Перспективы применения новых антидиабетических препаратов в ревматологии
https://doi.org/10.47360/1995-4484-2026-315-334
Аннотация
В спектре коморбидной патологии при ревматических и мышечно-скелетных заболеваниях (РМЗ) особое внимание привлекают метаболические нарушения, в первую очередь ожирение, ассоциирующееся с увеличением в популяции риска развития аутоиммунных заболеваний, в том числе РМЗ. В ревматологии проблема применения антидиабетических препаратов, снижающих риск развития ожирения, рассматривается не только с точки зрения лечения сахарного диабета 2-го типа, но и как более широкая проблема, связанная с перспективами репозиционирования как стратегии поиска новых медицинских показаний для уже существующих, разрешенных к применению или исследованных препаратов, что особенно актуально для гармонизации терапии комплексных РМЗ. В последние годы для лечения сахарного диабета 2-го типа и его осложнений разработаны новые классы препаратов – агонисты рецепторов глюкагоноподобного пептида 1-го типа (арГПП-1) и ингибиторы натрий-глюкозного котранспортера 2 (иНГЛТ-2; глифлозины).
Наряду с классическими антидиабетическими эффектами, арГПП-1 и иНГЛТ-2 обладают широким спектром антивоспалительных и иммуномодулирующих механизмов действия, которые могут потенциировать эффективность противоспалительной терапии РМЗ и сдерживать развитие коморбидной патологии. В статье обсуждаются данные, касающиеся механизмов антивоспалительной активности антидиабетических препаратов и их эффективности при РМЗ. Для того чтобы определить истинное место этих препаратов в отношении персонификации терапии РМЗ, в первую очередь снижения риска различных коморбидной патологии, необходимы дальнейшие исследования, направленные на прямое сравнение эффективности препаратов при различных клинических сценариях.
Ключевые слова
Об авторах
Е. Л. НасоновРоссия
Насонов Евгений Львович
115522, Москва, Каширское шоссе, 34а; 117997, Москва, ул. Островитянова, 1
Конфликт интересов:
Все авторы заявляют об отсутствии потенциального конфликта интересов, требующего раскрытия, в данной статье
М. В. Шестакова
Россия
117036, Москва, ул. Дмитрия Ульянова, 11;119192, Москва, Ломоносовский просп., 27, корп. 1
Конфликт интересов:
Все авторы заявляют об отсутствии потенциального конфликта интересов, требующего раскрытия, в данной статье
Л. В. Кондратьева
Россия
115522, Москва, Каширское шоссе, 34а
Конфликт интересов:
Все авторы заявляют об отсутствии потенциального конфликта интересов, требующего раскрытия, в данной статье
М. С. Елисеев
Россия
115522, Москва, Каширское шоссе, 34а
Конфликт интересов:
Все авторы заявляют об отсутствии потенциального конфликта интересов, требующего раскрытия, в данной статье
Список литературы
1. van der Heijde D, Daikh DI, Betteridge N, Burmester GR, Hassett AL, Matteson EL, et al. Common language description of the term rheumatic and musculoskeletal diseases (RMDs) for use in communication with the lay public, healthcare providers and other stakeholders endorsed by the European League Against Rheumatism (EULAR) and the American College of Rheumatology (ACR). Ann Rheum Dis. 2018;77(6):829-832. doi: 10.1136/annrheumdis-2017-212565
2. Abend AH, He I, Bahroos N, Christianakis S, Crew AB, Wise LM, et al. Estimation of prevalence of autoimmune diseases in the United States using electronic health record data. J Clin Invest. 2024;135(4):e178722. doi: 10.1172/JCI178722
3. Conrad N, Misra S, Verbakel JY, Verbeke G, Molenberghs G, Taylor PN, et al. Incidence, prevalence, and co-occurrence of autoimmune disorders over time and by age, sex, and socioeconomic status: A population-based cohort study of 22 million individuals in the UK. Lancet. 2023;401(10391):1878-1890. doi: 10.1016/S0140-6736(23)00457-9
4. Насонов ЕЛ. Достижения фармакотерапии иммуновоспалительных ревматических заболеваний в XXI веке. Терапевтический архив. 2025;97(5):401-411. doi: 10.26442/00403660.2025.05.203213
5. Burmester GR, Pope JE. Novel treatment strategies in rheumatoid arthritis. Lancet. 2017;389(10086):2338-2348. doi: 10.1016/S01406736(17)31491-5
6. Li M, Wu C, Yin P, Qian J, Zhao J, Wang Q, et al. Mortalityrelated health metrics in systemic autoimmune diseases: An epidemiological analysis of a nationwide register-based cohort. Sci Bull (Beijing). 2025;70(4):492-495. doi: 10.1016/j.scib.2024.12.021
7. Kolasinski SL, Neogi T, Hochberg MC, Oatis C, Guyatt G, Block J, et al. 2019 American College of Rheumatology/Arthritis Foundation guideline for the management of osteoarthritis of the hand, hip, and knee. Arthritis Care Res (Hoboken). 2020;72(2):149-162. doi: 10.1002/acr.24131
8. Brooks RT, England BR, Kronzer VL, Crowson CS. The evolving comorbidity landscape of rheumatoid arthritis. Nat Rev Rheumatol. 2026;22(7):447-458. doi: 10.1038/s41584-026-01386-2
9. Yu CY, Kuo CF, Chou IJ, Chen JS, Lu HY, Wu CY, et al. Comorbidities of systemic lupus erythematosus prior to and following diagnosis in different age-at-onset groups. Lupus. 2022;31(8):963-973. doi: 10.1177/09612033221100908
10. Hässler S, Lorenzon R, Binvignat M, Ribet C, Roux A, Johanet C, et al. Clinical correlates of lifetime and current comorbidity patterns in autoimmune and inflammatory diseases. J Autoimmun. 2024;149:103318. doi: 10.1016/j.jaut.2024.103318
11. Jalali-Najafabadi F, Bailey R, Lyons J, Akbari A, Ba Dhafari T, Azadbakht N, et al. 10-year multimorbidity patterns among people with and without rheumatic and musculoskeletal diseases: An observational cohort study using linked electronic health records from Wales, UK. BMJ Open. 2024;14(6):e079169. doi: 10.1136/bmjopen-2023-079169
12. Porsch F, Binder CJ. Autoimmune diseases and atherosclerotic cardiovascular disease. Nat Rev Cardiol. 2024;21(11):780-807. doi: 10.1038/s41569-024-01045-7
13. van de Vyver M. Immunology of chronic low-grade inflammation: Relationship with metabolic function. J Endocrinol. 2023;257(1):e220271. doi: 10.1530/JOE-22-0271
14. Huang S, Chen J, Zhang H, Wu W, Xue S, Zhu Z, et al. Inflammatory mechanisms underlying metabolic syndrome-associated and potential treatments. Osteoarthr Cartil Open. 2025;7(2):100614. doi: 10.1016/j.ocarto.2025.100614
15. Lin L, Shan Y, Lei F, Zhang J, Zhang L, Zhang XJ, et al. Cardiovascular health, genetic susceptibility, and the risk of incident autoimmune disorders in the UK Biobank: A prospective cohort study. J Am Heart Assoc. 2025;14(10):e039451. doi: 10.1161/jAHA.124.039451
16. Spatocco I, Mele G, De Rosa G, Fusco C, Ruggiero K, Pellegrini V, et al. Obesity as a risk factor for autoimmune diseases: A systematic review and meta-analysis. Obesity (Silver Spring). 2026;34(1):36-50. doi: 10.1002/oby.70044
17. Nikiphorou E, Fragoulis GE. Inflammation, obesity and rheumatic disease: Common mechanistic links. A narrative review. Ther Adv Musculoskelet Dis. 2018;10(8):157-167. doi: 10.1177/1759720X18783894
18. Turner L, Wanasinghe AI, Brunori P, Santosa S. Is adipose tissue inflammation the culprit of obesity-associated comorbidities? Obes Rev. 2025;26(11):e13956. doi: 10.1111/obr.13956
19. Schleh MW, Caslin HL, Garcia JN, Mashayekhi M, Srivastava G, Bradley AB, et al. Metaflammation in obesity and its therapeutic targeting. Sci Transl Med. 2023;15(723):eadf9382. doi: 10.1126/scitranslmed.adf9382
20. Matarese G. The link between obesity and autoimmunity. Science. 2023;379(6639):1298-1300. doi: 10.1126/science.ade0113
21. Alonso-Pérez A, Guillán-Fresco M, López-Fagúndez M, PazosPérez A, Crespo-Golmar A, Piñeiro-Ramil M, et al. Effect and regulation of obesity-associated low-grade chronic inflammation in major rheumatic diseases. Rheumato. 2022;2(4):114-125. doi: 10.3390/rheumato2040016
22. Blüher M. An overview of obesity-related complications: The epidemiological evidence linking body weight and other markers of obesity to adverse health outcomes. Diabetes Obes Metab. 2025;27(Suppl 2):3-19. doi: 10.1111/dom.16263
23. Castrejón I, Shakoor N, Block J, Pincus T. AB1132 Higher rates of obesity and associations with poorer clinical status in patients with RA, OA and SLE: A cross-sectional study from routine care. Ann Rheum Dis. 2017;76:1451-1451. doi: 10.1136/annrheumdis2017-eular.3812
24. Ogdie A, Eder L. The need for strategies to address obesity and psoriatic arthritis prevention in psoriasis. Br J Dermatol. 2020;182(3):523-524. doi: 10.1111/bjd.18595
25. Corrado A, Guadagni I, Picarelli G, Variola A. Obesity and chronic inflammation: Implications for rheumatoid arthritis, spondyloarthritis, and ulcerative colitis. Immun Inflamm Dis. 2025;13(1):e70080. doi: 10.1002/iid3.70080
26. Sattar N, Sattar LJ, McInnes IB, Siebert S, Ferguson LD. Obesity substantially impacts rheumatic and musculoskeletal diseases: Time to act. Ann Rheum Dis. 2025;84(6):894-898. doi: 10.1016/j.ard.2025.02.013
27. Bray GA, Heisel WE, Afshin A, Jensen MD, Dietz WH, Long M, et al. The science of obesity management: An Endocrine Society scientific statement. Endocr Rev. 2018;39(2):79-132. doi: 10.1210/ er.2017-00253
28. Kloock S, Ziegler CG, Dischinger U. Obesity and its comorbidities, current treatment options and future perspectives: Challenging bariatric surgery? Pharmacol Ther. 2023;251:108549. doi: 10.1016/j.pharmthera.2023.108549
29. Galindo RJ, Trujillo JM, Low Wang CC, McCoy RG. Advances in the management of type 2 diabetes in adults. BMJ Med. 2023;2(1):e000372. doi: 10.1136/bmjmed-2022-000372
30. Drucker DJ. GLP-1 physiology informs the pharmacotherapy of obesity. Mol Metab. 2022;57:101351. doi: 10.1016/j.molmet.2021.101351
31. Nauck MA, Tuttle KR, Tschöp MH, Blüher M. Glucagon-like receptor agonists and next-generation incretin-based medications: Metabolic, cardiovascular, and renal benefits. Lancet. 2026; 407(10531):892-908. doi: 10.1016/S0140-6736(25)02105-1
32. Patel S, Niazi SK. Emerging frontiers in GLP-1 therapeutics: A comprehensive evidence base. Pharmaceutics. 2025;17(8):1036. doi: 10.3390/pharmaceutics17081036
33. Kong F, Zhao Y, Zhang W, Wang X, Wu T, Zhou Z, et al. Comprehensive evaluation of GLP-1 receptor agonists: An umbrella review of clinical outcomes across multiple diseases. Nat Commun. 2026;17(1):972. doi: 10.1038/s41467-025-67701-9
34. Dharia A, Khan A, Sridhar VS, Cherney DZI. SGLT2 inhibitors: The sweet success for kidneys. Annu Rev Med. 2023;74:369-384. doi: 10.1146/annurev-med-042921-102135
35. Stielow M, Fijałkowski Ł, Alaburda A, Grześk G, Grześk E, Nowaczyk J, et al. SGLT2 inhibitors: From molecular mechanisms to clinical outcomes in cardiology and diabetology. Molecules. 2025;30(15):3112. doi: 10.3390/molecules30153112
36. Kingsmore KM, Grammer AC, Lipsky PE. Drug repurposing to improve treatment of rheumatic autoimmune inflammatory diseases. Nat Rev Rheumatol. 2020;16(1):32-52. doi: 10.1038/s41584019-0337-0
37. Hogan AE, Davis C, Jenkins BJ, Jones N, O’Shea D. Repurposing metabolic drugs as anti-inflammatory agents. Trends Endocrinol Metab. 2026;37(4):313-327. doi: 10.1016/j.tem.2025.07.003
38. Kyriazi N, Vassilakis KD, Bakiri A, Iliopoulos A, Fragoulis GE. Antiobesity medications in rheumatology. Quo vadis? Ann Rheum Dis. 2026;85(3):412-416. doi: 10.1016/j.ard.2025.08.013
39. Karacabeyli D, Lacaille D. Cardioprotective mechanisms and effects of glucagon-like peptide-1 receptor agonists in autoimmune rheumatic diseases. Rheumatology (Oxford). 2026;65(4):keag147. doi: 10.1093/rheumatology/keag147
40. Karacabeyli D, Lacaille D. Glucagon-like peptide-1 receptor agonists in arthritis: Current insights and future directions. Nat Rev Rheumatol. 2025;21(11):671-683. doi: 10.1038/s41584-02501302-0
41. Bilgin E, Venerito V, Bogdanos DP. Glucagon-like peptide-1 (GLP-1) receptor agonists in rheumatology: A review of current evidence and future directions. Autoimmun Rev. 2025;24(9):103864. doi: 10.1016/j.autrev.2025.103864
42. Karpouzas GA, Husni ME. Cardiovascular comorbidities in inflammatory rheumatic diseases. Rheum Dis Clin North Am. 2023;49(1):xv-xvi. doi: 10.1016/j.rdc.2022.09.001
43. Jogani VG, Mohamed Elfadil O, Edakkanambeth Varayil J, Mundi MS. Exploring the role of glucagon-like peptide-1 receptor agonists in critical illness: Mechanisms, benefits, and clinical implications. Curr Opin Crit Care. 2025;31(4):370-378. doi: 10.1097/MCC.0000000000001294
44. Насонов ЕЛ, Лысенко МА, Мутовина ЗЮ, Загребнева АИ, Николаева ЕВ, Ананьева ЛП, и др. Перспективы терапии системных аутоиммунных ревматических заболеваний. Что необходимо знать врачам отделений интенсивной терапии. Научно-практическая ревматология. 2026;64(2):109-125. doi: 10.47360/1995-4484-2026-109-125
45. Mehdi SF, Pusapati S, Anwar MS, Lohana D, Kumar P, Nandula SA, et al. Glucagon-like peptide-1: A multi-faceted anti-inflammatory agent. Front Immunol. 2023;14:1148209. doi: 10.3389/fimmu.2023.1148209
46. Chen J, Mei A, Wei Y, Li C, Qian H, Min X, et al. GLP-1 receptor agonist as a modulator of innate immunity. Front Immunol. 2022;13:997578. doi: 10.3389/fimmu.2022.997578
47. Bendotti G, Montefusco L, Lunati ME, Usuelli V, Pastore I, Lazzaroni E, et al. The anti-inflammatory and immunological properties of GLP-1 receptor agonists. Pharmacol Res. 2022;182:106320. doi: 10.1016/j.phrs.2022.106320
48. Quintana L, Tabaza N, Kurt B, Kahles F. Anti-inflammatory effects of GLP1-RA drugs. J Clin Endocrinol Metab. 2026:dgag218. doi: 101210/clinem/dgag218
49. Wong CK, Drucker DJ. Antiinflammatory actions of glucagon-like peptide-1-based therapies beyond metabolic benefits. J Clin Invest. 2025;135(21):e194751. doi: 10.1172/JCI194751
50. Drucker DJ. The benefits of GLP-1 drugs beyond obesity. Science. 2024;385(6706):258-260. doi: 10.1126/science.adn4128
51. Ullah A, Shen B. Immunomodulatory effects of anti-diabetic therapies: Cytokine and chemokine modulation by metformin, sodium-glucose cotransporter 2 inhibitors, and glucagon-like peptide-1 receptor agonists (2013–2025). Eur J Med Chem. 2025;299:118065. doi: 10.1016/j.ejmech.2025.118065
52. Feijóo-Bandín S, Aragón-Herrera A, Otero-Santiago M, AnidoVarela L, Moraña-Fernández S, Tarazón E, et al. Role of sodiumglucose co-transporter 2 inhibitors in the regulation of inflammatory processes in animal models. Int J Mol Sci. 2022;23(10):5634. doi: 10.3390/ijms23105634
53. Shu B, Chen X, Liu Z, Tang H, Yang B, Fu C. Pleiotropic effects of SGLT2 inhibitors: A focus on macrophage-mediated action. Pharmacol Res. 2025;222:108046. doi: 10.1016/j.phrs.2025.108046
54. Ansari S, Khoo B, Tan T. Targeting the incretin system in obesity and type 2 diabetes mellitus. Nat Rev Endocrinol. 2024;20(8):447-459. doi: 10.1038/s41574-024-00979-9
55. Wong CK, McLean BA, Baggio LL, Koehler JA, Hammoud R, Rittig N, et al. Central glucagon-like peptide 1 receptor activation inhibits Toll-like receptor agonist-induced inflammation. Cell Metab. 2024;36(1):130-143.e5. doi: 10.1016/j.cmet.2023.11.009
56. Zaiss MM, Joyce Wu HJ, Mauro D, Schett G, Ciccia F. The gutjoint axis in rheumatoid arthritis. Nat Rev Rheumatol. 2021;17(4):224-237. doi: 10.1038/s41584-021-00585-3
57. Gong B, Li C, Shi Z, Wang F, Dai R, Chen G, et al. GLP-1 receptor agonists: Exploration of transformation from metabolic regulation to multi-organ therapy. Front Pharmacol. 2025;16:1675552. doi: 10.3389/fphar.2025.1675552
58. Quodling N, Carrick FR, Hoffman N, Jemni M. The potential indirect impact of GLP-1 receptor agonists in the management of fibromyalgia. J. Clin. Med. 2026;15:3330 doi: 10.20944/preprints202603.0756.v1
59. Kim JA, Yoo HJ. Exploring the side effects of GLP-1 receptor agonist: To ensure its optimal positioning. Diabetes Metab J. 2025;49(4):525-541. doi: 10.4093/dmj.2025.0242
60. Vallon V. State-of-the-art-review: Mechanisms of action of SGLT2 inhibitors and clinical implications. Am J Hypertens. 2024;37(11):841-852. doi: 10.1093/ajh/hpae092
61. Abdollahi E, Keyhanfar F, Delbandi AA, Falak R, Hajimiresmaiel SJ, Shafiei M. Dapagliflozin exerts anti-inflammatory effects via inhibition of LPS-induced TLR-4 overexpression and NF-κB activation in human endothelial cells and differentiated macrophages. Eur J Pharmacol. 2022;918:174715. doi: 10.1016/j.ejphar.2021.174715
62. Jenkins BJ, Blagih J, Ponce-Garcia FM, Canavan M, Gudgeon N, Eastham S, et al. Canagliflozin impairs T cell effector function via metabolic suppression in autoimmunity. Cell Metab. 2023;35(7):1132-1146.e9. doi: 10.1016/j.cmet.2023.05.001
63. O’Hara DV, Jardine MJ. A review of the safety of sodium-glucose co-transporter-2 inhibitors. Diabetes Obes Metab. 2025;27(7):35983606. doi: 10.1111/dom.16385
64. To D, Bradshaw S, Lipson J. Case report of empagliflozin-induced cutaneous polyarteritis nodosa. J Cutan Med Surg. 2018;22(5):516-518. doi: 10.1177/1203475418760457
65. Stella M, Biassoni E, Fiorillo C, Grandis M, Mattioli F, Del Sette M. A case of anti-HMGCR myopathy triggered by sodium/glucose co-transporter 2 (SGLT2) inhibitors. Neurol Sci. 2022;43(7):4567-4570. doi: 10.1007/s10072-022-06046-3
66. Smolen JS, Aletaha D, Barton A, Burmester GR, Emery P, Firestein GS, et al. Rheumatoid arthritis. Nat Rev Dis Primers. 2018;4:18001. doi: 10.1038/nrdp.2018.1
67. Massay R, Malani A, Stubbs A. Glucagon-like peptide-1 receptor agonists in rheumatoid arthritis. Curr Opin Rheumatol. 2026;38(4):250-254. doi: 10.1097/BOR.0000000000001153
68. Buonanno S, Gaggiano C, Baldi C, Cantarini L, Frediani B, Gentileschi S. Glucagon-like peptide-1 receptor agonists in rheumatoid arthritis: A scoping review of metabolic, anti-inflammatory, and cardioprotective effects. J Pers Med. 2026;16(6):284. doi: 10.3390/jpm16060284
69. Veale JD, Gorman Á, Veale DJ, Fearon U, Orr C, Marzaioli V. Investigation of serum biomarkers in rheumatoid and psoriatic arthritis patients for disease-specific signatures. Arthritis Res Ther. 2025;27(1):147. doi: 10.1186/s13075-025-03608-6
70. Tejera-Segura B, López-Mejías R, Domínguez-Luis MJ, de Vera-González AM, González-Delgado A, Ubilla B, et al. Incretins in patients with rheumatoid arthritis. Arthritis Res Ther. 2017;19(1):229. doi: 10.1186/s13075-017-1431-9
71. Sullivan C, Gaoatswe G, Gibney J, Healy ML, Doran M, Kane D, et al. Treatment with the glucagon-like peptide-1 analogue liraglutide is associated with amelioration of disease activity in a prospective cohort study of patients with inflammatory arthritis. Proceedings of the 2013 ACR/ARHP Annual Meeting (San Diego, CA, USA, 25–30 October 2013). 2013.
72. Gavazova V, Pashkunova S. New therapeutic opportunities shared by obesity, type 2 diabetes and rheumatoid arthritis. Endocrine Abstracts; Bioscientifica. Bristol;2024.
73. Stipho F, Hindosh Y, Sayegh J, Hindosh A, Mitri B, Batarseh I, et al. Association of semaglutide prescription with improved joint outcomes in rheumatoid arthritis patients. Arthritis Rheumatol. 2025;77(Suppl 9).
74. Dente E, Kellner D, Tran V, Welsh T, Tran V, Saha A, et al. Effects of anti-obesity medications in RA patients. Arthritis Rheumatol. 2024;(76):4543-4544.
75. Kellner DA, Dente E, Tran V, Welsh T, Tran V, Saha A, et al. Effect of glucagon-like peptide 1 receptor agonists on patients with rheumatoid arthritis. ACR Open Rheumatol. 2025;7(9):e70103. doi: 10.1002/acr2.70103
76. Wang Q, Anthony DD. Glucagon-like peptide-1 receptor analog use is associated with reduced thromboembolic events compared with dipeptidyl peptidase-4 inhibitors in rheumatoid arthritis patients: A global retrospective cohort study. Clin Rheumatol. 2025;44(11):4479-4485. doi: 10.1007/s10067-025-07709-0
77. Beltagy A, Eshak N, Chhaya S. OP0069 GLP1 agonists mitigate the risk of cardiovascular events in rheumatoid arthritis patients treated with JAK inhibitors. Ann Rheum Dis. 2025;(84):61-62. doi: 10.1016/j.ard2025.05.092
78. Loizidis G, Summer R. GLP-1-based therapy and ICD-10-documented heart failure or respiratory failure events in non-diabetic adults with rheumatoid arthritis and obesity: A TriNetX federated cohort study. Clin Rheumatol. 2026 Jun 11. doi: 10.1007/s10067026-08212-w
79. Ambrosio ML, Monami M, Sati L, Marchionni N, Di Bari M, Mannucci E. GLP-1 receptor agonist-induced polyarthritis: A case report. Acta Diabetol. 2014;51(4):673-674. doi: 10.1007/s00592013-0525-3
80. Lee YJ, Fang YW, Chen MT, Liou HH, Li TH, Tsai MH. Association between autoimmune diseases and glucagon-like peptide-1 receptor agonists: A real-world evidence study. J Autoimmun. 2025;155:103453. doi: 10.1016/j.jaut.2025.103453
81. Yen FS, Wang SI, Hwu CM, Huang CW, Chang R, Hsu CC, et al. Comparative risk of rheumatoid arthritis between glucagon-like peptide-1 receptor agonists and sodium-glucose cotransporter-2 inhibitors in type 2 diabetes. J Autoimmun. 2025;157:103493. doi: 10.1016/j.jaut.2025.103493
82. Karacabeyli D, Lacaille D, Lu N, Xie H, Aviña-Zubieta JA. Glucagon-like peptide 1 receptor agonists, sodium-glucose cotransporter 2 inhibitors, and risk of autoimmune rheumatic diseases. Arthritis Rheumatol. 2026;78(3):654-664. doi: 10.1002/art.70044
83. Nassar M, Nassar O, Abosheaishaa H, Misra A. Comparative outcomes of systemic diseases in people with type 2 diabetes, or obesity alone treated with and without GLP-1 receptor agonists: A retrospective cohort study from the Global Collaborative Network. J Endocrinol Invest. 2025;48(2):483-497. doi: 10.1007/s40618-024-02466-4
84. Dobashi N, Sada KE, Kudo M, Morishita S, Sasaki S, Suganuma N. Risk of urinary tract infections associated with SGLT2 inhibitor use in patients with RA: A target trial emulation study. Rheumatology (Oxford). 2026;65(2):keaf580. doi: 10.1093/ rheumatology/keaf580
85. 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):435-449. doi: 10.47360/1995-44842023-435-449
86. Kalantari E, Zolbanin NM, Ghasemnejad-Berenji M. Protective effects of empagliflozin on methotrexate induced hepatotoxicity in rats. Biomed Pharmacother. 2024;170:115953. doi: 10.1016/j.biopha.2023.115953
87. Torres GA, Campoli F, Prasad A, Bhuvan F, Pandey K, Gelagutashvili G, et al. SGLT2 inhibitor use and cardiovascular outcomes in rheumatoid arthritis-associated interstitial lung disease: A propensity-matched Trinetx analysis. Amer J Respir Crit Care Medi. 2026;212(S1):S2143.
88. Насонов ЕЛ, Соловьев СК, Аршинов АВ. Системная красная волчанка: история и современность. Научно-практическая ревматология. 2022;60(4):397-412. doi: 10.47360/19954484-2022-397-412
89. Kaul A, Gordon C, Crow MK, Touma Z, Urowitz MB, van Vollenhoven R, et al. Systemic lupus erythematosus. Nat Rev Dis Primers. 2016;2:16039. doi: 10.1038/nrdp.2016.39
90. Jiang MY, Hwang JC, Feng IJ. Impact of diabetes mellitus on the risk of end-stage renal disease in patients with systemic lupus erythematosus. Sci Rep. 2018;8(1):6008. doi: 10.1038/s41598-018-24529-2
91. Hansen RB, Falasinnu T, Faurschou M, Jacobsen S, Simard JF. Risk of end-stage renal disease in patients with systemic lupus erythematosus and diabetes mellitus: A Danish nationwide cohort study. Arthritis Care Res (Hoboken). 2023;75(9):1871-1877. doi: 10.1002/acr.25091
92. Yen FS, Wang SI, Hsu CC, Hwu CM, Wei JC. Sodium-glucose cotransporter-2 inhibitors and nephritis among patients with systemic lupus erythematosus. JAMA Netw Open. 2024;7(6):e2416578. doi: 10.1001/jamanetworkopen.2024.16578
93. Ma KS, Lo JE, Kyttaris VC, Tsokos GC, Costenbader KH. Efficacy and safety of sodium-glucose cotransporter 2 inhibitors for the primary prevention of cardiovascular, renal events, and safety outcomes in patients with systemic lupus erythematosus and comorbid type 2 diabetes: A population-based target trial emulation. Arthritis Rheumatol. 2025;77(4):414-422. doi: 10.1002/art.43037
94. Anders HJ, Saxena R, Zhao MH, Parodis I, Salmon JE, Mohan C. Lupus nephritis. Nat Rev Dis Primers. 2020;6(1):7. doi: 10.1038/s41572-019-0141-9
95. Tektonidou MG, Dasgupta A, Ward MM. Risk of end-stage renal disease in patients with lupus nephritis, 1971–2015: A systematic review and bayesian meta-analysis. Arthritis Rheumatol. 2016;68(6):1432-1441. doi: 10.1002/art.39594
96. Соловьев СК, Козловская НЛ, Асеева ЕА, Баранов АА, Никишина НЮ, Насонов ЕЛ. Волчаночный нефрит – современные аспекты диагностики и терапии. Часть I. Научнопрактическая ревматология. 2024;62(1):55-64. doi: 10.47360/1995-4484-2024-55-64
97. Fanouriakis A, Kostopoulou M, Anders HJ, Andersen J, Aringer M, Beresford MW, et al. EULAR recommendations for the management of systemic lupus erythematosus with kidney involvement: 2025 update. Ann Rheum Dis. 2026;85(1):75-90. doi: 10.1016/j.ard.2025.09.007
98. Zhao XY, Li SS, He YX, Yan LJ, Lv F, Liang QM, et al. SGLT2 inhibitors alleviated podocyte damage in lupus nephritis by decreasing inflammation and enhancing autophagy. Ann Rheum Dis. 2023;82(10):1328-1340. doi: 10.1136/ard-2023-224242
99. Hakroush S, Tampe D, Kluge IA, Baier E, Korsten P, Tampe B. Comparative analysis of SGLT-2 expression in renal vasculitis and lupus nephritis. Ann Rheum Dis. 2022;81(7):1048-1050. doi: 10.1136/annrheumdis-2022-222167
100. Morales E, Galindo M. SGLT2 inhibitors in lupus nephropathy, a new therapeutic strategy for nephroprotection. Ann Rheum Dis. 2022;81(9):1337-1338. doi: 10.1136/annrheumdis-2022-222512
101. Vajgel G, Júnior BMDS, Filho CRSM, de Oliveira CBL, Costa DMDN, de Lima CAD, et al. Efficacy and safety of dapagliflozin in inactive lupus nephritis: A randomized crossover trial. Nephrol Dial Transplant. 2026;41(7):1253-1261. doi: 10.1093/ndt/gfaf257
102. Wang H, Li T, Sun F, Liu Z, Zhang D, Teng X, et al. Safety and efficacy of the SGLT2 inhibitor dapagliflozin in patients with systemic lupus erythematosus: A phase I/II trial. RMD Open. 2022;8(2):e002686. doi: 10.1136/rmdopen-2022-002686
103. Tayer-Shifman OE, Kenis I, Benchetrit S, Bar-Ziv D, PriPaz Basson Y, Levy Y, et al. Clinical experience with sodium-glucose transport 2 (SGLT2) inhibitors in patients with systemic lupus erythematosus. Int Urol Nephrol. 2026 58(5):1783-1791. doi: 10.1007/s11255-025-04815-5
104. Badawi MH, Nagy E, Wafa EW, El-Husseini A, Mohamed N, El-Ghar MA, et al. Impact of SGLT2i on bone health in patients with lupus nephritis: Randomized double blinded placebo-controlled clinical trial. J Nephrol. 2025;38(7):1865-1875. doi: 10.1007/s40620-025-02351-0
105. Sagy I, Shitrit I, Abuhasira R, David RB, Haviv YS, Tayer-Shifman O, et al. Kidney outcomes of systemic lupus erythematosus patients treated with SGLT2 inhibitors: A national cohort study. Semin Arthritis Rheum. 2025;73:152746. doi: 10.1016/j.semarthrit.2025.152746
106. Ramírez-Mulhern I, Navarro-Sánchez V, Rivero-Otamendi E, Sánchez-Mejía DE, Zavala-Miranda MF, Mejia-Vilet JM. Effects of sodium-glucose transporter 2 inhibitors in patients with lupus nephritis: A before-and-after retrospective cohort study. Rheumatology (Oxford). 2026;65(1):keaf548. doi: 10.1093/rheumatology/keaf548
107. Pope J, Karacabeyi D, Avina-Zubieta A. Target trial emulations of sodium-glucose cotransporter 2 inhibitors in systemic lupus erythematosus. Arthritis Rheum 2025;77(4):390-392. Doi:10.1002/art.43130.
108. Jorge A, Patel AV, Zhou B, Zhang L, Choi H. Glucagon-like peptide-1 receptor agonist use and the risk of adverse cardiac and kidney outcomes among patients with systemic lupus erythematosus and lupus nephritis. Arthritis Rheumatol. 2026;78(3):665671. doi: 10.1002/art.43403
109. Carlucci PM, Cohen B, Saxena A, Belmont HM, Masson M, Gold HT, et al. A retrospective evaluation of glucagon-like peptide-1 receptor agonists in systemic lupus erythematosus patients. Rheumatology (Oxford). 2025;64(5):3085-3089. doi: 10.1093/rheumatology/keae547
110. Nazzicone K, Sidiropoulos M, O’Toole A. From prescription to predicament: A case of semaglutide-induced discoid lupus erythematosus in an adult male patient. Cureus. 2025;17(4):e81663. doi: 10.7759/cureus.81663
111. Pinheiro MM, de Souza LG, Nunes GP, Martin IF, de Oliveira YU, Pinheiro FMM, et al. The first report of leukocytoclastic vasculitis induced by once-weekly subcutaneous semaglutide. Curr Med Res Opin. 2024;40(9):1525-1531. doi: 10.1080/03007995.2024.2386047
112. Castellanos V, Workneh H, Malik A, Mehta B. Semaglutideinduced lupus erythematosus with multiorgan involvement. Cureus. 2024;16(3):e55324. doi: 10.7759/cureus.55324
113. Stamellou E, Seikrit C, Tang SCW, Boor P, Tesař V, Floege J, et al. IgA nephropathy. Nat Rev Dis Primers. 2023;9(1):67. doi: 10.1038/s41572-023-00476-9
114. Wheeler DC, Stefánsson BV, Jongs N, Chertow GM, Greene T, Hou FF, et al. Effects of dapagliflozin on major adverse kidney and cardiovascular events in patients with diabetic and non-diabetic chronic kidney disease: A prespecified analysis from the DAPA-CKD trial. Lancet Diabetes Endocrinol. 2021;9(1):2231. doi: 10.1016/S2213-8587(20)30369-7
115. The EMPA-KIDNEY Collaborative Group; Herrington WG, Staplin N, Wanner C, Green JB, Hauske SJ, et al. Empagliflozin in patients with chronic kidney disease. N Engl J Med. 2023;388(2):117-127. doi: 10.1056/NEJMoa2204233
116. Насонов ЕЛ, Елисеев МС. Роль интерлейкина 1 в развитии заболеваний человека. Научно-практическая ревматология. 2016;54(1):60-77. doi: 10.14412/19954484-2016-60-77
117. Liu Z, Kong H, Zhang B. Narrative literature review of antidiabetic drugs’ effect on hyperuricemia: Elaborating actual data and mechanisms. Endocr Connect. 2024;13(6):e240070. doi: 10.1530/EC-24-0070
118. MacFarlane LA, Liu CC, Solomon DH. The effect of initiating pharmacologic insulin on serum uric acid levels in patients with diabetes: A matched cohort analysis. Semin Arthritis Rheum. 2015;44(5):592-596. doi: 10.1016/j.semarthrit.2014.10.008
119. Паневин ТС, Елисеев МС, Шестакова МВ, Насонов ЕЛ. Преимущества терапии ингибиторами натрий-глюкозного котранспортера 2-го типа у пациентов с сахарным диабетом 2-го типа в сочетании с гиперурикемией и подагрой. Терапевтический архив. 2020;92(5):110-118. doi: 10.26442/00403660.2020.05.000633
120. Lotfy M, Singh J, Rashed H, Tariq S, Zilahi E, Adeghate E. The effect of glucagon-like peptide-1 in the management of diabetes mellitus: Cellular and molecular mechanisms. Cell Tissue Res. 2014;358(2):343-358. doi: 10.1007/s00441-014-1959-9
121. Pereira MJ, Eriksson JW. Emerging role of SGLT-2 inhibitors for the treatment of obesity. Drugs. 2019;79(3):219-230. doi: 10.1007/s40265-019-1057-0
122. Fralick M, Chen SK, Patorno E, Kim SC. Assessing the risk for gout with sodium-glucose cotransporter-2 inhibitors in patients with type 2 diabetes: A population-based cohort study. Ann Intern Med. 2020;172(3):186-194. doi: 10.7326/M19-2610
123. Tesfaye H, Wang KM, Zabotka LE, Wexler DJ, Schmedt N, Koeneman L, et al. Empagliflozin and risk of incident gout: Analysis from the EMPagliflozin Comparative Effectiveness and SafEty (EMPRISE) Cohort Study. J Gen Intern Med. 2024;39(10):1870-1879. doi: 10.1007/s11606-024-08793-9
124. Lund LC, Højlund M, Henriksen DP, Hallas J, Kristensen KB. Sodium-glucose cotransporter-2 inhibitors and the risk of gout: A Danish population based cohort study and symmetry analysis. Pharmacoepidemiol Drug Saf. 2021;30(10):1391-1395. doi: 10.1002/pds.5252
125. Preston FG, Anson M, Riley DR, Ibarburu GH, Henney A, Lip GYH, et al. SGLT2 Inhibitors, but not GLP-1 receptor agonists, reduce incidence of gout in people living with type 2 diabetes across the therapeutic spectrum. Clin Ther. 2024;46(11):835840. doi: 10.1016/j.clinthera.2024.06.021
126. Dutour A, Abdesselam I, Ancel P, Kober F, Mrad G, Darmon P, et al. Exenatide decreases liver fat content and epicardial adipose tissue in patients with obesity and type 2 diabetes: A prospective randomized clinical trial using magnetic resonance imaging and spectroscopy. Diabetes Obes Metab. 2016;18(9):882-891. doi: 10.1111/dom.12680
127. Tonneijck L, Muskiet MHA, Smits MM, Bjornstad P, Kramer MHH, Diamant M, et al. Effect of immediate and prolonged GLP-1 receptor agonist administration on uric acid and kidney clearance: Post-hoc analyses of four clinical trials. Diabetes Obes Metab. 2018;20(5):1235-1245. doi: 10.1111/dom.13223
128. Moreno-Pérez O, Tejera-Muñoz A, Carreño-Valdivia R, Rodríguez-Bedoya M, Guillén-Morote C, Roldán-Sánchez A, et al. Impact of oral semaglutide on serum urate levels in people with type 2 diabetes: A retrospective real-world analysis (URISEMA study). Semin Arthritis Rheum. 2025;74:152807. doi: 10.1016/j.semarthrit.2025.152807
129. Okamoto A, Yokokawa H, Nagamine T, Fukuda H, Hisaoka T, Naito T. Efficacy and safety of semaglutide in glycemic control, body weight management, lipid profiles and other biomarkers among obese type 2 diabetes patients initiated or switched to semaglutide from other GLP-1 receptor agonists. J Diabetes Metab Disord. 2021;20(2):2121-2128. doi: 10.1007/s40200-02100899-9
130. Sattar N, Scilletta S, Stefanski A, Wang H, Daly JW, Linetzky B. Tirzepatide and change in uric acid and its association with weight reduction: Post hoc analyses of the SURMOUNT-1 randomised placebo-controlled trial. Ann Rheum Dis. 2026;85(3):558-565. doi: 10.1016/j.ard.2025.10.009
131. Doblado M, Moley KH. Facilitative glucose transporter 9, a unique hexose and urate transporter. Am J Physiol Endocrinol Metab. 2009;297(4):E831-E835. doi: 10.1152/ajpendo.00296.2009
132. Hatano M, Okada A, Yasunaga H. Comment on: Gout incidence in metformin versus sodium-glucose co-transporter-2 inhibitor users: A retrospective cohort study: Reply. Rheumatology (Oxford). 2025;64(9):5197. doi: 10.1093/rheumatology/keaf262
133. Елисеев МС, Паневин ТС, Желябина ОВ, Насонов ЕЛ. Перспективы применения метформина у пациентов с нарушением уратного обмена. Терапевтический архив. 2021; 93(5):628-634. doi: 10.26442/00403660.2021.05.200795
134. Davies MJ, Trujillo A, Vijapurkar U, Damaraju CV, Meininger G. Effect of canagliflozin on serum uric acid in patients with type 2 diabetes mellitus. Diabetes Obes Metab. 2015;17(4):426-429. doi: 10.1111/dom.12439
135. Choi HK, McCormick N, Yokose C. Excess comorbidities in gout: The causal paradigm and pleiotropic approaches to care. Nat Rev Rheumatol. 2022;18(2):97-111. doi: 10.1038/s41584-02100725-9
136. Wang A, Shi W, Zhang N, Tang H, Feng X. Newer glucose-lowering drugs and risk of gout: A network meta-analysis of randomized outcomes trials. Clin Ther. 2024;46(11):851-854. doi: 10.1016/j.clinthera.2024.04.013
137. Katsoula G, Kreitmaier P, Zeggini E. Insights into the molecular landscape of osteoarthritis in human tissues. Curr Opin Rheumatol. 2022;34(1):79-90. doi: 10.1097/BOR.0000000000000853
138. Hunter DJ, Bierma-Zeinstra S. Osteoarthritis. Lancet. 2019; 393(10182):1745-1759. doi: 10.1016/S0140-6736(19)30417-9
139. Weng Q, Chen Q, Jiang T, Zhang Y, Zhang W, Doherty M, et al. Global burden of early-onset osteoarthritis, 1990–2019: Results from the Global Burden of Disease Study 2019. Ann Rheum Dis. 2024;83(7):915-925. doi: 10.1136/ard-2023-225324
140. Duong V, Abdel Shaheed C, Ferreira ML, Narayan SW, Venkatesha V, Hunter DJ, et al. Risk factors for the development of knee osteoarthritis across the lifespan: A systematic review and metaanalysis. Osteoarthritis Cartilage. 2025;33(10):1162-1179. doi: 10.1016/j.joca.2025.03.003
141. Lawrence KW, Sobba W, Rajahraman V, Schwarzkopf R, Rozell JC. Does body mass index influence improvement in patient reported outcomes following total knee arthroplasty? A retrospective analysis of 3918 cases. Knee Surg Relat Res. 2023;35(1):21. doi: 10.1186/s43019-023-00195-1
142. Weijers JM, Müskens WD, van Riel PLCM. Effect of significant weight loss on disease activity: Reason to implement this nonpharmaceutical intervention in daily clinical practice. RMD Open. 2021;7:e001498. doi: 10.1136/rmdopen-2020-001498
143. Wijesinghe SN, Badoume A, Nanus DE, Sharma-Oates A, Farah H, Certo M, et al. Obesity defined molecular endotypes in the synovium of patients with osteoarthritis provides a rationale for therapeutic targeting of fibroblast subsets. Clin Transl Med. 2023;13(4):e1232. doi: 10.1002/ctm2.1232
144. Messier SP, Beavers DP, Queen K, Mihalko SL, Miller GD, Losina E, et al. Effect of diet and exercise on knee pain in patients with osteoarthritis and overweight or obesity: A randomized clinical trial. JAMA. 2022;328(22):2242-2251. doi: 10.1001/jama.2022.21893
145. Pan F, Wang Y, Lim YZ, Urquhart DM, Estee MM, Wluka AE, et al. Metformin for knee osteoarthritis in patients with overweight or obesity: A randomized clinical trial. JAMA. 2025;333(20):1804-1812. doi: 10.1001/jama.2025.3471
146. Насонов ЕЛ, Паневин ТС, Трошина ЕА. Агонисты рецепторов глюкагоноподобного пептида-1: перспективы применения в ревматологии. Научно-практическая ревматология. 2024;62(2):135-144. doi: 10.47360/1995-4484-2024-135-144
147. Zheng M, Zhao J, Wang Y, Cui Z, Qiao Z, Wu H, et al. Exploring new therapeutic drugs for osteoarthritis and osteoporosis: Glucagon-like peptide-1 receptor agonists: A review. Medicine (Baltimore). 2025;104(29):e43239. doi: 10.1097/MD.0000000000043239
148. Jamal N, Hollabaugh W, Scott L, Takkouche S. Unravelling the ties that bind: The intersection of obesity, osteoarthritis, and inflammatory pathways with emphasis on glucagon-like peptide-1 agonists. Clin Obes. 2025;15(1):e12700. doi: 10.1111/cob.12700
149. Bliddal H, Bays H, Czernichow S, Uddén Hemmingsson J, Hjelmesæth J, Hoffmann Morville T, et al.; STEP 9 Study Group. Once-weekly semaglutide in persons with obesity and knee osteoarthritis. N Engl J Med. 2024;391(17):1573-1583. doi: 10.1056/NEJMoa2403664
150. Gudbergsen H, Overgaard A, Henriksen M, Wæhrens EE, Bliddal H, Christensen R, et al. Erratum to “Liraglutide after dietinduced weight loss for pain and weight control in knee osteoarthritis: A randomized controlled trial”. Am J Clin Nutr. 2021;113:314-323. Am J Clin Nutr. 2025;122(3):901. doi: 10.1016/j.ajcnut.2025.07.013
151. Zhu H, Zhou L, Wang Q, Cai Q, Yang F, Jin H, et al. Glucagonlike peptide-1 receptor agonists as a disease-modifying therapy for knee osteoarthritis mediated by weight loss: Findings from the Shanghai Osteoarthritis Cohort. Ann Rheum Dis. 2023;82(9):1218-1226. doi: 10.1136/ard-2023-223845
152. Yang Y, Hao C, Jiao T, Yang Z, Li H, Zhang Y, et al. Osteoarthritis treatment via the GLP-1-mediated gut-joint axis targets intestinal FXR signaling. Science. 2025;388(6742):eadt0548. doi: 10.1126/science.adt0548
153. Porto JR, Lavu MS, Hecht CJ 2nd, Kaelber DC, Sculco PK, Heckmann ND, et al. The impact of contemporary glucagon-like peptide-1 receptor agonists on the onset, severity, and conversion to arthroplasty in hip and knee osteoarthritis. Orthop J Sports Med. 2025;13(1):23259671241297157. doi: 10.1177/23259671241297157
154. Samajdar SS, Bhaduri G, Ghoshal PK, Mukherjee S, Pal J, Chatterjee N, et al. Dual effects of dulaglutide on glycemic control and knee osteoarthritis pain in elderly patients with type 2 diabetes. Pain Manag. 2024;14(7):365-373. doi: 10.1080/ 17581869.2024.2402214
155. Jeon M, Hong B, Ko HY, Song HJ, Kwak SH, Kim JH, et al. Glucagon-like peptide-1 receptor agonists and risk of osteoarthritis among individuals with type 2 diabetes: A population-based cohort study. Diabetes Res Clin Pract. 2026;232:113091. doi: 10.1016/j.diabres.2026.113091
156. Ursini F, Ciaffi J, Caporali R. If the evidence is there, why are GLP-1 receptor agonists not on-label for hip and knee osteoarthritis in overweight patients? RMD Open. 2025;11(3):e006025. doi: 10.1136/rmdopen-2025-006025
157. Zhong S, Li F, Li D, Cheng Y, Wang X, Gao Y, et al. The braingut-joint axis in arthritis: Crosstalk, treatment, and future perspectives. J Orthop Translat. 2026;56:101045. doi: 10.1016/j.jot.2025.101045
158. Magruder ML, Yao VJH, Rodriguez AN, Ng MK, Sasson V, Erez O. Does semaglutide use decrease complications and costs following total knee arthroplasty? J Arthroplasty. 2023;38(11):2311-e23151.
159. Magruder ML, Miskiewicz MJ, Rodriguez AN, Mont MA. Semaglutide use prior to total hip arthroplasty results in fewer postoperative prosthetic joint infections and readmissions. J Arthroplasty. 2024;39(3):716-720.
160. Mashayekhi Y, Asgari AM, Pahlevan-Fallahy MT, Karimi MA, Jalali R, Shaker F. Impact of glucagon-like peptide-1 receptor agonists on postoperative complications after total joint arthroplasty: A systematic review and meta-analysis. J Orthop Surg (Hong Kong). 2025;33(3):10225536251391959. doi: 10.1177/10225536251391959
161. Kim BI, LaValva SM, Parks ML, Sculco PK, Della Valle AG, Lee GC. Glucagon-like peptide-1 receptor agonists decrease medical and surgical complications in morbidly obese patients undergoing primary TKA. J Bone Jt Surg Am. 2025;107(4):348-355.
162. Chan YC, Chuang SH, Kuo YJ, Lian YZ, Chen YP. The association between glucagon-like peptide-1 receptor agonists and postoperative complications after arthroplasty: A systematic review and meta-analysis. J Arthroplasty. 2025;40(12):3080-3088.e7. doi: 10.1016/j.arth.2025.06.083
163. Xu JJ, Johnson MC, Lama G, Budin JS, Tabbaa A, Chen AZ, et al. The effect of body mass index on the efficacy of semaglutide use at the time of total knee arthroplasty. J Arthroplasty. 2026;41(5):1333-1339. doi: 10.1016/j.arth.2025.09.056
164. Box MW, Puga TB, Werthmann NJ, Jen A, Liu Y, Riehl JT. Association of preoperative GLP-1 receptor agonist use with outcomes after primary total knee arthroplasty. Knee. 2026;58:104272. doi: 10.1016/j.knee.2025.10.026
165. Karmacharya P, Chakradhar R, Ogdie A. The epidemiology of psoriatic arthritis: A literature review. Best Pract Res Clin Rheumatol. 2021;35(2):101692. doi: 10.1016/j.berh.2021.101692
166. Toussirot E, Gallais-Sérézal I, Aubin F. The cardiometabolic conditions of psoriatic disease. Front Immunol. 2022;13:970371. doi: 10.3389/fimmu.2022.970371
167. Ciancio G, Maranini B, Sandri G, Amati G, Bortoluzzi A, Silvagni E, et al. Glucagon-like peptide-1 receptor agonists in psoriasis and psoriatic arthritis: Emerging evidence and future research opportunities. Front Immunol. 2026;17:1744308. doi: 10.3389/fimmu.2026.1744308
168. Лила АМ, Коротаева ТВ, Паневин ТС, Зоткин ЕГ. Агонисты рецептора глюкагоноподобного пептида 1 как потенциальный путь преодоления резистентности к терапии при псориазе и псориатическом артрите. Современная ревматология. 2026;20(3):84-90. doi: 10.14412/1996-7012-2026-3-84-90
169. Atiquzzaman N, Razdolsky N, Parmar MS. GLP-1 receptor agonists: Emerging therapeutic potential in psoriasis management – current evidence and future outlook. Eur J Clin Pharmacol. 2025;81(11):1569-1581. doi: 10.1007/s00228-025-03898-4
170. Buonanno S, Gaggiano C, Terribili R, Cantarini L, Frediani B, Gentileschi S. The potential role of GLP-1 receptor agonists in the management of psoriatic disease: A scoping review. Inflamm Res. 2025;74(1):167. doi: 10.1007/s00011-025-02140-2
171. Karacabeyli D, Lacaille D. Glucagon-like peptide 1 receptor agonists in patients with inflammatory arthritis or psoriasis: A scoping review. J Clin Rheumatol. 2024;30(1):26-31. doi: 10.1097/RHU.0000000000001949
172. Nicolau J, Nadal A, Ros I, Masmiquel L. Effects of liraglutide among patients with psoriatic arthritis and obesity. Reumatol Clin (Engl Ed). 2025;21(1):501809. doi: 10.1016/j.reumae.2025.501809
173. Haberman RH, Rice AL, Chen K, Scher U, Thib S, Scher JU, et al. Glucagon-like peptide-1 receptor agonist therapy is associated with improvement in psoriatic arthritis-related and metabolic outcomes: A retrospective analysis of two cohorts. Arthritis Rheumatol. 2026:10.1002/art.70170. doi: 10.1002/art.70170
174. Merola JF, Mease P, Kivitz A, Sattar N, Coates LC, Aletaha D, et al. Ixekizumab with tirzepatide achieved greater disease control than ixekizumab alone in adults with psoriatic arthritis and overweight or obesity: Results from a randomized clinical trial. Arthritis Rheumatol. 2026 Mar 28. doi: 10.1002/art.70134
175. Gao S, Xie X, Fan L, Yu L. Efficacy and safety of IL-17, IL-12/23, and IL-23 inhibitors for psoriatic arthritis: A network meta-analysis of randomized controlled trials. Front Immunol. 2025;16:1654343. doi: 10.3389/fimmu.2025.1654343
176. Hogan AE, Tobin AM, Ahern T, Corrigan MA, Gaoatswe G, Jackson R, et al. Glucagon-like peptide-1 (GLP-1) and the regulation of human invariant natural killer T cells: Lessons from obesity, diabetes and psoriasis. Diabetologia. 2011;54(11):2745-54. doi: 10.1007/s00125-011-2232-3
177. Buysschaert M, Baeck M, Preumont V, Marot L, Hendrickx E, Van Belle A, et al. Improvement of psoriasis during glucagon-like peptide-1 analogue therapy in type 2 diabetes is associated with decreasing dermal γδ T-cell number: A prospective case-series study. Br J Dermatol. 2014;171(1):155-161. doi: 10.1111/bjd.12886
178. Gatto A, Liu K, Milan N, Wong S. The effects of GLP-1 agonists on musculoskeletal health and orthopedic care. Curr Rev Musculoskelet Med. 2025;18(10):469-480. doi: 10.1007/s12178-02509978-3
179. Mabilleau G, Mieczkowska A, Chappard D. Use of glucagon-like peptide-1 receptor agonists and bone fractures: A meta-analysis of randomized clinical trials. J Diabetes. 2014;6(3):260-266. doi: 10.1111/1753-0407.12102
180. Driessen JH, Henry RM, van Onzenoort HA, Lalmohamed A, Burden AM, Prieto-Alhambra D, et al. Bone fracture risk is not associated with the use of glucagon-like peptide-1 receptor agonists: A population-based cohort analysis. Calcif Tissue Int. 2015;97(2):104-112. doi: 10.1007/s00223-015-9993-5
181. Cheng L, Hu Y, Li YY, Cao X, Bai N, Lu TT, et al. Glucagonlike peptide-1 receptor agonists and risk of bone fracture in patients with type 2 diabetes: A meta-analysis of randomized controlled trials. Diabetes Metab Res Rev. 2019;35(7):e3168. doi: 10.1002/dmrr.3168
182. Su B, Sheng H, Zhang M, Bu L, Yang P, Li L, et al. Risk of bone fractures associated with glucagon-like peptide-1 receptor agonists’ treatment: A meta-analysis of randomized controlled trials. Endocrine. 2015;48(1):107-115. doi: 10.1007/s12020-014-0361-4
183. Venugopal N, Meshay I, Hagedorn J. Association of GLP-1 agonists on hip fractures in a real-world cohort. URL: https://ota.org/sites/files/abstracts/2024/AM%2092 (Accessed: 25th May 2026).
184. Denton CP, Khanna D. Systemic sclerosis. Lancet. 2017; 390(10103):1685-1699. doi: 10.1016/S0140-6736(17)30933-9
185. Lin CY, Chen HA, Chang TW, Hsu TC, Su YJ. Association of systemic sclerosis with incident clinically evident heart failure. Arthritis Care Res (Hoboken). 2023;75(7):1452-1461. doi: 10.1002/acr.25016
186. Guédon AF, Carrat F, Mouthon L, Launay D, Chaigne B, Pugnet G, et al. Heart and systemic sclerosis-findings from a national cohort study. Rheumatology (Oxford). 2024;63(12):3380-3389. doi: 10.1093/rheumatology/kead599
187. Augusto SN Jr, Kaelber DC, Chatterjee S, Tang WHW. Sodium glucose co-transporter-2 inhibitors in patients with systemic sclerosis with or without heart failure. Am J Med. 2026;139(1):76-83. doi: 10.1016/j.amjmed.2025.08.009
188. González-López MA. Hidradenitis suppurativa. Med Clin (Barc). 2024;162(4):182-189. doi: 10.1016/j.medcli.2023.09.018
189. Ross Y, Ballou S. Association of hidradenitis suppurativa with autoimmune disease and autoantibodies. Rheumatol Adv Pract. 2021;6(2):rkab108. doi: 10.1093/rap/rkab108
190. Mintoff D, Agius R, Fava S, Pace NP. Investigating adiposityrelated metabolic health phenotypes in patients with hidradenitis suppurativa: A cross-sectional study. J Clin Med. 2023;12(14):4847. doi: 10.3390/jcm12144847
191. Nicolau J, Nadal A, Sanchís P, Pujol A, Masmiquel L, Nadal C. Liraglutide for the treatment of obesity among patients with hidradenitis suppurativa. Med Clin (Barc). 2024;162(3):118-122. doi: 10.1016/j.medcli.2023.11.007
192. Henry T, Cahn B, Haber R, Landers JT, Berger-Fleishman R, Alam M, et al. Therapeutic potential of GLP-1 agonists for hidradenitis suppurativa. Int J Dermatol. 2023;62(12):15431544. doi: 10.1111/ijd.16892
193. Findeisen K, Guymer E, Littlejohn G. Neuroinflammatory and immunological aspects of fibromyalgia. Brain Sci. 2025;15(2):206. doi: 10.3390/brainsci15020206
194. Eshak N, Bellagy A, Bazigh N, Chaisrimaneepan N. Exploring GLP-1 agonists effects in fibromyalgia patients: A propensity matched analysisusinf TriNetX database. Ann Rheum Dis. 2025:84(Suppl 1):232. doi: 10.1136/annrheumdis-2025-eularB639
195. He Y, Xu B, Zhang M, Chen D, Wu S, Gao J, et al. Advances in GLP-1 receptor agonists for pain treatment and their future potential. J Headache Pain. 2025;26(1):46. doi: 10.1186/s10194025-01979-4
196. Rosa S, Martins D, Martins M, Guimarães B, Cabral L, Horta L. Body mass index and musculoskeletal pain: A cross-sectional study. Cureus. 2021;13(2):e13400. doi: 10.7759/cureus.13400
197. Kaka B, Maharaj SS, Fatoye F. Prevalence of musculoskeletal disorders in patients with diabetes mellitus: A systematic review and meta-analysis. J Back Musculoskelet Rehabil. 2019;32(2):223-235. doi: 10.3233/BMR-171086
198. Karacabeyli D, Lacaille D, Lu N, McCormick N, Xie H, Choi HK, et al. Mortality and major adverse cardiovascular events after glucagon-like peptide-1 receptor agonist initiation in patients with immune-mediated inflammatory diseases and type 2 diabetes: A population-based study. PLoS One. 2024;19(8):e0308533. doi: 10.1371/journal.pone.0308533
199. Dai H, Lee YA, Natalie A, Jackson W, Pham A, et al. Glucagonlike peptide-1 receptor agonists and cardiovascular events in adults with obesity and autoimmune disease a target trial emalation, J Am Heart Assoc 2026;15:e047893. doi:10.1161/jAHA.125.047893.
200. Maretty L, Gill D, Simonsen L, Soh K, Zagkos L, Galanakis M, et al. Proteomic changes upon treatment with semaglutide in individuals with obesity. Nat Med. 2025;31(1):267-277. doi: 10.1038/s41591-024-03355-2
201. McLean BA, Wong CK, Campbell JE, Hodson DJ, Trapp S, Drucker DJ. Revisiting the complexity of GLP-1 action from sites of synthesis to receptor activation. Endocr Rev. 2021;42(2):101-132. doi: 10.1210/endrev/bnaa032
202. Mashayekhi M, Safa BI, Gonzalez MSC, Kim SF, EchouffoTcheugui JB. Systemic and organ-specific anti-inflammatory effects of sodium-glucose cotransporter-2 inhibitors. Trends Endocrinol Metab. 2024;35(5):425-438. doi: 10.1016/j.tem.2024.02.003
203. Mazzieri A, Basta G, Calafiore R, Luca G. GLP-1 Ras and SGLT2i: Two antidiabetic agents associated with immune and inflammation modulatory properties through the common AMPK pathway. Front Immunol. 2023;14:1163288. doi: 10.3389/fimmu.2023.1163288
204. Honing DY, Luiten RM, Matos TR. Regulatory T cell dysfunction in autoimmune diseases. Int J Mol Sci. 2024;25(13):7171. doi: 10.3390/ijms25137171
205. Насонов ЕЛ, Решетняк ТМ, Клименко АА, Николаева ЕВ. Катастрофический антифосфолипидный синдром: прототип аутоиммунного тромбовоспаления. Научно-практическая ревматология. 2026;64(3):227-248. doi: 10.47360/1995-4484-2026-227-248
Рецензия
Для цитирования:
Насонов Е.Л., Шестакова М.В., Кондратьева Л.В., Елисеев М.С. Перспективы применения новых антидиабетических препаратов в ревматологии. Научно-практическая ревматология. 2026;64(4):315-334. https://doi.org/10.47360/1995-4484-2026-315-334
For citation:
Nasonov E.L., Shestakova M.V., Kondratyeva L.V., Eliseev M.S. Prospects for the use of new antidiabetic drugs in rheumatology. Rheumatology Science and Practice. 2026;64(4):315-334. (In Russ.) https://doi.org/10.47360/1995-4484-2026-315-334
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