Sarebanhassanabadi Mohammadtaghi, Mahvash Shakiba, Marques-Vidal Pedro, Mirjalili Seyed Reza, Namayandeh Seyedeh Mahdieh, Mihanpour Hamideh, Mirshamsi Aida, Mirshamsi Ali
Yazd Cardiovascular Research Center, Non-Communicable Diseases Research Institute, Shahid Sadoughi University of Medical Sciences, Jomhouri Blvd, Yazd, 8917945556, Iran.
Department of Internal Medicine, BH10-642, Rue du Bugnon 46, Lausanne, CH-1011, Switzerland.
BMC Cardiovasc Disord. 2025 May 20;25(1):386. doi: 10.1186/s12872-025-04866-7.
The role of serum uric acid (SUA) as an independent risk factor for coronary artery disease (CAD) remains controversial, particularly in understudied Middle Eastern populations with distinct metabolic and dietary profiles.
To investigate the association between SUA levels and 10-year CAD incidence in a healthy Iranian cohort, adjusting for cardiometabolic confounders and exploring sex-specific relationships.
A 10-year prospective cohort study was conducted using data from the Yazd Healthy Heart Project. Cluster-random sampling recruited adults aged 20-74 years free of baseline cardiovascular disease. Participants with existing coronary artery disease, insufficient data, or loss to follow-up were excluded. Serum uric acid levels were stratified into quartiles, and Cox proportional hazards models adjusted for demographic, lifestyle, and metabolic variables were analyzed using SPSS (version 27.0).
Over 15,420 person-years, 225 incident CAD cases occurred (14.5% cumulative incidence). In crude analysis, the highest SUA quartile (Q4: > 5.2 mg/dL) was associated with increased CAD risk (HR = 1.66, 95% CI: 1.14-2.43). However, this association attenuated after adjustment for confounders (fully adjusted HR = 1.03, 95% CI: 0.62-1.69). Sex-stratified analysis revealed a transient association in women (crude HR = 2.13, 95% CI: 1.14-3.96), which dissipated post-adjustment, while no significant association was observed in men.
Elevated SUA levels were not independently associated with CAD risk in this healthy Middle Eastern cohort. Initial associations were attributable to confounding by metabolic factors such as obesity, dyslipidemia, and hypertension. These findings underscore the importance of contextualizing SUA's role within population-specific risk profiles and highlight the need for nuanced risk stratification strategies.
血清尿酸(SUA)作为冠状动脉疾病(CAD)的独立危险因素,其作用仍存在争议,尤其是在代谢和饮食特征独特但研究较少的中东人群中。
在一个健康的伊朗队列中,研究SUA水平与10年CAD发病率之间的关联,校正心血管代谢混杂因素,并探讨性别特异性关系。
利用亚兹德健康心脏项目的数据进行了一项为期10年的前瞻性队列研究。采用整群随机抽样方法招募了20-74岁无基线心血管疾病的成年人。排除患有现患冠状动脉疾病、数据不足或失访的参与者。血清尿酸水平被分为四分位数,并使用SPSS(版本27.0)分析校正了人口统计学、生活方式和代谢变量的Cox比例风险模型。
在超过15420人年的随访中,发生了22例CAD病例(累积发病率为14.5%)。在粗分析中,最高的SUA四分位数(Q4:>5.2mg/dL)与CAD风险增加相关(HR=1.66,95%CI:1.14-2.43)。然而,在调整混杂因素后,这种关联减弱(完全调整后的HR=1.03,95%CI:0.62-1.69)。按性别分层分析显示,女性存在短暂关联(粗HR=2.13,95%CI:1.14-3.96),调整后消失,而男性未观察到显著关联。
在这个健康的中东队列中,SUA水平升高与CAD风险无独立关联。最初的关联归因于肥胖、血脂异常和高血压等代谢因素的混杂作用。这些发现强调了在特定人群风险特征中确定SUA作用的重要性,并突出了需要细致入微的风险分层策略。