Response to biological treatment and subsequent risk of coronary events in rheumatoid arthritis

医学 类风湿性关节炎 风湿病 内科学 急性冠脉综合征 队列 比例危险模型 人口 危险系数 物理疗法 心肌梗塞 置信区间 环境卫生
作者
Lotta Ljung,Solbritt Rantapää‐Dahlqvist,Lennart Jacobsson,Johan Askling
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:75 (12): 2087-2094 被引量:73
标识
DOI:10.1136/annrheumdis-2015-208995
摘要

Objectives

Whether the increased risk of comorbidities, such as cardiovascular disease, in rheumatoid arthritis (RA) can be reverted by particular antirheumatic therapies, or response to these, is unclear but of critical clinical importance. We wanted to investigate whether response to tumour necrosis factor inhibitors (TNFi) translates into a reduced risk for acute coronary syndrome (ACS).

Methods

A cohort of patients with RA initiating a first TNFi 2001–2012 was identified in the Swedish Biologics Register. The association between European League Against Rheumatism (EULAR) response after 3–8 months of treatment (assessed using the first, the best and the measurement closest to 5 months, respectively), and the risk of incident ACS during the subsequent year was analysed in Cox regression models. Adjustments included cardiovascular risk factors, joint surgery, RA duration, education and work disability.

Results

During 6592 person-years among TNFi initiators (n=6864, mean age 55 years, 77% women), 47 ACS occurred. The adjusted HRs (95% CI), which were similar to the crude HRs, of the 1-year risk of ACS among EULAR good responders compared with non-responders were 0.5 (0.2 to 1.4), 0.4 (0.2 to 0.9) and 0.5 (0.2 to 1.2), for the first, the best and the evaluation closest to 5 months, respectively. EULAR moderate responders had equal risk to that of EULAR non-responders, who, compared with the general population referents (n=34 229), had a more than twice the risk of ACS. For good responders, there was no statistically significant difference in risk versus the general population.

Conclusions

Optimised RA disease control has the potential to revert otherwise increased risks for ACS in RA.

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