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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">10.47360/1995-4484-2021-394-400</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-3055</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>Оценка эффективности тофацитиниба при ревматоидном артрите в реальной клинической практике: взаимосвязь между снижением боли в первые 4 недели и активностью заболевания через 3–6 месяцев</article-title><trans-title-group xml:lang="en"><trans-title>Evaluation of the effectiveness of Tofacitinib in rheumatoid arthritis in real clinical practice: The relationship between pain relief in the first 4 weeks and disease activity after 3–6 months</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1391-0711</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каратеев</surname><given-names>А. 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Насоновой»; ФГБОУ ДПО «Российская медицинская академия непрерывного профессионального образования» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.A. Nasonova Research Institute of Rheumatology; Russian Medical Academy&#13;
of Continuous Professional Education of the Ministry of Healthcare of the Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>ФГБОУ ВО «Северо-Западный государственный медицинский университет им. И.И. Мечникова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>North-Western State Medical University named after I.I. Mechnikov</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>ФГБОУ ВО «Ярославский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Yaroslavl State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-5"><aff xml:lang="ru"><institution>ГБУЗ города Москвы «Научно-практический клинический центр диагностики и телемедицинских технологий Департамента здравоохранения города Москвы»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of Moscow Health Care Department</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-6"><aff xml:lang="ru"><institution>ФГБУ «Национальный медико-хирургический Центр им. Н.И. Пирогова» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical and Surgical Center named after N.I. Pirogov</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-7"><aff xml:lang="ru"><institution>ГБУЗ Ставропольского края «Ставропольская краевая клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Stavropol Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-8"><aff xml:lang="ru"><institution>ГБУЗ Астраханской области «Александро-Мариинская областная клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Aleksandro-Mariinskaya Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-9"><aff xml:lang="ru"><institution>ГБУЗ «Научно-исследовательский институт – Краевая клиническая больница № 1 им. проф. С.В. Очаповского» Министерства здравоохранения Краснодарского края</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Research Institute – Professor S.V. Ochapovsky Regional Clinical Hospital N 1</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-10"><aff xml:lang="ru"><institution>ФГБОУ ВО «Самарский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Samara State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-11"><aff xml:lang="ru"><institution>ФГБОУ ВО «Чувашский государственный университет им. И.Н. Ульянова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Chuvash State University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-12"><aff xml:lang="ru"><institution>ГБУЗ Тюменской области «Областная клиническая больница № 1»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tyumen Regional Clinical Hospital N 1</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-13"><aff xml:lang="ru"><institution>ГБУЗ города Москвы «Московский клинический научно-практический центр им. А.С. Логинова Департамента здравоохранения города Москвы»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Loginov Moscow Clinical Scientific Center</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-14"><aff xml:lang="ru"><institution>ГАУЗ «Кузбасская областная клиническая больница им. С.В. Беляева»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>S.V. Belyaev Kuzbass Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-15"><aff xml:lang="ru"><institution>ФГБОУ ВО «Волгоградский государственный медицинский&#13;
университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Volgograd State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-16"><aff xml:lang="ru"><institution>ГУЗ Тульской области «Тульская областная клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tula Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-17"><aff xml:lang="ru"><institution>ФГБОУ ВО «Петрозаводский государственный университет»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Petrozavodsk State University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-18"><aff xml:lang="ru"><institution>ГБУЗ «Самарская областная клиническая больница им. В.Д. Середавина»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>V.D. Seredavin Samara Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-19"><aff xml:lang="ru"><institution>ГУЗ Ульяновская областная клиническая больница</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Ulyanovsk Regional Clinical Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-20"><aff xml:lang="ru"><institution>ФГБОУ ВО «Смоленский государственный медицинский университет» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Smolensk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>05</day><month>09</month><year>2021</year></pub-date><volume>59</volume><issue>4</issue><elocation-id>394–400</elocation-id><permissions><copyright-statement>Copyright &amp;#x00A9; Каратеев А.Е., Погожева Е.Ю., Амирджанова В.Н., Филатова Е.С., Лила А.М., Мазуров В.И., Самигуллина Р.Р., Дадалова А.М., Дё А.Ю., Чакиева Д.С., Баранов А.А., Лапкина Н.А., Кольцова Е.Н., Кирюхина Н.А., Щендригин И.Н., Расевич Т.Г., Давыдова А.Ф., Семизарова И.В., Шафиева И.А., Башкова И.Б., Бобрикова Д.А., Муртазалиева Д.А., Кушнир И.Н., Калинина Е.В., Сальникова Т.С., Марусенко И.М., Семагина О.В., Виноградова И.Б., Кречикова Д.Г., Семченкова М.Ю., Насонов Е.Л., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Каратеев А.Е., Погожева Е.Ю., Амирджанова В.Н., Филатова Е.С., Лила А.М., Мазуров В.И., Самигуллина Р.Р., Дадалова А.М., Дё А.Ю., Чакиева Д.С., Баранов А.А., Лапкина Н.А., Кольцова Е.Н., Кирюхина Н.А., Щендригин И.Н., Расевич Т.Г., Давыдова А.Ф., Семизарова И.В., Шафиева И.А., Башкова И.Б., Бобрикова Д.А., Муртазалиева Д.А., Кушнир И.Н., Калинина Е.В., Сальникова Т.С., Марусенко И.М., Семагина О.В., Виноградова И.Б., Кречикова Д.Г., Семченкова М.Ю., Насонов Е.Л.</copyright-holder><copyright-holder xml:lang="en">Karateev A.E., Pogozheva E.Y., Amirjanova V.N., Filatova E.S., Lila A.M., Mazurov V.I., Samigullina R.R., Dadalova A.M., Dyo A.Y., Chakieva D.S., Baranov A.A., Lapkina N.A., Koltsova E.N., Kiryukhina N.A., Shchendrigin I.N., Rasevich T.G., Davydova A.F., Semizarova I.V., Shafieva I.A., Bashkova I.B., Bobrikova D.A., Murtazalieva D.A., Kushnir I.N., Kalinina E.V., Salnikova T.S., Marusenko I.M., Semagina O.V., Vinogradova I.B., Krechikova D.G., Semchenkova M.Y., 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/3055">https://rsp.mediar-press.net/rsp/article/view/3055</self-uri><abstract><p>Ингибитор JAK тофацитиниб (ТОФА) блокирует внутриклеточный сигнальный путь, активирующий синтез цитокинов и медиаторов, участвующих в развитии боли и центральной сенситизации (ЦС), что определяет быстрый анальгетический эффект. Однако не ясно, как снижение боли ассоциируется с достижением низ- кой активности ревматоидного артрита (РА).</p><p>Цель исследования – оценить связь между ранним клиническим ответом на тофацитиниб и снижением активности ревматоидного артрита через 3 и 6 месяцев.</p><sec><title>Материал и методы</title><p>Материал и методы. Исследуемую группу составили 88 больных РА (возраст – 53±11,5 года; 79,3% женщин), которые получали базисные противовоспалительные препараты (59,5% – метотрексат, 19,8% – лефлуномид) и которым был назначен ТОФА в дозе 10 мг/сут. Серопозитивность по ревматоидному фактору составила 89,8%; значение индекса DAS28-СРБ – 5,2±1,2. Оценивалась выраженность боли с помощью опросника Brief Pain Inventory, невропатический компонент боли (НКБ) – с помощью опросника PainDETECT, признаки ЦС – с помощью опросника Central Sensitisation Inventory (CSI) на ранних сроках после назначения ТОФА, активность РА – с помощью индекса DAS28-СРБ через 3 и 6 месяцев.</p></sec><sec><title>Результаты</title><p>Результаты. Средняя выраженность боли исходно составила 5,3±2,0 по визуальной аналоговой шкале (ВАШ); 51,1% пациентов имели признаки ЦС (CSI≥40), 15,9% имели НКБ (PainDETECT≥18). Через 7 дней после начала терапии отмечалось существенное снижение боли – до 4,1±1,8 по ВАШ (р&lt;0,05) и ЦС – 40,4±13,5 до 36,5±12,5 по CSI (р=0,01). Через 28 дней эффект был еще существеннее: уровень боли по ВАШ составил 2,8±1,6 (р=0,000), НКБ снизился с 11,8±5,6 до 6,8±3,1 (р=0,000), ЦС – до 31,6±13,9 (р=0,000). Значение индекса DAS28-СРБ через 3 и 6 месяцев составило соответственно 3,7±1,3 и 3,6±1,2. Число больных со снижением боли ≥50% через 28 дней составило 59,9%, низкая активность РА через 3 мес. (DAS28- СРБ≤3,2) была достигнута у 64,4% больных. Имелась четкая корреляция между числом пациентов с уменьшением боли ≥50% через 28 дней и числом пациентов, достигших низкой активности РА через 3 и 6 мес. (rS=0,548, p=0,000 и rS=0,790, p=0,000 соответственно). 6 больных выбыли из исследования вследствие неэффективности или социальных причин. Серьезных нежелательных реакций отмечено не было.</p></sec><sec><title>Выводы</title><p>Выводы. Использование ингибитора JAK ТОФА позволяет достичь быстрого анальгетического эффекта и снижения признаков ЦС. Ранний клинический ответ на ТОФА (уменьшение боли) позволяет прогнозировать снижение активности РА через 3 и 6 месяцев терапии.</p></sec></abstract><trans-abstract xml:lang="en"><p>The JAK inhibitor tofacitinib (TOFA) blocks the intracellular signaling pathway that activates the synthesis of cytokines and mediators involved in the development of pain and central sensitization (CS), which determines the rapid analgesic effect. However, it is not clear how pain reduction is associated with achieving low activity in rheumatoid arthritis (RA).</p><p>The aim of the study was to assess the relationship between the early clinical response to tofacitinib and a decrease in rheumatoid arthritis activity after 3 and 6 months.</p><sec><title>Material and methods</title><p>Material and methods. The study group consisted of 88 RA patients (age – 53±11.5 years; 79.3% of women) who received basic anti-inflammatory drugs (59.5% – methotrexate, 19.8% – leflunomide) and who were prescribed TOFA in a dose 10 mg/day. Seropositivity for rheumatoid factor was 89.8%; the value of the DAS28 index is 5.2±1.2. The severity of pain was assessed using the Brief Pain Inventory questionnaire, the neuropathic component of pain (NCP) – using the PainDETECT questionnaire, signs of CS – using the Central Sensitization Inventory (CSI) questionnaire in the early stages after the administration of TOFA, RA activity – using the DAS28-CRP index after 3 and 6 months.</p></sec><sec><title>Results</title><p>Results. The mean severity of pain at baseline was 5.3±2.0 on the visual analogue scale (VAS); 51.1% of patients had signs of CS (CSI&gt;40), 15.9% had NCP (PainDETECT&gt;18). 7 days after the start of therapy, there was a significant decrease in pain – to 4.1±1.8 according to VAS (p&lt;0.05) and CS – 40.4±13.5 to 36.5±12.5 according to CSI (p=0.01). After 28 days, the effect was even more significant: the level of pain according to the VAS was 2.8±1.6 (p=0.000), the NCP decreased from 11.8±5.6 to 6.8±3.1 (p=0.000), CS – up to 31.6±13.9 (p=0.000). The value of the DAS28-CRP index after 3 and 6 months was 3.7±1.3 and 3.6±1.2, respectively. The number of patients with pain relief ≥50% after 28 days was 59.9%, low RA activity after 3 months. (DAS28-CRP≤3.2) was acieved in 64.4% of patients. There was a clear correlation between the number of patients with a pain reduction of ≥50% at 28 days and the number of patients who achieved low RA activity at 3 and 6 months. (rS=0.548, p=0.000 and rS=0.790, p=0.000). 6 patients dropped out of the study due to inefficiency or social reasons. No serious adverse reactions were noted.</p></sec><sec><title>Conclusions</title><p>Conclusions. The use of the JAK inhibitor TOFA allows achieving a quick analgesic effect and reducing the signs of CS. An early clinical response to TOFA (pain relief) predicts a decrease in RA activity after 3 and 6 months of therapy.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>ревматоидный артрит</kwd><kwd>тофацитиниб</kwd><kwd>боль</kwd><kwd>центральная сенситизация</kwd><kwd>активность</kwd><kwd>корреляция</kwd></kwd-group><kwd-group xml:lang="en"><kwd>rheumatoid arthritis</kwd><kwd>tofacitinib</kwd><kwd>pain</kwd><kwd>central sensitization</kwd><kwd>activity</kwd><kwd>correlation</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Статья спонсируется компанией «Пфайзер»</funding-statement></funding-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, Авдеева АС, Лила АМ. Эффективность и безопасность тофацитиниба при иммуновоспалительных ревматических заболеваниях (часть I). 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