Adusumalli Srikanth, McCarthy Cian P, Magaret Craig A, Rhyne Rhonda F, Jaffer Farouc A, Januzzi James L
Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.
Prevencio, Inc, Kirkland, Washington.
Am J Cardiol. 2025 May 1;242:25-31. doi: 10.1016/j.amjcard.2024.12.037. Epub 2025 Jan 6.
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.
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。