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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="en"><front><journal-meta><journal-id journal-id-type="publisher-id">sechenov</journal-id><journal-title-group><journal-title xml:lang="en">Sechenov Medical Journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Сеченовский вестник</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2218-7332</issn><issn pub-type="epub">2658-3348</issn><publisher><publisher-name>Сеченовский Университет</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">sechenov-38</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>КЛИНИЧЕСКАЯ МЕДИЦИНА</subject></subj-group></article-categories><title-group><article-title>MARKERS OF SEVERE DESTRUCTION RHEUMATOID ARTHRITIS</article-title><trans-title-group xml:lang="ru"><trans-title>МАРКЕРЫ ТЯЖЕЛОГО ДЕСТРУКТИВНОГО ТЕЧЕНИЯ РЕВМАТОИДНОГО АРТРИТА</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>Комарова</surname><given-names>Е. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Komarova</surname><given-names>E. B.</given-names></name></name-alternatives><email xlink:type="simple">elbelcom@ua.fm</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Государственное учреждение «Луганский государственный медицинский университет» Луганской народной республики</institution><country>Россия</country></aff><aff xml:lang="en"><institution>State Institution «Lugansk State Medical University» of the Lugansk Peopleʼs Republic</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>30</day><month>12</month><year>2017</year></pub-date><volume>0</volume><issue>4</issue><fpage>30</fpage><lpage>34</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Komarova E.B., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Комарова Е.Б.</copyright-holder><copyright-holder xml:lang="en">Komarova E.B.</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.sechenovmedj.com/jour/article/view/38">https://www.sechenovmedj.com/jour/article/view/38</self-uri><abstract><p>In the examined patients with rheumatoid arthritis (RA), the VEGF level in blood was 2 times higher than the control and 30 % higher in the high-positive patients with anti-CCP. VEGF correlated with clinical parameters of severe RA, high disease activity, effusion to the joint cavity and hypervascularization of the synovial lining. The concentration of FGF in the blood in RA patients was 2.5 times higher than control and 25 % higher in the high-positive patients with anti-CCP. FGF correlated with the duration of the disease, parameters of clinical course, the synovial thickening, the presence of pannus and osteochondral erosion. High levels of VEGF, FGF in the blood can be used as markers of severe destruction diseases in RA patients</p></abstract><trans-abstract xml:lang="ru"><p>У обследованных больных ревматоидным артритом (РА) уровень VEGF в крови был в 2 раза выше контроля и на 30 % больше у больных, высокопозитивных по АЦЦП. VEGF коррелировал с клиническими показателями тяжелого течения РА, высокой активности заболевания, выпотом в полость сустава и гиперваскуляризацией синовии. Концентрация FGF в крови у больных РА была в 2,5 раза выше контроля и на 25 % больше у высокопозитивных по АЦЦП. FGF коррелировал с длительностью заболевания, показателями клинического течения, утолщением синовии, наличием паннуса и костно-хрящевых эрозий. Высокие уровни VEGF, FGF в крови могут быть использованы как маркеры тяжелого деструктивного течения заболевания у больных РА.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>ревматоидный артрит</kwd><kwd>деструкция суставов</kwd><kwd>сосудистый эндотелиальный фактор роста</kwd><kwd>фактор роста фибробластов</kwd><kwd>ангиогенез</kwd></kwd-group><kwd-group xml:lang="en"><kwd>rheumatoid arthritis</kwd><kwd>joint destruction</kwd><kwd>vascular endothelial growth factor</kwd><kwd>fibroblast growth factor</kwd><kwd>angiogenesis</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">Чичасова Н.В., Владимиров С.А., Иголкина Е.В., Имаметдинова Г.Р. Бремя ревматоидного артрита: медицинские и социальные проблемы. Научно-практическая ревматология. 2009; 47(1): 4-10.</mixed-citation><mixed-citation xml:lang="en">Чичасова Н.В., Владимиров С.А., Иголкина Е.В., Имаметдинова Г.Р. 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