Okan Taha, Altın Cihan, Topaloglu Caner, Doruk Mehmet, Yılmaz Mehmet Birhan
Cardiology Department, Kardiya Medical Center, 35550 Izmir, Turkey.
Cardiology Department, Faculty of Medicine, Izmir Economy University, 35550 Izmir, Turkey.
Diagnostics (Basel). 2025 Jan 17;15(2):206. doi: 10.3390/diagnostics15020206.
: As an endocrine organ, adipose tissue produces adipokines that influence coronary artery disease (CAD). The objective of this study was to assess the potential value of CTRP5 and chemerin in differentiating coronary computed tomography angiography (CCTA)-confirmed coronary artery disease (CAD) versus non-CAD. Secondarily, within the CCTA-confirmed CAD group, the aim was to investigate the relationship between the severity and extent of CAD, as determined by coronary artery calcium score (CACS), and the levels of CTRP5 and chemerin. : Consecutive individuals with chest pain underwent CCTA to evaluate coronary artery anatomy and were divided into two groups. The CCTA-confirmed CAD group included patients with any atherosclerotic plaque (soft, mixed, or calcified) regardless of calcification, while the non-CAD group consisted of individuals without plaques on CCTA, with zero CACS, and without ischemia on stress ECG. Secondarily, in the CCTA-confirmed CAD group, the severity and extent of CAD were evaluated using CACS. Blood samples were collected and stored at -80 °C for analysis of CTRP5 and chemerin levels via ELISA. : Serum CTRP5 and chemerin levels were significantly higher in the CAD group compared to the non-CAD group (221.83 ± 103.81 vs. 149.35 ± 50.99 ng/mL, = 0.003 and 105.02 ± 35.62 vs. 86.07 ± 19.47 ng/mL, = 0.005, respectively). Receiver operating characteristic (ROC) analysis showed that a CTRP5 cutoff of 172.30 ng/mL had 70% sensitivity and 73% specificity for identifying CAD, while a chemerin cutoff of 90.46 ng/mL had 61% sensitivity and 62% specificity. A strong positive correlation was observed between CTRP5 and chemerin, but neither adipokine showed a correlation with the Agatston score, a measure of CAD severity and extent, nor with coronary artery stenosis as determined by CCTA. : CTRP5 and chemerin were significantly elevated in the CCTA-confirmed CAD group compared to the non-CAD group, with CTRP5 showing greater sensitivity and specificity. However, neither adipokine was linked to CAD severity and extent, differing from findings based on invasive coronary angiography (ICA). CTRP5 may serve as a promising "all-or-none biomarker" for CAD presence.
作为一个内分泌器官,脂肪组织会产生影响冠状动脉疾病(CAD)的脂肪因子。本研究的目的是评估C1q/TNF相关蛋白5(CTRP5)和趋化素在鉴别冠状动脉计算机断层扫描血管造影(CCTA)确诊的冠状动脉疾病(CAD)与非CAD方面的潜在价值。其次,在CCTA确诊的CAD组中,目的是研究由冠状动脉钙化积分(CACS)确定的CAD严重程度和范围与CTRP5和趋化素水平之间的关系。
连续的胸痛患者接受CCTA以评估冠状动脉解剖结构,并被分为两组。CCTA确诊的CAD组包括有任何动脉粥样硬化斑块(软斑块、混合斑块或钙化斑块)的患者,无论有无钙化,而非CAD组由CCTA上无斑块、CACS为零且负荷心电图无缺血的个体组成。其次,在CCTA确诊的CAD组中,使用CACS评估CAD的严重程度和范围。采集血样并储存在-80°C,通过酶联免疫吸附测定(ELISA)分析CTRP5和趋化素水平。
与非CAD组相比,CAD组的血清CTRP5和趋化素水平显著更高(分别为221.83±103.81 vs. 149.35±50.99 ng/mL,P = 0.003;以及105.02±35.62 vs. 86.07±19.47 ng/mL,P = 0.005)。受试者工作特征(ROC)分析表明,CTRP5临界值为172.30 ng/mL时,识别CAD的敏感性为70%,特异性为73%,而趋化素临界值为90.46 ng/mL时,敏感性为61%,特异性为62%。观察到CTRP5和趋化素之间存在强正相关,但这两种脂肪因子均与CAD严重程度和范围的测量指标阿加特斯顿积分无相关性,也与CCTA确定的冠状动脉狭窄无相关性。
与非CAD组相比,CCTA确诊的CAD组中CTRP5和趋化素显著升高,CTRP5表现出更高的敏感性和特异性。然而,这两种脂肪因子均与CAD的严重程度和范围无关,这与基于有创冠状动脉造影(ICA)的研究结果不同。CTRP5可能是一种有前景的用于诊断CAD的“全或无生物标志物”。