Tumour necrosis factor antagonist use and associated risk reduction of cardiovascular events among patients with rheumatoid arthritis

被引:281
|
作者
Greenberg, Jeffrey D. [1 ]
Kremer, Joel M. [2 ]
Curtis, Jeffrey R. [3 ]
Hochberg, Marc C. [4 ]
Reed, George [5 ]
Tsao, Peter [6 ]
Farkouh, Michael E. [7 ]
Nasir, Adeel [1 ]
Setoguchi, Soko [8 ]
Solomon, Daniel H. [6 ,8 ]
机构
[1] NYU, Hosp Joint Dis, Dept Rheumatol, New York, NY 10003 USA
[2] Albany Med Coll, Div Rheumatol, Albany, NY 12208 USA
[3] Univ Alabama, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[4] Univ Maryland, Div Clin Immunol & Rheumatol, Baltimore, MD 21201 USA
[5] Univ Massachusetts, Sch Med, Div Prevent & Behav Med, Worcester, MA USA
[6] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[7] Mt Sinai Heart, Clin Trials Unit, New York, NY USA
[8] Brigham & Womens Hosp, Div Pharmacoepidemiol, Boston, MA 02115 USA
基金
美国医疗保健研究与质量局; 美国国家卫生研究院;
关键词
FACTOR-ALPHA BLOCKADE; C-REACTIVE PROTEIN; MYOCARDIAL-INFARCTION; INSULIN-RESISTANCE; CORRONA DATABASE; TNF-ALPHA; DISEASE; MORTALITY; THERAPY; ATHEROSCLEROSIS;
D O I
10.1136/ard.2010.129916
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To examine the association of cardiovascular events with tumour necrosis factor (TNF) a antagonist use compared with non-biological disease-modifying antirheumatic drug (DMARD) utilisation in patients with rheumatoid arthritis (RA). Methods The study population included 10 156 patients enrolled in the Consortium of Rheumatology Researchers of North America RA registry. Three study cohorts were defined based on three mutually exclusive drug use categories, including TNF antagonists, methotrexate and other non-biological DMARDs. HR were calculated adjusting for cardiovascular risk factors, RA disease characteristics and prednisone use. The primary study outcome was a composite of non-fatal myocardial infarction (MI), transient ischaemic attack (TIA) or stroke and cardiovascular-related death. Results There were 88 cardiovascular events, including 26 MI, 45 TIA/strokes and 17 cardiovascular-related deaths. After adjusting for age, gender, cardiovascular risk factors and RA disease characteristics, patients using a TNF antagonist experienced a reduced risk of the primary composite cardiovascular endpoint (HR 0.39, 95% CI 0.19 to 0.82) compared with users of non-biological DMARDs. Methotrexate was not associated with a reduced risk (HR 0.94, 95% CI 0.49 to 1.80). Prednisone use was associated with a dose-dependent increased risk (p=0.04). The risk reduction associated with TNF antagonists was also observed for non-fatal cardiovascular events (HR 0.35, 95% CI 0.16 to 0.74). Conclusion TNF antagonist use was associated with a reduced risk of cardiovascular events in patients with RA.
引用
收藏
页码:576 / 582
页数:7
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