Brodov Yafim, Chouraqui Pierre, Goldenberg Ilan, Boyko Valentina, Mandelzweig Lori, Behar Shlomo
Heart Institute, Sheba Medical Center, Tel Hashomer, Israel.
Cardiology. 2009;114(4):300-5. doi: 10.1159/000239860. Epub 2009 Sep 23.
In patients with coronary artery disease (CAD), elevated serum uric acid (SUA) levels may predict worse cardiovascular outcomes. It is known that SUA levels are influenced by renal function. We aimed to assess the predictive value of SUA while taking into account patients' renal function.
The primary end point (PEP) risk, including fatal or nonfatal myocardial infarction (MI) or sudden death, was assessed by SUA quintiles before and after adjustment for the estimated glomerular filtration rate (eGFR) in 2,796 nondiabetic CAD patients enrolled in the Bezafibrate Infarction Prevention study.
The PEP risk increased from the lowest (11.8%) to highest SUA quintile (18.0%), p < 0.005, respectively. After adjustment for age, sex, smoking, prior MI, metabolic syndrome variables, NYHA classes II-IV, heart rate and treatment with bezafibrate, diuretics, angiotensin-converting enzyme inhibitors, beta-blockers, calcium channel blockers and antiplatelets, the highest SUA quintile exhibited the highest PEP risk [hazard ratio (HR): 1.47 (95% CI: 1.06-2.04)]. Patients in the highest - compared with those in the lowest - quintiles continued to demonstrate an increased PEP risk [HR: 1.46 (95% CI: 1.04-2.06)], even after additional adjustment for the eGFR.
In nondiabetic patients with CAD, elevated SUA levels are associated with an increased risk of cardiac events, independent of renal function.
在冠状动脉疾病(CAD)患者中,血清尿酸(SUA)水平升高可能预示着更差的心血管结局。已知SUA水平受肾功能影响。我们旨在评估在考虑患者肾功能的情况下SUA的预测价值。
在苯扎贝特预防心肌梗死研究中纳入的2796例非糖尿病CAD患者中,通过估计肾小球滤过率(eGFR)调整前后的SUA五分位数评估主要终点(PEP)风险,包括致命或非致命性心肌梗死(MI)或猝死。
PEP风险分别从最低SUA五分位数的11.8%增加到最高五分位数的18.0%,p<0.005。在调整年龄、性别、吸烟、既往MI、代谢综合征变量、纽约心脏协会II-IV级、心率以及使用苯扎贝特、利尿剂、血管紧张素转换酶抑制剂、β受体阻滞剂、钙通道阻滞剂和抗血小板药物治疗后,最高SUA五分位数显示出最高的PEP风险[风险比(HR):1.47(95%CI:1.06-2.04)]。即使在进一步调整eGFR后,最高五分位数的患者与最低五分位数的患者相比,仍显示出增加的PEP风险[HR:1.46(95%CI:1.04-2.06)]。
在非糖尿病CAD患者中,SUA水平升高与心脏事件风险增加相关,且独立于肾功能。