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多种生物标志物预测冠状动脉慢性完全闭塞患者的主要不良心血管事件

Multiple Biomarkers to Predict Major Adverse Cardiovascular Events in Patients With Coronary Chronic Total Occlusions.

作者信息

Adusumalli Srikanth, McCarthy Cian P, Magaret Craig A, Rhyne Rhonda F, Jaffer Farouc A, Januzzi James L

机构信息

Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Prevencio, Inc, Kirkland, Washington.

出版信息

Am J Cardiol. 2025 May 1;242:25-31. doi: 10.1016/j.amjcard.2024.12.037. Epub 2025 Jan 6.

Abstract

There are limited tools available to predict the long-term prognosis of persons with coronary chronic total occlusions (CTO). A previously described blood biomarker panel to predict cardiovascular (CV) events was evaluated in patients with CTO. From 1,251 patients in the CASABLANCA study, 241 participants with a CTO were followed for an average of 4 years for occurrence of major adverse CV events (MACE, CV death, nonfatal myocardial infarction or stroke) and CV death/heart failure (HF) hospitalization. Results of a biomarker panel (kidney injury molecule-1, N-terminal pro-B-type natriuretic peptide, osteopontin, and tissue inhibitor of metalloproteinase-1) from baseline samples were expressed as low-, medium-, and high-risk. By 4 years, a total of 67 (27.8%) MACE and 56 (23.2%) CV death/HF hospitalization events occurred. The C-statistic of the panel for MACE through 4 years was 0.79 (p < 0.001). Considering the low-risk group as referent, the hazard ratio (HR) of MACE by 4 years was 6.65 (95% confidence interval [CI]: 2.98 to 14.8) and 12.4 (95% CI:5.17 to 29.6) for the medium and high-risk groups (both p < 0.001). The C-statistic for CVD/HF hospitalization by 4 years was 0.84 (p < 0.001). Compared to the low-risk score group, the medium and high-risk groups had HR of 5.61 (95% CI: 2.33 to 13.5) and 15.6 (95% CI: 6.18, 39.2; both p value <0.001). In conclusion, a multiple biomarker panel assisted in discriminating a broad range of risk for adverse outcomes in patients with coronary CTO. These results may have implications for risk stratification, patient care and could have a role for clinical trial enrichment.

摘要

目前可用于预测冠状动脉慢性完全闭塞(CTO)患者长期预后的工具有限。我们对先前描述的一种用于预测心血管(CV)事件的血液生物标志物组合在CTO患者中进行了评估。在卡萨布兰卡研究的1251名患者中,对241名患有CTO的参与者平均随访4年,观察主要不良心血管事件(MACE,包括CV死亡、非致命性心肌梗死或中风)以及CV死亡/心力衰竭(HF)住院情况。来自基线样本的生物标志物组合(肾损伤分子-1、N末端B型利钠肽原、骨桥蛋白和基质金属蛋白酶-1组织抑制剂)结果被分为低、中、高风险。到4年时,共发生了67例(27.8%)MACE和56例(23.2%)CV死亡/HF住院事件。该生物标志物组合在4年内对MACE的C统计量为0.79(p<0.001)。以低风险组作为参照,4年时中风险组和高风险组发生MACE的风险比(HR)分别为6.65(95%置信区间[CI]:2.98至14.8)和12.4(95%CI:5.17至29.6)(均p<0.001)。4年时CV死亡/HF住院的C统计量为0.84(p<0.001)。与低风险评分组相比,中风险组和高风险组的HR分别为5.61(95%CI:2.33至13.5)和15.6(95%CI:6.18至39.2;均p值<0.001)。总之,一种多种生物标志物组合有助于区分冠状动脉CTO患者不良结局的广泛风险范围。这些结果可能对风险分层、患者护理有影响,并且可能在临床试验富集方面发挥作用。

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