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To treat RA, we must go to
Rheumatoid arthritis (RA) is a common disease in the department of rheumatology and immunology, and the basic pathology is manifested as synovitis, vascular filament formation, and gradual destruction of joint cartilage and bone, which eventually leads to joint deformity and loss of function, which seriously affects the patient's physical function and quality of life [1
The triggers for CVD in patients with RA can be divided into two broad categories, namely traditional risk factors and non-traditional risk factors
In January 2017, the European Federation against Rheumatism (EULAR) updated its recommendations for CVD risk management in patients with RA and other inflammatory joint diseases [7].
Systemic inflammation plays an important role in the development of CVD in patients with RA, and therapeutic drugs targeting inflammatory mediators may reduce the risk
The data suggest that patients with RA treated with b/tsDMARDs have a generally lower
Multiple studies have shown that abatacept may be more effective at reducing the risk of CVD in patients with RA than csDMARDs and TNF inhibitors
In the process of clinical practice, it is necessary to consider the specific situation of patients with different RA, and select DMARDs with different mechanisms of action for patients with different risk factors to reduce the risk
Professor Zhu Jing
Director of the Department of Rheumatology and Immunology, Sichuan Provincial People's Hospital
Chief Physician Master Tutor
President of the Rheumatology and Immunology Branch of Sichuan Medical Doctor Association
Chairman of the Rheumatology Committee of sichuan Medical Health and Health Promotion Association
Vice Chairman of the Rheumatology and Immunology Branch of Sichuan Medical Association
Member of the Standing Committee of the Rheumatology Physician Branch of the Chinese Medical Doctor Association
Member of the Standing Committee of the Rheumatology and Immunology Committee of the Cross-Strait Medical and Health Exchange Association, Deputy Leader of the Science Popularization Education Group, and Member of the Standing Committee of the Chronic Disease Management Group
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Comparative Risk of Cardiovascular Events With Biologic and Synthetic Disease-Modifying Antirheumatic Drugs in Patients With Rheumatoid Arthritis: A Systematic Review and Meta-Analysis[J].
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NOT ALL THE SAME? REACHING REMISSION REDUCES THE RISK OF CVD IN PATIENTS WITH RA, BUT PATIENTS ON BIOLOGICS MAY BE BETTER PROTECTED[J].
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J Rheumatol.
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[12]Singh S, Fumery M, Singh AG, et al.
Comparative Risk of Cardiovascular Events With Biologic and Synthetic Disease-Modifying Antirheumatic Drugs in Patients With Rheumatoid Arthritis: A Systematic Review and Meta-Analysis[J].
Arthritis Care Res (Hoboken).
2020, 72(4):561-576.
[13]Hsieh MJ, Lee CH, Tsai ML, et al.
Biologic Agents Reduce Cardiovascular Events in Rheumatoid Arthritis Not Responsive to Tumour Necrosis Factor Inhibitors: A National Cohort Study[J].
Can J Cardiol.
2020, 36(11):1739-1746.
[14]Ursini F, Russo E, Letizia Hribal M, et al.
Abatacept improves whole-body insulin sensitivity in rheumatoid arthritis: an observational study[J].
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[15]Galiuto L, Patrono C.
Differential cardiovascular effects of disease-modifying antirheumatic drugs in rheumatoid arthritis[J].
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[16]Atzeni F, Rodríguez-Carrio J, Popa CD, et al.
Cardiovascular effects of approved drugs for rheumatoid arthritis[J].
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Increased cardiovascular risk in rheumatoid arthritis: mechanisms and implications[J].
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Triggers of Cardiovascular Diseases in Rheumatoid Arthritis[J].
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[19]Fazeli MS, Khaychuk V, Wittstock K, et al.
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Clin Med Insights Arthritis Musculoskelet Disord.
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This article is only used to provide scientific information to healthcare professionals and does not represent the position of the
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