Xiong Xinlin, Yuan Li, Long Xiaobin, An Minsheng, Huang Shen, Liu Liang
Department of cardiology, Clinical Medical College& Affiliated Hospital of Chengdu University, Chengdu city, PR China.
Clin Appl Thromb Hemost. 2025 Jan-Dec;31:10760296251324201. doi: 10.1177/10760296251324201. Epub 2025 Apr 15.
BackgroundCystatin C is a cysteine protease inhibitor, synthesized by nucleated cells, and released into various body fluids. Lots of studies have reported an association between cystatin C and atherosclerotic cardiovascular disease. However, the association of cystatin C with high-risk patients with acute coronary syndrome(ACS) has not been well studied. In this study, we investigated potential association of cystatin C with high-risk patients with ACS, and assessed whether cystatin C provide discriminating power of clinical risk stratification in patients with ACS.MethodsWe enrolled 219 patients with ACS in the present study. The cystatin C concentration was measured in clinical laboratory. The global registry of acute coronary events (GRACE) scores was calculated to assess risk stratification. The high-risk patients with ACS were defined based on GRACE scores and killip classification.ResultsThe cystatin C levels were significantly higher in high-risk patients compared to non-high-risk patients, both in the overall ACS group and its subtypes, including non-ST elevation ACS (NSTE-ACS) and ST elevation ACS (STE-ACS)(< 0.05). The receiver operating characteristic (ROC) curve analysis showed that cystatin C had a discriminative performance for identifying high-risk patients across these groups(< 0.05). After adjusting for potential confounders, multivariate logistic regression confirmed that the elevated cystatin C levels were independently associated with high-risk patients with ACS(< 0.05).ConclusionsThe cystatin C was obviously elevated in high-risk group in the patients with ACS and its subgroups. Cystatin C appears to be a valuable biomarker for distinguishing and predicting high-risk patients with ACS, suggesting its relevance in clinical risk stratification.
背景
胱抑素C是一种由有核细胞合成并释放到各种体液中的半胱氨酸蛋白酶抑制剂。许多研究报告了胱抑素C与动脉粥样硬化性心血管疾病之间的关联。然而,胱抑素C与急性冠状动脉综合征(ACS)高危患者的关联尚未得到充分研究。在本研究中,我们调查了胱抑素C与ACS高危患者之间的潜在关联,并评估了胱抑素C是否能为ACS患者提供临床风险分层的鉴别能力。
方法
我们在本研究中纳入了219例ACS患者。在临床实验室测量胱抑素C浓度。计算急性冠状动脉事件全球注册(GRACE)评分以评估风险分层。根据GRACE评分和Killip分级定义ACS高危患者。
结果
在整个ACS组及其亚型,包括非ST段抬高型ACS(NSTE-ACS)和ST段抬高型ACS(STE-ACS)中,高危患者的胱抑素C水平均显著高于非高危患者(<0.05)。受试者工作特征(ROC)曲线分析表明,胱抑素C在识别这些组中的高危患者方面具有鉴别性能(<0.05)。在调整潜在混杂因素后,多因素逻辑回归证实,胱抑素C水平升高与ACS高危患者独立相关(<0.05)。
结论
ACS患者及其亚组的高危组中胱抑素C明显升高。胱抑素C似乎是区分和预测ACS高危患者的有价值生物标志物,表明其在临床风险分层中的相关性。