Menshikova IV. Hyaluronic acid in the treatment of osteoarthritis: innovations in injection therapy. A review. Terapevticheskii Arkhiv (Ter. Arkh.). 2024;96(8):820–825. DOI: 10.26442/00403660.2024.08.202916
Гиалуроновая кислота в лечении остеоартрита: инновации в инъекционной терапии
Меньшикова И.В. Гиалуроновая кислота в лечении остеоартрита: инновации в инъекционной терапии. Терапевтический архив. 2024;96(8):820–825. DOI: 10.26442/00403660.2024.08.202916
Menshikova IV. Hyaluronic acid in the treatment of osteoarthritis: innovations in injection therapy. A review. Terapevticheskii Arkhiv (Ter. Arkh.). 2024;96(8):820–825. DOI: 10.26442/00403660.2024.08.202916
В обзоре кратко представлено современное понимание гетерогенности остеоартрита (ОА), в основе которой лежат патофизиологические особенности различных его вариантов. Эти различия отражены в концепции фенотипов и эндотипов ОА. В клинических рекомендациях по лечению ОА сделан акцент на место препаратов гиалуроновой кислоты, подробно изучены механизмы действия гиалуроната натрия с различной молекулярной массой. Приведены результаты исследований российских и зарубежных авторов по эффективности и безопасности применения разных форм этих препаратов. Персонализированная терапия пациентов с разными фенотипами ОА показана на примере линейки препаратов Флексотрон.
The review briefly presents modern understanding heterogeneity of osteoarthritis (OA) which is based on pathophysiological features of its variants. The concept of the phenotypes and endotypes of OA reflects these differences. In clinical recommendations description the emphasis on the place of hyaluronic acid is made. The mechanisms of action of sodium hyaluronate with different molecular mass are studied in detail. The results of foreign and Russian studies on efficacy and safety of different forms of hyaluronic acid are given. Personalized treatment of patients with different phenotypes of OA is shown by an example of a line of Flexotron series.
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26. Yasuda T. Hyaluronan inhibits prostaglandin E2 production via CD44 in U937 human macrophages. Tohoku J Exp Med. 2010;220(3):229-35. DOI:10.1620/tjem.220.229
27. Sasaki A, Sasaki K, Konttinen YT, et al. Hyaluronate inhibits the interleukin-1beta-induced expression of matrix metalloproteinase (MMP)-1 and MMP-3 in human synovial cells. Tohoku J Exp Med. 2004;204(2):99-107. DOI:10.1620/tjem.204.99
28. Altman RD, Manjoo A, Fierlinger A, et al. The mechanism of action for hyaluronic acid treatment in the osteoarthritic knee: a systematic review. DMC Musculoskelt Disord. 2015;16:321.
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2024;20(10):12-6 (in Russian)]. DOI:10.33978/2307-3586-2024-20-10-12-16
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________________________________________________
1. Rossiiskie klinicheskie rekomendatsii. Revmatologiia. Pod red. EL Nasonova. Moscow: GEOTAR-Media, 2020 (in Russian).
2. Loeser EF, Goldring SR, Scanzello CR. Osteoarthritis: a disease of the joint as an organ. Arthritis Rheum. 2012;64(6):1697-707.
3. Sharma I. Osteoarthritis of the knee. N Engl J Med. 2021;384(1):51-9.
4. Zhang W, Doherty M, Peat G, et al. EULAR evidence-based recommendations for the diagnosis of knee osteoarthritis. Ann Rheum Dis. 2010;69(3):483-9. DOI:10.1136/ard.2009.113100
5. McAlindon TE, Bannuru RR, Sullivan MC, et al. OARSI guidelines for the non-surgical management of knee osteoarthritis. Osteoarthritis Cartilage.
2014;22(3):363-88. DOI:10.1016/j.joca.2014.01.003
6. Waarsing JH, Bierma-Zeinstra SM, Weinana H. Distinct subtypes of knee osteoarthritis: data from the osteoarthritis initiative. Rheumatology (Oxford). 2015;54(9):1650-8.
7. Dell’Isola A, Allan R, Smith SL, et al. Identification of clinical phenotypes in knee osteoarthritis: a systematic review of the literature. BMC Musculoskelet Disord. 2016;17(1):425. DOI:10.1186/s12891-016-1286-2
8. Dell’Isola A, Steultjens M. Classification of patients with knee osteoarthritis in clinical phenotypes: data from the osteoarthritis initiative. PLoS One. 2018;13(1):e0191045. DOI:10.1371/journal.pone.0191045.eCollection 2018
9. Jameson JL, Longo DL. Precision medicine – personalized, problematic and promising. N Engl J Med. 2015;372(23):229-34.
10. Oo WM, Little C, Duong V, Hunter DJ. The development of disease-modifying therapies for osteoarthritis (DMOADs): the evidence to date. Drug Des Devel Ther. 2021;15:2921-45.
11. Im GI, Moon JY. Emerging Concepts of Endotypes/Phenotypes in Pegenerative Medicine for Osteoarthritis. Tissue Eng Regen Med. 2022;19(2):321-24.
12. Mobasheri A, Rayman MP, Gualillo O, et al. The role of metabolism in the pathogenesis of osteoarthritis. Nat Rev Rheumatol. 2017;13:302-11.
13. Karsdal MA, Christiansen C, Ladel C, et al. Osteoarthritis – a case for personalized health care? Osteoarthritis Cartilage. 2014;22(1):7-16.
14. Herreo-Beaumont G, Roman-Bias JA, Bruyere O, et al. Clinical settings in knee osteoarthritis: Pathphysiology guides treatment. Maturitas. 2017;96:54-7.
15. Lila AM, Alekseeva LI, Taskina EA. Modern approaches to osteoarthritis therapy taking into account updated international guidelines. RMJ. Medical Review. 2019;11(11-2):48-5 (in Russian).
16. Arden NK, Perry TA, Bannuri RR, et al. Non-surgical management of knee osteoarthritis: comparison of ESCEO and OARSI 2019 guidelines. Nat Rev Rhematol. 2021;17(1):59-66. DOI:10.1038/s41584-020-00523-9
17. Kroon FPB, Carmona I, Schoones JW, Kloppenburg M. Efficacy and safety of non-pharmacological, pharmacological and surgical treatment for hand osteoarthritis: a systematic literature review informing the 2018 update of the EULAR recommendationsfor the management of hand osteoarthritis. RMD Open. 2018;4(2):e000734.
DOI:10.1136/rmdopen-2018-000734
18. Karateev DE, Luchikhina LV, Luchikhina EL, Golukhov G.N. Current Management Strategy for Osteoarthritis Patients: a Review. Bulletin of Rehabilitation Medicine. 2022;21(6):30-41 (in Russian). DOI:10.38025/2078-1962-2022-21-6-30-41
19. Park D, Park YM, Ko SH, et al. Association between knee osteoarthritis and the risk of cardiovascular disease and synergistic adverse effects of lack of exercise. Sci Rep. 2023;13(1):2777.
20. Chichasova NV. Modern approaches to the treatment of osteoarthritis. Meditsinskiy sovet = Medical Council. 2020;(4):126-35 (in Russian). DOI:10.21518/2079-701X-2020-4-126-135
21. Fransen M, Agaliotis M, Nairn L, et al. Glucosamine and chondroitin for knee placebo-controlled clinical trial evaluating osteoarthritis: a double-blind randomised single and combination regimens. Ann Rheum Dis. 2015;74(5):851-8. DOI:10.1136/annrheumdis-2013-203954
22. Lila AM, Mazurov VI, Martynov AI, et al. Resolution of the consensus of the Russian Federation experts on the diagnosis and treatment of osteoarthritis, 2022. Sovremennaya Revmatologiya=Modern Rheumatology Journal. 2022;16(6):106-16 (in Russian). DOI:10.14412/1996-7012-2022-6-106-116
23. Bruyere O, Honvo G, Veronese N, et al. An updated algorithm recommendation for the management of knee osteoarthritis from the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO). Semin Arthritis Rheum. 2019;49(3):337-50.
24. Garatziotis S, Savani RC. Hyaluronan biology: a complex balancing act of structure, function, location and context. Matrix Biol. 2019;78-79:1-10. DOI:10.1016/j.matbio.2019.02.002
25. Wang C-T, Lin Y-T, Chiang B-L, et al. High molecular weight hyaluronic acid down-regulates the gene expression of osteoarthritis-associated cytokines and enzymes in fibroblast-like synoviocytes from patients with early osteoarthritis. Osteoarthr Cartilage. 2006;14(12):1237-47. DOI:10.1016/j.joca.2006.05.009
26. Yasuda T. Hyaluronan inhibits prostaglandin E2 production via CD44 in U937 human macrophages. Tohoku J Exp Med. 2010;220(3):229-35. DOI:10.1620/tjem.220.229
27. Sasaki A, Sasaki K, Konttinen YT, et al. Hyaluronate inhibits the interleukin-1beta-induced expression of matrix metalloproteinase (MMP)-1 and MMP-3 in human synovial cells. Tohoku J Exp Med. 2004;204(2):99-107. DOI:10.1620/tjem.204.99
28. Altman RD, Manjoo A, Fierlinger A, et al. The mechanism of action for hyaluronic acid treatment in the osteoarthritic knee: a systematic review. DMC Musculoskelt Disord. 2015;16:321.
29. Gotoh S, Onaya J, Abe M, et al. Effects of the molecular weight of hyaluronic acid and its action mechanisms on experimental joint pain in rats. Ann Rheum Dis. 1993;52(11):817-22. DOI:10.1136/ard.52.11.817
30. Ghosh P, Guidolin D. Potential mechanism of action of intra-articular hyaluronan therapy in osteoarthritis: are the effects molecular weight dependent? Semin Arthritis Rheum. 2002;32(1):10-37.
31. Bannuri RR, Vaysbrot EE, Sullivan MC, McAlindon TE. Relative efficacy of hyaluronic acid in comparison with NSAIDs for knee osteoarthritis: a systematic review and meta-analysis. Semin Arthritis Rheum. 2013;43(5):593-99. DOI:10.1016/j.semarthrit.2013.10.002
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Авторы
И.В. Меньшикова*
ФГАОУ ВО «Первый Московский государственный медицинский университет им. И.М. Сеченова» Минздрава России (Сеченовский Университет), Москва, Россия
*ivmenshikova@mail.ru
________________________________________________
Irina V. Menshikova*
Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia
*ivmenshikova@mail.ru