Department of Cardiology, School of Medicine, Zhongshan Hospital of Xiamen University, Xiamen University, Xiamen, Fujian, China.
Shengli Clinical Medical College, Fujian Medical University, Fuzhou, Fujian, China.
Clin Cardiol. 2024 Feb;47(2):e24229. doi: 10.1002/clc.24229.
After acute coronary syndrome (ACS), inflammation aids healing but may harm the heart. Interleukin (IL)-18 and IL-1β are pivotal proinflammatory cytokines released during pyroptosis, a process that initiates and sustains inflammation. This study aimed to evaluate the levels of circulating IL-18 and IL-1β during the progression of ACS and to determine their association with subsequent clinical events in ACS patients.
Circulating levels of IL-18 and IL-1β are associated with subsequent clinical events in ACS patients.
Employing immunoassays, we examined plasma levels of IL-1β and IL-18 in 159 ACS patients and matched them with 159 healthy controls. The primary composite endpoint included recurrent unstable angina, myocardial infarction, heart failure exacerbation, stroke, or cardiovascular death.
ACS patients exhibited a significant increase in plasma IL-18 levels, measuring 6.36 [4.46-9.88] × 10 pg/mL, in contrast to the control group with levels at 4.04 [3.21-4.94] × 10 pg/mL (p < 0.001). Conversely, plasma levels of IL-1β remained unchanged compared to the control group. Following a 25-month follow-up, IL-18 levels exceeding the median remained an important prognostic factor for adverse clinical events in ACS patients (hazard ratio = 2.37, 95% confidence interval: 1.14-4.91, p = 0.021). Besides, IL-18 displayed a nonlinear association with adverse clinical events (p nonlinear = 0.044). Subgroup analysis revealed that the correlation between IL-18 and the risk of adverse clinical events was not significantly affected by factors such as age, sex, history of diabetes, smoking, Gensini score, or ACS type (all p interaction >0.05).
IL-18 appears to hold potential as a predictive marker for anticipating clinical outcomes in patients with ACS.
急性冠状动脉综合征(ACS)后,炎症有助于愈合,但也可能损害心脏。白细胞介素(IL)-18 和 IL-1β 是细胞焦亡过程中释放的关键促炎细胞因子,该过程起始并维持炎症。本研究旨在评估 ACS 进展过程中循环 IL-18 和 IL-1β 的水平,并确定它们与 ACS 患者随后的临床事件的关系。
循环 IL-18 和 IL-1β 水平与 ACS 患者随后的临床事件相关。
我们采用免疫测定法检测了 159 例 ACS 患者和 159 例健康对照者的血浆 IL-1β 和 IL-18 水平。主要复合终点包括复发性不稳定型心绞痛、心肌梗死、心力衰竭加重、卒中和心血管死亡。
ACS 患者的血浆 IL-18 水平显著升高,为 6.36[4.46-9.88]×10pg/ml,而对照组为 4.04[3.21-4.94]×10pg/ml(p<0.001)。相反,与对照组相比,血浆 IL-1β 水平无变化。在 25 个月的随访后,IL-18 水平超过中位数仍然是 ACS 患者不良临床事件的重要预后因素(危险比=2.37,95%置信区间:1.14-4.91,p=0.021)。此外,IL-18 与不良临床事件呈非线性关系(p非线性=0.044)。亚组分析显示,IL-18 与不良临床事件风险之间的相关性不受年龄、性别、糖尿病史、吸烟、Gensini 评分或 ACS 类型等因素的显著影响(所有 p 交互值>0.05)。
IL-18 似乎可作为预测 ACS 患者临床结局的标志物。