Division of Nephrology, Department of Medicine I, University of Bonn, Germany.
Atherosclerosis. 2013 Aug;229(2):541-8. doi: 10.1016/j.atherosclerosis.2013.04.027. Epub 2013 May 3.
Cystatin C is a well established marker of kidney function. There is evidence that cystatin C concentrations are also associated with mortality. The present analysis prospectively evaluated the associations of cystatin C with all-cause and cardiovascular (CV) mortality in a well-characterized cohort of persons undergoing angiography, but without overt renal insufficiency.
Cystatin C was available in 2998 persons (mean age: 62.7 ± 10.5 years; 30.3% women). Of those 2346 suffered from coronary artery disease (CAD) and 652 (controls) did not. Creatinine (mean ± SD: 83.1 ± 47.8 vs. 74.1 ± 24.7 μmol/L, p = 0.036) but not Cystatin C (mean ± SD: 1.02 ± 0.44 vs. 0.92 ± 0.26 mg/L, p = 0.065) was significantly higher in patients with CAD. After a median follow-up of 9.9 years, in total 898 (30%) deaths occurred, 554 (18.5%) due to CV disease and 326 (10.9%) due to non-CV causes. Multivariable-adjusted Cox analysis (adjusting for eGFR and established cardiovascular risk factors, lipid lowering therapy, angiographic coronary artery disease, and C-reactive protein) revealed that patients in the highest cystatin C quartile were at an increased risk for all-cause (hazard ratio (HR) 1.93, 95% CI 1.50-2.48) and CV mortality (HR 2.05 95% CI 1.48-2.84) compared to those in the lowest quartile. The addition of cystatin C to a model consisting of established cardiovascular risk factors increased the area under the receiver-operating characteristic curve for CV and all-cause mortality, but the difference was statistically not significant. However, reclassification analysis revealed significant improvement by addition of cystatin C for CV and all-cause mortality (p < 0.001), respectively.
The concentration of cystatin C is strongly associated with long-term all-cause and cardiovascular mortality in patients referred to coronary angiography, irrespective of creatinine-based renal function.
胱抑素 C 是肾功能的一个既定标志物。有证据表明,胱抑素 C 浓度也与死亡率相关。本分析前瞻性评估了胱抑素 C 与接受血管造影但无明显肾功能不全的患者全因和心血管(CV)死亡率的相关性。
在一个经过充分特征描述的接受血管造影的人群中,2998 人(平均年龄:62.7 ± 10.5 岁;30.3%为女性)可获得胱抑素 C 数据。其中 2346 人患有冠状动脉疾病(CAD),652 人(对照组)未患有 CAD。CAD 患者的肌酐(平均值 ± 标准差:83.1 ± 47.8 比 74.1 ± 24.7 μmol/L,p = 0.036)但不是胱抑素 C(平均值 ± 标准差:1.02 ± 0.44 比 0.92 ± 0.26 mg/L,p = 0.065)明显更高。中位随访 9.9 年后,共有 898 人(30%)死亡,554 人(18.5%)死于心血管疾病,326 人(10.9%)死于非心血管原因。多变量调整 Cox 分析(调整肾小球滤过率和已确立的心血管危险因素、降脂治疗、血管造影冠状动脉疾病和 C 反应蛋白)显示,胱抑素 C 最高四分位的患者全因死亡(危险比(HR)1.93,95%置信区间(CI)1.50-2.48)和心血管死亡(HR 2.05 95% CI 1.48-2.84)的风险增加,与最低四分位相比。将胱抑素 C 添加到包含已确立的心血管危险因素的模型中,增加了 CV 和全因死亡率的受试者工作特征曲线下面积,但统计学上无显著差异。然而,重新分类分析显示,添加胱抑素 C 对 CV 和全因死亡率的分类有显著改善(p < 0.001)。
在接受冠状动脉造影的患者中,胱抑素 C 的浓度与长期全因和心血管死亡率密切相关,而与基于肌酐的肾功能无关。