Integrating the GRACE Score with the Ceramide Risk Score Enhances the Predictive Accuracy of Major Adverse Cardiac Events in Patients with Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention.

IF 1.3 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Reviews in cardiovascular medicine Pub Date : 2024-12-31 eCollection Date: 2025-01-01 DOI:10.31083/RCM25984
Xiaofei Wang, Chengzhe Liu, Fu Yu, Zizhuo Zhang, Jiale Wang, Xiaoyu Shi, Tianyou Xu, Qiang Deng, Liping Zhou, Wanyue Sang, Hong Jiang, Lilei Yu
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Abstract

Background: Ceramide, a key molecule in sphingolipid metabolism, is recognized as a standalone predictor of long-term major adverse cardiac events (MACE). We explore if integrating the global registry of acute coronary events (GRACE) score with the ceramide risk score (ceramide test 1, CERT1) improves MACE prediction in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI).

Methods: This cohort study included 210 participants with ACS undergoing PCI. MACE was defined as the recurrence of non-fatal acute myocardial infarction, repeat coronary revascularization procedures (PCI or coronary artery bypass grafting, CABG), or death excluding the initial event qualifying the patient for the study. The cumulative incidence of MACE was analyzed using the Kaplan-Meier method. Both univariate and multivariate Cox regression analyses identified MACE predictors. The predictive accuracy of combining the GRACE score with the CERT1 score was assessed using the area under the receiver operating characteristic curve (AUC), integrated discrimination improvement (IDI), and net reclassification improvement (NRI).

Results: During the 12-month follow-up period, 35 of the 210 participants experienced a MACE. The Kaplan-Meier analysis revealed a significant variation in MACE incidence stratified by the CERT1 score (χ2 = 21.344, p < 0.001). Multivariate Cox regression analysis identified low-density lipoprotein (p = 0.002), quantitative flow ratio (p = 0.013), the CERT1 score (p = 0.005), and the GRACE score (p = 0.007) as independent predictors for MACE. Integrating the GRACE score with the CERT1 score improved prediction accuracy, raising the AUC from 0.733 to 0.834. This adjustment provided a more precise risk reclassification and discrimination between patients likely and unlikely to experience MACE (NRI: 0.526, p = 0.004; IDI: 0.120, p < 0.001).

Conclusions: The CERT1 score independently predicts long-term MACE for individuals diagnosed with ACS undergoing PCI. Including the CERT1 score significantly enhances the GRACE score's capacity to risk-stratify these patients.

Clinical trial registration: Registration number: ChiCTR2300068491 (https://www.chictr.org.cn/showproj.html?proj=180370).

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将GRACE评分与神经酰胺风险评分相结合可提高急性冠状动脉综合征患者经皮冠状动脉介入治疗时主要心脏不良事件的预测准确性。
神经酰胺是神经鞘脂代谢的关键分子,被认为是长期主要心脏不良事件(MACE)的独立预测因子。我们探讨是否将全球急性冠状动脉事件登记(GRACE)评分与神经酰胺风险评分(神经酰胺测试1,CERT1)相结合可以改善急性冠状动脉综合征(ACS)患者经皮冠状动脉介入治疗(PCI)的MACE预测。方法:本队列研究纳入210例ACS患者行PCI治疗。MACE定义为非致死性急性心肌梗死复发、重复冠状动脉血运重建术(PCI或冠状动脉旁路移植术,CABG)或排除符合研究条件的初始事件的死亡。采用Kaplan-Meier法分析MACE的累积发生率。单因素和多因素Cox回归分析确定了MACE预测因子。采用受试者工作特征曲线下面积(AUC)、综合判别改善(IDI)和净重分类改善(NRI)评估GRACE评分与CERT1评分结合的预测准确性。结果:在12个月的随访期间,210名参与者中有35人经历了MACE。Kaplan-Meier分析显示,按CERT1评分分层的MACE发生率存在显著差异(χ2 = 21.344, p < 0.001)。多因素Cox回归分析发现,低密度脂蛋白(p = 0.002)、定量血流比(p = 0.013)、CERT1评分(p = 0.005)和GRACE评分(p = 0.007)是MACE的独立预测因子。将GRACE评分与CERT1评分相结合,提高了预测精度,AUC由0.733提高到0.834。这种调整提供了更精确的风险重新分类和可能和不可能经历MACE的患者之间的区分(NRI: 0.526, p = 0.004;IDI: 0.120, p < 0.001)。结论:CERT1评分独立预测诊断为ACS接受PCI的个体的长期MACE。纳入CERT1评分可显著提高GRACE评分对这些患者进行风险分层的能力。临床试验注册:注册号:ChiCTR2300068491 (https://www.chictr.org.cn/showproj.html?proj=180370)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reviews in cardiovascular medicine
Reviews in cardiovascular medicine 医学-心血管系统
CiteScore
2.70
自引率
3.70%
发文量
377
审稿时长
1 months
期刊介绍: RCM is an international, peer-reviewed, open access journal. RCM publishes research articles, review papers and short communications on cardiovascular medicine as well as research on cardiovascular disease. We aim to provide a forum for publishing papers which explore the pathogenesis and promote the progression of cardiac and vascular diseases. We also seek to establish an interdisciplinary platform, focusing on translational issues, to facilitate the advancement of research, clinical treatment and diagnostic procedures. Heart surgery, cardiovascular imaging, risk factors and various clinical cardiac & vascular research will be considered.
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