Wang Di, Mao Lin, Li Kun, Wang Lu, Wang Yan, Yang Longyan
Center for Endocrine Metabolism and Immune Diseases, Beijing Luhe Hospital, Capital Medical University, Beijing, People's Republic of China.
Beijing Key Laboratory of Diabetes Research and Care, Beijing, People's Republic of China.
Diabetes Metab Syndr Obes. 2024 Dec 21;17:4857-4865. doi: 10.2147/DMSO.S478526. eCollection 2024.
Coronary artery stenosis caused by atherogenesis is a major pathological link in coronary heart disease (CHD), which is a leading cause of global morbidity and mortality. Junctional adhesion molecule C (JAM-C) presents more and more association with atherosclerosis. However, no studies have shown the relationship between soluble JAM-C (sJAM-C) and the degree of coronary artery stenosis. This study aimed to analyze the effect of sJAM-C on coronary artery stenosis and to verify whether sJAM-C could be a biomarker for coronary artery stenosis.
The participants registered at the Beijing Luhe Hospital, Capital Medical University in the cross-sectional study. A total of 121 patients without coronary stenosis and 408 patients with coronary artery stenosis were enrolled after matching age and sex. Demographic information, medication history, and laboratory data were collected. The level of serum sJAM-C was detected by enzyme-linked immunosorbent assay (ELISA) kits. We used the logistic regression model to evaluate the association between sJAM-C and coronary artery stenosis. Furthermore, the receiver operating characteristic (ROC) curve and area under curve (AUC) were used to evaluate the diagnostic value of sJAM-C on coronary artery stenosis.
The serum level of sJAM-C was remarkably higher in patients with coronary artery stenosis than those without stenosis (p < 0.0001). Logistic regression models showed that there were positive association between serum sJAM-C level and coronary artery stenosis after adjustment, with corresponding ORs were 3.088 (95% CI 1.922-4.960, p < 0.0001). And the ROC curve revealed a sensitivity of 65.7% and specificity of 60.3% with AUC of 0.676 (95% CI 0.622-0.730) for the diagnosis of coronary artery stenosis with serum sJAM-C at a cut-off value of 18.1 pg/mL, indicating a certain diagnostic value.
In summary, higher serum sJAM-C level was possibly associated with the more severe coronary artery stenosis. Additionally, sJAM-C demonstrates a certain diagnostic value of coronary artery stenosis. These findings suggest sJAM-C may be a biomarker for coronary artery stenosis.
动脉粥样硬化所致冠状动脉狭窄是冠心病(CHD)的主要病理环节,冠心病是全球发病和死亡的主要原因。连接黏附分子C(JAM-C)与动脉粥样硬化的关联日益增多。然而,尚无研究表明可溶性JAM-C(sJAM-C)与冠状动脉狭窄程度之间的关系。本研究旨在分析sJAM-C对冠状动脉狭窄的影响,并验证sJAM-C是否可作为冠状动脉狭窄的生物标志物。
在横断面研究中,选取首都医科大学附属北京潞河医院登记的参与者。在匹配年龄和性别后,共纳入121例无冠状动脉狭窄患者和408例冠状动脉狭窄患者。收集人口统计学信息、用药史和实验室数据。采用酶联免疫吸附测定(ELISA)试剂盒检测血清sJAM-C水平。我们使用逻辑回归模型评估sJAM-C与冠状动脉狭窄之间的关联。此外,采用受试者工作特征(ROC)曲线和曲线下面积(AUC)评估sJAM-C对冠状动脉狭窄的诊断价值。
冠状动脉狭窄患者的血清sJAM-C水平显著高于无狭窄患者(p < 0.0001)。逻辑回归模型显示,调整后血清sJAM-C水平与冠状动脉狭窄呈正相关,相应的比值比为3.088(95%可信区间1.922 - 4.960,p < 0.0001)。ROC曲线显示,血清sJAM-C诊断冠状动脉狭窄的截断值为18.1 pg/mL时,灵敏度为65.7%,特异度为60.3%,AUC为0.676(95%可信区间0.622 - 0.730),表明具有一定的诊断价值。
综上所述,较高的血清sJAM-C水平可能与更严重的冠状动脉狭窄相关。此外,sJAM-C对冠状动脉狭窄具有一定的诊断价值。这些发现提示sJAM-C可能是冠状动脉狭窄的生物标志物。