Academic Journal
Enhancing the Efficacy and Safety of Methotrexate Treatment: A Focus on Drug Interactions (Review) ; Повышение эффективности и безопасности использования метотрексата: фокус на лекарственные взаимодействия (обзор)
العنوان: | Enhancing the Efficacy and Safety of Methotrexate Treatment: A Focus on Drug Interactions (Review) ; Повышение эффективности и безопасности использования метотрексата: фокус на лекарственные взаимодействия (обзор) |
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المؤلفون: | S. A. Doktorova, Yu. Yu. Grabovetskaya, M. Stefanov, V. V. Rafalskiy, С. А. Докторова, Ю. Ю. Грабовецкая, М. Стефанов, В. В. Рафальский |
المساهمون: | This research was supported by funds provided to the Immanuel Kant Baltic Federal University through the Russian Federal Academic Leadership Programme “Priority 2030” (project No. 123102600004-1)., Данная работа была поддержана из средств программы стратегического академического лидерства «Приоритет 2030» БФУ им. И. Канта, научный проект № 123102600004-1. |
المصدر: | Safety and Risk of Pharmacotherapy; 2024: Online First ; Безопасность и риск фармакотерапии; 2024: Online First ; 2619-1164 ; 2312-7821 ; undefined |
بيانات النشر: | Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’) |
سنة النشر: | 2024 |
المجموعة: | Safety and Risk of Pharmacotherapy (E-Journal) / Безопасность и риск фармакотерапии |
مصطلحات موضوعية: | нестероидные противовоспалительные препараты, drug interactions, adverse drug reactions, pharmacokinetics, pharmacodynamics, safety, rheumatoid arthritis, disease-modifying antirheumatic drugs, biologicals, proton pump inhibitors, non-steroidal anti-inflammatory drugs, лекарственные взаимодействия, нежелательные реакции, фармакокинетика, фармакодинамика, безопасность лекарственных средств, ревматоидный артрит, базисные противовоспалительные препараты, биологические препараты, ингибиторы протонной помпы |
الوصف: | INTRODUCTION. Methotrexate (MTX) is the main disease-modifying antirheumatic drug (DMARD) and the gold standard for the safety and efficacy evaluation of biologicals and targeted small molecules. However, its narrow therapeutic range, interpatient variability in pharmacokinetics and pharmacodynamics, and potential clinically relevant drug–drug interactions (DDIs) may lead to treatment failure and increase the risk of adverse drug reactions (ADRs).AIM. The study aimed to describe the main clinically significant DDIs associated with MTX used in rheumatic disease therapy and determine possible approaches to addressing this issue based on a literature review.DISCUSSION. MTX is characterised by pharmacokinetic DDIs during absorption, cell penetration, and elimination. Some non-steroidal anti-inflammatory drugs (NSAIDs), theophylline, sulfasalazine, antibacterial agents, and proton pump inhibitors (PPIs) affect MTX elimination and therapeutic effects. The main ADRs associated with MTX include haematotoxicity, hepatotoxicity, lung tissue damage (interstitial pneumonitis and pulmonary fibrosis), and renal dysfunction. The severity of these ADRs depends on the dose, comorbidities, and concomitant therapy. The toxicity of MTX may be increased by the concomitant administration of medicinal products that exhibit haematotoxicity and affect renal function (impair the elimination of medicines). When co-administering MTX and medicines having clinically significant DDIs described in the literature, healthcare providers should consider the risk factors for each individual patient. The most significant risk factors include moderate to severe renal and hepatic impairment, older age, polypharmacy, and hypoalbuminemia.CONCLUSIONS. This article describes potential clinically significant interactions between MTX and certain NSAIDs, antibacterial agents, and PPIs that depend on individual patient characteristics and may increase the toxicity or decrease the effectiveness of MTX. MTX deprescribing, short-term withdrawal, and dosing ... |
نوع الوثيقة: | article in journal/newspaper |
وصف الملف: | application/pdf |
اللغة: | Russian |
Relation: | https://www.risksafety.ru/jour/article/view/416/1034; https://www.risksafety.ru/jour/article/view/416/1043; https://www.risksafety.ru/jour/article/view/416/1044; https://www.risksafety.ru/jour/article/view/416/1045; https://www.risksafety.ru/jour/article/view/416/1048; https://www.risksafety.ru/jour/article/view/416/1050; https://www.risksafety.ru/jour/article/view/416/1052; https://www.risksafety.ru/jour/article/view/416/1059; https://www.risksafety.ru/jour/article/view/416/1067; https://www.risksafety.ru/jour/article/view/416/1074; https://www.risksafety.ru/jour/article/view/416/1081; https://www.risksafety.ru/jour/article/view/416/1087; https://www.risksafety.ru/jour/article/downloadSuppFile/416/447; https://www.risksafety.ru/jour/article/downloadSuppFile/416/448; https://www.risksafety.ru/jour/article/downloadSuppFile/416/473; Weinblatt ME. Methotrexate in rheumatoid arthritis: a quarter century of development. Trans Am Clin Climatol Assoc. 2013;124:16–25. PMID: 23874006; Насонов ЕЛ, Каратеев ДЕ, Сатыбалдыев АМ, Лучихина ЕЛ, Лукина ГВ, Николенко МВ и др. Ревматоидный артрит в Российской Федерации по данным Российского регистра больных артритом (сообщение I). Научно-практическая ревматология. 2016;54:50–62. https://doi.org/10.14412/1995-4484-2016-50-62; Braun J, Kästner P, Flaxenberg P, Währisch J, Hanke P, Demary W, et al. Comparison of the clinical efficacy and safety of subcutaneous versus oral administration of methotrexate in patients with active rheumatoid arthritis: results of a six-month, multicenter, randomized, double-blind, controlled, phase IV trial. Arthritis Rheum. 2008;58(1):73–81. https://doi.org/10.1002/art.23144; Anghel L-A. Utilization patterns of disease-modifying antirheumatic drugs (DMARDs) in patients with autoimmune rheumatic diseases. Farmacia. 2019;67(1):184–92. https://doi.org/10.31925/farmacia.2019.1.25; Левитан АИ, Решетько ОВ. Реальная клиническая практика фармакотерапии ревматоидного артрита. Клиническая фармакология и терапия. 2019;28(1):44–9. https://doi.org/10.32756/0869-5490-2019-1-44-49; Насонов ЕЛ, Мазуров ВИ, Каратеев ДЕ, Лукина ГВ, Жиляев ЕВ, Амирджанова ВН и др. Проект рекомендаций по лечению ревматоидного артрита Общероссийской общественной организации «Ассоциация ревматологов России» — 2014 (часть 1). Научно-практическая ревматология. 2014;52(5):477–94. https://doi.org/10.14412/1995-4484-2014-477-494; Fraenkel L, Bathon JM, England BR, St Clair EW, Arayssi T, Carandang K, et al. 2021 American College of Rheumatology Guideline for the treatment of rheumatoid arthritis. Arthritis Rheumatol. 2021;73(7):1108–23. https://doi.org/10.1002/acr.24596; Lau CS, Chia F, Dans L, Harrison A, Hsieh TY, Jain R, et al. 2018 update of the APLAR recommendations for treatment of rheumatoid arthritis. Int J Rheum Dis. 2019;22(3):357–75. https://doi.org/10.1111/1756-185x.13513; Smolen JS, Landewé RBM, Bergstra SA, Kerschbaumer A, Sepriano A, Aletaha D, et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2022 update. Ann Rheum Dis. 2023;82(1):3–18. https://doi.org/10.1136/ard-2022-223356; Насонов ЕЛ, Амирджанова ВН, Олюнин ЮА, Муравьев ЮВ, Баранов АА, Зонова ЕВ и др. Применение метотрексата при ревматоидном артрите. Рекомендации Общероссийской общественной организации «Ассоциация ревматологов России». Научно-практическая ревматология. 2023;61(4):435–49. https://doi.org/10.47360/1995-4484-2023-435-449; Насонов ЕЛ, Каратеев ДЕ, Чичасова НВ. Новые рекомендации по лечению ревматоидного артрита (EULAR, 2013): место метотрексата. Научно-практическая ревматология. 2015;53(5s):32–50. https://doi.org/10.14412/1995-4484-2015-32-50; Tarp S, Jorgensen TS, Furst DE, Dossing A, Taylor PC, Choy EH, et al. Added value of combining methotrexate with a biological agent compared to biological monotherapy in rheumatoid arthritis patients: a systematic review and meta-analysis of randomised trials. Semin Arthritis Rheum. 2019;48(6):958–66. https://doi.org/10.1016/j.semarthrit.2018.10.002; Silva MF, Ribeiro C, Goncalves VMF, Tiritan ME, Lima A. Liquid chromatographic methods for the therapeutic drug monitoring of methotrexate as clinical decision support for personalized medicine: a brief review. Biomed Chromatogr. 2018;32(5):e4159. https://doi.org/10.1002/bmc.4159; Bagatini F, Blatt CR, Maliska G, Trespash GV, Pereira IA, Zimmermann AF, et al. Potential drug interactions in patients with rheumatoid arthritis. Rev Bras Reumatol. 2011;51(1):20–39. English, Portuguese. PMID: 21412604; Ma SN, Zaman Huri H, Yahya F. Drug-related problems in patients with rheumatoid arthritis. Ther Clin Risk Manag. 2019;15:505–24. https://doi.org/10.2147/TCRM.S194921; Jeong H, Baek SY, Kim SW, Eun YH, Kim IY, Kim H, et al. Comorbidities of rheumatoid arthritis: results from the Korean National Health and Nutrition Examination Survey. PLoS One. 2017;12(4):e0176260. https://doi.org/10.1371/journal.pone.0176260; Bechman K, Clarke BD, Rutherford AI, Yates M, Nikiphorou E, Molokhia M, et al. Polypharmacy is associated with treatment response and serious adverse events: results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Rheumatology. 2019;58(10):1767–76. https://doi.org/10.1093/rheumatology/kez037; Ye L, Yang-Huang J, Franse CB, Rukavina T, Vasiljev V, Mattace-Raso F, et al. Factors associated with polypharmacy and the high risk of medication-related problems among older community-dwelling adults in European countries: a longitudinal study. BMC Geriatr. 2022;22(1):841. https://doi.org/10.1186/s12877-022-03536-z; Bourré-Tessier J, Haraoui B. Methotrexate drug interactions in the treatment of rheumatoid arthritis: a systematic review. J Rheumatol. 2010;37(7):1416–21. https://doi.org/10.3899/jrheum.090153; Hall JJ, Bolina M, Chatterley T, Jamali F. Interaction between low-dose methotrexate and non-steroidal anti-inflammatory drugs, penicillins, and proton pump inhibitors. Ann Pharmacother. 2016;51(2):163–78. https://doi.org/10.1177/1060028016672035; Pflugbeil S, Böckl K, Pongratz R, Leitner M, Graninger W, Ortner A. Drug interactions in the treatment of rheumatoid arthritis and psoriatic arthritis. Rheumatol Int. 2020;40(4):511–21. https://doi.org/10.1007/s00296-020-04526-3; Leveque D, Santucci R, Gourieux B, Herbrecht R. Pharmacokinetic drug-drug interactions with methotrexate in oncology. Expert Rev Clin Pharmacol. 2011;4(6):743–50. https://doi.org/10.1586/ecp.11.57; Patane M, Ciriaco M, Chimirri S, Ursini F, Naty S, Grembiale RD, et al. Interactions among low dose of methotrexate and drugs used in the treatment of rheumatoid arthritis. Adv Pharmacol Sci. 2013;2013:313858. https://doi.org/10.1155/2013/313858; Desmoulin SK, Hou Z, Gangjee A, Matherly LH. The human proton-coupled folate transporter: biology and therapeutic applications to cancer. Cancer Biol Ther. 2012;13(14):1355–73. https://doi.org/10.4161/cbt.22020; Bedoui Y, Guillot X, Selambarom J, Guiraud P, Giry C, Jaffar-Bandjee MC, et al. Methotrexate an old drug with new tricks. Int J Mol Sci. 2019;20(20).5023. https://doi.org/10.3390/ijms20205023; Bannwarth B, Pehourcq F, Schaeverbeke T, Dehais J. Clinical pharmacokinetics of low-dose pulse methotrexate in rheumatoid arthritis. Clin Pharmacokinet. 1996;30(3):194–210. https://doi.org/10.2165/00003088-199630030-00002; Hoekstra M, Haagsma C, Neef C, Proost J, Knuif A, van de Laar M. Bioavailability of higher dose methotrexate comparing oral and subcutaneous administration in patients with rheumatoid arthritis. J Rheumatol. 2004;31(4):645–8. PMID: 15088287; Bianchi G, Caporali R, Todoerti M, Mattana P. Methotrexate and rheumatoid arthritis: current evidence regarding subcutaneous versus oral routes of administration. Adv Ther. 2016;33(3):369–78. https://doi.org/10.1007/s12325-016-0295-8; Maksimovic V, Pavlovic-Popovic Z, Vukmirovic S, Cvejic J, Mooranian A, Al-Salami H, et al. Molecular mechanism of action and pharmacokinetic properties of methotrexate. Mol Biol Rep. 2020;47(6):4699–708. https://doi.org/10.1007/s11033-020-05481-9; Bezabeh S, Mackey AC, Kluetz P, Jappar D, Korvick J. Accumulating evidence for a drug–drug interaction between methotrexate and proton pump inhibitors. Oncologist. 2012;17(4):550–4. https://doi.org/10.1634/theoncologist.2011-0431; Inoue K, Yuasa H. Molecular basis for pharmacokinetics and pharmacodynamics of methotrexate in rheumatoid arthritis therapy. Drug Metab Pharmacokinet. 2014;29(1):12–9. https://doi.org/10.2133/dmpk.dmpk-13-rv-119; Seideman P, Beck O, Eksborg S, Wennberg M. The pharmacokinetics of methotrexate and its 7-hydroxy metabolite in patients with rheumatoid arthritis. Br J Clin Pharmacol. 1993;35(4):409–12. https://doi.org/10.1111/j.1365-2125.1993.tb04158.x; Lima A, Sousa H, Monteiro J, Azevedo R, Medeiros R, Seabra V. Genetic polymorphisms in low-dose methotrexate transporters: current relevance as methotrexate therapeutic outcome biomarkers. Pharmacogenomics. 2014;15(12):1611–35. https://doi.org/10.2217/pgs.14.116; Mikkelsen TS, Thorn CF, Yang JJ, Ulrich CM, French D, Zaza G, et al. PharmGKB summary: methotrexate pathway. Pharmacogenet Genomics. 2011;21(10):679–86. https://doi.org/10.1097/FPC.0b013e328343dd93; Валиев ТТ, Семенова ВВ, Иконникова АЮ, Петрова АА, Белышева ТС, Наседкина ТВ. Роль фармакогенетических факторов в развитии побочных эффектов метотрексата при лечении злокачественных опухолей. Современная онкология. 2021;23(4):622–7. https://doi.org/10.26442/18151434.2021.4.201127; Murakami T, Mori N. Involvement of multiple transporters-mediated transports in mizoribine and methotrexate pharmacokinetics. Pharmaceuticals (Basel). 2012;5(8):802–36. https://doi.org/10.3390/ph5080802; Chabner BA, Allegra CJ, Curt GA, Clendeninn NJ, Baram J, Koizumi S, et al. Polyglutamation of methotrexate. Is methotrexate a prodrug? J Clin Invest. 1985;76(3):907–12. https://doi.org/10.1172/JCI112088; Neuman MG, Cameron RG, Haber JA, Katz GG, Malkiewicz IM, Shear NH. Inducers of cytochrome P450 2E1 enhance methotrexate-induced hepatocytoxicity. Clin Biochem. 1999;32(7):519–36. https://doi.org/10.1016/s0009-9120(99)00052-1; Thyss A, Milano G, Kubar J, Namer M, Schneider M. Clinical and pharmacokinetic evidence of a life-threatening interaction between methotrexate and ketoprofen. Lancet. 1986;1(8475):256–8. https://doi.org/10.1016/s0140-6736(86)90786-5; Ушкалова ЕА, Зырянов СК, Бутранова ОИ, Самсонова КИ. Метамизол натрия: регуляторный статус в разных странах мира, проблемы безопасности и ошибки применения. Безопасность и риск фармакотерапии. 2022;10(4):396–410. https://doi.org/10.30895/2312-7821-2022-10-4-396-410; Nozaki Y, Kusuhara H, Kondo T, Iwaki M, Shiroyanagi Y, Nakayama H, et al. Species difference in the inhibitory effect of nonsteroidal anti-inflammatory drugs on the uptake of methotrexate by human kidney slices. J Pharmacol Exp Ther. 2007;322(3):1162–70. https://doi.org/10.1124/jpet.107.121491; Glynn-Barnhart AM, Erzurum SC, Leff JA, Martin RJ, Cochran JE, Cott GR, Szefler SJ. Effect of low-dose methotrexate on the disposition of glucocorticoids and theophylline. J Allergy Clin Immunol. 1991;88(2):180–6. https://doi.org/10.1016/0091-6749(91)90326-j; Okada M, Fujii H, Suga Y, Morito S, Okada M, Nishigami J, et al. Drug interaction between methotrexate and salazosulfapyridine in Japanese patients with rheumatoid arthritis. J Pharm Health Care Sci. 2017;3:7. https://doi.org/10.1186/s40780-017-0073-z; Ronchera CL, Hernández T, Peris JE, Torres F, Granero L, Jiménez NV, Plá JM. Pharmacokinetic interaction between high-dose methotrexate and amoxycillin. Ther Drug Monit. 1993;15(5):375–9. https://doi.org/10.1097/00007691-199310000-00004; Al-Quteimat OM, Al-Badaineh MA. Methotrexate and trimethoprim-sulphamethoxazole: extremely serious and life-threatening combination. J Clin Pharm Ther. 2013;38(3):203–5. https://doi.org/10.1111/jcpt.12060; Hamid M, Lashari B, Ahsan I, Micaily I, Sarwar U, Crocetti J. A deadly prescription: combination of methotrexate and trimethoprim-sulfamethoxazole. J Community Hosp Intern Med Perspect. 2018;8(3):149–51. https://doi.org/10.1080/20009666.2018.1466598; Haider L, Sharif S, Hasan A, McFarlane IM. Low-dose methotrexate toxicity in the setting of vancomycin-induced acute kidney injury. Am J Med Case Rep. 2020;8(7):206–9. PMID: 32775622; Reid T, Yuen A, Catolico M, Carlson RW. Impact of omeprazole on the plasma clearance of methotrexate. Cancer Chemother Pharmacol. 1993;33(1):82–4. https://doi.org/10.1007/BF00686028; Tröger U, Stötzel B, Martens-Lobenhoffer J, Gollnick H, Meyer FP. Drug points: severe myalgia from an interaction between treatments with pantoprazole and methotrexate. BMJ. 2002;324(7352):1497. https://doi.org/10.1136/bmj.324.7352.1497; Bannwarth B, Labat L, Moride Y, Schaeverbeke T. Methotrexate in rheumatoid arthritis. An update. Drugs. 1994;47(1):25–50. https://doi.org/10.2165/00003495-199447010-00003; Miller DR, Letendre PW, DeJong DJ, Fiechtner JJ. Methotrexate in rheumatoid arthritis: an update. Pharmacotherapy. 1986;6(4):170–8. https://doi.org/10.1002/j.1875-9114.1986.tb03472.x; Kawase A, Yamamoto T, Egashira S, Iwaki M. Stereoselective inhibition of methotrexate excretion by glucuronides of nonsteroidal anti-inflammatory drugs via multidrug resistance proteins 2 and 4. J Pharmacol Exp Ther. 2016;356(2):366–74. https://doi.org/10.1124/jpet.115.229104; Frenia ML, Long KS. Methotrexate and nonsteroidal antiinflammatory drug interactions. Ann Pharmacother. 1992;26(2):234–7. https://doi.org/10.1177/106002809202600219; van Roon EN, van de Laar MA. Methotrexate bioavailability. Clin Exp Rheumatol. 2010;28(5 Suppl 61):S27–32. PMID: 21044430; Grim J, Chládek J, Martínková J. Pharmacokinetics and pharmacodynamics of methotrexate in non-neoplastic diseases. Clin Pharmacokinet. 2003;42(2):139–51. https://doi.org/10.2165/00003088-200342020-00003; Wang W, Zhou H, Liu L. Side effects of methotrexate therapy for rheumatoid arthritis: a systematic review. Eur J Med Chem. 2018;158:502–16. https://doi.org/10.1016/j.ejmech.2018.09.027; Gremese E, Alivernini S, Tolusso B, Zeidler MP, Ferraccioli G. JAK inhibition by methotrexate (and csDMARDs) may explain clinical efficacy as monotherapy and combination therapy. J Leukoc Biol. 2019;106(5):1063–8. https://doi.org/10.1002/JLB.5RU0519-145R; Hasko G, Cronstein B. Regulation of inflammation by adenosine. Front Immunol. 2013;4:85. https://doi.org/10.3389/fimmu.2013.00085; Friedman B, Cronstein B. Methotrexate mechanism in treatment of rheumatoid arthritis. Joint Bone Spine. 2019;86(3):301–7. https://doi.org/10.1016/j.jbspin.2018.07.004; Thomas S, Fisher KH, Snowden JA, Danson SJ, Brown S, Zeidler MP. Methotrexate is a JAK/STAT pathway inhibitor. PLoS One. 2015;10(7):e0130078. https://doi.org/10.1371/journal.pone.0130078; Chinnaiya K, Lawson MA, Thomas S, Haider MT, Down J, Chantry AD, et al. Low-dose methotrexate in myeloproliferative neoplasm models. Haematologica. 2017;102(9):e336–e9. https://doi.org/10.3324/haematol.2017.165738; Solipuram V, Mohan A, Patel R, Ni R. Effect of Janus kinase inhibitors and methotrexate combination on malignancy in patients with rheumatoid arthritis: a systematic review and meta-analysis of randomized controlled trials. Auto Immun Highlights. 2021;12(1):8. https://doi.org/10.1186/s13317-021-00153-5; Panja S, Khatua DK, Halder M. Simultaneous binding of folic acid and methotrexate to human serum albumin: insights into the structural changes of protein and the location and competitive displacement of drugs. ACS Omega. 2018;3(1):246–53. https://doi.org/10.1021/acsomega.7b01437; Liu Y, Zhou S, Nissel J, Wu A, Lau H, Palmisano M. The pharmacokinetic effect of coadministration of apremilast and methotrexate in individuals with rheumatoid arthritis and psoriatic arthritis. Clin Pharmacol Drug Dev. 2014;3(6):456–65. https://doi.org/10.1002/cpdd.109; Tanaka Y, Suzuki M, Nakamura H, Toyoizumi S, Zwillich SH, Tofacitinib Study I. Phase II study of tofacitinib (CP-690,550) combined with methotrexate in patients with rheumatoid arthritis and an inadequate response to methotrexate. Arthritis Care Res (Hoboken). 2011;63(8):1150–8. https://doi.org/10.1002/acr.20494; Payne C, Zhang X, Shahri N, Williams W, Cannady E. AB0492 Evaluation of potential drug–drug interactions with baricitinib. Annals of the Rheumatic Diseases. 2015;74(Suppl 2):1063. https://doi.org/10.1136/annrheumdis-2015-eular.1627; Hazlewood GS, Barnabe C, Tomlinson G, Marshall D, Devoe DJ, Bombardier C. Methotrexate monotherapy and methotrexate combination therapy with traditional and biologic disease modifying anti-rheumatic drugs for rheumatoid arthritis: a network meta-analysis. Cochrane Database Syst Rev. 2016;2016(8):CD010227. https://doi.org/10.1002/14651858.CD010227.pub2; Xu Z, Davis HM, Zhou H. Clinical impact of concomitant immunomodulators on biologic therapy: pharmacokinetics, immunogenicity, efficacy and safety. J Clin Pharmacol. 2015;55 Suppl 3:S60–74. https://doi.org/10.1002/jcph.380; Schaeverbeke T, Truchetet ME, Kostine M, Barnetche T, Bannwarth B, Richez C. Immunogenicity of biologic agents in rheumatoid arthritis patients: lessons for clinical practice. Rheumatology (Oxford). 2016;55(2):210–20. https://doi.org/10.1093/rheumatology/kev277; Iwaki M, Shimada H, Irino Y, Take M, Egashira S. Inhibition of methotrexate uptake via organic anion transporters OAT1 and OAT3 by glucuronides of nonsteroidal anti-inflammatory drugs. Biol Pharm Bull. 2017;40(6):926–31. https://doi.org/10.1248/bpb.b16-00970; Tracy TS, Krohn K, Jones DR, Bradley JD, Hall SD, Brater DC. The effects of a salicylate, ibuprofen, and naproxen on the disposition of methotrexate in patients with rheumatoid arthritis. Eur J Clin Pharmacol. 1992;42(2):121–5. https://doi.org/10.1007/BF00278469; Stewart CF, Fleming RA, Arkin CR, Evans WE. Coadministration of naproxen and low-dose methotrexate in patients with rheumatoid arthritis. Clin Pharmacol Ther. 1990;47(4):540–6. https://doi.org/10.1038/clpt.1990.69; Skeith KJ, Russell AS, Jamali F, Coates J, Friedman H. Lack of significant interaction between low dose methotrexate and ibuprofen or flurbiprofen in patients with arthritis. J Rheumatol. 1990;17(8):1008–10. PMID: 2213774; Combe B, Edno L, Lafforgue P, Bologna C, Bernard JC, Acquaviva P, et al. Total and free methotrexate pharmacokinetics, with and without piroxicam, in rheumatoid arthritis patients. Br J Rheumatol. 1995;34(5):421–8. https://doi.org/10.1093/rheumatology/34.5.421; Hubner G, Sander O, Degner FL, Turck D, Rau R. Lack of pharmacokinetic interaction of meloxicam with methotrexate in patients with rheumatoid arthritis. J Rheumatol. 1997;24(5):845–51. PMID: 9150070; Iqbal MP, Baig JA, Ali AA, Niazi SK, Mehboobali N, Hussain MA. The effects of non-steroidal anti-inflammatory drugs on the disposition of methotrexate in patients with rheumatoid arthritis. Biopharm Drug Dispos. 1998;19(3):163–7. https://doi.org/10.1002/(sici)1099-081x(199804)19:33.0.co;2-l; Karim A, Tolbert DS, Hunt TL, Hubbard RC, Harper KM, Geis GS. Celecoxib, a specific COX-2 inhibitor, has no significant effect on methotrexate pharmacokine tics in patients with rheumatoid arthritis. J Rheumatol. 1999;26(12):2539–43. PMID: 10606360; Hartmann SN, Rordorf CM, Milosavljev S, Branson JM, Chales GH, Juvin RR, et al. Lumiracoxib does not affect methotrexate pharmacokinetics in rheumatoid arthritis patients. Ann Pharmacother. 2004;38(10):1582–7. https://doi.org/10.1345/aph.1E044; Schwartz JI, Agrawal NG, Wong PH, Miller J, Bachmann K, Marbury T, ey al. Examination of the effect of increasing doses of etoricoxib on oral methotrexate pharmacokinetics in patients with rheumatoid arthritis. J Clin Pharmacol. 2009;49(10):1202–9. https://doi.org/10.1177/0091270009338939; Каратеев АЕ, Ермакова ЮА, Березюк АН, Соловьева ЕС. Метотрексат и ингибиторы протонной помпы — имеется ли негативное фармакологическое взаимодействие? Научно-практическая ревматология. 2013;51(6):662–5. https://doi.org/10.14412/1995-4484-2013-662-5; Joerger M, Huitema AD, van den Bongard HJ, Baas P, Schornagel JH, Schellens JH, Beijnen JH. Determinants of the elimination of methotrexate and 7-hydroxy-methotrexate following high-dose infusional therapy to cancer patients. Br J Clin Pharmacol. 2006;62(1):71–80. https://doi.org/10.1111/j.1365-2125.2005.02513.x; Vakily M, Amer F, Kukulka MJ, Andhivarothai N. Coadministration of lansoprazole and naproxen does not affect the pharmacokinetic profile of methotrexate in adult patients with rheumatoid arthritis. J Clin Pharmacol. 2005;45(10):1179–86. https://doi.org/10.1177/0091270005280100; Shimada T, Nishimura Y, Funada Y, Takenaka K, Kobayashi K, Urata Y, et al. [A case of Pneumocystis carinii pneumonia associated with low dose methotrexate treatment for rheumatoid arthritis and trimethoprim-sulphamethoxazole induced pancytopenia]. Arerugi. 2004;53(6):575–81. PMID: 15247519; Blum R, Seymour JF, Toner G. Significant impairment of high-dose methotrexate clearance following vancomycin administration in the absence of overt renal impairment. Ann Oncol. 2002;13(2):327–30. https://doi.org/10.1093/annonc/mdf021; Tobon GJ, Canas C, Jaller JJ, Restrepo JC, Anaya JM. Serious liver disease induced by infliximab. Clin Rheumatol. 2007;26(4):578–81. https://doi.org/10.1007/s10067-005-0169-y; Garces S, Demengeot J, Benito-Garcia E. The immunogenicity of anti-TNF therapy in immune-mediated inflammatory diseases: a systematic review of the literature with a meta-analysis. Ann Rheum Dis. 2013;72(12):1947–55. https://doi.org/10.1136/annrheumdis-2012-202220; Cohen S, Zwillich SH, Chow V, Labadie RR, Wilkinson B. Co-administration of the JAK inhibitor CP-690,550 and methotrexate is well tolerated in patients with rheumatoid arthritis without need for dose adjustment. Br J Clin Pharmacol. 2010;69(2):143–51. https://doi.org/10.1111/j.1365-2125.2009.03570.x; Zhu T, Moy S, Valluri U, Cao Y, Zhang W, Sawamoto T, et al. Investigation of potential drug–drug interactions between peficitinib (ASP015K) and methotrexate in patients with rheumatoid arthritis. Clin Drug Investig. 2020;40(9):827–38. https://doi.org/10.1007/s40261-020-00937-z; Gnjidic D, Le Couteur DG, Hilmer SN. Discontinuing drug treatments. BMJ. 2014;349:g7013. https://doi.org/10.1136/bmj.g7013; Akkara Veetil BM, Bongartz T. Perioperative care for patients with rheumatic diseases. Nat Rev Rheumatol. 2011;8(1):32–41. https://doi.org/10.1038/nrrheum.2011.171; Park JK, Kim MJ, Choi Y, Winthrop K, Song YW, Lee EB. Effect of short-term methotrexate discontinuation on rheumatoid arthritis disease activity: post-hoc analysis of two randomized trials. Clin Rheumatol. 2020;39(2):375–9. https://doi.org/10.1007/s10067-019-04857-y; Lee J, Singh N, Gray SL, Makris UE. Optimizing medication use in older adults with rheumatic musculoskeletal diseases: deprescribing as an approach when less may be more. ACR Open Rheumatol. 2022;4(12):1031–41. https://doi.org/10.1002/acr2.11503; Сычев ДА, Остроумова ОД, Переверзев АП, Кочетков АИ, Остроумова ТМ, Клепикова МВ, Эбзеева ЕЮ. Пожилой и старческий возраст пациентов как фактор риска развития лекарственно-индуцированных заболеваний. Безопасность и риск фармакотерапии. 2021;9(1):15–24. https://doi.org/10.30895/2312-7821-2021-9-1-15-24; Garfinkel D, Mangin D. Feasibility study of a systematic approach for discontinuation of multiple medications in older adults: addressing polypharmacy. Arch Inter Med. 2010;170(18): 1648–54. https://doi.org/10.1001/archinternmed.2010.355; Park JK, Lee MA, Lee EY, Song YW, Choi Y, Winthrop KL, Lee EB. Effect of methotrexate discontinuation on efficacy of seasonal influenza vaccination in patients with rheumatoid arthritis: a randomised clinical trial. Ann Rheum Dis. 2017;76(9):1559–65. https://doi.org/10.1136/annrheumdis-2017-211128; Гриднева ГИ, Муравьев ЮВ, Лучихина ЕЛ, Демидова НВ, Каратеев ДЕ. Вопросы оптимизации терапии метотрексатом у больных ревматоидным артритом. Научно-практическая ревматология. 2017;55(1):41–7. https://doi.org/10.14412/1995-4484-2017-41-47; Hu Q, Wang H, Xu T. Predicting hepatotoxicity associated with low-dose methotrexate using machine learning. J Clin Med. 2023;12(4):1599. https://doi.org/10.3390/jcm12041599; Samal L, Khasnabish S, Foskett C, Zigmont K, Faxvaag A, Chang F, et al. Comparison of a voluntary safety reporting system to a global trigger tool for identifying adverse events in an oncology population. J Patient Saf. 2022;18(6):611–6. https://doi.org/10.1097/PTS.0000000000001050; https://www.risksafety.ru/jour/article/view/416 |
DOI: | 10.30895/2312-7821-2024-416 |
الاتاحة: | https://www.risksafety.ru/jour/article/view/416 https://doi.org/10.30895/2312-7821-2024-416 |
Rights: | Authors who have their articles published in this journal agree to the following terms:Authors retain copyright for their work and grant the journal with the right of first publication under Creative Commons Attribution Licensethat allows others to pass on the work provided they include references to the authors and the original publication.Authors retain the right to enter into non-exclusive distribution arrangements allowing the distribution of the original publication (e.g., adding it to an institutional repository or publishing it in a book), provided all the necessary references are included.Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their personal websites) prior to and during the submission process, as it can lead to a productive discussion and higher citation rates (See The Effect of Open Access). ; Авторы, публикующие статьи в данном журнале, соглашаются со следующим:Авторы сохраняют за собой авторские права на работу и предоставляют журналу право первой публикации работы на условиях лицензии Creative Commons Attribution License, которая позволяет другим распространять данную работу с обязательным сохранением ссылок на авторов оригинальной работы и оригинальную публикацию в этом журнале.Авторы имеют право размещать препринты и постпринты своих работ, а также исследовательские данные из них в институтском хранилище или публичных репозиториях, согласно политике журнала. |
رقم الانضمام: | edsbas.FE7CA3AD |
قاعدة البيانات: | BASE |
DOI: | 10.30895/2312-7821-2024-416 |
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