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1Academic Journal
Authors: A. V. Rudakova, Т. V. Korotaeva, А. В. Рудакова, Т. В. Коротаева
Source: FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology; Vol 17, No 4 (2024); 504-512 ; ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология; Vol 17, No 4 (2024); 504-512 ; 2070-4933 ; 2070-4909
Subject Terms: таргетные синтетические базисные противовоспалительные препараты, psoriatic arthritis, netakimab, biological disease-modifying antirheumatic drugs, targeted synthetic disease-modifying antirheumatic drugs, псориатический артрит, нетакимаб, генно-инженерные биологические препараты
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Relation: https://www.pharmacoeconomics.ru/jour/article/view/1139/590; Псориаз артропатический. Псориатический артрит. Клинические рекомендации. 2024. URL: https://cr.minzdrav.gov.ru/view-cr/562_3 (дата обращения 25.11.2024).; Gladman D.D., Antoni C., Mease P., et al. Psoriatic arthritis: epidemiology, clinical features, course, and outcome. Ann Rheum Dis. 2005; 64 (Suppl. 2): ii14–7. https://doi.org/10.1136/ard.2004.032482.; Толкачева Д.Г., Младов В.В., Соколова В.Д. Эффективность генно-инженерных биологических и таргетных синтетических препаратов, зарегистрированных в России для терапии взрослых пациентов с активным псориатическим артритом: систематический обзор и сетевой метаанализ. Медицинские технологии. Оценка и выбор. 2021; 2: 51–66. https://doi.org/10.17116/medtech20214302151.; Румянцева Е.И., Железнякова И.А., Плахотник О.С. и др. Основные изменения в модели оплаты медицинской помощи по клиникостатистическим группам в Российской Федерации в 2024 году. Медицинские технологии. Оценка и выбор. 2024; 2: 10–21. https://doi.org/10.17116/medtech20244602110.; Lu C., Wallace B.I., Waljee A.K., et al. Comparative efficacy and safety of targeted DMARDs for active psoriatic arthritis during induction therapy: a systematic review and network meta analysis. Semin Arthritis Rheum. 2019; 49 (3): 381–8. https://doi.org/10.1016/j.semarthrit.2019.06.001.; Ruyssen-Witrand A., Perry R., Watkins C., et al. Efficacy and safety of biologics in psoriatic arthritis: a systematic literature review and network meta-analysis. RMD Open. 2020; 6 (1): e001117. https://doi.org/10.1136/rmdopen-2019-001117.; Рудакова А.В., Толкачева Д.Г., Соколова В.Д. Фармакоэкономические аспекты терапии псориатического артрита среднетяжелой и тяжелой степени. ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология. 2021; 14 (2): 116–23. https://doi.org/10.17749/2070-4909/farmakoekonomika.2021.095.; https://www.pharmacoeconomics.ru/jour/article/view/1139
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2Academic Journal
Authors: D. Novikova S., H. Udachkina V., I. Kirillova G., T. Popkova V., Д. Новикова С., Е. Удачкина В., И. Кириллова Г., Т. Попкова В.
Source: Rational Pharmacotherapy in Cardiology; Vol 15, No 6 (2019); 820-830 ; Рациональная Фармакотерапия в Кардиологии; Vol 15, No 6 (2019); 820-830 ; 2225-3653 ; 1819-6446
Subject Terms: rheumatoid arthritis, chronic heart failure, conventional synthetic disease-modifying anti-rheumatic drugs, targeted conventional synthetic disease-modifying anti-rheumatic drugs, biological disease-modifying anti-rheumatic drugs, cardiac function, N-terminal prohormone of brain natriuretic peptide, ревматоидный артрит, хроническая сердечная недостаточность, синтетические базисные противовоспалительные препараты, таргетные синтетические базисные противовоспалительные препараты, генно-инженерные биологические препараты, функция сердца, N-концевой предшественник мозгового натрийуретического пептида
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Relation: https://www.rpcardio.com/jour/article/view/2074/1889; Новикова Д.С., Кириллова И.Г., Удачкина Е.В., Попкова Т.В. Хроническая сердечная недостаточность у больных ревматоидным артритом (часть 1): распространенность, особенности этиологии и патогенеза. Рациональная Фармакотерапия в Кардиологии. 2018;14(5):703-10. DOI:10.20996/1819-6446-2018-14-5-703-710.; Новикова Д.С., Удачкина Е.В., Кириллова И.Г., Попкова Т.В. Хроническая сердечная недостаточность у больных ревматоидным артритом (часть II): трудности диагностики. Рациональная Фармакотерапия в Кардиологии. 2018;14(6):870-8. DOI:10.20996/18196446-2018-14-6-870-878.; Ridker P.M., Everett B.M., Thuren T., et al. Antiinflammatory therapy with canakinumab for atherosclerotic disease. N Engl J Med. 2017;377:1119-31. DOI:10.1056/NEJMoa1707914.; Zhang Y., Lu N., Peloquin C., et al. Improved survival in rheumatoidarthritis: a general population-based cohort study. Ann Rheum Dis. 2017;76(2):408-13. DOI:10.1136/annrheumdis-2015-209058.; Kerola A.M., Nieminen T.V., Virta L.J., et al. No increased cardiovascular mortality among early rheumatoid arthritis patients: a nationwide register study in 2000-2008. Clin Exp Rheumatol. 2015; 33(3):391-8. PMID: 25936374.; Solomon D.H., Reed G.W., Kremer J.M., et al. Disease activity in rheumatoid arthritis and the risk of cardiovascular events. Arthritis Rheumatol. 2015;67:1449-55. DOI:10.1002/art.39098.; Logstrup B.B., Ellingsen T., Pedersen A.B., et al. Development of heart failure in patients with rheumatoid arthritis: A Danish population-based study. Eur J Clin Invest. 2018;48(5):e12915. DOI:10.1111/eci.12915.; Arts E.E., Fransen J., denBroeder A.A., et al. Low disease activity (DAS28≤3.2) reduces the risk of first cardiovascular event in rheumatoid arthritis: a time-dependent Cox regression analysis in a large cohort study. Ann Rheum Dis. 2017;76(10):1693-9. DOI:10.1136/annrheumdis-2016-210997.; Bradham W., Ormseth M.J., Elumogo C., et al. Absence of fibrosis and inflammation by cardiac magnetic resonance imaging in rheumatoid arthritis patients with low to moderate disease activity. J Rheumatol. 2018;45(8):1078-84. DOI:10.3899/jrheum.170770.; Popkova T.V., Novikova D.S., Gasparyan A.Y., Nasonov E.L. Cardiovascular effects of methotrexate in rheumatoid arthritis revisited. Curr Med Chem. 2015;22(16):1903-10. PMID:25876749. DOI:10.2174/0929867322666150415122039.; Roubille C., Richer V., Starnino T., et al. The effects of tumour necrosis factor inhibitors, methotrexate, non-steroidal anti-inflammatory drugs and corticosteroids on cardiovascular events in rheumatoid arthritis, psoriasis and psoriatic arthritis: a systematic review and meta-analysis. Ann Rheum Dis. 2015; 74(3):480-9. DOI:10.1136/annrheumdis-2014-206624.; Ridker P.M., Everett B.M., Pradhan A., et al. Low-Dose Methotrexate for the Prevention of Atherosclerotic Events. N Engl J Med. 2019;21;380(8):752-2. DOI:10.1056/NEJMoa1809798.; Zhang Z., Zhao P., Li A., et al. Effects of methotrexate on plasma cytokines and cardiac remodeling and function in postmyocarditis rats. Mediators Inflamm. 2009;2009:389720. DOI:10.1155/2009/389720.; Li W., Gong K., Ding Y., et al. Effects of triptolide and methotrexate nanosuspensions on left ventricular remodeling in autoimmune myocarditis rats. Int J Nanomedicine. 2019;14:851-63. DOI:10.2147/IJN.S191267.; Campochiaro C., De Luca G., Sartorelli S., et al. Efficacy and Safety of Methotrexate for the Treatment of Autoimmune Virus-Negative Myocarditis: A Case Series. J ClinRheumatol 2018; [Epub ahead of print]. DOI:10.1097/RHU.0000000000000897.; Gong K., Zhang Z., Sun X., et al. The nonspecific anti-inflammatory therapy with methotrexate for patients with chronic heart failure. Am Heart J. 2006;151(1):62-8. DOI:10.1016/j.ahj.2005.02.040.; Bernatsky S., Hudson M., Suissa S. Anti-rheumatic drug use and risk of hospitalization for congestive heart failure in rheumatoid arthritis. Rheumatology (Oxford). 2005;44(5):677-80. DOI:10.1093/rheumatology/keh610.; Myasoedova E., Crowson C.S., Nicola P.J., et al. The influence of rheumatoid arthritis disease characteristics on heart failure. J Rheumatol. 2011;38(8):1601-6. DOI:10.3899/jrheum.100979.; Logstrup B.B., Masic D., Laurbjerg T.B., et al. Left ventricular function at two-year follow-up in treatmentnaive rheumatoid arthritis patients is associated with anti-cyclic citrullinated peptide antibody status: a cohort study. Scand J Rheumatol. 2017;46(6):432-40. DOI:10.1080/03009742.2016.1249941.; Baker J.F., Sauer B., Teng C.C., et al. Initiation of disease-modifying therapies in rheumatoid arthritis is associated with changes in blood pressure. J Clin Rheumatol. 2018;24(4):203-209. DOI:10.1097/RHU.0000000000000736.; Mangoni A.A., Baghdadi L.R., Shanahan E.M., et al. Methotrexate, blood pressure and markers of arterial function in patients with rheumatoid arthritis: a repeated cross-sectional study. Ther Adv Musculoskel Dis. 2017;9(9):213-29. DOI:10.1177/1759720X17719850.; Gasparyan A.Y., Ayvazyan L., Cocco G., Kitas G.D. Adverse cardiovascular effects of antirheumatic drugs: implications for clinical practice and research. Curr Pharm Des. 2012;18(11):1543-55. DOI:10.2174/138161212799504759.; Minoretti P., Bruno A., Di Vito C., Emanuele E. Leflunomide as an antiatherogenic drug. Med Hypotheses. 2007;68(5):1175-6. DOI:10.1016/j.mehy.2006.10.036.; Nielsen C.B., Nielsen C., Nybo M., et al. The in vitro effect of antirheumatic drugs on platelet function. Platelets. 2019;2:1-10. DOI:10.1080/09537104.2019.1609665.; Ma Z.G., Zhang X., Yuan Y.P., et al. A77 1726 (leflunomide) blocks and reverses cardiac hypertrophy and fibrosis in mice. Clin Sci (Lond.) 2018;132:685-99. DOI:10.1042/CS20180160.; Suissa S., Bernatsky S., Hudson M. Antirheumatic drug use and the risk of acute myocardial infarction. Arthritis Rheum. 2006;55:531-6. DOI:10.1002/art.22094.; Naranjo A., Sokka T., Descalzo M.A., et al.; f-RA Group. Cardiovascular disease in patients with rheumatoid arthritis: results from the QUEST-RA study. Arthritis Res Ther. 2008;10(2):R30. DOI:10.1186/ar2383.; Solomon D.H., Avorn J., Katz J.N. Immunosuppressive medications and hospitalization for cardiovascular events in patients with rheumatoid arthritis. Arthritis Rheum. 2006;54:3790-8. DOI:10.1002/art.22255.; Serelis J., Panagiotakos D.B., Mavrommati M., Skopouli F.N. Cardioascular disease is related to hypertension in patients with RA: a greek cohort study. J Rheumatol. 2011;38(2):236-41. DOI:10.3899/jrheum.100564.; Новикова Д.С., Попкова Т.В., Герасимов А.Н. и др. Высокая частота сердечных сокращений как потенциальный фактор риска развития сердечно-сосудистых заболеваний у женщин с ревматоидным артритом. 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DOI:10.2147/DDDT.S166893.; Chatre C., Roubille F., Vernhet H., et al. Cardiac Complications Attributed to Chloroquine and Hydroxychloroquine: A Systematic Review of the Literature Drug Saf. 2018;41(10):919-31. DOI:10.1007/s40264-018-0689-4.; Baniaamam M., Paulus W.J., Blanken A.B., Nurmohamed M.T. The effect of biological DMARDs on the risk of congestive heart failure in rheumatoid arthritis: a systematic review. Expert Opin Biol Ther. 2018;18(5):585-94. DOI:10.1080/14712598.2018.1462794.; Kotyla P.J. Bimodal function of anti-TNF treatment: shall we be concerned about anti-TNF treatment in patients with rheumatoid arthritis and heart failure? Int J Mol Sci. 2018;12;19(6). pii:E1739. DOI:10.3390/ijms19061739.; Hartman M.H.T., Groot H.E., Leach I.M., et al. Trends Cardiovasc Med. 2018l;28(6):369-79. DOI:10.1016/j.tcm.2018.02.003.; Pascale V., Finelli R., Giannotti R., et al. Cardiac eccentric remodeling in patients with rheumatoid arthritis. Sci Rep. 2018;8(1):5867. DOI:10.1038/s41598-018-24323-0.; Ntusi N.A.B., Francis J.M., Sever E., et al. Anti-TNF modulation reduces myocardial inflammation and improves cardiovascular function in systemic rheumatic diseases. Int J Cardiol. 2018;270:253-59. DOI:10.1016/j.ijcard.2018.06.099.; Mann D.L., McMurray J.J., Packer M., et al. Targeted anti cytokine therapy in patients with chronic heart failure: results of the Randomized Etanercept Worldwide Evaluation (RENEWAL). Circulation. 2004;109:1594-602. DOI:10.1161/01.CIR.0000124490.27666.B2.; Chung E.S., Packer M., Lo K.H., et al. Anti-TNF therapy against congestive heart failure investigators. Randomized, double-blind, placebo-controlled, pilot trial of infliximab, a chimeric monoclonal antibody to tumor necrosis factor-alpha, in patients with moderate to-severe heart failure: results of the anti-TNF Therapy Against Congestive Heart Failure (ATTACH) trial. Circulation. 2003;107:3133-40. DOI:10.1161/01.CIR.0000077913.60364.D2.; Setoguchi S., Schneeweiss S., Avorn J., et al. Tumor necrosis factor-alpha antagonist use and heart failure in elderly patients with rheumatoid arthritis. Am Heart J. 2008;156(2):336-41. DOI:10.1016/j.ahj.2008.02.025.; Curtis J.R., Kramer J.M., Martin C., et al. Heart failure among younger rheumatoid arthritis and Crohn's patients exposed to TNF-alpha antagonists. Rheumatology (Oxford). 2007;46(11):168893. DOI:10.1093/rheumatology/kem212.; Santos R.C., Figueiredo V.N., Martins L.C., et al. Infliximab reduces cardiac output in rheumatoid arthritis patients without heart failure. Rev Assoc Med Bras. 2012;58(6):698-702.; Al-Aly Z., Pan H., Zeringue A., et al. Tumor necrosis factor-αblockade, cardiovascular outcomes, and survival in rheumatoid arthritis. Translational Research. 2011;157(1):10-8. DOI:10.1016/j.trsl.2010.09.005.; Jensen T.B., Tsao N., Pawar A., et al. Risk of heart failure following exposure to non-TNFi compared to TNFi biologics in us patients with rheumatoid arthritis. Ann Rheum Dis. 2019;78 suppl. 2:A1392. DOI:10.1136/annrheumdis-2019-eular.1384; Schau T., Gottwald M., Arbach O., et al. Increased prevalence of diastolic heart failure in patients with rheumatoid arthritis correlates with active disease, but not with treatment type. J Rheumatol. 2015;42(11):2029-37. DOI:10.3899/jrheum.141647.; Solomon D.H., Rassen J.A., Kuriya B., et al. Heart failure risk among patients with rheumatoid arthritis starting a TNF antagonist. Ann Rheum Dis. 2013;72:1813-8. DOI:10.1136/annrheumdis-2012-202136.; Tomaš L., Lazurova I., Oetterova M., et al. Left ventricular morphology and function in patients with rheumatoid arthritis. Wien Klin Wochenschr. 2013;125(9-10):233-8. DOI:10.1007/s00508-0130349-8.; Vizzardi E., Cavazzana I., Franceschini F. Left ventricular function in rheumatoid arthritis during anti-TNF-treatment: a speckle tracking prospective echocardiographic study Monaldi Arch Chest Dis. 2016;84(1-2):716. DOI:10.4081/monaldi.2015.716.; Wolfe F., Michaud K. Heart failure in rheumatoid arthritis: rates, predictors, and the effect of antitumor necrosis factor therapy. 2004;116(5):305-11. DOI:10.1016/j.amjmed.2003.09.039; Morgan C.L., Emery P., Porter D., et al. Treatment of rheumatoid arthritis with etanercept with reference to disease-modifying anti-rheumatic drugs: Long-term safety and survival using prospective, observational data. Rheumatology. 2014;53(1):186-94. DOI:10.1093/rheumatology/ket333.; Peters M.J.L., Welsh P., McInnes I.B., et al. Tumour necrosis factor α blockade reduces circulating Nterminal pro-brain natriuretic peptide levels in patients with active rheumatoid arthritis: Results from a prospective cohort study. Ann Rheum Dis. 2010;69(7):1281-85. 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Left ventricular Structure and Function in Patients With Rheumatoid Arthritis, As Assessed by Cardiac Magnetic Resonance Imaging. Arthritis and Rheumatism. 2010;62(4):940-51. DOI:10.1002/art.27349.; Ikonomidis I., Lekakis J.P., Nikolaou M., et al. Inhibition of interleukin-1 by anakinra improves vascular and left ventricular function in patients with rheumatoid arthritis. Circulation. 2008;117:2662-9. DOI:10.1161/CIRCULATIONAHA.107.731877.; Ikonomidis I., Tzortzis S., Andreadou I., et al. Increased benefit of interleukin-1 inhibition on vascular function, myocardial deformation, and twisting in patients with coronary artery disease and coexisting rheumatoid arthritis. Circ Cardiovasc Imaging. 2014;7:619-28. DOI:10.1161/CIRCIMAGING.113.001193.; Van Tassell B.W., Arena R., Biondi-Zoccai G., et al. Effects of interleukin-1 blockade with anakinra on aerobic exercise capacity in patients with heart failure and preserved ejection fraction (from the DHART pilot study). 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Interleukin-1b lockade with canakinumab to improve exercise capacity in patients with chronic systolic heart failure and elevated high sensitivity c-reactive protein (Hs-CRP). [cited by Sep 20, 2019]. Available from: https://clinicaltrials.gov/ct2/show/NCT01900600.; Yokoe I., Kobayashi H., Kobayashi Y., et al. Impact of tocilizumab on N-terminal pro-brain natriuretic peptide levels in patients with active rheumatoid arthritis without cardiac symptoms. Scand J Rheumatol. 2018;47(5):364-70. DOI:10.1080/03009742.2017.1418424.; Generali E., Carrara C., Selmi G., et. al. Comparison of the risks of hospitalisation for cardiovascular events in patients with rheumatoid arthritis treated with tocilizumab and etanercept. Clinical and Experimental Rheumatology. 2018;36:310-3.; Xie F., Yun H., Levitan E.B., et al. Tocilizumab and the risk for cardiovascular disease: a direct comparison among biologic disease-modifying antirheumatic drugs for rheumatoid arthritis patients. 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Five-year administration of tocilizumab to a patient with rheumatoid arthritis complicated by severe chronic heart failure. Nihon Rinsho Meneki Gakkai Kaishi. 2014;37(6):488-92. DOI:10.2177/jsci.37.488.; Nevers T., Salvador A.M., Grodecki-Pena A., et al. Left ventricular T-cell recruitment contributes to the pathogenesis of heart failure. Circ Heart Fail. 2015;8(4):776-87. DOI:10.1161/CIRCHEARTFAILURE.115.002225.; Kallikourdis M., Martini E., Carullo P. T cell costimulation blockade blunts pressure overload-induced heart failure. Nat Commun. 2017;8:14680. DOI:10.1038/ncomms14680.; Generali E., Carrara G., Kallikourdis M., et al. Risk of hospitalization for heart failure in rheumatoid arthritis patients treated with etanercept and abatacept. Rheumatol Int. 2019;39(2):239-43. DOI:10.1007/s00296-018-4196-9.; Jin Y., Kang E.H., Brill G., et al. Cardiovascular (CV) Risk after Initiation of Abatacept versus TNF Inhibitors in Rheumatoid Arthritis Patients with and without Baseline CV Disease. J Rheumatol. 2018;45(9):1240-8. DOI:10.3899/jrheum.170926.; Novikova D.S., Popkova T.V., Nasonov E.L. The effect of anti-B-cell therapy on the development of atherosclerosis in patients with rheumatoid arthritis. Curr Pharm Des. 2012;18:1512-8. DOI:10.2174/138161212799504768.; Novikova D.S., Popkova T.V., Lukina G.V., et al. The effects of rituximab on lipids, arterial stiffness and carotid Intima-media thickness in rheumatoid arthritis. J Korean Med Sci, 2016;31(2):202-7. DOI:10.3346/jkms.2016.31.2.202.; Sanchez-Trujillo L., Jerjes-Sanchez C., Rodriguez D., et al. Phase II clinical trial testing the safety of a humanised monoclonal antibody anti-CD20 in patients withheart failure with reduced ejection fraction, ICFEr-RITU2: study protocol. BMJ Open. 2019;9:e022826. DOI:10.1136/bmjopen-2018022826.; Youker K.A., Assad-Kottner C., Cordero-Reyes A.M., et al. High proportion of patients with endstage heart failure regardless of aetiology demonstrates anti-cardiac antibody deposition in failing myocardium: humoral activation, a potential contributor of disease progression. Eur Heart J. 2014;35:1061-8. DOI:10.1093/eurheartj/eht506.; Sanchez-Trujillo L., Vazquez-Garza E., Castillo E.C., et al. Role of adaptive immunity in the development and progression of heart failure: new evidence. Arch Med Res. 2017;48:1-11. DOI:10.1016/j.arcmed.2016.12.008.; Lee S. Safe Use of Rituximab in an Elderly Patient With Rheumatoid Arthritis and Severe Heart Failure A Case Report. J Clin Rheumatol. 2018;24(3):167-9.; Charles-Schoeman C., Wicker P., Gonzalez-Gay M.A., et al. Cardiovascular safety findings in patients with rheumatoid arthritis treated with tofacitinib, an oral Janus kinase inhibitor. Semin Arthritis Rheum. 2016;46(3):261-71. DOI:10.1016/j.semarthrit.2016.05.014.; Kremer J., Bingham C., Cappelli L., et al. Post-approval comparative safety study of tofacitinib and biologic DMARDS: five-year results from a US-based rheumatoid arthritis registry Ann Rheum Dis. 2019;78 suppl 2:A82. DOI:10.1136/annrheumdis-2019-eular.621.; Novikova D.S., Udachkina H.V., Markelova E.I., et al. Dynamics of body mass index and visceral adiposity index in patients with rheumatoid arthritis treated with tofacitinib. Rheumatol Int. 2019;39(7):1181-9. DOI:10.1007/s00296-019-04303-x.; Novikova D., Kirillova I., Markelova E., et al. The first report of significantly improvement of NT-proBNP level in rheumatoid arthritis patients treated with tofacitinib during 12-month follow-up. Ann Rheum Dis. 2019;78 suppl 2:pA368. DOI:10.1136/annrheumdis-2019-eular.2865.; Taylor P.C., Weinblatt M.E., Burmester G.R., et al. Cardiovascular safety during treatment with baricitinib in rheumatoid arthritis. Arthritis Rheumatol. 2019;71(7):1042-55. DOI:10.1002/art.40841.; https://www.rpcardio.com/jour/article/view/2074
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3Academic Journal
Authors: T. V. Korotaeva, E. Yu. Loginova, E. E. Gubar, Yu. L. Korsakova, M. V. Sedunova, I. N. Pristavsky, I. N. Kushnir, I. F. Umnova, S. S. Kudishina, Т. В. Коротаева, Е. Ю. Логинова, Е. Е. Губарь, Ю. Л. Корсакова, М. В. Седунова, И. Н. Приставский, И. Н. Кушнир, И. Ф. Умнова, С. С. Кудишина
Contributors: This article has been supported by Sandoz, Статья спонсируется компанией «Сандоз»
Source: Modern Rheumatology Journal; Том 15, № 1 (2021); 27-31 ; Современная ревматология; Том 15, № 1 (2021); 27-31 ; 2310-158X ; 1996-7012
Subject Terms: метотрексат, minimal disease activity, synthetic disease-modifying antirheumatic drugs, methotrexate, минимальная активность болезни, синтетические базисные противовоспалительные препараты
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Relation: https://mrj.ima-press.net/mrj/article/view/1096/1053; https://mrj.ima-press.net/mrj/article/view/1096/1061; Насонов ЕЛ, редактор. Ревматология. Российские клинические рекомендации. Москва: ГЭОТАР-Медиа; 2017. 456 с.; Gladman DD, Thavaneswaran A, Chandran V, et al. Do patients with psoriatic arthritis who present early fare better than those presenting later in the disease? Ann Rheum Dis. 2011 Dec;70(12):2152-4. doi:10.1136/ard.2011.150938. Epub 2011 Sep 12.; Theander E, Husmark T, Alenius GM, et al. Early psoriatic arthritis: short symptom duration, male gender and preserved physical functioning at presentation predict favorable outcome at 5-year follow-up. Results from the Swedish Early Psoriatic Arthritis Register (SwePsA). Ann Rheum Dis. 2014;73(2):407-13. doi:10.1136/annrheumdis-2012-201972.; Коротаева ТВ, Логинова ЕЮ, Гетия ТС, Насонов ЕЛ. Результаты применения стратегии «Лечение до достижения цели» у больных ранним псориатическим артритом через 1 год после начала терапии: данные исследования РЕМАРКА. Терапевтический архив. 2018;90(5):22-9.; Gossec L, Baraliakos X, Kerschbaumer A, et al. EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2019 update. Ann Rheum Dis. 2020 Jun;79(6):700-12. doi:10.1136/annrheumdis-2020-217159.; Huynh DH, Boyd TA, Etzel CJ, et al. Persistence of low disease activity after tumour necrosis factor inhibitor (TNFi) discontinuation in patients with psoriatic arthritis. RMD Open. 2017 Jan 16;3(1):e000395. doi:10.1136/rmdopen-2016-000395. eCollection 2017.; Логинова EЮ, Коротаева TВ, Губарь ЕЕ и др. Влияние длительности псориатического артрита на достижение ремиссии и минимальной активности болезни на фоне терапии генно-инженерными биологическими препаратами. Данные Общероссийского регистра пациентов с псориатическим артритом. Научно-практическая ревматология. 2020;58(6):695-700.; Логинова ЕЮ, Коротаева ТВ, Корсакова ЮЛ и др. Клинический статус и трудоспособность пациентов, включенных в Общероссийский регистр пациентов с псориатическим артритом. Современная ревматология. 2020;14(3):19-26. doi:10.14412/1996-7012-2020-3-19-26.; Sheane BJ, Thavaneswaran A, Gladman DD, Chandran V. Attainment of Minimal Disease Activity Using Methotrexate in Psoriatic Arthritis. J Rheumatol. 2016 Sep;43(9):1718- 23. doi:10.3899/jrheum.160111. Epub 2016 Jul 15.; Coates LC, Helliwell PS. Methotrexate efficacy in the Tight Control in Psoriatic Arthritis study. J Rheumatol. 2016 Feb;43(2): 356-61. doi:10.3899/jrheum.150614. Epub 2015 Dec 15.; Vena GA, Cassano N, Iannone F. Update on subcutaneous methotrexate for inflammatory arthritis and psoriasis. Ther Clin Risk Manag. 2018 Jan 9;14:105-16. doi:10.2147/TCRM.S154745. eCollection 2018.; Bianchi G, Caporali R, Mattana P. Methotrexate and rheumatoid arthritis: current evidence regarding subcutaneous versus oral routes of administration. Adv Ther. 2016 Mar;33(3):369-78. doi:10.1007/s12325-016-0295-8. Epub 2016 Feb 4.; Hazlewood GS, Thorne JC, Pope JE, et al. The comparative effectiveness of oral versus subcutaneous methotrexate for the treatment of early rheumatoid arthritis. Ann Rheum Dis. 2016 Jun;75(6):1003-8. doi:10.1136/annrheumdis-2014-206504. Epub 2015 May 15.; Mease PJ, Gladman DD, Collier DH, et al. Etanercept and methotrexate as monotherapy or in combination for psoriatic arthritis: primary results from a randomized, controlled phase III trial. Arthritis Rheumatol. 2019 Jul; 71(7):1112-24. doi:10.1002/art.40851. Epub 2019 May .
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4Academic Journal
Authors: E. Yu. Loginova, T. V. Korotaeva, E. E. Gubar, Yu. L. Korsakova, S. I. Glukhova, E. A. Vasilenko, A. A. Vasilenko, N. A. Kuznetsova, I. M. Patrikeyeva, E. L. Nasonov, Е. Ю. Логинова, Т. В. Коротаева, Е. Е. Губарь, Ю. Л. Корсакова, С. И. Глухова, Е. А. Василенко, А. А. Василенко, Н. А. Кузнецова, И. М. Патрикеева, Е. Л. Насонов
Source: Modern Rheumatology Journal; Том 15, № 3 (2021); 35–42 ; Современная ревматология; Том 15, № 3 (2021); 35–42 ; 2310-158X ; 1996-7012
Subject Terms: минимальная активность болезни, tofacitinib, adalimumab, biologic disease-modifying antirheumatic drug, targeted synthetic disease-modifying antirheumatic drug, remission, minimal disease activity, тофацитиниб, адалимумаб, генно-инженерные биологические препараты, таргетные синтетические базисные противовоспалительные препараты, ремиссия
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Relation: https://mrj.ima-press.net/mrj/article/view/1145/1104; https://mrj.ima-press.net/mrj/article/view/1145/1109; Gladman DD, Antoni C, Mease P, et al. Psoriatic arthritis: epidemiology, clinical features, course, and outcome. Ann Rheum Dis. 2005 Mar;64 Suppl 2(Suppl 2):ii14-7. doi:10.1136/ard.2004.032482.; Coates LC, Kavanaugh A, Mease PJ, et al. Group for Research and Assessment of Psoriasis and Psoriatic Arthritis 2015 treatment recommendations for psoriatic arthritis. Arthritis Rheumatol. 2016 May;68(5):1060-71. doi:10.1002/art.39573. Epub 2016 Mar 23.; Gossec L, Baraliakos X, Kerschbaumer A, et al. European League Against Rheumatism (EULAR) recommendations for the management of psoriatic arthritis with pharmacological therapies: 2019 update. Ann Rheum Dis. 2020 Jun;79(6):700-12. doi:10.1136/annrheumdis-2020-217159.; Murray K, Turk M, Alammari Y, et al. Long-term remission and biologic persistence rates: 12-year real-world data. Arthritis Res Ther. 2021 Jan 13;23(1):25. doi:10.1186/s13075-020-02380-z.; Haddad A, Gazitt T, Feldhamer I, et al. Treatment persistence of biologics among patients with psoriatic arthritis. Arthritis Res Ther. 2021 Jan 29;23(1):44. doi:10.1186/s13075-021-02417-x.; Merola JF, Lockshin B, Mody EA. Switching biologics in the treatment of psoriatic arthritis. Semin Arthritis Rheum. 2017 Aug; 47(1):29-37. doi:10.1016/j.semarthrit.2017.02.001. Epub 2017 Feb 8.; Choy E. Clinical significance of Janus Kinase inhibitor selectivity. Rheumatology (Oxford). 2020 Mar 1;59(3):487-94. doi:10.1093/rheumatology/kez664.; Virtanen AT, Haikarainen T, Raivola J, Silvennoinen O. Selective JAKinibs: prospects in Inflammatory and Autoimmune diseases. BioDrugs. 2019 Feb;33(1):15-32. doi:10.1007/s40259-019-00333-w.; Colbert RA, Ward MM. JAK inhibitors taking on psoriatic arthritis. N Engl J Med. 2017 Oct 19;377(16):1582-4. doi:10.1056/NEJMe1709907.; Mease P, Hall S, Fitzgerald O, et al. Tofacitinib or adalimumab versus placebo for psoriatic arthritis. N Engl J Med. 2017 Oct 19; 377(16):1537-50. doi:10.1056/NEJMoa1615975.; Gladman D, Rigby W, Azevedo VF, et al. Tofacitinib for psoriatic arthritis in patients with an inadequate response to TNF inhibitors. N Engl J Med. 2017 Oct 19;377(16):1525-36. doi:10.1056/NEJMoa1615977.; Nash P, Coates LC, Fleischmann R, et al. Efficacy of Tofacitinib for the Treatment of Psoriatic Arthritis: Pooled Analysis of Two Phase 3 Studies. Rheumatol Ther. 2018 Dec; 5(2):567-82. doi:10.1007/s40744-018-0131-5. Epub 2018 Nov 9.; Castro S, Masmitja J, Carlos M. Efficacy of Tofacitinib in the Treatment of Psoriatic Arthritis: A Systematic Review. Adv Ther. 2021 Feb;38(2):868-84. doi:10.1007/s12325-020-01585-7. Epub 2020 Dec 17.; Насонов ЕЛ. Новые подходы к фармакотерапии ревматоидного артрита: тофацитиниб. Научно-практическая ревматология. 2014;52(2):209-21.; Dhillon S. Tofacitinib: A Review in Rheumatoid Arthritis. Drugs. 2017 Dec;77(18): 1987-2001. doi:10.1007/s40265-017-0835-9.; Berekmeri A, Mahmood F, Wittmann M, Helliwell P. Tofacitinib for the treatment of psoriasis and psoriatic arthritis. Expert Rev Clin Immunol. 2018 Sep;14(9):719-30. doi:10.1080/1744666X.2018.1512404.; Логинова ЕЮ, Корсакова ЮЛ, Губарь ЕЕ и др. Эффективность и безопасность то- фацитиниба у больных псориатическим артритом в реальной клинической практике. Научно-практическая ревматология. 2020;58(3):268-75.; Helliwell P, Coates LC, FitzGerald O, et al. Disease-specific composite measures for psoriatic arthritis are highly responsive to a Janus kinase inhibitor treatment that targets multiple domains of disease. Arthritis Res Ther. 2018 Oct 29;20(1):242. doi:10.1186/s13075-018-1739-0.; Smolen JS, Mease P, Tahir H, et al. Multicentre, randomised, open-label, parallel- group study evaluating the efficacy and safety of ixekizumab versus adalimumab in patients with psoriatic arthritis naive to biological disease-modifying antirheumatic drug: final results by week 52. Ann Rheum Dis. 2020 Oct;79(10):1310-19. doi:10.1136/annrheumdis-2020-217372. Epub 2020 Jul 13.; McInnes IB, Behrens F, Mease PJ, et al. Secukinumab versus adalimumab for treatment of active psoriatic arthritis (EXCEED): a double-blind, parallel-group, randomised, active-controlled, phase 3b trial. Lancet. 2020 May 9;395(10235):1496-505. doi:10.1016/S0140-6736(20)30564-X.; Mease P, Gladman DD, Collier DH, et al. Etanercept and Methotrexate as Monotherapy or in Combination for Psoriatic Arthritis: Primary Results From a Randomized, Controlled Phase III Trial. Arthritis Rheumatol. 2019 Jul;71(7):1112-24. doi:10.1002/art.40851. Epub 2019 May 28.; Lu C, Wallaceb BI, Waljee AK, et al. Comparative efficacy and safety of targeted DMARDs for active psoriatic arthritis during induction therapy: A systematic review and network meta-analysis. Semin Arthritis Rheum. 2019 Dec;49(3):381-8. doi:10.1016/j.semarthrit.2019.06.001. Epub 2019 Jun 10.; Deodhar A, Sliwinska-Stanczyk P, Xu H, et al. Tofacitinib for the treatment of ankylosing spondylitis: a phase III, randomised, double- blind, placebocontrolled study. Ann Rheum Dis. 2021 Apr 27;annrheumdis-2020-219601. doi:10.1136/annrheumdis-2020-219601. Online ahead of print.; Gubar E, Korotaeva T, Korsakova Y, et al. Effect of tofacitinib treatment on active MRI sacroiliitis and disease activity reduction in psoriatic arthritis patients. Data from clinical practice. Ann Rheum Dis. 2020;79:1162.; www.pfizer.com/news/press-release/press-release-detail/pfizer-shares-co-primary-endpoint-results-post-marketing; Инструкция по медицинскому применению препарата тофацитиниб (Яквинус) № ЛП-002026-200820.
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5Academic Journal
Authors: A. E. Karateev, А. Е. Каратеев
Contributors: Исследование выполнено в рамках фундаментальной научной темы № 394 0514-2019-0015 «Контроль боли при ревматических заболеваниях: консервативная терапия и хирургические методы коррекции» (АААА-А19-119021190148-3).
Source: Rheumatology Science and Practice; Vol 58, No 4 (2020); 420-427 ; Научно-практическая ревматология; Vol 58, No 4 (2020); 420-427 ; 1995-4492 ; 1995-4484
Subject Terms: барицитиниб, chronic pain, fatigue, targeted synthetic basic anti-inflammatory drugs, JAK kinase, baricitinib, хроническая боль, утомляемость, таргетные синтетические базисные противовоспалительные препараты, Янус киназа
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Patient-Reported Outcomes in Rheumatoid Arthritis. Rheum Dis Clin North Am. 2016; 42(2):219-37. doi:10.1016/j.rdc.2016.01.010; Fautrel B, Alten R, Kirkham B, et al. Call for action: how to improve use of patient-reported outcomes to guide clinical decision making in rheumatoid arthritis. Rheumatol Int. 2018; 38(6):935-947. doi:10.1007/s00296-018-4005-5; Smolen JS, Strand V, Koenig AS, Szumski A, Kotak S, Jones TV. Discordance between patient and physician assessments of global disease activity in rheumatoid arthritis and association with work productivity. Arthritis Res Ther. 2016; 18(1):114. doi:10.1186/s13075-016-1004-3; Zhang A, Lee YC. Mechanisms for Joint Pain in Rheumatoid Arthritis (RA): from Cytokines to Central Sensitization. Curr Osteoporos Rep. 2018;16(5):603-610. doi:10.1007/s11914-018-0473-5; Sharma J, Bhar S, Devi CS. A review on interleukins: The key manipulators in rheumatoid arthritis. Mod Rheumatol. 2017; 27(5):723-746. doi:10.1080/14397595.2016.1266071; Ge C, Holmdahl R. The structure, specificity and function of anti-citrullinated protein antibodies. Nat Rev Rheumatol. 2019;15(8):503-508. doi:10.1038/s41584-019-0244-4; Gong T, Liu L, Jiang W, Zhou R. DAMP-sensing Receptors in Sterile Inflammation and Inflammatory Diseases. Nat Rev Immunol. 2020; 20(2):95-112. doi:10.1038/s41577-019-0215-7; Takeuchi Y, Hirota K, Sakaguch S. Synovial Tissue Inflammation Mediated by Autoimmune T Cells. Front Immunol. 2019;10:1989. doi:10.3389/fimmu.2019.01989.; Nagata S. Apoptosis and Clearance of Apoptotic Cells. Annu Rev Immunol. 2018 Apr 26;36:489-517. doi:10.1146/annurev-immunol-042617-053010; Smith Jr T, Tharakan A, Martin R. Targeting ADAM10 in Cancer and Autoimmunity. Front Immunol. 2020; 11:499. doi:10.3389/fimmu.2020.00499; Deane K, Holers V. The Natural History of Rheumatoid Arthritis. Clin Ther. 2019;41(7):1256-1269. doi:10.1016/j.clinthera.2019.04.028; Uciechowski P, Dempke W. Interleukin-6: A Masterplayer in the Cytokine Network. Oncology. 2020; 98(3):131-137. doi:10.1159/000505099; Crotti C, Agape E, Becciolini A, Biggioggero M, Favalli EG. Targeting Granulocyte-Monocyte Colony-Stimulating Factor Signaling in Rheumatoid Arthritis: Future Prospects. Drugs. 2019; 79(16):1741-1755. doi:10.1007/s40265-019-01192-z; Katz EJ, Gold MS. Inflammatory hyperalgesia: a role for the C-fiber sensory neuron cell body? J Pain. 2006; 7(3):170-8. doi:10.1016/j.jpain.2005.10.003; Chen X, Alessandri-Haber N, Levine JD. Marked attenuation of inflammatory mediator-induced C-fiber sensitization for mechanical and hypotonic stimuli in TRPV4-/- mice. Mol Pain. 2007; 3:31. doi:10.1186/1744-8069-3-31; Lee C-H, Giuliani F. The Role of Inflammation in Depression and Fatigue. Front Immunol. 2019 Jul 19;10:1696. doi:10.3389/fimmu.2019.01696; Kim K-H, Seo H-J, Abdi S., Huh B. All About Pain Pharmacology: What Pain Physicians Should Know. Korean J Pain. 2020;33(2):108-120. doi:10.3344/kjp.2020.33.2.108; Harth M, Nielson WR. Pain and affective distress in arthritis: relationship to immunity and inflammation. Expert Rev Clin Immunol. 2019; 15(5):541-552. doi:10.1080/1744666X.2019.1573675; Yang S, Chang M. Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States. Int J Mol Sci. 2019; 20(13):3130. doi:10.3390/ijms20133130; Zhao SS, Duffield SJ, Goodson NJ. The prevalence and impact of comorbid fibromyalgia in inflammatory arthritis. Best Pract Res Clin Rheumatol. 2019;33(3):101423. doi:10.1016/j.berh.2019.06.005; Dougados M, Perrot S. Fibromyalgia and central sensitization in chronic inflammatory joint diseases. Joint Bone Spine. 2017; 84(5):511-513. doi:10.1016/j.jbspin.2017.03.001; Druce KL, Basu N. Predictors of fatigue in rheumatoid arthritis. Rheumatology (Oxford). 2019;58(Suppl 5): v29-v34. doi:10.1093/rheumatology/kez346; Daviu N, Bruchas M, Moghaddam B, Sandi C, Beyeler A. Neurobiological Links Between Stress and Anxiety. Neurobiol Stress. 2019; 11:100191. doi:10.1016/j.ynstr.2019.100191.; Maloley PM, England BR, Sayles H, et al. Post-traumatic stress disorder and serum cytokine and chemokine concentrations in patients with rheumatoid arthritis. Semin Arthritis Rheum. 2019; 49(2):229-235. doi:10.1016/j.semarthrit.2019.02.002; Tiosano S, Yavne Y, Watad A, et al. The impact of tocilizumab on anxiety and depression in patients with rheumatoid arthritis.Eur J Clin Invest. 2020 Jun 1:e13268. doi:10.1111/eci.13268; Arendt-Nielsen L, Morlion B, Perrot S, et al. Assessment and manifestation of central sensitisation across different chronic pain conditions. Eur J Pain. 2018;22(2):216-241. doi:10.1002/ejp.1140; Kaplan C, Minc A, Basu N, Schrepf A. Inflammation and the Central Nervous System in Inflammatory Rheumatic Disease. Curr Rheumatol Rep. 2019;21(12):67. doi:10.1007/s11926-019-0870-5; Kiguchi N, Kobayashi D, Saika F, Matsuzaki S, Kishioka S. Pharmacological Regulation of Neuropathic Pain Driven by Inflammatory Macrophages. Int J Mol Sci. 2017;18(11):2296. doi:10.3390/ijms18112296; Siouti E, Andreakos E. The many facets of macrophages in rheumatoid arthritis. Biochem Pharmacol. 2019;165:152-169. doi:10.1016/j.bcp.2019.03.029; Kothari P, Pestana R, Mesraoua R, et al. IL-6-mediated induction of matrix metalloproteinase-9 is modulated by JAKdependent IL-10 expression in macrophages. J Immunol. 2014;192(1):349-57. doi:10.4049/jimmunol.1301906; Salaffi F, Giacobazzi G, Di Carlo M. Chronic Pain in Inflammatory Arthritis: Mechanisms, Metrology, and Emerging Targets-A Focus on the JAK-STAT Pathway. Pain Res Manag. 2018;2018:8564215; Насонов ЕЛ, Лила АМ. Ингибиторы Янус-киназ при иммуно-воспалительных ревматических заболеваниях: новые возможности и перспективы. Научно-практическая ревматология. 2019;57(1):8-16. doi:10.14412/1995-4484-2019-8-16.; Virtanen A, Haikarainen T, Raivola J, Silvennoinen O. Selective JAKinibs: Prospects in Inflammatory and Autoimmune Diseases. BioDrugs. 2019;33(1):15-32. doi:10.1007/s40259-019-00333-w; Park SJ, Lee JH, Kim HY, et al. Astrocytes, but not microglia, rapidly sense H₂O₂via STAT6 phosphorylation, resulting in cyclooxygenase-2 expression and prostaglandin release. J Immunol. 2012;188(10):5132-5141. doi:10.4049/jimmunol.1101600; Ding CP, Guo YJ, Li HN, et al. Red nucleus interleukin-6 participates in the maintenance of neuropathic pain through JAK/ STAT3 and ERK signaling pathways. Exp Neurol. 2018 Feb;300:212-221. DOI:10.1016/j.expneurol.2017.11.012; Xu Z, Wu H, Zhang H, Bai J, Zhang Z. Interleukins 6/8 and cyclooxygenase-2 Release and Expressions Are Regulated by Oxidative stress-JAK2/STAT3 Signaling Pathway in Human Bronchial Epithelial Cells Exposed to Particulate Matter ≤2.5 μm. J Appl Toxicol. 2020 Mar 24. doi:10.1002/jat.3977; Choy EHS, Miceli-Richard C, González-Gay MA, et al. The effect of JAK1/JAK2 inhibition in rheumatoid arthritis: efficacy and safety of baricitinib. Clin Exp Rheumatol. 2019;37(4):694- 704; Smolen JS, Landewé RBM, Bijlsma JWJ, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update. Ann Rheum Dis. 2020;79(6):685-699. doi:10.1136/annrheumdis-2019-216655; Насонов ЕЛ, Лила АМ. Барицитиниб: новые возможности фармакотерапии ревматоидного артрита и других иммуновоспалительных ревматических заболеваний. Научно-практическая ревматология. 2020;58(3):304-316. doi:10.14412/1995-4484-2020-304-316; Pope J, Sawant R, Tundia N, et al. Comparative Efficacy of JAK Inhibitors for Moderate-To-Severe Rheumatoid Arthritis: A Network Meta-Analysis. Adv Ther. 2020;37(5):2356-2372. doi:10.1007/s12325-020-01303-3; Taylor PC, Keystone EC, van der Heijde D, et al. Baricitinib versus Placebo or Adalimumab in Rheumatoid Arthritis. N Engl J Med. 2017;376(7):652-662. doi:10.1056/NEJMoa1608345; Keystone EC, Taylor PC, Tanaka Y., et al. Patient-reported Outcomes From a Phase 3 Study of Baricitinib Versus Placebo or Adalimumab in Rheumatoid Arthritis: Secondary Analyses From the RA-BEAM Study. Ann Rheum Dis. 2017;76(11):1853-1861. doi:10.1136/annrheumdis-2017-211259; Taylor PC, Lee YC, Fleischmann R, et al. Achieving Pain Control in Rheumatoid Arthritis with Baricitinib or Adalimumab Plus Methotrexate: Results from the RA-BEAM Trial. J Clin Med. 2019;8(6). pii: E831. doi:10.3390/jcm8060831; Smolen JS, Kremer JM, Gaich CL, et al. Patient-reported Outcomes From a Randomised Phase III Study of Baricitinib in Patients With Rheumatoid Arthritis and an Inadequate Response to Biological Agents (RA-BEACON). Ann Rheum Dis. 2017;76(4):694-700. doi:10.1136/annrheumdis-2016-209821; Fautrel B, Zhu B, Taylor PC, et al. Comparative effectiveness of improvement in pain and physical function for baricitinib versus adalimumab, tocilizumab and tofacitinib monotherapies in rheumatoid arthritis patients who are naïve to treatment with biologic or conventional synthetic disease-modifying antirheumatic drugs: a matching-adjusted indirect comparison. RMD Open. 2020;6(1). pii: e001131. doi:10.1136/rmdopen-2019-001131
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6Academic Journal
Source: Rheumatology Science and Practice; Vol 57, No 1 (2019); 75-82 ; Научно-практическая ревматология; Vol 57, No 1 (2019); 75-82 ; 1995-4492 ; 1995-4484
Subject Terms: генно-инженерные биологические препараты, nonsteroidal anti-inflammatory drugs, glucocorticoids, disease modifying anti-rheumatic drugs, biologicals, нестероидные противовоспалительные препараты, глюкокортикоиды, синтетические и таргетные синтетические базисные противовоспалительные препараты
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