Zheng Liu-Chang, Liu Fang, Zheng Pei-Ming, Xiao Zheng, Cui Fa-Cai
Department of Clinical Laboratory, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Department of Medical Imaging, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Clin Interv Aging. 2025 Apr 25;20:495-504. doi: 10.2147/CIA.S519437. eCollection 2025.
Acute myocardial infarction (AMI) in the elderly is associated with high morbidity and mortality, with major adverse cardiovascular events (MACE) remaining a major concern despite early revascularization. This study aimed to evaluate the association of soluble suppression of tumorigenicity 2 (sST2), interleukin-33 (IL-33), and homocysteine (Hcy) with coronary stenosis severity and their predictive value for MACE in elderly AMI patients.
A retrospective analysis was conducted on 143 elderly AMI patients (≥65 years) admitted between June 2022 and June 2024. Patients were divided into two groups based on MACE occurrence: Group A (no MACE, n=56) and Group B (MACE, n=87). Serum sST2, IL-33, and Hcy levels were measured using ELISA, and coronary stenosis severity was assessed using the Gensini score. Statistical analyses included Spearman correlation, multivariate logistic regression, and receiver operating characteristic (ROC) curve analysis to evaluate predictive performance.
Serum sST2, IL-33, and Hcy levels were significantly higher in the MACE group compared to the non-MACE group (72.37±10.68 vs 38.76±11.15, p<0.05; 60.61±10.89 vs 33.74±11.23, p<0.05; 32.76±4.15 vs 15.38±4.62, p<0.05, respectively). Biomarker levels positively correlated with coronary stenosis severity (sST2: r=0.647, p<0.05; IL-33: r=0.659, p<0.05; Hcy: r=0.582, p<0.05). Multivariate logistic regression confirmed that sST2 (OR=1.056, 95% CI: 1.015-1.094, p=0.005), IL-33 (OR=1.069, 95% CI: 1.024-2.016, p=0.001), and Hcy (OR=1.037, 95% CI: 1.008-1.077, p=0.033) were independent risk factors for MACE. ROC analysis showed that sST2, IL-33, and Hcy had AUCs of 0.841 (95% CI: 0.762-0.915, p<0.001), 0.803 (95% CI: 0.724-0.878, p<0.001), and 0.729 (95% CI: 0.642-0.812, p<0.001), respectively. Combined detection of all three biomarkers significantly improved MACE prediction (AUC=0.910, 95% CI: 0.851-0.956, p<0.001).
Serum sST2, IL-33, and Hcy levels are positively correlated with coronary stenosis severity and independently associated with MACE in elderly AMI patients. Their combined detection significantly enhances MACE prediction, providing a potential strategy for improved risk stratification and management in this high-risk population.
老年急性心肌梗死(AMI)的发病率和死亡率较高,尽管早期进行了血运重建,但主要不良心血管事件(MACE)仍是主要关注点。本研究旨在评估可溶性肿瘤抑制因子2(sST2)、白细胞介素-33(IL-33)和同型半胱氨酸(Hcy)与老年AMI患者冠状动脉狭窄严重程度的相关性及其对MACE的预测价值。
对2022年6月至2024年6月收治的143例老年AMI患者(≥65岁)进行回顾性分析。根据MACE发生情况将患者分为两组:A组(无MACE,n = 56)和B组(有MACE,n = 87)。采用酶联免疫吸附测定法(ELISA)检测血清sST2、IL-33和Hcy水平,并用Gensini评分评估冠状动脉狭窄严重程度。统计分析包括Spearman相关性分析、多因素逻辑回归分析和受试者工作特征(ROC)曲线分析,以评估预测性能。
与无MACE组相比,有MACE组的血清sST2、IL-33和Hcy水平显著更高(分别为72.37±10.68 vs 38.76±11.15,p<0.05;60.61±10.89 vs 33.74±11.23,p<0.05;32.76±4.15 vs 15.38±4.62,p<0.05)。生物标志物水平与冠状动脉狭窄严重程度呈正相关(sST2:r = 0.647,p<0.05;IL-33:r = 0.659,p<0.