solov’eva</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Соловьева Наталья Алексеевна – к.м.н., н.с. </p></bio><bio xml:lang="en"><p>Solov’eva Natal’ya Alekseevna – cms, temporary acting chief scientific officer - head of the Laboratory of Population Genetics</p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>8 (924) 171 34 89 </p></bio><email xlink:type="simple">sonata608@yandex.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>Кононова</surname><given-names>С. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Kononova</surname><given-names>S. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кононова Сардана Кононовна – к.б.н., с.н.с. </p></bio><bio xml:lang="en"><p>Kononova Sardana Kononovna - senior researcher of the laboratory of molecular genetics </p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>8 (924) 166 06 77 </p></bio><email xlink:type="simple">konsard@rambler.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>Куртанов</surname><given-names>Х. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kurtanov</surname><given-names>Kh. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Куртанов Харитон Алексеевич – к.м.н., гл.н.с.–руковод. отд. </p></bio><bio xml:lang="en"><p>Kurtanov Khariton Alekseevich – cms, Chief Scientific Officer - Head of the Department of Molecular Genetics</p><p>677010, Republic of Sakha (Yakutia), Yakutsk, Sergelyahskoe St, 4 </p><p>+7 (914) 106 00 30 </p></bio><email xlink:type="simple">hariton_kurtanov@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ЯНЦ КМП</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Budgetary Institution “Yakut science center of complex medical problems”</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>29</day><month>08</month><year>2025</year></pub-date><volume>0</volume><issue>4</issue><fpage>102</fpage><lpage>105</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Терентьев И.Т., Варламова М.А., Павлова Н.И., Дьяконова А.Т., Соловьева Н.А., Кононова С.К., Куртанов Х.А., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Терентьев И.Т., Варламова М.А., Павлова Н.И., Дьяконова А.Т., Соловьева Н.А., Кононова С.К., Куртанов Х.А.</copyright-holder><copyright-holder xml:lang="en">Terentiev I.T., Varlamova M.A., Pavlova N.I., D’yakonova A.T., Solov’eva N.A., Kononova S.K., Kurtanov K.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://ymj.elpub.ru/jour/article/view/1196">https://ymj.elpub.ru/jour/article/view/1196</self-uri><abstract><p>Клопидогрел остаётся основным препаратом для антитромбоцитарной терапии у пациентов, которым проведено стентирование коронарных сосудов по поводу острого коронарного синдрома. Представлены обоснование и дизайн наблюдательного исследования, направленного на проверку гипотезы о том, что высокая частота генетического полиморфизма цитохрома CYP2С19*2 ассоциирована с тромбозом коронарного стента.</p></abstract><trans-abstract xml:lang="en"><p>The relevance of this article is due to the fact that cardiovascular diseases are currently the leading cause of death and disability worldwide. The leading role in the structure of mortality from cardiovascular diseases belongs to coronary heart disease. Ischemic heart disease (IHD) is a chronic disease that develops with insufficient oxygen supply to the myocardium. The main cause (more than 90% of cases) of insufficient intake of oxygen is the formation of atherosclerotic plaques in the lumen of the coronary arteries, the arteries of the blood supplying the heart muscle (myocardium). One of the main drugs for antiplatelet therapy in cardiology is clopidogrel, the use of which can reduce the incidence of thrombotic complications. Clopidogrel is the most famous member of the thienopyridine group. Clopidogrel remains the main drug for antiplatelet therapy in patients who received stenting of the coronary vessels for acute coronary syndrome. The rationale and design of the observational study aimed at testing the hypothesis that the high frequency of the genetic polymorphism of cytochrome CYP2C19*2 is associated with coronary stent thrombosis is presented.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>клопидогрел</kwd><kwd>стентирование коронарных сосудов</kwd><kwd>острый коронарный синдром</kwd><kwd>персонализированная терапия</kwd><kwd>резистентность к клопидогрелу</kwd><kwd>парадоксальный ответ</kwd><kwd>генетические полиморфизмы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Clopidogrel</kwd><kwd>coronary stenting</kwd><kwd>the acute coronary syndrome</kwd><kwd>personalized therapy</kwd><kwd>clopidogrel resistance</kwd><kwd>paradoxical response</kwd><kwd>genetic polymorphisms</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">Ассоциация генов, кодирующих белки гемостаза, с параметрами периферического гемостаза и предрасположенностью к атеротромбозам у пациентов с сердечно-сосудистыми заболеваниями / Г.И. 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