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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">10.14412/1995-4484-2019-523-527</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-2785</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>Длительность  ремиссии  и  минимальной активности болезни  после  инициации и отмены генно-инженерных  биологических  препаратов у  больных  ранним  псориатическим  артритом (данные  Общероссийского  регистра псориатического  артрита)</article-title><trans-title-group xml:lang="en"><trans-title>The duration of remission and minimal disease activity after initiation and discontinuation of biological agents in patients with early psoriatic arthritis (data from the all-russian psoriatic arthritis registry)</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>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.</p><p>115522, Москва, Каширское шоссе, 34А.</p></bio><bio xml:lang="en"><p>34A, Kashirskoe Shosse, Moscow 115522.</p></bio><email xlink:type="simple">eyloginova@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>Коротаева</surname><given-names>T. 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>115522, Москва, Каширское шоссе, 34А.</p></bio><bio xml:lang="en"><p>34A, Kashirskoe Shosse, Moscow 115522.</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>Глухова</surname><given-names>С. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Glukhova</surname><given-names>S. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34А.</p></bio><bio xml:lang="en"><p>34A, Kashirskoe Shosse, Moscow 115522.</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>Насонов</surname><given-names>Е. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Nasonov</surname><given-names>E. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>115522, Москва, Каширское шоссе, 34А;119991, Москва,ул. Трубецкая, 8, стр. 2ю.</p></bio><bio xml:lang="en"><p>34A, Kashirskoe Shosse, Moscow 115522; 8, Trubetskaya St., Build. 2, Moscow 119991.</p></bio><xref ref-type="aff" rid="aff-2"/></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><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Научно-исследовательский институт ревматологии им. В.А. Насоновой; Первый Московский государственный медицинский университет им. И.М. Сеченова Минздрава России (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova  Research Institute of Rheumatology; I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>15</day><month>11</month><year>2019</year></pub-date><volume>57</volume><issue>5</issue><fpage>523</fpage><lpage>527</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Логинова Е.Ю., Коротаева T.В., Глухова С.И., Насонов Е.Л., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Логинова Е.Ю., Коротаева T.В., Глухова С.И., Насонов Е.Л.</copyright-holder><copyright-holder xml:lang="en">Loginova E.Y., Korotaeva T.V., Glukhova S.I., Nasonov E.L.</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/2785">https://rsp.mediar-press.net/rsp/article/view/2785</self-uri><abstract><p>Длительность  ремиссии  и минимальной активности болезни (МАБ) при лечении  генно-инженерными биологическими препаратами (ГИБП) и после их отмены у больных ранним  псориатическим артритом (ПсА) изучены недостаточно.</p><p>Цель исследования – изучить сроки наступления и длительность ремиссии  и МАБ после назначения и отмены ГИБП у больных ранним  ПсА, наблюдавшихся по принципам стратегии «Лечение до достижения цели» (treattotarget, Т2Т).</p><sec><title>Материал и методы</title><p>Материал и методы. В исследование включено  34 больных ранним  ПсА (18 мужчин, 16 женщин), соответствующих критериям CASPAR, принимавших участие во Всероссийском регистре, наблюдавшихся по принципам стратегии Т2Т. Средний  возраст больных составил 38±11 лет, длительность ПсА – 12,0±10,0 мес, псориаза – 89,8±91,1 мес. В начале наблюдения медиана DAS составляла 4,05 [3,72; 5,10], DAPSA – 33,55 [28,34;41,77]. Всем больным назначался ГИБП (адалимумаб – 21 пациенту,  устекинумаб – 8, цертолизумаба пэгол – 3, этанерцепт – 2) в комбинации с метотрексатом. Медиана  длительности  терапии составила 9 [6,5; 15] мес. Оценивали активность  и эффективность терапии ПсА по DAS, DAPSA и критериям MAБ (число болезненных суставов ≤1, число припухших суставов ≤1, PASI ≤1 или BSA ≤3, оценка боли пациентом ≤15 мм, оценка активности заболевания пациентом ≤20 мм по визуальной аналоговой  шкале, HAQ ≤0,5,  энтезиты≤1) в начале исследования и каждые 3 мес. Определяли количество  больных, достигших ремиссии  (DAS&lt;1,6, DAPSA ≤4) или МАБ (5 критериев  из 7) на фоне терапии ГИБП хотя бы 1 раз за 24 мес наблюдения. Обострением считали отсутствие ремиссии  или МАБ к моменту осмотра. Определяли длительность ремиссии и МАБ после отмены ГИБП на основании индексов  активности в момент осмотра врачом 1 раз в 3 мес. </p></sec><sec><title>Результаты и обсуждение</title><p>Результаты и обсуждение. В течение 24 мес наблюдения ремиссия  по DAS/DAPSA  была достигнута хотя бы1 раз у 28 (82%) / 27 (79%) больных соответственно, МАБ – у 28 (82%). Первая ремиссия  по DAS/DAPSA  наступала в среднем через 4,8±2,2  / 5,8±3,2  мес, МАБ – 4,0±1,9  мес. Средняя  длительность ремиссии  по DAS/DAPSA  составила 9,1±5,0  / 8,3±5,0  мес соответственно, МАБ – 11,0±5,5  мес. Ответили на терапию,но не достигли ремиссии  по DAPSA 7 (21%), по DAS и МАБ – по 6 (18%) пациентов. Продолжали получатьГИБП до конца наблюдения 8 пациентов, сохраняя ремиссию.  Прекратили терапию по разным причинам19 пациентов. Обострение после отмены ГИБП было зафиксировано врачом по DAS у 11 (55%) пациентов в среднем через 6,5±2,3  мес и по DAPSA у 12 (60%) через 5,8±2,3  мес. Со слов больных, обострение  после отмены ГИБП развилось  в среднем через 3,5±3,4  мес. У 5 (15%) пациентов наблюдалось обострение  по DAS/DAPSA  на фоне терапии ГИБП в среднем через 11,5±4,7  / 12,0±4,7  мес.</p></sec></abstract><trans-abstract xml:lang="en"><p>Remission duration and minimal disease activity (MDA) during treatment with biological agents (BA) and after their discontinuation in patients with early psoriatic arthritis (PsA) have been insufficiently studied.</p><sec><title>Objective</title><p>Objective: to study the timing of the onset and duration of remission and MDA after BA initiation and discontinuation in patients with early PsA, followed up according to the Treat-to-Target (T2T) principles.</p></sec><sec><title>Subjects and methods</title><p>Subjects and methods. The investigation enrolled 34 patients (18 men, 16 women) with early PsA who met the CASPAR criteria, had participated  in the All-Russian Registry and followed up according to the T2T principles.The patients' mean age was 38±11 years; the duration of PsA and psoriasis was 12.0±10.0 and 89.8±91.1 months, respectively. At the beginning of the follow-up, the median DAS and DAPSA scores were 4.05 [3.72; 5.10] and 33.55[28.34; 41.77], respectively. All the patients were prescribed BAs (adalimumab  (n=21), ustekinumab  (n=8), certolizumab  pegol (n=3)  or etanercept (n=2)) in combination  with methotrexate. The median therapy duration was 9 [6.5; 15] months. The activity of the disease and efficiency of PsA therapy were evaluated using DAS, DAPSA and the criteria for MDA (tender joint count of ≤1, swollen joint count of ≤1, PASI score ≤1 or BSA ≤3, pain intensity on visual analogue scale (VAS) ≤15 mm, patient's assessment of disease activity on VAS ≤20 mm; HAQ score ≤0.5; enthesitis index ≤1) at the beginning of the investigation and then every 3 months. The number of patients who had achieved remission (DAS &lt;1.6; DAPSA ≤4) or MDA (5 of 7 criteria) during BA therapy at least once during the 24-month follow-up was determined.  The absence of remission or MDA at the time of examination  was considered to be an exacerbation. The duration of remission and MDA was estimated after BA discontinuation according to the activity indices at the time of examination  by a physician every 3 months.</p></sec><sec><title>Results and discussion</title><p>Results and discussion. During the 24-month follow-up, DAS/DAPSA  remissions were achieved at least once by 28 (82%)/27 (79%) patients, respectively; and MDA was seen in 28 (82%). The first DAS/DAPSA  remission occurred after an average of 4.8±2.2/5.8±3.2 months; MDA – after 4.0±1.9 months. The average DAS/DAPSA  remission duration was 9.1±5.0/8.3±5.0 months,  respectively, and MDA – 11.0±5.5 months. Seven (21%) patients responded to therapy, but did not achieve neither DAPSA, nor DAS remission and 6 (18%) patients did not have MDA. 8 patients in remission continued  to receive BAs until the end of the follow-up. Nineteen  patients discontinued therapy for various reasons. After discontinuation of BAs, the physician recorded DAS exacerbation in 11 (55%) patients after an average of 6.5±2.3 months and DAPSA exacerbation in 12 (60%)after 5.8±2.3 months. According to the patient assessment, an exacerbation developed in an average of 3.5±3.4 months after BA discontinuation. A DAS/DAPSA  exacerbation was observed in 5 (15%) patients during BA therapy after an average of 11.5±4.7/12.0±4.7 months.</p></sec><sec><title>Conclusion</title><p>Conclusion. During BA therapy, the majority of patients with early PsA achieved remission and MDA following an average of 5 months after the start of treatment using the T2T strategy. After BA discontinuation, an exacerbation occurs in more than half of patients. Following BA discontinuation, the remission duration recorded by the physician according to the activity indices averages 6 months; the duration of subjective improvement  according to the patient assessment was 3 months. With continued  BA treatment, 15% were observed to have lost its efficiency after an average of 12 months.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ранний  псориатический артрит</kwd><kwd>генно-инженерные биологические препараты</kwd><kwd>ремиссия</kwd><kwd>минимальная активность  болезни</kwd><kwd>обострение  болезни</kwd></kwd-group><kwd-group xml:lang="en"><kwd>early psoriatic arthritis</kwd><kwd>biological agents</kwd><kwd>remission</kwd><kwd>minimal disease activity</kwd><kwd>disease exacerbation</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование проводилось в рамках выполнения научной темы №398 «Патогенетические особенности и персонифицированная терапия анкилозирующего спондилита и псориатического артрита», утвержденной Ученым советом ФГНБУ «НИИР им. В.А. 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