Pagidipati Neha J, Hess Connie N, Clare Robert M, Akerblom Axel, Tricoci Pierluigi, Wojdyla Daniel, Keenan Robert T, James Stefan, Held Claes, Mahaffey Kenneth W, Klein Alyssa B, Wallentin Lars, Roe Matthew T
Duke University Health System, Duke Clinical Research Institute, Durham, NC.
University of Colorado School of Medicine, Aurora, CO.
Am Heart J. 2017 May;187:53-61. doi: 10.1016/j.ahj.2017.02.023. Epub 2017 Feb 21.
Studies have suggested a relationship between higher baseline serum uric acid (sUA) levels and an elevated risk of subsequent ischemic cardiovascular outcomes among acute coronary syndrome (ACS) patients; this relationship may be modified by a clinical history of gout and has not been studied in large patient cohorts. We sought to understand the effect of sUA and gout on ACS outcomes.
Using PLATO and TRACER data on 27,959 ACS patients, we evaluated baseline sUA levels in relation to a composite of cardiovascular death, myocardial infarction (MI), or stroke. We assessed interaction terms to determine if a baseline clinical diagnosis of gout modified this putative relationship; 46% (n=12,882) had sUA levels elevated >6.0 mg/dL.
Patients with elevated levels were more often male with a history of prior MI, diabetes, and heart failure compared with those with sUA <6.0 mg/dL. The unadjusted risk of the composite endpoint increased with corresponding elevations in sUA levels (per 1 mg/dL increase) (HR=1.23 [95% CI: 1.20-1.26]) above the statistical inflection point of 5.0 mg/dL. After adjustment, the association between sUA level and the composite outcome remained significant (HR=1.07 [95% CI: 1.04-1.10]), and baseline gout did not modify this relationship.
In patients with ACS, increasing levels of sUA are associated with an elevated risk of cardiovascular events, regardless of a clinical diagnosis of gout. Further investigation is warranted to determine the mechanism behind this relationship and to delineate whether sUA is an appropriate therapeutic target to reduce cardiovascular risk.
研究表明,急性冠状动脉综合征(ACS)患者较高的基线血清尿酸(sUA)水平与随后发生缺血性心血管事件的风险升高之间存在关联;这种关系可能会因痛风病史而改变,且尚未在大型患者队列中进行研究。我们试图了解sUA和痛风对ACS预后的影响。
利用来自27959例ACS患者的PLATO和TRACER数据,我们评估了基线sUA水平与心血管死亡、心肌梗死(MI)或中风的综合情况之间的关系。我们评估了交互项,以确定痛风的基线临床诊断是否改变了这种假定的关系;46%(n = 12882)的患者sUA水平升高>6.0mg/dL。
与sUA<6.0mg/dL的患者相比,sUA水平升高的患者更常为男性,有既往MI、糖尿病和心力衰竭病史。在5.0mg/dL的统计拐点以上,复合终点的未调整风险随着sUA水平的相应升高(每升高1mg/dL)而增加(HR = 1.23 [95%CI:1.20 - 1.26])。调整后,sUA水平与复合结局之间的关联仍然显著(HR = 1.07 [95%CI:1.04 - 1.10]),且基线痛风并未改变这种关系。
在ACS患者中,无论痛风的临床诊断如何,sUA水平升高均与心血管事件风险升高相关。有必要进一步研究以确定这种关系背后的机制,并确定sUA是否是降低心血管风险的合适治疗靶点。