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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">rpcardio</journal-id><journal-title-group><journal-title xml:lang="en">Rational Pharmacotherapy in Cardiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Рациональная Фармакотерапия в Кардиологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1819-6446</issn><issn pub-type="epub">2225-3653</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20996/1819-6446-2018-14-5-711-715</article-id><article-id custom-type="elpub" pub-id-type="custom">rpcardio-1760</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="en"><subject>ASSOCIATED PROBLEMS OF CARDIOLOGY</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>СМЕЖНЫЕ ВОПРОСЫ КАРДИОЛОГИИ</subject></subj-group></article-categories><title-group><article-title>Dynamics of Carotid Intima-Media Thickness, Parameters of Arterial Stiffness and Ambulatory Blood Pressure Monitoring during Therapy with  Inhibitor of Tumor Necrosis Factor-Alpha in Patients with  Early Psoriatic Arthritis</article-title><trans-title-group xml:lang="ru"><trans-title>Динамика показателей толщины  комплекса интима-медиа, жесткости сосудистой стенки, суточного мониторирования артериального давления у больных ранним псориатическим артритом в результате терапии ингибитором фактора некроза опухоли-альфа</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>Маркелова</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Markelova</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Маркелова Евгения Иннокентьевна – кандидат медицинских наук, старший научный сотрудник, лаборатория ревмокардиологии, НИИР им. В.А. Насоновой.</p><p>115522, Москва, Каширское шоссе,  34а.</p></bio><bio xml:lang="en"><p>Evgenia I. Markelova – MD, PhD, Senior Researcher,  Rheumocardiology Laboratory.</p><p>Kashirskoe shosse 34A, Moscow  115522.</p><p> </p></bio><email xlink:type="simple">evgenia-i.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>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><bio xml:lang="ru"><p>Новикова Диана Сергеевна – доктор медицинских наук, ведущий научный сотрудник, лаборатория ревмокардиологии, НИИР им. В.А. Насоновой.</p><p>115522, Москва, Каширское шоссе,  34а.</p></bio><bio xml:lang="en"><p>Diana S. Novikova – MD, PhD, Leading Researcher,  Rheumocardiology Laboratory.</p><p>Kashirskoe shosse 34A, Moscow  115522.</p><p> </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>Коротаева</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Korotaeva</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Коротаева Татьяна Викторовна – доктор медицинских наук, заведующая лаборатории диагностики и инновационных методов лечения псориатического артрита, НИИР им. В.А. Насоновой.</p><p>115522, Москва, Каширское шоссе,  34а.</p></bio><bio xml:lang="en"><p>Tatiana V. Korotaeva – MD, PhD, Head of Laboratory of Diagnostics and Innovative Methods of Psoriatic Arthritis Treatment.</p><p>Kashirskoe shosse 34A, Moscow  115522.</p><p> </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>Логинова</surname><given-names>Е. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Loginova</surname><given-names>E. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Логинова Елена Юрьевна – кандидат медицинских наук, старший научный сотрудник, лаборатория диагностики и инновационных методов лечения псориатического артрита, НИИР им. В.А. Насоновой.</p><p>115522, Москва, Каширское шоссе,  34а.</p></bio><bio xml:lang="en"><p>Elena Yu. Loginova – MD, PhD, Senior Researcher,  Laboratory of Diagnostics and Innovative Methods of Psoriatic Arthritis Treatment.</p><p>Kashirskoe shosse 34A, Moscow  115522.</p><p> </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт ревматологии им. В.А. Насоновой</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>03</day><month>11</month><year>2018</year></pub-date><volume>14</volume><issue>5</issue><fpage>711</fpage><lpage>715</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Markelova E.I., Novikova D.S., Korotaeva T.V., Loginova E.Y., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Маркелова Е.И., Новикова Д.С., Коротаева Т.В., Логинова Е.Ю.</copyright-holder><copyright-holder xml:lang="en">Markelova E.I., Novikova D.S., Korotaeva T.V., Loginova E.Y.</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.rpcardio.online/jour/article/view/1760">https://www.rpcardio.online/jour/article/view/1760</self-uri><abstract><sec><title>Background</title><p>Background. Patients with psoriatic arthritis (PsA) have increased risk of cardiovascular diseases (CVD). Anti-tumor necrosis factor (TNF) therapy is an effective in PsA but its cardiovascular effects are poorly understood.</p></sec><sec><title>Aim</title><p>Aim. To study the changes in carotid intima-media thickness (c-IMT), parameters of arterial stiffness (AS), ambulatory blood pressure monitoring (AMBP) in early PsA (EPsA) patients during the anti-TNF therapy with adalimumab (ADA).</p></sec><sec><title>Material and methods</title><p>Material and methods. Patients with EPsA (n=16; 11 females, 5 males; median age 45.5 years, EPsA duration – 7.7  months) were included into the study. All patients were treated with ADA 40 mg every other week up to 3 months. At baseline and after 3 months of therapy all patients were assessed  for conventional cardiovascular risk factors, DAS (Disease Activity Score) and  HAQ (Health Assessment Questionnaire) indices, C-reactive protein (CRP), c-IMT, ABPM. At baseline the  4 patients had  arterial hypertension, and  all patients received effective antihypertensive therapy. All patients were assessed for AS parameters: carotid-femoral pulse wave velocity (PWVcf) and index of wave reflection (rigidity index; RI, %). c-IMT was measured using a high-resolution B-mode ultrasound machine. The results are presented in the form of a median – Me (25; 75 percentiles).</p></sec><sec><title>Results</title><p>Results. By the end of the 3rd month of therapy, a decrease in the activity of early PsA was observed as compared to baseline values: DAS decreased from 4.6 (2.9; 1.9) to 1.6 (1.3; 1.9), p=0,001; HAQ from 0.93 (0.81; 1.31) to 0.25 (0; 0.56), p=0,001; CRP from 27.2 (9.7; 33.7) to 1.8 (0.8; 3.1) mg/l, p=0.001. EPsA remission (DAS&lt;1.6) was achieved in 94% of patients. By the end of therapy c-IMT decreased from 0.8 (0.74; 0.85) to 0.73 (0.58; 0.77) mm, p=0,01; as well as AS parameters: PWVcf from 9.9 (7.7; 17.7) to 9.2 (7.4; 10.6) m/s, p&lt;0.05; RI from 69.5 (58; 74) to 49.5 (44; 64)%, p&lt;0.05. AMBPs parameters didn't change significantly. We found significant (p=0.03) decrease in the frequency of the increase in 24-hour diastolic blood pressure.</p></sec><sec><title>Conclusions</title><p>Conclusions. Anti-TNF treatment with ADA improves arterial wall state by decreasing inflammation. These data confirm the idea that inflammation involves in acceleration of atherosclerosis in EPsA patients. </p></sec></abstract><trans-abstract xml:lang="ru"><p>Псориатический артрит (ПсА) – хроническое воспалительное заболевание, ассоциирующееся с высоким  риском  развития сердечно-сосудистых заболеваний (ССЗ). Изучение кардиоваскулярных эффектов биологической терапии, направленной на подавление активности ПсА, является важной задачей.</p><sec><title>Цель</title><p>Цель. Оценить динамику толщины комплекса интима-медиа (КИМ) сонных артерий, показателей артериальной ригидности (АР), суточного мониторирования артериального давления (СМАД) во время терапии адалимумабом в течение 3 мес наблюдения у пациентов с ранним ПсА. Материал и методы. В исследование включены  16  больных  ранним ПсА (11 женщин, 5 мужчин), медиана (Me) возраста – 45,5 лет, длительности заболевания – 7,7  мес.  Оценивали индексы  DAS (Disease Activity Score) и HAQ (Health Assessment Questionnaire), уровень С-реактивного белка  (СРБ), традиционные факторы риска  ССЗ. Артериальная гипертония в анамнезе была  у 4 человек, получавших эффективную антигипертензивную терапию.  Всем больным выполнено СМАД, ультразвуковое дуплексное сканирование сонных артерий с оценкой толщины  КИМ, оценка  АР с измерением индекса отражения (ИО, %) и скорости  распространения пульсовой волны  аорты (СРПВ аорты,  м/с). Адалимумаб вводился подкожно по 40  мг 1 р/2 нед  в течение  3 мес.  Результаты  представлены в виде  медианы – Ме (25; 75 перцентили).</p></sec><sec><title>Результаты</title><p>Результаты. К концу 3-го мес лечения  наблюдали снижение показателей активности  раннего  ПсА по сравнению с исходными значениями: DAS c 4,61 (2,92; 5,33) до 1,6  (1,3; 1,9), p=0,001; HAQ с 0,93 (0,81; 1,31) до 0,25 (0; 0,56), p=0,001; СРБ с 27,2 (9,7; 33,7) до 1,8  (0,8; 3,1) мг/л,  p=0,001. У 94% больных  отмечена полная  ремиссия раннего  ПсА. Выявлено  снижение толщины  КИМ сонных  артерий с 0,8  (0,74; 0,85) до 0,73 (0,58; 0,77) мм, p=0,01; показателей АР: СРПВ аорты с 9,9  (7,7; 17,7) до 9,2  (7,4; 10,6) м/с, p&lt;0,05; ИО с 69,5 (58; 74) до 49,5 (44; 64)%, p&lt;0,05. Не выявлено значимой динамики параметров СМАД. Отмечено  статистически  значимое (p=0,03) уменьшение частоты повышения среднесуточных (24 ч) показателей диастолического артериального давления.</p></sec><sec><title>Заключение</title><p>Заключение. Снижение воспалительной активности раннего ПсА на фоне терапии адалимумабом сопровождалось улучшением состояния сосудистой стенки.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ранний псориатический артрит</kwd><kwd>ингибитор фактора некроза опухолей альфа</kwd><kwd>комплекс интима-медиа</kwd><kwd>артериальная ригидность</kwd><kwd>суточное мониторирование артериального давления</kwd></kwd-group><kwd-group xml:lang="en"><kwd>early psoriatic arthritis</kwd><kwd>inhibitor of tumor  necrosis factor-alpha</kwd><kwd>carotid intima-media thickness</kwd><kwd>arterial stiffness</kwd><kwd>ambulatory blood pressure monitoring</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">Sritheran D., Leung Y.Y. Making the next steps in psoriatic arthritis management: current status and future directions. 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