Koton Silvia, Howard Sally C, Warlow Charles P, Murphy Michael F G, Rothwell Peter M
Stanley Steyer School of Health Professions, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Cerebrovasc Dis. 2008;26(5):517-24. doi: 10.1159/000155990. Epub 2008 Sep 23.
Several studies have shown serum urate to be an independent risk factor for vascular disease, but others have not, although a stronger association in women than in men has been a consistent finding. Studies of stroke patients have shown possible associations between urate level and stroke severity, but there have been no large cohort studies of the effect of urate on the long-term risk of future vascular events in patients with a transient ischaemic attack (TIA) or stroke. We studied this relationship in 2 independent cohorts.
Individual data on 15,483 patient-years of follow-up from the UK-TIA trial (13,182 patient-years) and the Oxford TIA study (2,301 patient-years) were analyzed. Hazard ratios (per unit increase of baseline urate in mg/dl) for the risks of stroke and acute coronary events (ACE) were obtained from Cox models stratified by study, with and without adjustment for potential confounders. Potential interactions between urate and baseline characteristics were also assessed.
Linear associations between urate and risk of ACE were found in both studies: pooled age- and sex-adjusted hazard ratio = 1.17, 95% CI 1.06-1.30, per unit increase of urate (p = 0.003). Sex, body mass index and previous myocardial infarction or angina were effect modifiers, but only the effect of sex remained after adjustment for other risk factors (p = 0.002), with a 5th:1st quintile hazard ratio of 4.23 (1.97-9.07, p < 0.0001) in women and 1.09 (0.70-1.71, p = 0.69) in men. These findings were consistent across the 2 studies. No associations were found between urate level and either risk or severity of stroke.
High urate levels were independent predictors of long-term risk of ACE in women who had a TIA or stroke, but not in men, in 2 independent studies. Urate levels could be useful in identifying women at high risk of coronary events in routine practice.
多项研究表明血清尿酸是血管疾病的独立危险因素,但其他一些研究则未发现此关联,尽管女性中尿酸与血管疾病的关联比男性更强这一发现较为一致。对中风患者的研究显示尿酸水平与中风严重程度之间可能存在关联,但尚无关于尿酸对短暂性脑缺血发作(TIA)或中风患者未来发生血管事件长期风险影响的大型队列研究。我们在两个独立队列中研究了这种关系。
分析了来自英国TIA试验(13,182患者年)和牛津TIA研究(2,301患者年)的15,483患者年随访的个体数据。通过按研究分层的Cox模型,在调整和未调整潜在混杂因素的情况下,获得中风和急性冠状动脉事件(ACE)风险的风险比(每单位基线尿酸增加mg/dl)。还评估了尿酸与基线特征之间的潜在相互作用。
两项研究均发现尿酸与ACE风险之间存在线性关联:合并年龄和性别调整后的风险比=1.17,95%可信区间1.06 - 1.30,尿酸每单位增加(p = 0.003)。性别、体重指数以及既往心肌梗死或心绞痛是效应修饰因素,但在调整其他危险因素后,仅性别效应仍然显著(p = 0.002),女性中第5分位数:第1分位数的风险比为4.23(1.97 - 9.07,p < 0.0001),男性为1.09(0.70 - 1.71,p = 0.69)。这些发现在两项研究中是一致的。未发现尿酸水平与中风风险或严重程度之间存在关联。
在两项独立研究中,高尿酸水平是发生TIA或中风女性发生ACE长期风险的独立预测因素,但在男性中并非如此。在常规实践中,尿酸水平可能有助于识别有冠状动脉事件高风险的女性。