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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">mrj</journal-id><journal-title-group><journal-title xml:lang="ru">Современная ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Modern Rheumatology Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1996-7012</issn><issn pub-type="epub">2310-158X</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1996-7012-2019-1-108-113</article-id><article-id custom-type="elpub" pub-id-type="custom">mrj-895</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>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Насколько эффективна «средняя терапевтическая доза» нестероидного противовоспалительного препарата при остеоартрите?</article-title><trans-title-group xml:lang="en"><trans-title>How effective is the average therapeutic dose of a nonsteroidal anti-inflammatory drug in osteoarthritis?</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>Каратеев</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Karateev</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Андрей Евгеньевич Каратеев</p><p>115522, Москва, Каширское шоссе, 34А</p></bio><bio xml:lang="en"><p>Andrey Evgenyevich Karateev</p><p>34A, Kashirskoe Shosse, Moscow 115522</p></bio><email xlink:type="simple">aekarat@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ 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>2019</year></pub-date><pub-date pub-type="epub"><day>27</day><month>03</month><year>2019</year></pub-date><volume>13</volume><issue>1</issue><fpage>108</fpage><lpage>113</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Каратеев А.Е., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Каратеев А.Е.</copyright-holder><copyright-holder xml:lang="en">Karateev A.E.</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://mrj.ima-press.net/mrj/article/view/895">https://mrj.ima-press.net/mrj/article/view/895</self-uri><abstract><p>Международное многоцентровое исследование PRECISION, посвященное оценке кардиоваскулярной безопасности целекоксиба, на-проксена и ибупрофена, находится под пристальным вниманием критиков. Одно из замечаний, которое высказывается в отношении этого исследования — применение относительно низкой дозы целекоксиба (в среднем чуть выше 200 мг/сут), которая, по мнению ряда экспертов, может быть недостаточно эффективной. Однако так ли это на самом деле?</p><p>В настоящем обзоре приведены данные многочисленных международных исследований, посвященных лечению остеоартрита (ОА), в которых целекоксиб в дозе 200 мг/сут сравнивали с парацетамолом 4000 мг/сут, опиоидами, диклофенаком 100—150 мг/сут, на-проксеном 1000 мг/сут, ибупрофеном 2400 мг/сут, медленно действующими противовоспалительными средствами (глюкозамин, хондроитин и их комбинация). Практически во всех этих работах показано хорошее и быстрое анальгетическое действие целекоксиба 200 мг, не уступающее таковому препаратов контроля или превышающее его. Целекоксиб 200 мг/сут позволял контролировать боль при ОА на протяжении многих месяцев и препятствовать развитию рецидивов этого заболевания. Низкий риск осложнений со стороны желудочно-кишечного тракта и сердечно-сосудистой системы, подтвержденный исследованием PRECISION, делает целекоксиб 200 мг/сут средством выбора для длительной терапии ОА, в том числе у больных с серьезным коморбидным фоном.</p></abstract><trans-abstract xml:lang="en"><p>The international multicenter PRECISION study evaluating the cardiovascular safety of celecoxib, naproxen, and ibuprofen is under close scrutiny by critics. One of the criticisms about this study was that the use of relatively low dose (on average just above 200 mg/day) may not be effective enough. But is it really so?</p><p>This review gives data from numerous international studies dealing with the treatment of osteoarthritis (OA), in which celecoxib 200 mg/day is compared with paracetamol 4000 mg/day, diclofenac 100—150 mg/day, naproxen 1000 mg/day, ibuprofen 2400 mg/day and slow-acting antirheumatic drugs (glucosamine, chondroitin, and their combination). Almost all studies demonstrate that celecoxib 200 mg has a good and rapid analgesic effect that is not inferior to or exceed that of the reference drugs.</p><p>Celecoxib 200 mg/day could relieve pain in OA for many months and prevent disease recurrences. The low risk of gastrointestinal and cardiovascular complications, which has been confirmed by the PRECISION study, makes celecoxib 200 mg/day the drug of choice for long-term OA therapy, including in patients with serious comorbid conditions.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>нестероидные противовоспалительные препараты</kwd><kwd>целекоксиб</kwd><kwd>эффективность</kwd><kwd>осложнения</kwd><kwd>кардиоваскулярный риск</kwd><kwd>желудочно-кишечный тракт</kwd><kwd>остеоартрит</kwd></kwd-group><kwd-group xml:lang="en"><kwd>nonsteroidal anti-inflammatory drugs</kwd><kwd>celecoxib</kwd><kwd>efficacy</kwd><kwd>complications</kwd><kwd>cardiovascular risk</kwd><kwd>gastrointestinal tract</kwd><kwd>osteoarthritis</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">Nissen S, Yeomans N, Solomon D, et al. Cardiovascular Safety of Celecoxib, Naproxen, or Ibuprofen for Arthritis. N Engl JMed. 2016 Dec 29;375(26):2519-29. doi: 10.1056/NEJMoa1611593. Epub 2016 Nov 13.</mixed-citation><mixed-citation xml:lang="en">Nissen S, Yeomans N, Solomon D, et al. Cardiovascular Safety of Celecoxib, Naproxen, or Ibuprofen for Arthritis. N Engl JMed. 2016 Dec 29;375(26):2519-29. doi: 10.1056/NEJMoa1611593. Epub 2016 Nov 13.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Fitzgerald GA. Imprecision: Limitations to Interpretation of a Large Randomized Clinical Trial. Circulation. 2017 Jan 10; 135(2):113-115. doi: 10.1161/CIRCULA-TIONAHA.116.026324. Epub 2016 Nov 13.</mixed-citation><mixed-citation xml:lang="en">Fitzgerald GA. Imprecision: Limitations to Interpretation of a Large Randomized Clinical Trial. Circulation. 2017 Jan 10; 135(2):113-115. doi: 10.1161/CIRCULA-TIONAHA.116.026324. Epub 2016 Nov 13.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Patrono C, Baigent C. Coxibs, Traditional NSAIDs, and Cardiovascular Safety Post-PRECISION: What We Thought We Knew Then and What We Think We Know Now. Clin Pharmacol Ther. 2017 Aug; 102(2):238-245. doi: 10.1002/cpt.696. Epub 2017 May 26.</mixed-citation><mixed-citation xml:lang="en">Patrono C, Baigent C. Coxibs, Traditional NSAIDs, and Cardiovascular Safety Post-PRECISION: What We Thought We Knew Then and What We Think We Know Now. Clin Pharmacol Ther. 2017 Aug; 102(2):238-245. doi: 10.1002/cpt.696. Epub 2017 May 26.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Rane MA, Foster JG, Wood SK, et al. Benefits and Risks of Nonsteroidal Anti-inflammatory Drugs: Methodologic Limitations Lead to Clinical Uncertainties. Ther Innov Regul Sci. 2018 Sep 3: 2168479018794159. doi: 10.1177/2168479018794159. [Epub ahead of print]</mixed-citation><mixed-citation xml:lang="en">Rane MA, Foster JG, Wood SK, et al. Benefits and Risks of Nonsteroidal Anti-inflammatory Drugs: Methodologic Limitations Lead to Clinical Uncertainties. Ther Innov Regul Sci. 2018 Sep 3: 2168479018794159. doi: 10.1177/2168479018794159. [Epub ahead of print]</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Муравьев ЮВ. Почему исследование комплексной безопасности целекоксиба при артритах, названное PRECISION, является последним по счету, а не по значимости? Научно-практическая ревматология. 2017;55(3):324-6. doi: 10.14412/1995-4484-2017-324-326</mixed-citation><mixed-citation xml:lang="en">Murav'ev YuV. Why is the study of the complex safety of celecoxib for arthritis, which is called PRECISION, last but not least? Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2017;55(3):324-6. (In Russ.). doi: 10.14412/1995-4484-2017-324-326</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Довгань ЕВ. Результаты исследования PRECISION: удалось ли ответить на вопрос, насколько безопасны коксибы в сравнении с «традиционными» нестероидными противовоспалительными препаратами у пациентов с высоким риском развития сердечно-сосудистых осложнений? Современная ревматология. 2017; 11(3):129—31. doi: 10.14412/1996-7012-2017-3-129-131</mixed-citation><mixed-citation xml:lang="en">Dovgan' EV. Results of the PRECISION study: Could an answer be given to the question of how safe coxibs versus traditional NSAIDs are in treating patients at high risk for cardiovascular events? Sovremennaya revmatologiya = Modern Rheumatology Journal. 2017;11(3):129—31. (In Russ.). doi: 10.14412/1996-7012-2017-3-129-131</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Yeomans ND, Graham DY, Husni ME, et al. Randomised clinical trial: gastrointestinal events in arthritis patients treated with celecoxib, ibuprofen or naproxen in the PRECISION trial. Aliment Pharmacol Ther. 2018 Jun;47(11):1453-1463. doi: 10.1111/apt.14610. Epub 2018 Apr 17.</mixed-citation><mixed-citation xml:lang="en">Yeomans ND, Graham DY, Husni ME, et al. Randomised clinical trial: gastrointestinal events in arthritis patients treated with celecoxib, ibuprofen or naproxen in the PRECISION trial. Aliment Pharmacol Ther. 2018 Jun;47(11):1453-1463. doi: 10.1111/apt.14610. Epub 2018 Apr 17.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Гайдукова ИЗ, Ребров АП, Лапшина СА и др. Применение нестероидных противовоспалительных препаратов и генно-инженерных биологических препаратов для лечения аксиальных спондилоартритов. Рекомендации Экспертной группы по изучению спондилоартритов при Общероссийской общественной организации «Ассоциация ревматологов России». Научно-практическая ревматология. 2017; 55(5):474-84. doi: 10.14412/1995-4484-2017-474-484</mixed-citation><mixed-citation xml:lang="en">Gaidukova IZ, Rebrov AP, Lapshina SA, et al. Use of nonsteroidal antiinflammatory drugs and biological agents for the treatment of axial spondyloarthritides. recommendations of the spondyloarthritis study group of experts, All-russian public organization «The association of rheumatology of Russia». Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2017;55(5):474-84. (In Russ.). doi: 10.14412/1995-4484-2017-474-484</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Зонова ЕВ, Каратеев АЕ. Обоснованный подход к выбору нестероидных противовоспалительных препаратов при остеоартрите. Современная ревматология. 2018;12(4):47-53. doi: 10.14412/1996-7012-2018-4-47-53</mixed-citation><mixed-citation xml:lang="en">Zonova EV, Karateev AE. A sound approach to choosing nonsteroidal anti-inflammatory drugs for osteoarthritis. Sovremennaya revmatologiya = Modern Rheumatology Journal. 2018;12(4):47-53. (In Russ.). doi: 10.14412/1996-7012-2018-4-47-53</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Robinson WH, Lepus CM, Wang Q, et al. Low-grade inflammation as a key mediator of the pathogenesis of osteoarthritis. Nat Rev Rheumatol. 2016 Oct;12(10):580-92. doi: 10.1038/nrrheum.2016.136. Epub 2016 Aug 19.</mixed-citation><mixed-citation xml:lang="en">Robinson WH, Lepus CM, Wang Q, et al. Low-grade inflammation as a key mediator of the pathogenesis of osteoarthritis. Nat Rev Rheumatol. 2016 Oct;12(10):580-92. doi: 10.1038/nrrheum.2016.136. Epub 2016 Aug 19.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Mathiessen A, Conaghan PG. Synovitis in osteoarthritis: current understanding with therapeutic implications. Arthritis Res Ther. 2017 Feb 2;19(1):18. doi: 10.1186/s13075-017-1229-9.</mixed-citation><mixed-citation xml:lang="en">Mathiessen A, Conaghan PG. Synovitis in osteoarthritis: current understanding with therapeutic implications. Arthritis Res Ther. 2017 Feb 2;19(1):18. doi: 10.1186/s13075-017-1229-9.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Dell'Isola A, Allan R, Smith SL. Identification of clinical phenotypes in knee osteoarthritis: a systematic review of the literature. BMC Musculoskelet Disord. 2016 Oct 12;17(1):425.</mixed-citation><mixed-citation xml:lang="en">Dell'Isola A, Allan R, Smith SL. Identification of clinical phenotypes in knee osteoarthritis: a systematic review of the literature. BMC Musculoskelet Disord. 2016 Oct 12;17(1):425.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Ong SM, Hadadi E, Dang TM, et al. The pro-inflammatory phenotype of the human non-classical monocyte subset is attributed to senescence. Cell Death Dis. 2018 Feb 15;9(3):266. doi: 10.1038/s41419-018-0327-1.</mixed-citation><mixed-citation xml:lang="en">Ong SM, Hadadi E, Dang TM, et al. The pro-inflammatory phenotype of the human non-classical monocyte subset is attributed to senescence. Cell Death Dis. 2018 Feb 15;9(3):266. doi: 10.1038/s41419-018-0327-1.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Timur UT, Caron MM, Bastiaansen-Jenniskens YM, et al. Celecoxib-mediated reduction of prostanoid release in Hoffa's fat pad from donors with cartilage pathology results in an attenuated inflammatory phenotype. Osteoarthritis Cartilage. 2018 May;26(5): 697-706. doi: 10.1016/j.joca.2018.01.025. Epub 2018 Feb 7.</mixed-citation><mixed-citation xml:lang="en">Timur UT, Caron MM, Bastiaansen-Jenniskens YM, et al. Celecoxib-mediated reduction of prostanoid release in Hoffa's fat pad from donors with cartilage pathology results in an attenuated inflammatory phenotype. Osteoarthritis Cartilage. 2018 May;26(5): 697-706. doi: 10.1016/j.joca.2018.01.025. Epub 2018 Feb 7.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Song GG, Seo YH, Kim JH, et al. Relative efficacy and tolerability of etoricoxib, celecoxib, and naproxen in the treatment of osteoarthritis: A Bayesian network metaanalysis of randomized controlled trials based on patient withdrawal. Z Rheumatol. 2016 Jun;75(5):508-16. doi: 10.1007/s00393-015-0023-9.</mixed-citation><mixed-citation xml:lang="en">Song GG, Seo YH, Kim JH, et al. Relative efficacy and tolerability of etoricox-ib, celecoxib, and naproxen in the treatment of osteoarthritis: A Bayesian network metaanalysis of randomized controlled trials based on patient withdrawal. Z Rheumatol. 2016	Jun;75(5):508-16. doi: 10.1007/s00393-015-0023-9.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Deeks JJ, Smith LA, Bradley MD. Efficacy, tolerability, and upper gastrointestinal safety of celecoxib for treatment of osteoarthritis and rheumatoid arthritis: systematic review of randomised controlled trials. BMJ. 2002 Sep 21;325(7365):619</mixed-citation><mixed-citation xml:lang="en">Deeks JJ, Smith LA, Bradley MD. Efficacy, tolerability, and upper gastrointestinal safety of celecoxib for treatment of osteoarthritis and rheumatoid arthritis: systematic review of randomised controlled trials. BMJ. 2002 Sep 21;325(7365):619</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Zweers MC, de Boer TN, van Roon J, et al. Celecoxib: considerations regarding its potential disease-modifying properties in osteoarthritis. Arthritis Res Ther. 2011;13(5): 239. doi: 10.1186/ar3437. Epub 2011 Sep 21.</mixed-citation><mixed-citation xml:lang="en">Zweers MC, de Boer TN, van Roon J, et al. Celecoxib: considerations regarding its potential disease-modifying properties in osteoarthritis. Arthritis Res Ther. 2011;13(5): 239. doi: 10.1186/ar3437. Epub 2011 Sep 21.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Frampton JE, Keating GM. Celecoxib: a review of its use in the management of arthritis and acute pain. Drugs. 2007;67(16): 2433-72.</mixed-citation><mixed-citation xml:lang="en">Frampton JE, Keating GM. Celecoxib: a review of its use in the management of arthritis and acute pain. Drugs. 2007;67(16): 2433-72.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Xu C, Gu K, Yasen Y, Hou Y. Efficacy and Safety of Celecoxib Therapy in Osteoarthritis: A Meta-Analysis of Randomized Controlled Trials. Medicine (Baltimore). 2016 May;95(20):e3585. doi: 10.1097/MD.0000000000003585.</mixed-citation><mixed-citation xml:lang="en">Xu C, Gu K, Yasen Y, Hou Y. Efficacy and Safety of Celecoxib Therapy in Osteoarthritis: A Meta-Analysis of Randomized Controlled Trials. Medicine (Baltimore). 2016 May;95(20):e3585. doi: 10.1097/MD.0000000000003585.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu X, Wu D, Sang L, et al. Comparative effectiveness of glucosamine, chondroitin, acetaminophen or celecoxib for the treatment of knee and/or hip osteoarthritis: a network meta-analysis. Clin Exp Rheumatol. 2018 Jul-Aug;36(4):595-602. Epub 2018 Jan 31.</mixed-citation><mixed-citation xml:lang="en">Zhu X, Wu D, Sang L, et al. Comparative effectiveness of glucosamine, chondroitin, acetaminophen or celecoxib for the treatment of knee and/or hip osteoarthritis: a network meta-analysis. Clin Exp Rheumatol. 2018 Jul-Aug;36(4):595-602. Epub 2018 Jan 31.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Puljak L, Marin A, Vrdoljak D. Celecoxib for osteoarthritis. Cochrane Database Syst Rev. 2017 May 22;5:CD009865. doi: 10.1002/14651858.CD009865.pub2.</mixed-citation><mixed-citation xml:lang="en">Puljak L, Marin A, Vrdoljak D. Celecoxib for osteoarthritis. Cochrane Database Syst Rev. 2017	May 22;5:CD009865. doi: 10.1002/14651858.CD009865.pub2.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Alvarez-Soria MA, Herrero-Beaumont G, Moreno-Rubio J, et al. Longterm NSAID treatment directly decreases COX-2 and mPGES-1 production in the articular cartilage of patients with osteoarthritis. Osteoarthritis Cartilage. 2008 Dec;16(12): 1484-93. doi: 10.1016/j.joca.2008.04.022. Epub 2008 Jun 10.</mixed-citation><mixed-citation xml:lang="en">Alvarez-Soria MA, Herrero-Beaumont G, Moreno-Rubio J, et al. Long-term NSAID treatment directly decreases COX-2 and mPGES-1 production in the articular cartilage of patients with osteoarthritis. Osteoarthritis Cartilage. 2008 Dec;16(12): 1484-93. doi: 10.1016/j.joca.2008.04.022. Epub 2008 Jun 10.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Wang G, Li J, Zhang L, et al. Celecoxib induced apoptosis against different breast cancer cell lines by down-regulated NF-kB pathway. Biochem Biophys Res Commun. 2017 Aug 26;490(3):969-976. doi: 10.1016/j.bbrc.2017.06.148. Epub 2017 Jun 27.</mixed-citation><mixed-citation xml:lang="en">Wang G, Li J, Zhang L, et al. Celecoxib induced apoptosis against different breast cancer cell lines by down-regulated NF-kB pathway. Biochem Biophys Res Commun. 2017 Aug 26;490(3):969-976. doi: 10.1016/j.bbrc.2017.06.148. Epub 2017 Jun 27.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Zuo C, Hong Y, Qiu X, et al. Celecoxib suppresses proliferation and metastasis of pancreatic cancer cells by down-regulating STAT3 / NF-kB and L1CAM activities. Pan-creatology. 2018 Apr;18(3):328-333. doi: 10.1016/j.pan.2018.02.006. Epub 2018 Feb 15.</mixed-citation><mixed-citation xml:lang="en">Zuo C, Hong Y, Qiu X, et al. Celecoxib suppresses proliferation and metastasis of pancreatic cancer cells by down-regulating STAT3 / NF-kB and L1CAM activities. Pan-creatology. 2018 Apr;18(3):328-333. doi: 10.1016/j.pan.2018.02.006. Epub 2018 Feb 15.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Matsuyama A, Higashi S, Tanizaki S, et al. Celecoxib inhibits osteoblast differentiation independent of cyclooxygenase activity. Clin Exp Pharmacol Physiol. 2018 Jan;45(1): 75-83. doi: 10.1111/1440-1681.12846. Epub 2017 Sep 20.</mixed-citation><mixed-citation xml:lang="en">Matsuyama A, Higashi S, Tanizaki S, et al. Celecoxib inhibits osteoblast differentiation independent of cyclooxygenase activity. Clin Exp Pharmacol Physiol. 2018 Jan;45(1): 75-83. doi: 10.1111/1440-1681.12846. Epub 2017 Sep 20.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Chan PC, Hsiao FC, Chang HM, et al. Importance of adipocyte cyclooxygenase-2 and prostaglandin E2-prostaglandin E receptor 3 signaling in the development of obesity-induced adipose tissue inflammation and insulin resistance. FASEB J. 2016 Jun;30(6): 2282-97. doi: 10.1096/fj.201500127. Epub 2016 Mar 1.</mixed-citation><mixed-citation xml:lang="en">Chan PC, Hsiao FC, Chang HM, et al. Importance of adipocyte cyclooxygenase-2 and prostaglandin E2-prostaglandin E receptor 3 signaling in the development of obesity-induced adipose tissue inflammation and insulin resistance. FASEB J. 2016 Jun;30(6): 2282-97. doi: 10.1096/fj.201500127. Epub 2016 Mar 1.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Ilhan N, Gungor H, Gul HF, Eroksuz H. Expression of Endoglin and Vascular Endothelial Growth Factor as Prognostic Markers in Experimental Colorectal Cancer. Anticancer Res. 2016 Aug;36(8):3953-9.</mixed-citation><mixed-citation xml:lang="en">Ilhan N, Gungor H, Gul HF, Eroksuz H. Expression of Endoglin and Vascular Endothelial Growth Factor as Prognostic Markers in Experimental Colorectal Cancer. Anticancer Res. 2016 Aug;36(8):3953-9.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Pincus T, Koch G, Lei H, et al. Patient Preference for Placebo, Acetaminophen (paracetamol) or Celecoxib Efficacy Studies (PACES): two randomised, double blind, placebo controlled, crossover clinical trials in patients with knee or hip osteoarthritis. Ann Rheum Dis. 2004 Aug;63(8):931-9. Epub 2004 Apr 13.</mixed-citation><mixed-citation xml:lang="en">Pincus T, Koch G, Lei H, et al. Patient Preference for Placebo, Acetaminophen (paracetamol) or Celecoxib Efficacy Studies (PACES): two randomised, double blind, placebo controlled, crossover clinical trials in patients with knee or hip osteoarthritis. Ann Rheum Dis. 2004 Aug;63(8):931-9. Epub 2004 Apr 13.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Smith SR, Deshpande BR, Collins JE, et al. Comparative pain reduction of oral non-steroidal anti-inflammatory drugs and opioids for knee osteoarthritis: systematic analytic review. Osteoarthritis Cartilage. 2016 Jun;24(6):962-72. doi: 10.1016/j.joca.2016.01.135. Epub 2016 Feb 1.</mixed-citation><mixed-citation xml:lang="en">Smith SR, Deshpande BR, Collins JE, et al. Comparative pain reduction of oral non-steroidal anti-inflammatory drugs and opioids for knee osteoarthritis: systematic analytic review. Osteoarthritis Cartilage. 2016 Jun;24(6):962-72. doi: 10.1016/j.joca.2016.01.135. Epub 2016 Feb 1.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Kellner HL, Li C, Essex MN. Celecoxib and Diclofenac Plus Omeprazole are Similarly Effective in the Treatment of Arthritis in Patients at High GI Risk in the CONDOR Trial. Open Rheumatol J. 2013 Nov 13;7:96-100. doi: 10.2174/1874312901307010096.eCollection2013.</mixed-citation><mixed-citation xml:lang="en">Kellner HL, Li C, Essex MN. Celecoxib and Diclofenac Plus Omeprazole are Similarly Effective in the Treatment of Arthritis in Patients at High GI Risk in the CONDOR Trial. Open Rheumatol J. 2013 Nov 13;7:96-100. doi: 10.2174/1874312901307010096.eCollection2013.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Clegg DO, Reda DJ, Harris CL, et al. Glucosamine, chondroitin sulfate, and the two in combination for painful knee osteoarthritis. N Engl J Med. 2006 Feb 23; 354(8):795-808.</mixed-citation><mixed-citation xml:lang="en">Clegg DO, Reda DJ, Harris CL, et al. Glucosamine, chondroitin sulfate, and the two in combination for painful knee osteoarthritis. N Engl J Med. 2006 Feb 23; 354(8):795-808.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Hochberg MC, Martel-Pelletier J, Monfort J, et al. Combined chondroitin sulfate and glucosamine for painful knee osteoarthritis: a multicentre, randomised, double-blind, non-inferiority trial versus cele-coxib. Ann Rheum Dis. 2016 Jan;75(1):37-44. doi: 10.1136/annrheumdis-2014-206792. Epub 2015 Jan 14.</mixed-citation><mixed-citation xml:lang="en">Hochberg MC, Martel-Pelletier J, Monfort J, et al. Combined chondroitin sulfate and glucosamine for painful knee osteoarthritis: a multicentre, randomised, double-blind, non-inferiority trial versus cele-coxib. Ann Rheum Dis. 2016 Jan;75(1):37-44. doi: 10.1136/annrheumdis-2014-206792. Epub 2015 Jan 14.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Reginster JY, Dudler J, Blicharski T, Pavelka K. Pharmaceutical-grade Chondroitin sulfate is as effective as celecoxib and superior to placebo in symptomatic knee osteoarthritis: the ChONdroitin versus CElecoxib versus Placebo Trial (CONCEPT). Ann Rheum Dis. 2017 Sep;76(9):1537-1543. doi: 10.1136/annrheumdis-2016-210860. Epub 2017 May 22.</mixed-citation><mixed-citation xml:lang="en">Reginster JY, Dudler J, Blicharski T, Pavelka K. Pharmaceutical-grade Chondroitin sulfate is as effective as celecoxib and superior to placebo in symptomatic knee osteoarthritis: the ChONdroitin versus CElecoxib versus Placebo Trial (CONCEPT). Ann Rheum Dis. 2017 Sep;76(9):1537-1543. doi: 10.1136/annrheumdis-2016-210860. Epub 2017 May 22.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Strand V, Simon LS, Dougados M, et al. Treatment of osteoarthritis with continuous versus intermittent celecoxib. J Rheumatol. 2011 Dec;38(12):2625-34. doi: 10.3899/jrheum.110636. Epub 2011 Nov 1.</mixed-citation><mixed-citation xml:lang="en">Strand V, Simon LS, Dougados M, et al. Treatment of osteoarthritis with continuous versus intermittent celecoxib. J Rheumatol. 2011 Dec;38(12):2625-34. doi: 10.3899/jrheum.110636. Epub 2011 Nov 1.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Emery P, Koncz T, Pan S, Lowry S. Analgesic effectiveness of celecoxib and diclofenac in patients with osteoarthritis of the hip requiring joint replacement surgery: a 12-week, multicenter, randomized, doubleblind, parallel-group, double-dummy, noninferiority study. Clin Ther. 2008 Jan;30(1): 70-83. doi: 10.1016/j.clinthera.2008.01.016.</mixed-citation><mixed-citation xml:lang="en">Emery P, Koncz T, Pan S, Lowry S. Analgesic effectiveness of celecoxib and diclofenac in patients with osteoarthritis of the hip requiring joint replacement surgery: a 12-week, multicenter, randomized, doubleblind, parallel-group, double-dummy, noninferiority study. Clin Ther. 2008 Jan;30(1): 70-83. doi: 10.1016/j.clinthera.2008.01.016.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">McKenna F, Borenstein D, Wendt H, et al. Celecoxib versus diclofenac in the management of osteoarthritis of the knee. Scand J Rheumatol. 2001;30(1):11-8.</mixed-citation><mixed-citation xml:lang="en">McKenna F, Borenstein D, Wendt H, et al. Celecoxib versus diclofenac in the management of osteoarthritis of the knee. Scand J Rheumatol. 2001;30(1):11-8.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Kivitz AJ, Moskowitz RW, Woods E, et al. Comparative Efficacy and Safety of Celecoxib and Naproxen in the Treatment of Osteoarthritis of the Hip. J Int Med Res. 2001 Nov-Dec;29(6):467-79.</mixed-citation><mixed-citation xml:lang="en">Kivitz AJ, Moskowitz RW, Woods E, et al. Comparative Efficacy and Safety of Celecoxib and Naproxen in the Treatment of Osteoarthritis of the Hip. J Int Med Res. 2001 Nov-Dec;29(6):467-79.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Gordo AC, Walker C, Armada B, Zhou D. Efficacy of celecoxib versus ibuprofen for the treatment of patients with osteoarthritis of the knee: A randomized double-blind, non-inferiority trial. J Int Med Res. 2017 Feb;45(1): 59-74. doi: 10.1177/0300060516673707. Epub 2017 Jan 12.</mixed-citation><mixed-citation xml:lang="en">Gordo AC, Walker C, Armada B, Zhou D. Efficacy of celecoxib versus ibuprofen for the treatment of patients with osteoarthritis of the knee: A randomized double-blind, non-inferiority trial. J Int Med Res. 2017 Feb;45(1): 59-74. doi: 10.1177/0300060516673707. Epub 2017 Jan 12.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Singh G, Fort JG, Goldstein JL, et al. Celecoxib versus naproxen and diclofenac in osteoarthritis patients: SUCCESS-I Study. Am J Med. 2006 Mar;119(3):255-66.</mixed-citation><mixed-citation xml:lang="en">Singh G, Fort JG, Goldstein JL, et al. Celecoxib versus naproxen and diclofenac in osteoarthritis patients: SUCCESS-I Study. Am J Med. 2006 Mar;119(3):255-66.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Bingham CO3rd, Sebba AI, Rubin BR, et al. Efficacy and safety of etoricoxib 30 mg and celecoxib 200 mg in the treatment of osteoarthritis in two identically designed, randomized, placebo-controlled, non-inferiority studies. Rheumatology (Oxford). 2007 Mar; 46(3):496-507. Epub 2006 Aug 27.</mixed-citation><mixed-citation xml:lang="en">Bingham CO3rd, Sebba AI, Rubin BR, et al. Efficacy and safety of etoricoxib 30 mg and celecoxib 200 mg in the treatment of osteoarthritis in two identically designed, randomized, placebo-controlled, non-inferiority studies. Rheumatology (Oxford). 2007 Mar; 46(3):496-507. Epub 2006 Aug 27.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Каратеев АЕ, Лила АМ, Чурюканов МВ и др. Оценка эффективности алгоритма назначения нестероидных противовоспалительных препаратов (НПВП), основанного на анализе факторов риска лекарственных осложнений, в реальной клинической практике. Результаты всероссийского проекта «ПРИНЦИП» (Применение Рекомендаций по Использованию НПВП: Целенаправленное Изменение Практики). Научно-практическая ревматология. 2017;55(5):485-92. doi: 10.14412/1995-4484-2017-485-492</mixed-citation><mixed-citation xml:lang="en">Karateev AE, Lila AM, Churyukanov MV, et al. Evaluation of the effectiveness of a nonsteroidal anti-inflammatory drug (NSAID) selection algorithm based on the analysis of risk factors for drug-induced complications in real clinical practice: the results of the all-russian PRINCIPLE project (application of recommendations for NSAID use: a goal-oriented change of practice). Nauchno-prakticheskaya revmatologiya = Rheumatology Science and Practice. 2017;55(5):485-92. (In Russ.). doi: 10.14412/1995-4484-2017-485-492</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
