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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">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1995-4484-2014-283-289</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-1940</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL RESEARCH</subject></subj-group></article-categories><title-group><article-title>Коморбидность при ревматоидном артрите</article-title><trans-title-group xml:lang="en"><trans-title>COMORBIDITY IN RHEUMATOID ARTHRITIS</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>Панафидина</surname><given-names>Т. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Panafidina</surname><given-names>T. A.</given-names></name></name-alternatives><email xlink:type="simple">panafidina@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>Кондратьева</surname><given-names>Л. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kondratyeva</surname><given-names>L. V.</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>Герасимова</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Gerasimova</surname><given-names>E. V.</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>Новикова</surname><given-names>Д. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Novikova</surname><given-names>D. S.</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>Попкова</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Popkova</surname><given-names>T. V.</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>ФГБУ «Научно- исследовательский институт ревматологии им. В.А. Насоновой» РАН, Москва, Россия</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Nasonova Research Institute of Rheumatology, Moscow, Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>20</day><month>06</month><year>2014</year></pub-date><volume>52</volume><issue>3</issue><issue-title>№3 (2014)</issue-title><fpage>283</fpage><lpage>289</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Панафидина Т.А., Кондратьева Л.В., Герасимова Е.В., Новикова Д.С., Попкова Т.В., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Панафидина Т.А., Кондратьева Л.В., Герасимова Е.В., Новикова Д.С., Попкова Т.В.</copyright-holder><copyright-holder xml:lang="en">Panafidina T.A., Kondratyeva L.V., Gerasimova E.V., Novikova D.S., Popkova T.V.</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://rsp.mediar-press.net/rsp/article/view/1940">https://rsp.mediar-press.net/rsp/article/view/1940</self-uri><abstract><p>Пик начала ревматоидного артрита (РА) приходится на 30–55 лет. В этом возрасте пациенты имеют и другие сопутствующие (коморбидные) заболевания, которые оказывают влияние на течение и прогноз РА, выбор тактики лечения и качество жизни больных. Цель настоящего исследования – выявить наиболее значимые и часто встречающиеся коморбидные состоя- ния у пациентов с РА. Материал и методы. Включено 200 пациентов в возрасте 55 [46; 61] лет, преобладали женщины (82,5%), с дли- тельным течением заболевания (5 [1; 10] лет), серопозитивные по IgM ревматоидному фактору (83,0%) и ан- тителам к циклическому цитруллинированному пептиду (81,6%), с умеренной и высокой клинической актив- ностью болезни (DAS28=3,9 [3,1; 4,9]). У 71,2% пациентов рентгенологически выявлялись деструктивные из- менения суставов кистей или стоп различной степени выраженности, 64,5% больных имели II функциональ- ный класс. Основным базисным противовоспалительным препаратом (БПВП) был метотрексат, его получали 69,5% пациентов, терапия генно-инженерными биологическими препаратами (ГИБП) применялась в 21,0% случаев. 15,5% пациентов не получали БПВП и ГИБП. Глюкокортикоиды принимали 43,0% больных РА. Результаты. Сопутствующие заболевания имели 72,0% пациентов с РА. Чаще всего встречалась артериальная гипертензия (АГ; 60,0%), дислипидемия (ДЛП; 45,0%), переломы разной локализации (29,5%) и ишемиче- ская болезнь сердца (21,0%). Инфаркт миокарда и инсульт наблюдались в 1,5 и 1,0% случаев соответственно. Сахарный диабет (СД) выявлен в 7,5% случаев, остеопороз – у 15,5% пациентов. 81,7% пациентов с РА и АГ и 80,0% пациентов с РА и СД получали гипотензивную и сахароснижающую терапию соответственно. В то же время больные РА, имеющие ДЛП и остеопороз, принимали специфические препараты гораздо реже (30,0 и 29,0% соответственно). Выводы. Коморбидные состояния при РА встречаются часто. Учитывая, что кардиоваскулярные заболевания являются основной причиной летальности при РА, необходимо адекватно и своевременно корректировать традиционные факторы риска (АГ, ДЛП, СД). Курация больных РА требует междисциплинарного подхода и взаимодействия между врачами разных специальностей. </p></abstract><trans-abstract xml:lang="en"><p>The peak onset of rheumatoid arthritis (RA) is at 30-55 years of age. At this age, the patients have also other concomi- tant diseases (comorbidities) that affect the course and prognosis of RA, the choice of its treatment policy, quality of life of the patients. Objective: to identify the most important and common comorbidities in patients with RA. Subjects and methods. Two hundred patients (median age 55 [46; 61] years) were enrolled; there was a preponderance of women (82.5%) with median disease duration 5 [1; 10] years, seropositive for IgM rheumatoid factor (83.0%) and anti-cyclic citrullinated peptide antibodies (81.6%) with moderate and high disease activity (median DAS28 value 3.9 [3.1; 4.9]). Varying degrees of destructive changes in hand and foot joints were radiologically detected in 71.2% of the patients; 64.5% of the patients had Functional Class II. Methotrexate was given to 69.5% of the patients; therapy with biological agents was used in 21.0% of the cases. 15.5% of the patients did not receive DMARD or biologics. 43.0% of the patients with RA received glucocorticoids. Results. Comorbidities were present in 72.0% of the patients with RA. The most common diseases were hypertension (60.0%), dyslipidemia (45.0%), fractures at various sites (29.5%), and coronary heart disease (21.0%). Myocardial infarction and stroke were observed in 1.5 and 1.0% of cases, respectively. There was diabetes mellitus (DM) in 7.5% of the cases and osteoporosis in 15.5% of the patients. 81.7% of the patients with RA and hypertension and 80.0% of those with RA and DM received antihypertensive and sugar-lowering therapy, respectively. At the same time the RA patients with dyslipidemia and osteoporosis received specific drugs far less frequently (30.0 and 29.0%, respectively). Conclusion. Comorbidities are frequently encountered in RA. By taking into account the fact that cardiovascular dis- eases are a main cause of death in RA; it is necessary to adequately and timely modify traditional risk factors (hyper- tension, dyslipidemia, and diabetes mellitus). Treatment patients with RA requires an interdisciplinary approach and an interaction between physicians of different specialties. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>ревматоидный артрит</kwd><kwd>сопутствующие (коморбидные) заболевания</kwd><kwd>артериальная гипер- тензия</kwd><kwd>дислипидемия</kwd><kwd>сахарный диабет</kwd><kwd>ишемическая болезнь сердца</kwd><kwd>остеопороз.</kwd></kwd-group><kwd-group xml:lang="en"><kwd>rheumatoid arthritis</kwd><kwd>concurrent diseases (comorbidities)</kwd><kwd>hypertension</kwd><kwd>dyslipidemia</kwd><kwd>diabetes mellitus</kwd><kwd>coronary heart disease</kwd><kwd>osteoporosis.</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">Насонов ЕЛ, редактор. Ревматология: клинические рекомендации. 2-е изд., испр. и доп. Москва: ГЭОТАР- Медиа; 2010. 752 c. [Nasonov EL, editor. 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