Smolen J.S., Aletaha D., McInnes I.B. Rheumatoid arthritis. Lancet. 2016;388(10055):2023–2038. doi: 10.1016/S0140-6736(16)30173-8..
DOI: 10.1016/S0140-6736(16)30173-8
Насонов Е.Л. Российские клинические рекомендации. Ревматология. М.: ГЭОТАР-Медиа; 2017. 464 с. Режим доступа: https://www.rosmedlib.ru/book/ISBN9785970442616.html.https://www.rosmedlib.ru/book/ISBN9785970442616.html
Насонов Е.Л. Российские клинические рекомендации. Ревматология. М.: ГЭОТАР-Медиа; 2017. 464 с. Режим доступа: https://www.rosmedlib.ru/book/ISBN9785970442616.html.https://www.rosmedlib.ru/book/ISBN9785970442616.html
Насонов Е.Л., Лила А.М., Мазуров В.И., Гордеев А.В., Белов Б.С., Жиляев Е.В. и др. Ревматоидный артрит Клинические рекомендации. M.; 2018. Режим доступа: http://cr.rosminzdrav.ru/#!/recomend/173.http://cr.rosminzdrav.ru/#!/recomend/173
Насонов Е.Л., Лила А.М., Мазуров В.И., Гордеев А.В., Белов Б.С., Жиляев Е.В. и др. Ревматоидный артрит Клинические рекомендации. M.; 2018. Режим доступа: http://cr.rosminzdrav.ru/#!/recomend/173.http://cr.rosminzdrav.ru/#!/recomend/173
Agca R., Hopman L.H.G.A., Laan K.J.C., van Halm V.P., Peters M.J.L., Smulders Y.M. et al. Cardiovascular Event Risk in Rheumatoid Arthritis Compared with Type 2 Diabetes: A 15-year Longitudinal Study. J Rheumatol. 2020;47(3):316–324. doi: 10.3899/jrheum.180726..
DOI: 10.3899/jrheum.180726
Подзолков В.И., Сафронова Т.А., Наткина Д.У. Эндотелиальная дисфункция у больных с контролируемой и неконтролируемой артериальной гипертензией. Терапевтический архив. 2019;91(9):108–114. doi: 10.2644 2/00403660.2019.09.000344..
DOI: 10.2644 2/00403660.2019.09.000344
Подзолков В.И., Сафронова Т.А., Наткина Д.У. Эндотелиальная дисфункция у больных с контролируемой и неконтролируемой артериальной гипертензией. Терапевтический архив. 2019;91(9):108–114. doi: 10.2644 2/00403660.2019.09.000344..
DOI: 10.26442/00403660.2019.09.000344
Бувальцев В.И. Дисфункция эндотелия как новая концепция профилактики и лечения сердечно-сосудистых заболеваний. Международный медицинский журнал. 2001;3(7):202–208. Режим доступа: https://medi.ru/info/9108/.https://medi.ru/info/9108/
Бувальцев В.И. Дисфункция эндотелия как новая концепция профилактики и лечения сердечно-сосудистых заболеваний. Международный медицинский журнал. 2001;3(7):202–208. Режим доступа: https://medi.ru/info/9108/.https://medi.ru/info/9108/
Трухан Д.И., Филимонов С.Н. Болезни сердечнососудистой системы: клиника, диагностика и лечение. СПб.: СпецЛит; 2016. 319 с.
Verma I., Syngle A., Krishan P. Predictors of endothelial dysfunction and atherosclerosis in rheumatoid arthritis in Indian population. Indian Heart J. 2017;69(2):200–206. doi: 10.1016/j.ihj.2016.10.013..
DOI: 10.1016/j.ihj.2016.10.013
Jagpal A., Navarro-Millán I. Cardiovascular co-morbidity in patients with rheumatoid arthritis: a narrative review of risk factors, cardiovascular risk assessment and treatment. BMC Rheumatol. 2018;2:10. doi: 10.1186/s41927-018-0014-y..
DOI: 10.1186/s41927-018-0014-y
Meyer P.W., Anderson R., Ker J.A., Ally M.T. Rheumatoid arthritis and risk of cardiovascular disease. Cardiovasc J Afr. 2018;29(5):317–321. doi: 10.5830/CVJA-2018-018..
DOI: 10.5830/CVJA-2018-018
Курак Т.А., Митьковская Н.П., Авдей Л.Л., Оганова Е.Г., Молочников М.Г., Ильина Т.В. и др. Металлопротеиназная активность у пациентов с ревматоидным артритом: роль системного воспаления и традиционных факторов риска кардиоваскулярных заболеваний. Кардиология в Беларуси. 2011;(3):34–44. Режим доступа: https://elibrary.ru/item.asp?id=16545061.https://elibrary.ru/item.asp?id=16545061
Курак Т.А., Митьковская Н.П., Авдей Л.Л., Оганова Е.Г., Молочников М.Г., Ильина Т.В. и др. Металлопротеиназная активность у пациентов с ревматоидным артритом: роль системного воспаления и традиционных факторов риска кардиоваскулярных заболеваний. Кардиология в Беларуси. 2011;(3):34–44. Режим доступа: https://elibrary.ru/item.asp?id=16545061.https://elibrary.ru/item.asp?id=16545061
Libby P., Ridker P.M., Maseri A. Inflammation and atherosclerosis. Circulation. 2002;105(9):1135–1143. doi: 10.1161/hc0902.104353..
DOI: 10.1161/hc0902.104353
Arend W.P. Physiology of cytokine pathways in rheumatoid arthritis. Arthritis Rheum. 2001;45(1):101–106. doi: 10.1002/1529-0131(200102)45:1<101:AIDANR90>3.0.CO;2-7..
DOI: 10.1002/1529-0131(200102)45:1<101:AIDANR90>3.0.CO;2-7
Robert M., Miossec P. Effects of Interleukin 17 on the cardiovascular system. Autoimmun Rev. 2017;16(9):984–991. doi: 10.1016/j.autrev.2017.07.009..
DOI: 10.1016/j.autrev.2017.07.009
McInnes I.B., Schett G. Cytokines in the pathogenesis of rheumatoid arthritis. Nat Rev Immunol. 2007;7(6):429–442. doi: 10.1038/nri2094..
DOI: 10.1038/nri2094
Meune C., Touzé E., Trinquart L., Allanore Y. High risk of clinical cardiovascular events in rheumatoid arthritis: Levels of associations of myocardial infarction and stroke through a systematic review and meta-analysis. Arch Cardiovasc Dis. 2010;103(4):253–261. doi: 10.1016/j.acvd.2010.03.007..
DOI: 10.1016/j.acvd.2010.03.007
Pober J.S., Cotran R.S. Cytokines and endothelial cell biology. Physiol Rev. 1990;70(2):427–451. doi: 10.1152/physrev.1990.70.2.427..
DOI: 10.1152/physrev.1990.70.2.427
Fossiez F., Djossou O., Chomarat P., Flores-Romo L., Ait-Yahia S., Maat C. et al. T cell interleukin-17 induces stromal cells to produce proinflammatory and hematopoietic cytokines. J Exp Med. 1996;183(6):2593–2603. doi: 10.1084/jem.183.6.2593..
DOI: 10.1084/jem.183.6.2593
Rodríguez-Carrio J., Alperi-López M., López P., Alonso-Castro S., CarroEsteban S.R., Ballina-García F.J., Suárez A. Red cell distribution width is associated with endothelial progenitor cell depletion and vascular-related mediators in rheumatoid arthritis. Atherosclerosis. 2015;240(1):131– 136. doi: 10.1016/j.atherosclerosis.2015.03.009..
DOI: 10.1016/j.atherosclerosis.2015.03.009
Slowikowski K., Wei K., Brenner M.B., Raychaudhuri S. Functional genomics of stromal cells in chronic inflammatory diseases. Curr Opin Rheumatol. 2018;30(1):65–71. doi: 10.1097/BOR.0000000000000455..
DOI: 10.1097/BOR.0000000000000455
Yuan S., Zhang S., Zhuang Y., Zhang H., Bai J., Hou Q. Interleukin-17 Stimulates STAT3-Mediated Endothelial Cell Activation for Neutrophil Recruitment. Cell Physiol Biochem. 2015;36(6):2340–2356. doi: 10.1159/000430197..
DOI: 10.1159/000430197
Li J.H., Pober J.S. The cathepsin B death pathway contributes to TNF plus IFN-gamma-mediated human endothelial injury. J Immunol. 2005;175(3):1858–1866. doi: 10.4049/jimmunol.175.3.1858..
DOI: 10.4049/jimmunol.175.3.1858
Zhu F., Wang Q., Guo C., Wang X., Cao X., Shi Y. et al. IL-17 induces apoptosis of vascular endothelial cells: a potential mechanism for human acute coronary syndrome. Clin Immunol. 2011;141(2):152–160. doi: 10.1016/j.clim.2011.07.003..
DOI: 10.1016/j.clim.2011.07.003
Bombeli T., Mueller M., Haeberli A. Anticoagulant properties of the vascular endothelium. Thromb Haemost. 1997;77(3):408–423. Available at: https://www.ncbi.nlm.nih.gov/pubmed/9065986.https://www.ncbi.nlm.nih.gov/pubmed/9065986
Bombeli T., Mueller M., Haeberli A. Anticoagulant properties of the vascular endothelium. Thromb Haemost. 1997;77(3):408–423. Available at: https://www.ncbi.nlm.nih.gov/pubmed/9065986.https://www.ncbi.nlm.nih.gov/pubmed/9065986
Yang X., Chang Y., Wei W. Endothelial Dysfunction and Inflammation: Immunity in Rheumatoid Arthritis. Mediators Inflamm. 2016;2016:6813016. doi: 10.1155/2016/6813016..
DOI: 10.1155/2016/6813016
Aubry M.C., Maradit-Kremers H., Reinalda M.S., Crowson C.S., Edwards W.D., Gabriel S.E. Differences in atherosclerotic coronary heart disease between subjects with and without rheumatoid arthritis. J Rheumatol. 2007;34(5):937– 942. Available at: https://www.ncbi.nlm.nih.gov/pubmed/17361987.https://www.ncbi.nlm.nih.gov/pubmed/17361987
Aubry M.C., Maradit-Kremers H., Reinalda M.S., Crowson C.S., Edwards W.D., Gabriel S.E. Differences in atherosclerotic coronary heart disease between subjects with and without rheumatoid arthritis. J Rheumatol. 2007;34(5):937– 942. Available at: https://www.ncbi.nlm.nih.gov/pubmed/17361987.https://www.ncbi.nlm.nih.gov/pubmed/17361987
Kitas G.D., Gabriel S.E. Cardiovascular disease in rheumatoid arthritis: state of the art and future perspectives. Ann Rheum Dis. 2011;70(1):8–14. doi: 10.1136/ard.2010.142133..
DOI: 10.1136/ard.2010.142133
Grignani G., Maiolo A. Cytokines and hemostasis. Haematologica. 2000;85(9):967–972. Available at: https://www.ncbi.nlm.nih.gov/pubmed/10980636.https://www.ncbi.nlm.nih.gov/pubmed/10980636
Grignani G., Maiolo A. Cytokines and hemostasis. Haematologica. 2000;85(9):967–972. Available at: https://www.ncbi.nlm.nih.gov/pubmed/10980636.https://www.ncbi.nlm.nih.gov/pubmed/10980636
Sohn R.H., Deming C.B., Johns D.C., Champion H.C., Bian C., Gardner K., Rade J.J. Regulation of endothelial thrombomodulin expression by inflammatory cytokines is mediated by activation of nuclear factor-kappa B. Blood. 2005;105(10):3910–3917. doi: 10.1182/blood-2004-03-0928..
DOI: 10.1182/blood-2004-03-0928
Hot A., Lenief V., Miossec P. Combination of IL-17 and TNFalpha induces a pro-inflammatory, pro-coagulant and pro-thrombotic phenotype in human endothelial cells. Ann Rheum Dis. 2012;71(5):768–776. doi: 10.1136/annrheumdis-2011-200468..
DOI: 10.1136/annrheumdis-2011-200468
Habets K.L., Trouw L.A., Levarht E.W., Korporaal S.J., Habets P.A., de Groot P. et al. Anti-citrullinated protein antibodies contribute to platelet activation in rheumatoid arthritis. Arthritis Res Ther. 2015;17(1):209. doi: 10.1186/s13075-015-0665-7..
DOI: 10.1186/s13075-015-0665-7
Habets K.L., Trouw L.A., Levarht E.W., Korporaal S.J., Habets P.A., de Groot P. et al. Anti-citrullinated protein antibodies contribute to platelet activation in rheumatoid arthritis. Arthritis Res Ther. 2015;17(1):209. doi: 10.1186/s13075-015-0665-7..
DOI: 10.1186/ s13075-015-0665-7
Manfredi A.A., Baldini M., Camera M., Baldissera E., Brambilla M., Peretti G. et al. Anti-TNFα agents curb platelet activation in patients with rheumatoid arthritis. Ann Rheum Dis. 2016;75(8):1511–1520. doi: 10.1136/annrheumdis-2015-208442..
DOI: 10.1136/annrheumdis-2015-208442
IL6R Genetics Consortium Emerging Risk Factors Collaboration, Sarwar N., Butterworth A.S., Freitag D.F., Gregson J., Willeit P., Gorman D.N. et al. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies. Lancet. 2012;379(9822):1205–1213. doi: 10.1016/S0140-6736(11)61931-4..
DOI: 10.1016/S0140-6736(11)61931-4
Hurlimann D., Forster A., Noll G., Enseleit F., Chenevard R., Distler O. et al. Anti-tumor necrosis factor-alpha treatment improves endothelial function in patients with rheumatoid arthritis. Circulation. 2002;106(17):2184–2187. doi: 10.1161/01.cir.0000037521.71373.44..
DOI: 10.1161/01.cir.0000037521.71373.44
Ridker P.M. From C-Reactive Protein to Interleukin-6 to Interleukin-1: Moving Upstream To Identify Novel Targets for Atheroprotection. Circ Res. 2016;118(1):145–156. doi: 10.1161/CIRCRESAHA.115.306656..
DOI: 10.1161/CIRCRESAHA.115.306656
Kleveland O., Kunszt G., Bratlie M., Ueland T., Broch K., Holte E. et al. Effect of a single dose of the interleukin-6 receptor antagonist tocilizumab on inflammation and troponin T release in patients with non-ST-elevation myocardial infarction: a double blind, randomized, placebo-controlled phase 2 trial. Eur Heart J. 2016;37(30):2406–2413. doi: 10.1093/eurheartj/ehw171..
DOI: 10.1093/eurheartj/ehw171
Schultz O., Oberhauser F., Saech J., Rubbert-Roth A., Hahn M., Krone W., Laudes M. Effects of inhibition of interleukin-6 signalling on insulin sensitivity and lipoprotein (a) levels in human subjects with rheumatoid diseases. PLoS One. 2010;5(12):e14328. doi: 10.1371/journal.pone.0014328..
DOI: 10.1371/journal.pone.0014328
Zúñiga L.A., Shen W.J., Joyce-Shaikh B., Pyatnova E.A., Richards A.G., Thom C. et al. IL-17 regulates adipogenesis, glucose homeostasis, and obesity. J Immunol. 2010;185(11):6947–6959. doi: 10.4049/jimmunol.1001269..
DOI: 10.4049/jimmunol.1001269
Liao K.P., Solomon D.H. Traditional cardiovascular risk factors, inflammation and cardiovascular risk in rheumatoid arthritis. Rheumatology (Oxford). 2013;52(1):45–52. doi: 10.1093/rheumatology/kes243..
DOI: 10.1093/rheumatology/kes243
Zhou S.F., Yuan J., Liao M.Y., Xia N., Tang T.T., Li J.J. et al. IL-17A promotes ventricular remodeling after myocardial infarction. J Mol Med (Berl). 2014;92(10):1105–1116. doi: 10.1007/s00109-014-1176-8..
DOI: 10.1007/s00109-014-1176-8
Su S.A., Yang D., Zhu W., Cai Z., Zhang N., Zhao L. et al. Interleukin-17A mediates cardiomyocyte apoptosis through Stat3-iNOS pathway. Biochim Biophys Acta. 2016;1863(11):2784–2794. doi: 10.1016/j.bbamcr.2016.08.013..
DOI: 10.1016/j.bbamcr.2016.08.013
Wu L., Ong S., Talor M.V., Barin J.G., Baldeviano G.C., Kass D.A. et al. Cardiac fibroblasts mediate IL-17A-driven inflammatory dilated cardiomyopathy. J Exp Med. 2014;211(7):1449–1464. doi: 10.1084/jem.20132126..
DOI: 10.1084/jem.20132126
Chung C.P., Oeser A., Solus J.F., Gebretsadik T., Shintani A., Avalos I. et al. Inflammation-associated insulin resistance: differential effects in rheumatoid arthritis and systemic lupus erythematosus define potential mechanisms. Arthritis Rheum. 2008;58(7):2105–2112. doi: 10.1002/art.23600..
DOI: 10.1002/art.23600
Giacomelli R., Ruscitti P., Alvaro S., Ciccia F., Liakouli V., Di Benedetto P. et al. IL-1β at the crossroad between rheumatoid arthritis and type 2 diabetes: may we kill two birds with one stone? Expert Rev Clin Immunol. 2016;12(8):849–855. doi: 10.1586/1744666X.2016.1168293..
DOI: 10.1586/1744666X.2016.1168293
Ruscitti P., Ursini F., Cipriani P., Greco M., Alvaro S., Vasiliki L. et al. IL-1 inhibition improves insulin resistance and adipokines in rheumatoid arthritis patients with comorbid type 2 diabetes: An observational study. Medicine (Baltimore). 2019;98(7):e14587. doi: 10.1097/MD.0000000000014587..
DOI: 10.1097/MD.0000000000014587
Corrado A., Colia R., Rotondo C., Sanpaolo E., Cantatore F.P. Changes in serum adipokines profile and insulin resistance in patients with rheumatoid arthritis treated with anti-TNF-α. Curr Med Res Opin. 2019;35(12):2197–2205. doi: 10.1080/03007995.2019.1654988..
DOI: 10.1080/03007995.2019.1654988
Cohen Tervaert J.W. Hypertension: an autoimmune disease? Hypertens Res. 2011;34(4):443–444. doi: 10.1038/hr.2011.15..
DOI: 10.1038/hr.2011.15
Datta D., Ferrell W.R., Sturrock R.D., Jadhav S.T., Sattar N. Inflammatory suppression rapidly attenuates microvascular dysfunction in rheumatoid arthritis. Atherosclerosis. 2007;192(2):391–395. doi: 10.1016/j.atherosclerosis.2006.05.034..
DOI: 10.1016/j.atherosclerosis.2006.05.034
Arosio E., De Marchi S., Rigoni A., Prior M., Delva P., Lechi A. Forearm haemodynamics, arterial stiffness and microcirculatory reactivity in rheumatoid arthritis. J Hypertens. 2007;25(6):1273–1278. doi: 10.1097/HJH.0b013e3280b0157e..
DOI: 10.1097/HJH.0b013e3280b0157e
Galarraga B., Khan F., Kumar PPullar T., Belch J.J. C-reactive protein: the underlying cause of microvascular dysfunction in rheumatoid arthritis. Rheumatology (Oxford). 2008;47(12):1780–1784. doi: 10.1093/rheumatology/ken386..
DOI: 10.1093/rheumatology/ken386
Jeong H., Baek S.Y., Kim S.W., Park E.J., Lee J., Kim H., Jeon C.H. C reactive protein level as a marker for dyslipidaemia, diabetes and metabolic syndrome: results from the Korea National Health and Nutrition Examination Survey. BMJ Open. 2019;9(8):e029861. doi: 10.1136/bmjopen-2019-029861..
DOI: 10.1136/bmjopen-2019-029861
Ciftci O., Yilmaz S., Topcu S., Caliskan M., Gullu H., Erdogan D. et al. Impaired coronary microvascular function and increased intimamedia thickness in rheumatoid arthritis. Atherosclerosis. 2008;198(2):332–337. doi: 10.1016/j.atherosclerosis.2007.11.013..
DOI: 10.1016/j.atherosclerosis.2007.11.013
Skeoch S., Cristinacce P.L.H., Williams H., Pemberton P., Xu D., Sun J. et al. Imaging atherosclerosis in rheumatoid arthritis: evidence for increased prevalence, altered phenotype and a link between systemic and localised plaque inflammation. Sci Rep. 2017;7(1):827. doi: 10.1038/s41598-017-00989-w..
DOI: 10.1038/s41598-017-00989-w
Emerging Risk Factors Collaboration, Kaptoge S., Di Angelantonio E., Lowe G., Pepys M.B., Thompson S.G., Collins R., Danesh J. C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant metaanalysis. Lancet. 2010;375(9709):132–140. doi: 10.1016/S0140-6736(09)61717-7..
DOI: 10.1016/S0140-6736(09)61717-7
Zegkos T., Kitas G., Dimitroulas T. Cardiovascular risk in rheumatoid arthritis: assessment, management and next steps. Ther Adv Musculoskelet Dis. 2016;8(3):86–101. doi: 10.1177/1759720X16643340..
DOI: 10.1177/1759720X16643340
Medina G., Vera-Lastra O., Peralta-Amaro A.L., Jiménez-Arellano M.P., Saavedra M.A., Cruz-Domínguez M.P., Jara L.J. Metabolic syndrome, autoimmunity and rheumatic diseases. Pharmacol Res. 2018;133:277–288. doi: 10.1016/j.phrs.2018.01.009..
DOI: 10.1016/j.phrs.2018.01.009
Francisco V., Ruiz-Fernández C., Pino J., Mera A., González-Gay M.A., Gómez R. et al. Adipokines: Linking metabolic syndrome, the immune system, and arthritic diseases. Biochem Pharmacol. 2019;165:196–206. doi: 10.1016/j.bcp.2019.03.030..
DOI: 10.1016/j.bcp.2019.03.030
Batún-Garrido J.A.J., Salas-Magaña M., Juárez-Rojop I.E., Hernández-Núñez E., Olán F. Relationship between leptin concentrations and disease activity in patients with rheumatoid arthritis. Med Clin (Barc). 2018;150(9):341– 344. doi: 10.1016/j.medcli.2017.10.020..
DOI: 10.1016/j.medcli.2017.10.020
Batún-Garrido J.A.J., Salas-Magaña M., Juárez-Rojop I.E. Association between leptin and IL-6 concentrations with cardiovascular risk in patients with rheumatoid arthritis. Clin Rheumatol. 2018;37(3):631–637. doi: 10.1007/s10067-017-3897-x..
DOI: 10.1007/s10067-017-3897-x
Agca R., Heslinga S.C., Rollefstad S., Heslinga M., McInnes I.B., Peters M.J. et al. EULAR recommendations for cardiovascular disease risk management in patients with rheumatoid arthritis and other forms of inflammatory joint disorders: 2015/2016 update. Ann Rheum Dis. 2017;76(1):17–28. doi: 10.1136/annrheumdis-2016-209775..
DOI: 10.1136/annrheumdis-2016-209775
Hollan I., Dessein P.H., Ronda N., Wasko M.C., Svenungsson E., Agewall S. et al. Prevention of cardiovascular disease in rheumatoid arthritis. Autoimmun Rev. 2015;14(10):952–969. doi: 10.1016/j.autrev.2015.06.004..
DOI: 10.1016/j.autrev.2015.06.004
Трухан Д.И. Рациональная фармакотерапия в кардиологии сквозь призму коморбидности и лекарственной безопасности. Справочник поликлинического врача. 2015;1:26–31. Режим доступа: https://con-med.ru/magazines/physician/physician-01-2015/ratsionalnaya_farmakoterapiya_v_kardiologii_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti/.https://con-med.ru/magazines/physician/physician-01-2015/ratsionalnaya_farmakoterapiya_v_kardiologii_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti/
Трухан Д.И. Рациональная фармакотерапия в кардиологии сквозь призму коморбидности и лекарственной безопасности. Справочник поликлинического врача. 2015;1:26–31. Режим доступа: https://con-med.ru/magazines/physician/physician-01-2015/ratsionalnaya_farmakoterapiya_v_kardiologii_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti/.https://con-med.ru/magazines/physician/physician-01-2015/ratsionalnaya_farmakoterapiya_v_kardiologii_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti/
Трухан Д.И. Нестероидные противовоспалительные препараты сквозь призму коморбидности и лекарственной безопасности: в фокусе – амтолметин гуацил. Consilium Medicum. 2015;17(2):27–33. Режим доступа: https://con-med.ru/magazines/consilium_medicum/consilium_medicum-02-2015/nesteroidnye_protivovospalitelnye_preparaty_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti_/.https://con-med.ru/magazines/consilium_medicum/consilium_medicum-02-2015/nesteroidnye_protivovospalitelnye_preparaty_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti_/
Трухан Д.И. Нестероидные противовоспалительные препараты сквозь призму коморбидности и лекарственной безопасности: в фокусе – амтолметин гуацил. Consilium Medicum. 2015;17(2):27–33. Режим доступа: https://con-med.ru/magazines/consilium_medicum/consilium_medicum-02-2015/nesteroidnye_protivovospalitelnye_preparaty_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti_/.https://conmed.ru/magazines/consilium_medicum/consilium_medicum-02-2015/nesteroidnye_protivovospalitelnye_preparaty_skvoz_prizmu_komorbidnosti_i_lekarstvennoy_bezopasnosti_/
Леонова М.В. Кардиотоксичность нестероидных противовоспалительных препаратов. Consilium Medicum. 2019;21(10):107–116. Режим доступа: https://consilium.orscience.ru/archive/2019/vol-21-10-2019/kardiotoksichnost-nesteroidnykh-protivovospalitelnykhpreparatov_6358/?element.https://consilium.orscience.ru/archive/2019/vol-21-10-2019/kardiotoksichnost-nesteroidnykh-protivovospalitelnykhpreparatov_6358/?element
Леонова М.В. Кардиотоксичность нестероидных противовоспалительных препаратов. Consilium Medicum. 2019;21(10):107–116. Режим доступа: https://consilium.orscience.ru/archive/2019/vol-21-10-2019/kardiotoksichnost-nesteroidnykh-protivovospalitelnykhpreparatov_6358/?element.https://consilium.orscience.ru/archive/2019/vol-21-10-2019/kardiotoksichnostnesteroidnykh-protivovospalitelnykh-preparatov_6358/?element
Lin T.C., Solomon D.H., Tedeschi S.K., Yoshida K., Kao Yang Y.H. Comparative Risk of Cardiovascular Outcomes Between Topical and Oral Nonselective NSAIDs in Taiwanese Patients With Rheumatoid Arthritis. J Am Heart Assoc. 2017;6(11):e006874. doi: 10.1161/JAHA.117.006874..
DOI: 10.1161/JAHA.117.006874
Grigoriou A., Ibrahim F., Chaabo K., Scott D.L., Steer S., Galloway J. Cardiovascular risk with NSAIDs in rheumatoid arthritis: an analysis using routinely collected data. Rheumatology (Oxford). 2016;55(4):763–764. doi: 10.1093/rheumatology/kev386..
DOI: 10.1093/rheumatology/kev386
Заводовский Б.В., Сивордова Л.Е. Кардиоваскулярная безопасность применения нестероидных противовоспалительных препаратов при хронических воспалительных ревматических заболеваниях. Терапевтический архив. 2018;90(8):101–106. doi: 10.26442/terarkh2018908101-106..
DOI: 10.26442/terarkh2018908101-106
Sparks J.A. Rheumatoid Arthritis. Ann Intern Med. 2019;170(1):ITC1–ITC16. doi: 10.7326/AITC201901010..
DOI: 10.7326/AITC201901010
Braun J., Baraliakos X., Westhoff T. Nonsteroidal anti-inflammatory drugs and cardiovascular risk – a matter of indication. Semin Arthritis Rheum. 2020;50(2):285–288. doi: 10.1016/j.semarthrit.2019.07.012..
DOI: 10.1016/j.semarthrit.2019.07.012
Rawla P. Cardiac and vascular complications in rheumatoid arthritis. Reumatologia. 2019;57(1):27–36. doi: 10.5114/reum.2019.83236..
DOI: 10.5114/reum.2019.83236
Dvirnik N., Belley-Cote E.P., Hanif H., Devereaux P.J., Lamy A., Dieleman J.M. et al. Steroids in cardiac surgery: a systematic review and meta-analysis. Br J Anaesth. 2018;120(4):657–667. doi: 10.1016/j.bja.2017.10.025..
DOI: 10.1016/j.bja.2017.10.025
Rincón del I., Battafarano D.F., Restrepo J.F., Erikson J.M., Escalante A. Glucocorticoid Dose Thresholds Associated With All-Cause and Cardiovascular Mortality in Rheumatoid Arthritis. Arthritis Rheumatol. 2014;66(2):264–272. doi: 10.1002/art.38210..
DOI: 10.1002/art.38210
Wei L., MacDonald T.M., Walker B.R. Taking glucocorticoids by prescription is associated with subsequent cardiovascular disease. Ann Intern Med. 2004;141(10):764–770. doi: 10.7326/0003-4819-141-10-200411160-00007..
DOI: 10.7326/0003-4819-141-10-200411160-00007
Suissa S., Bernatsky S., Hudson M. Antirheumatic drug use and the risk of acute myocardial infarction. Arthritis Rheum. 2006;55(4):531–536. doi: 10.1002/art.22094..
DOI: 10.1002/art.22094
Wolfe F., Michaud K. The risk of myocardial infarction and pharmacologic and nonpharmacologic myocardial infarction predictors in rheumatoid arthritis. A cohort and nested case–control analysis. Arthritis Rheum. 2008;58(9):2612–2621. doi: 10.1002/art.23811..
DOI: 10.1002/art.23811
Panoulas V.F., Douglas K.M., Milionis H.J., Stavropoulos-Kalinglou A., Nightingale P., Kita M.D. et al. Prevalence and associations of hypertension and its control in patients with rheumatoid arthritis. Rheumatology (Oxford). 2007;46(9):1477-82. doi: 10.1093/rheumatology/kem169..
DOI: 10.1093/rheumatology/kem169
Hafström I., Rohani M., Deneberg S., Wörnert M., Jogestrand T., Frostegård J. Effects of low-dose prednisolone on endothelial function, atherosclerosis, and traditional risk factors for atherosclerosis in patients with rheumatoid arthritis – a randomized study. J Rheumatol. 2007;34(9):1810–1816. Available at: https://www.researchgate.net/publication/6143870_.https://www.researchgate.net/publication/6143870_
Hafström I., Rohani M., Deneberg S., Wörnert M., Jogestrand T., Frostegård J. Effects of low-dose prednisolone on endothelial function, atherosclerosis, and traditional risk factors for atherosclerosis in patients with rheumatoid arthritis – a randomized study. J Rheumatol. 2007;34(9):1810–1816. Available at: https://www.researchgate.net/publication/6143870_.https://www.researchgate.net/publication/6143870_
Georgiadis A.N., Papavasiliou E.C., Lourida E.S., Alamanos Y., Kostara C., Tselepis A.D., Drosos A.A. Atherogenic lipid profile is a feature characteristic of patients with early rheumatoid arthritis: effect of early treatment – a prospective, controlled study. Arthritis Res Ther. 2006;8(3):R82. doi: 10.1186/ar1952..
DOI: 10.1186/ar1952
Davis J.M. 3rd, Maradit Kremers H., Crowson C.S., Nicola P.J., Ballman K.V., Therneau T.M. et al. Glucocorticoids and cardiovascular events in rheumatoid arthritis: a population-based cohort study. Arthritis Rheum. 2007;56(3):820–830. doi: 10.1002/art.22418..
DOI: 10.1002/art.22418
Naranjo A., Sokka T., Descalzo M.A., Calvo-Alén J., Hørslev-Petersen K., Luukkainen R.K. et al. QUEST-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..
DOI: 10.1186/ar2383
Sihnoven S., Korpela M., Mustonen J., Huhtala H., Karstila K., Pasternack A. Mortality in patients with rheumatoid arthritis treated with low-dose oral glucocorticoids. A population-based cohort study. J Rheumatol. 2006;33(9):1740–1746. Available at: https://www.ncbi.nlm.nih.gov/pubmed/16881099.https://www.ncbi.nlm.nih.gov/pubmed/16881099
Sihnoven S., Korpela M., Mustonen J., Huhtala H., Karstila K., Pasternack A. Mortality in patients with rheumatoid arthritis treated with low-dose oral glucocorticoids. A population-based cohort study. J Rheumatol. 2006;33(9):1740–1746. Available at: https://www.ncbi.nlm.nih.gov/pubmed/16881099.https://www.ncbi.nlm.nih.gov/pubmed/16881099
Van Halm V.P., Nurmohamed M.T., Twisk J.W., Dijkmans B.A., Voskuyl A.E. Disease-modifying antirheumatic drugs are associated with a reduced risk for cardiovascular disease in patients with rheumatoid arthritis: a case control study. Arthritis Res Ther. 2006;8(5):R151. doi: 10.1186/ar2045..
DOI: 10.1186/ar2045
Choi H.K., Hernan M.A., Seeger J.D., Robins J.M., Wolfe F. Methotrexate and mortality in patients with rheumatoid arthritis: a prospective study. Lancet. 2002;359(9313):1173–1177. doi: 10.1016/S0140-6736(02)08213-2..
DOI: 10.1016/S0140-6736(02)08213-2
Salliot C., van der Heijde D. Long-term safety of methotrexate monotherapy in patients with rheumatoid arthritis: a systematic literature research. Ann Rheum Dis. 2009;68:1100–1104. doi: 10.1136/ard.2008.093690..
DOI: 10.1136/ard.2008.093690
Smolen J.S., Landewé R., Breedveld F.C., Dougados M., Emery P., GaujouxViala C. et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs. Ann Rheum Dis. 2010;69(6):964–975. doi:10.1136/ard.2009.126532..
DOI: 10.1136/ard.2009.126532
Mori H., Okada Y., Kawaguchi M., Iwata S., Yoshikawa M., Sonoda S. et al. A Study of the Vascular Endothelial Function in Patients with Type 2 Diabetes Mellitus and Rheumatoid Arthritis. Intern Med. 2019;58(10):1383–1390. doi: 10.2169/internalmedicine.1564-18..
DOI: 10.2169/internalmedicine.1564-18
Westlake S.L., Colebatch A.N., Baird J., Kiely P., Quinn M., Choy E. et al. The effect of methotrexate on cardiovascular disease in patients with rheumatoid arthritis: a systematic literature review. Rheumatology (Oxford). 2010;49(2):295–307. doi: 10.1093/rheumatology/kep366..
DOI: 10.1093/rheumatology/kep366
Micha R., Imamura F., Wyler von Ballmoos M., Solomon D.H., Hernán M.A., Ridker P.M., Mozaffarian D. Systemic review and meta-analysis of methotrexate use and risk of cardiovascular disease. Am J Cardiol. 2011;108(9):1362–1370. doi: 10.1016/j.amjcard.2011.06.054..
DOI: 10.1016/j.amjcard.2011.06.054
Roubille C., Richer V., Starnino T., McCourt C., McFarlane A., Fleming P. 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):480–489. doi: 10.1136/annrheumdis-2014-206624..
DOI: 10.1136/annrheumdis-2014-206624
Mangoni A.A., Tommasi S., Zinellu A., Sotgia S., Bassu S., Piga M. et al. Methotrexate and Vasculoprotection: Mechanistic Insights and Potential Therapeutic Applications in Old Age. Curr Pharm Des. 2019;25(39):4175– 4184. doi: 10.2174/1381612825666191112091700..
DOI: 10.2174/1381612825666191112091700
Bălănescu A.R., Bojincă V.C., Bojincă M., Donisan T., Bălănescu S.M. Cardiovascular effects of methotrexate in immune-mediated inflammatory diseases. Exp Ther Med. 2019;17(2):1024–1029. doi: 10.3892/etm.2018.6992..
DOI: 10.3892/etm.2018.6992
Wallace D.J., Metzger A.L., Stecher V.J., Turnbull B.A., Kern P.A. Cholesterollowering effect of hydroxychloroquine in patients with rheumatic disease: reversal of deleterious effects of steroids on lipids. Am J Med. 1990;89(3):322–326. doi: 10.1016/0002-9343(90)90345-e..
DOI: 10.1016/0002-9343(90)90345-e
Atzeni F., Turiel M., Caporali R., Cavagna L., Tomasoni L., Sitia S., SarziPuttini P. The effect of pharmacological therapy on the cardiovascular system of patients with systemic rheumatic diseases. Autoimmun Rev. 2010;9(12):835–839. doi: 10.1016/j.autrev.2010.07.018..
DOI: 10.1016/j.autrev.2010.07.018
Shapiro M., Levy Y. The association between hydroxychloroquine treatment and cardiovascular morbidity among rheumatoid arthritis patients. Oncotarget. 2017;9(5):6615–6622. doi: 10.18632/oncotarget.23570..
DOI: 10.18632/oncotarget.23570
Rempenault C., Combe B., Barnetche T., Gaujoux-Viala C., Lukas C., Morel J., Hua C. Metabolic and cardiovascular benefits of hydroxychloroquine in patients with rheumatoid arthritis: a systematic review and meta-analysis. Ann Rheum Dis. 2018;77(1):98–103. doi: 10.1136/annrheumdis-2017-211836..
DOI: 10.1136/annrheumdis-2017-211836
Morris S.J., Wasko M.C., Antohe J.L., Sartorius J.A., Kirchner H.L., Dancea S., Bili A. Hydroxychloroquine use associated with improvement in lipid profiles in rheumatoid arthritis patients. Arthritis Care Res (Hoboken). 2011;63(4):530–534. doi: 10.1002/acr.20393..
DOI: 10.1002/acr.20393
Kerr G., Aujero M., Richards J., Sayles H., Davis L., Cannon G. et al. Associations of Hydroxychloroquine use with lipid profiles in rheumatoid arthritis: pharmacologic implications. Arthritis Care Res (Hoboken). 2014;66(11):1619–1626. doi: 10.1002/acr.22341..
DOI: 10.1002/acr.22341
Li C., Wang X.R., Ji H.J., Zhang X.Y., Li X.F., Wang L.Z. et al. Cardiovascular disease in rheumatoid arthritis: medications and risk factors in China. Clin Rheumatol. 2017;36(5):1023–1029. doi: 10.1007/s10067-017-3596-7..
DOI: 10.1007/s10067-017-3596-7
Wasko M.C., Hubert H.B., Lingala V.B., Elliott J.R., Luggen M.E., Fries J.F., Ward M.M. Hydroxychloroquine and risk of diabetes in patients with rheumatoid arthritis. JAMA. 2007;298(2):187–193. doi: 10.1001/jama.298.2.187..
DOI: 10.1001/jama.298.2.187
Nicolau J., Lequerré T., Bacquet H., Vittecoq O. Rheumatoid arthritis, insulin resistance, and diabetes. Joint Bone Spine. 2017;84(4):411–416. doi: 10.1016/j.jbspin.2016.09.001..
DOI: 10.1016/j.jbspin.2016.09.001
Bili A., Sartorius J.A., Kirchner H.L., Morris S.J., Ledwich L.J., Antohe J.L. et al. Hydroxychloroquine use and decreased risk of diabetes in rheumatoid arthritis patients. J Clin Rheumatol. 2011;17(3):115–120. doi: 10.1097/RHU.0b013e318214b6b5..
DOI: 10.1097/RHU.0b013e318214b6b5
Bili A., Sartorius J.A., Kirchner H.L., Morris S.J., Ledwich L.J., Antohe J.L. et al. Hydroxychloroquine use and decreased risk of diabetes in rheumatoid arthritis patients. J Clin Rheumatol. 2011;17(3):115–120. doi: 10.1097/RHU.0b013e318214b6b5..
DOI: 10.1097/ RHU.0b013e318214b6b5
Hung Y.M., Wang Y.H., Lin L., Wang P.Y.P., Chiou J.Y., Wei J.C. Hydroxychloroquine may be associated with reduced risk of coronary artery diseases in patients with rheumatoid arthritis: A nationwide population-based cohort study. Int J Clin Pract. 2018;72(5):e13095. doi: 10.1111/ijcp.13095..
DOI: 10.1111/ijcp.13095
Rho Y.H., Oeser A., Chung C.P., Milne G.L., Stein C.M. Drugs used in the treatment of rheumatoid arthritis: relationship between current use and cardiovascular risk factors. Arch Drug Inf. 2009;2(2):34–40. doi: 10.1111/j.1753-5174.2009.00019.x..
DOI: 10.1111/j.1753-5174.2009.00019.x
Wasko MC. Rheumatoid arthritis and cardiovascular disease. Curr Rheumatol Rep. 2008;10(5):390–397. doi: 10.1007/s11926-008-0063-0..
DOI: 10.1007/s11926-008-0063-0
Tam H.-W., Yeo K.-J., Leong P.-Y., Chen C.H., Li Y.C., Ma C.M. et al. Sulfasalazine might reduce risk of cardiovascular diseases in patients with ankylosing spondylitis: A nationwide population-based retrospective cohort study. Int J Rheum Dis. 2017;20(3):363–370. doi: 10.1111/1756-185X.12986..
DOI: 10.1111/1756-185X.12986
Vohra K., Krishan P., Varma S., Kalra H.S. Exploring the potential of lowdose sulfasalazine in stable coronary artery disease patients: randomized, double-blind, placebo-controlled study. Eur Heart J Cardiovasc Pharmacother. 2015;1(4):214–216. doi: 10.1093/ehjcvp/pvv021..
DOI: 10.1093/ehjcvp/pvv021
MacMullan P.A., Madigan A.M., Paul N., Peace A.J., Alagha A., Nolan K.B. et al. Sulfasalazine and its metabolites inhibit platelet function in patients with inflammatory arthritis. Clin Rheumatol. 2016;35(2):447–455. doi: 10.1007/s10067-014-2769-x..
DOI: 10.1007/s10067-014-2769-x
Woodworth T.G., den Broeder A.A. Treating to target in established rheumatoid arthritis: Challenges and opportunities in an era of novel targeted therapies and biosimilars. Best Pract Res Clin Rheumatol. 2015;29(4–5):543–549. doi: 10.1016/j.berh.2015.10.001..
DOI: 10.1016/j.berh.2015.10.001
Day A.L., Singh J.A. Cardiovascular Disease Risk in Older Adults and Elderly Patients with Rheumatoid Arthritis: What Role Can DiseaseModifying Antirheumatic Drugs Play in Cardiovascular Risk Reduction? Drugs Aging. 2019;36(6):493–510. doi: 10.1007/s40266-019-00653-0..
DOI: 10.1007/s40266-019-00653-0
Charles-Schoeman C., Wang X., Lee Y.Y., Shahbazian A., Navarro-Millán I., Yang S. et al. Association of Triple Therapy with Improvement in Cholesterol Profiles over Two-Year Followup in the Treatment of Early Aggressive Rheumatoid Arthritis Trial. Arthritis Rheumatol. 2016;68(3):577–586. doi: 10.1002/art.39502..
DOI: 10.1002/art.39502
Kisiel B., Kruszewski R., Juszkiewicz A., Raczkiewicz A., Bachta A., Tłustochowicz M. et al. Methotrexate, Cyclosporine A, and Biologics Protect against Atherosclerosis in Rheumatoid Arthritis. J Immunol Res. 2015;2015:759610. doi: 10.1155/2015/759610..
DOI: 10.1155/2015/759610
Van Doornum S., McColl G., Wicks I.P. Tumour necrosis factor antagonists improve disease activity but not arterial stiffness in rheumatoid arthritis. Rheumatology (Oxford). 2005;44(11):1428–1432. doi: 10.1093/rheumatology/kei033..
DOI: 10.1093/rheumatology/kei033
Tikiz H., Arslan O., Pirildar T., Tikiz C., Bayindir P. The effect of anti-tumor necrosis factor (TNF)-alpha therapy with etanercept on endothelial functions in patients with rheumatoid arthritis. Anadolu Kardiyol Derg. 2010;10(2):98–103. doi: 10.5152/akd.2010.031..
DOI: 10.5152/akd.2010.031
Gonzalez-Juanatey C., Testa A., Garcia-Castelo A., Garcia-Porrua C., Llorca J., Gonzalez-Gay M.A. Active but transient improvement of endothelial function in rheumatoid arthritis patients undergoing long-term treatment with anti-tumor necrosis factor alpha antibody. Arthritis Rheum. 2004;51(3):447–450. doi: 10.1002/art.20407..
DOI: 10.1002/art.20407
Mäki-Petäjä K.M., Hall F.C., Booth A.D., Wallace S.M., Yasmin, Bearcroft P.W., Harish S. et al. Rheumatoid arthritis is associated with increased aortic pulse-wave velocity, which is reduced by anti-tumor necrosis factor-alpha therapy. Circulation. 2006;114(11):1185–1192. doi: 10.1161/CIRCULATIONAHA.105.601641..
DOI: 10.1161/CIRCULATIONAHA.105.601641
Wong M., Oakley S.P., Young L., Jiang B.Y., Wierzbicki A., Panayi G. et al. Infliximab improves vascular stiffness in patients with rheumatoid arthritis. Ann Rheum Dis. 2009;68(8):1277–1284. doi: 10.1136/ard.2007.086157..
DOI: 10.1136/ard.2007.086157
Angel K., Provan S.A., Fagerhol M.K., Mowinckel P., Kvien T.K., Atar D. Effect of 1-year anti-TNF-α therapy on aortic stiffness, carotid atherosclerosis, and calprotectin in inflammatory arthropathies: a controlled study. Am J Hypertens. 2012;25(6):644–650. doi: 10.1038/ajh.2012.12..
DOI: 10.1038/ajh.2012.12
Dulai R., Perry M., Twycross-Lewis R., Morrissey D., Atzeni F., Greenwald S. The effect of tumor necrosis factor-α antagonists on arterial stiffness in rheumatoid arthritis: a literature review. Semin Arthritis Rheum. 2012;42(1):1–8. doi: 10.1016/j.semarthrit.2012.02.002..
DOI: 10.1016/j.semarthrit.2012.02.002
Vlachopoulos C., Gravos A., Georgiopoulos G., Terentes-Printzios D., Ioakeimidis N., Vassilopoulos D. et al. The effect of TNF-a antagonists on aortic stiffness and wave reflections: a meta-analysis. Clin Rheumatol. 2018;37(2):515–526. doi: 10.1007/s10067-017-3657-y..
DOI: 10.1007/s10067-017-3657-y
Del Porto F., Laganà B., Lai S., Nofroni I., Tinti F., Vitale M. et al. Response to anti-tumor necrosis factor alpha blockade is associated with reduction of carotid intima-media thickness in patients with active rheumatoid arthritis. Rheumatology (Oxford). 2007;46(7):1111–1115. doi: 10.1093/rheumatology/kem089..
DOI: 10.1093/rheumatology/kem089
Arida A., Protogerou A.D., Konstantonis G., Fragiadaki K., Kitas G.D., Sfikakis P.P. Atherosclerosis is not accelerated in rheumatoid arthritis of low activity or remission, regardless of antirheumatic treatment modalities. Rheumatology (Oxford). 2017;56(6):934–939. doi: 10.1093/rheumatology/kew506..
DOI: 10.1093/rheumatology/kew506
Jacobsson L.T., Turesson C., Gulfe A., Kapetanovic M.C., Petersson I.F., Saxne T., Geborek P. Treatment with tumor necrosis factor blockers is associated with a lower incidence of first cardiovascular events in patients with rheumatoid arthritis. J Rheumatol. 2005;32(7):1213–1218. Available at: https://www.ncbi.nlm.nih.gov/pubmed/15996054.https://www.ncbi.nlm.nih.gov/pubmed/15996054
Jacobsson L.T., Turesson C., Gulfe A., Kapetanovic M.C., Petersson I.F., Saxne T., Geborek P. Treatment with tumor necrosis factor blockers is associated with a lower incidence of first cardiovascular events in patients with rheumatoid arthritis. J Rheumatol. 2005;32(7):1213–1218. Available at: https://www.ncbi.nlm.nih.gov/pubmed/15996054.https://www.ncbi.nlm.nih.gov/pubmed/15996054
Dixon W.G., Watson K.D., Lunt M., Hyrich K.L., Silman A.J., Symmons D.P. Reduction in the incidence of myocardial infarction in patients with rheumatoid arthritis who respond to anti-tumor necrosis factor alpha therapy: results from the British Society for Rheumatology Biologics Register. Arthr Rheum. 2007;56(9):2905–2912. doi: 10.1002/art.22809..
DOI: 10.1002/art.22809
Lee J.L., Sinnathurai P., Buchbinder R., Hill C., Lassere M., March L. Biologics and cardiovascular events in inflammatory arthritis: a prospective national cohort study. Arthritis Res Ther. 2018;20(1):171. doi: 10.1186/s13075-018-1669-x..
DOI: 10.1186/s13075-018-1669-x
Low A.S.L., Symmons D.P.M., Lunt M., Mercer L.K., Gale C.P., Watson K.D. et al. Relationship between exposure to tumour necrosis factor inhibitor therapy and incidence and severity of myocardial infarction in patients with rheumatoid arthritis. Ann Rheum Dis. 2017;76(4):654–660. doi: 10.1136/annrheumdis-2016-209784..
DOI: 10.1136/annrheumdis-2016-209784
Di Micco P., Ferrazzi P., Librè L., Mendolicchio L., Quaglia I., De Marco M. et al. Intima-media thickness evolution after treatment with infliximab in patients with rheumatoid arthritis. Int J Gen Med. 2009;2:141–144. doi: 10.2147/ijgm.s5178..
DOI: 10.2147/ijgm.s5178
Lazzerini P.E., Acampa M., Hammoud M., Maffei S., Capecchi P.L., Selvi E. et al. Arrhythmic risk during acute infusion of infliximab: a prospective, singleblind, placebo-controlled, crossover study in patients with chronic arthritis. J Rheumatol. 2008;35(10):1958–1965. Available at: https://www.ncbi.nlm.nih.gov/pubmed/18709695.https://www.ncbi.nlm.nih.gov/pubmed/18709695
Lazzerini P.E., Acampa M., Hammoud M., Maffei S., Capecchi P.L., Selvi E. et al. Arrhythmic risk during acute infusion of infliximab: a prospective, singleblind, placebo-controlled, crossover study in patients with chronic arthritis. J Rheumatol. 2008;35(10):1958–1965. Available at: https://www.ncbi.nlm.nih.gov/pubmed/18709695.https://www.ncbi.nlm.nih.gov/pubmed/18709695
Chung E.S., Packer M., Lo K.H., Fasanmade A.A., Willerson J.T. Randomized, double-blind, placebocontrolled, pilot trial of infliximab, a chimeric monoclonal antibody to tumor necrosis factor-alpha, in patients with moderate-tosevere heart failure: results of the anti-TNF Therapy Against Congestive Heart Failure (ATTACH) trial. Circulation. 2003;107(25):3133– 3140. doi: 10.1161/01.CIR.0000077913.60364.D2..
DOI: 10.1161/01.CIR.0000077913.60364.D2
Widdifield J., Bernatsky S., Paterson J.M., Thorne J.C., Cividino A., Pope J. et al. Quality care in seniors with new-onset rheumatoid arthritis: a Canadian perspective. Arthritis Care Res (Hoboken). 2011;63(1):53–57. doi: 10.1002/acr.20304..
DOI: 10.1002/acr.20304
Singh J.A., Furst D.E., Bharat A., Curtis J.R., Kavanaugh A.F., Kremer J.M. et al. 2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis. Arthritis Care Res (Hoboken). 2012;64(5):625–639. doi: 10.1002/acr.21641..
DOI: 10.1002/acr.21641
Hassan S., Feld J., Cohen S., Zisman D. The effect of biologic therapy on the lipid profile of rheumatoid arthritis (ra), psoriatic arthritis (psa) and ankylosing spondylitis (as) patients. Harefuah. 2017;156(7):446–450. Available at: https://www.ncbi.nlm.nih.gov/pubmed/28786273.https://www.ncbi.nlm.nih.gov/pubmed/28786273
Hassan S., Feld J., Cohen S., Zisman D. The effect of biologic therapy on the lipid profile of rheumatoid arthritis (ra), psoriatic arthritis (psa) and ankylosing spondylitis (as) patients. Harefuah. 2017;156(7):446–450. Available at: https://www.ncbi.nlm.nih.gov/pubmed/28786273.https://www.ncbi.nlm.nih.gov/pubmed/28786273
Virone A., Bastard J.P., Fellahi S., Capeau J., Rouanet S., Sibilia J. et al. Comparative effect of tumour necrosis factor inhibitors versus other biological agents on cardiovascular risk-associated biomarkers in patients with rheumatoid arthritis. RMD Open. 2019;5(2):e000897. doi: 10.1136/rmdopen-2019-000897..
DOI: 10.1136/rmdopen-2019-000897
Castañeda S., Remuzgo-Martínez S., López-Mejías R., Genre F., Calvo-Alén J., Llorente I. et al. Rapid beneficial effect of the IL-6 receptor blockade on insulin resistance and insulin sensitivity in non-diabetic patients with rheumatoid arthritis. Clin Exp Rheumatol. 2019;37(3):465–473. Available at: https://www.ncbi.nlm.nih.gov/pubmed/30418124.https://www.ncbi.nlm.nih.gov/pubmed/30418124
Castañeda S., Remuzgo-Martínez S., López-Mejías R., Genre F., Calvo-Alén J., Llorente I. et al. Rapid beneficial effect of the IL-6 receptor blockade on insulin resistance and insulin sensitivity in non-diabetic patients with rheumatoid arthritis. Clin Exp Rheumatol. 2019;37(3):465–473. Available at: https://www.ncbi.nlm.nih.gov/pubmed/30418124.https://www.ncbi.nlm.nih.gov/pubmed/30418124
Provan S.A., Berg I.J., Hammer H.B., Mathiessen A., Kvien T.K., Semb A.G. The Impact of Newer Biological Disease Modifying Anti-Rheumatic Drugs on Cardiovascular Risk Factors: A 12-Month Longitudinal Study in Rheumatoid Arthritis Patients Treated with Rituximab, Abatacept and Tociliziumab. PLoS One. 2015;10(6):e0130709. doi: 10.1371/journal.pone.0130709..
DOI: 10.1371/journal.pone.0130709
Castagné B., Viprey M., Martin J., Schott A.M., Cucherat M., Soubrier M. Cardiovascular safety of tocilizumab: A systematic review and network metaanalysis. PLoS One. 2019;14(8):e0220178. doi: 10.1371/journal.pone.0220178..
DOI: 10.1371/journal.pone.0220178
Ursini F., Ruscitti P., Caio G.P.I., Manfredini R., Giacomelli R., De Giorgio R. The effect of non-TNF-targeted biologics on vascular dysfunction in rheumatoid arthritis: A systematic literature review. Autoimmun Rev. 2019;18(5):501–509. doi: 10.1016/j.autrev.2019.03.008..
DOI: 10.1016/j.autrev.2019.03.008
Cañete J.D., Hernández M.V., Sanmartí R. Safety profile of biological therapies for treating rheumatoid arthritis. Expert Opin Biol Ther. 2017;17(9):1089–1103. doi: 10.1080/14712598.2017.1346078..
DOI: 10.1080/14712598.2017.1346078
Fragoulis G.E., Panayotidis I., Nikiphorou E. Cardiovascular Risk in Rheumatoid Arthritis and Mechanistic Links: From Pathophysiology to Treatment. Curr Vasc Pharmacol. 2020;18(5):431–446. doi: 10.2174/1570161117666190619143842..
DOI: 10.2174/1570161117666190619143842
Reiss A.B., Silverman A., Khalfan M., Vernice N.A., Kasselman L.J., Carsons S.E., De Leon J. Accelerated Atherosclerosis in Rheumatoid Arthritis: Mechanisms and Treatment. Curr Pharm Des. 2019;25(9):969–986. doi: 10.2174/1381612825666190430113212..
DOI: 10.2174/1381612825666190430113212
Трухан Д.И., Иванова Д.С., Белус К.Д. Ревматоидный артрит и традиционные кардиоваскулярные факторы риска: актуальные аспекты реальной клинической практики. Consilium Medicum. 2020;22(1):19–25. doi: 10.26442/20751753.2020.1.200052..
DOI: 10.26442/20751753.2020.1.200052