Department of Cardiology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, No. 26 Shengli Street, Jiang'an District, Hubei, 430030, China.
Ir J Med Sci. 2022 Oct;191(5):2085-2090. doi: 10.1007/s11845-021-02836-4. Epub 2021 Nov 22.
Cell division cycle 42 (CDC42) regulates macrophage polarization, vascular inflammation, atherosclerosis progression, and modifies differentiation of T helper (Th) cells, while its potential as a biomarker in coronary heart disease (CHD) patients is still lacking. This study aimed to evaluate CDC42 expression, its correlation with Th1, Th2, and Th17 cells, adhesion molecules, and biochemical indexes in CHD patients.
One hundred two CHD patients and 50 controls were enrolled. CDC42 expression in peripheral blood mononuclear cells was assessed by reverse transcription quantitative polymerase chain reaction in all participants. In CHD patients, Th1, Th2, and Th17 cells were detected by flow cytometric analysis; meanwhile, serum levels of inflammatory cytokines and adhesion molecules were detected by enzyme-linked immunosorbent assay.
CDC42 was lower in CHD patients (median (interquartile range (IQR)) = 0.431 (0.304-0.722)) than in controls (median (IQR) = 0.985 (0.572-1.760)) (p < 0.001). CDC42 was positively associated with Th2 cells (p = 0.016) and interleukin (IL)-10 (p = 0.034), but negatively correlated with Th17 cells (p < 0.001) and IL-17A (p < 0.001) in CHD patients. However, no association was found in CDC42 with Th1 cells (p = 0.199) or interferon-γ (p = 0.367) in CHD patients. Besides, CDC42 was negatively correlated with vascular cell adhesion molecule-1 (p = 0.013) and intercellular cell adhesion molecule-1 (p = 0.001) in CHD patients. Additionally, CDC42 negatively associated with C-reactive protein (p < 0.001), Gensini score (p < 0.001), total cholesterol (p = 0.039), and low-density lipoprotein cholesterol (p = 0.014), but not with other biochemical indexes (p > 0.05) in CHD patients.
CDC42 correlates with Th2 cells, Th17 cells, and adhesion molecules, also reflects inflammation, coronary stenosis degree, and cholesterol level in CHD patients.
细胞分裂周期蛋白 42(CDC42)调节巨噬细胞极化、血管炎症、动脉粥样硬化进展,并改变辅助性 T 细胞(Th)的分化,但其作为冠心病(CHD)患者的生物标志物的潜力尚不清楚。本研究旨在评估 CDC42 在 CHD 患者中的表达及其与 Th1、Th2 和 Th17 细胞、黏附分子和生化指标的相关性。
纳入 102 例 CHD 患者和 50 例对照者。所有参与者均采用逆转录定量聚合酶链反应检测外周血单个核细胞中 CDC42 的表达。在 CHD 患者中,通过流式细胞术分析检测 Th1、Th2 和 Th17 细胞;同时,通过酶联免疫吸附试验检测血清炎症细胞因子和黏附分子水平。
CHD 患者的 CDC42 水平(中位数(四分位距(IQR))= 0.431(0.304-0.722))低于对照组(中位数(IQR)= 0.985(0.572-1.760))(p<0.001)。在 CHD 患者中,CDC42 与 Th2 细胞(p=0.016)和白细胞介素(IL)-10(p=0.034)呈正相关,与 Th17 细胞(p<0.001)和 IL-17A(p<0.001)呈负相关。然而,在 CHD 患者中,CDC42 与 Th1 细胞(p=0.199)或干扰素-γ(p=0.367)之间无相关性。此外,CDC42 与 CHD 患者的血管细胞黏附分子-1(p=0.013)和细胞间黏附分子-1(p=0.001)呈负相关。此外,CDC42 与 C 反应蛋白(p<0.001)、Gensini 评分(p<0.001)、总胆固醇(p=0.039)和低密度脂蛋白胆固醇(p=0.014)呈负相关,但与其他生化指标(p>0.05)无相关性。
CDC42 与 Th2 细胞、Th17 细胞和黏附分子相关,也反映了 CHD 患者的炎症、冠状动脉狭窄程度和胆固醇水平。