Department of Radiology, Charité - Universitätsmedizin Berlin, Germany.
J Magn Reson Imaging. 2011 Oct;34(4):816-23. doi: 10.1002/jmri.22683. Epub 2011 Jul 18.
To evaluate very small superparamagnetic iron oxide particles (VSOP-C184) as blood-pool contrast agent for coronary MR angiography (CMRA) in humans.
Six healthy volunteers and 14 patients with suspected coronary artery disease underwent CMRA after administration of VSOP-C184 at the following doses: 20 μmol Fe/kg (4 patients), 40 μmol Fe/kg (5 patients), 45 μmol Fe/kg (6 healthy volunteers), and 60 μmol Fe/kg (5 patients). In healthy volunteers, contrast-to-noise ratio (CNR), signal-to-noise ratio (SNR), and vessel edge definition (VED) of contrast-enhanced CMRA were compared with non-contrast-enhanced CMRA. In patients, a per-segment intention-to-diagnose evaluation of contrast-enhanced CMRA for detection of significant coronary stenosis (≥50%) was performed.
Three healthy volunteers (45 μmol Fe/kg VSOP-C184) and two patients (60 μmol Fe/kg VSOP-C184) had adverse events of mild or moderate intensity. VSOP-C184 significantly increased CNR (15.1 ± 4.6 versus 6.9 ± 1.9; P = 0.010), SNR (21.7 ± 5.3 versus 15.4 ± 1.6; P = 0.048), and VED (2.3 ± 0.6 versus 1.2 ± 0.2; P < 0.001) compared with non-contrast-enhanced CMRA. In patients, contrast-enhanced CMRA yielded sensitivity, specificity, and diagnostic accuracy for detection of significant coronary stenosis of 86.7%, 71.0%, 73.1%, respectively.
CMRA using VSOP-C184 was feasible and yielded moderate diagnostic accuracy for detection of significant coronary stenosis within this proof-of-concept setting.
评估超小超顺磁性氧化铁颗粒(VSOP-C184)作为人冠状动脉磁共振血管造影(CMRA)血池对比剂的效果。
6 名健康志愿者和 14 名疑似冠心病患者分别接受 20 μmol Fe/kg(4 例)、40 μmol Fe/kg(5 例)、45 μmol Fe/kg(6 例健康志愿者)和 60 μmol Fe/kg(5 例)VSOP-C184 剂量的 CMRA 检查。在健康志愿者中,比较了增强与非增强 CMRA 的对比噪声比(CNR)、信噪比(SNR)和血管边缘定义(VED)。在患者中,对增强 CMRA 检测显著冠状动脉狭窄(≥50%)的分段意向诊断评估进行了评估。
3 名(45 μmol Fe/kg VSOP-C184)健康志愿者和 2 名(60 μmol Fe/kg VSOP-C184)患者出现了轻度或中度不良反应。与非增强 CMRA 相比,VSOP-C184 显著增加了 CNR(15.1 ± 4.6 对 6.9 ± 1.9;P = 0.010)、SNR(21.7 ± 5.3 对 15.4 ± 1.6;P = 0.048)和 VED(2.3 ± 0.6 对 1.2 ± 0.2;P < 0.001)。在患者中,增强 CMRA 检测显著冠状动脉狭窄的敏感性、特异性和诊断准确性分别为 86.7%、71.0%和 73.1%。
在这一概念验证研究中,VSOP-C184 的 CMRA 是可行的,对检测显著冠状动脉狭窄具有中等的诊断准确性。