Sharma Rakesh
Atherosclerosis Division, Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Magn Reson Med Sci. 2002 Dec 15;1(4):217-32. doi: 10.2463/mrms.1.217.
To evaluate the potential role of carotid artery atherosclerosis plaque magnetic resonance (MR) microimaging as magnetic resonance imaging (MRI) marker, ex vivo MR images were acquired at optimized parameters on 9.4T Bruker animal imager for occluded tissue resected by carotid endarterectomy (CEA) and corresponding histopathological analysis was made.
For imaging, CEA tissues of size 2-6 cm long and 0.5-1.5 cm wide, were transferred to 15 ml co-polymer laboratory culture tubes containing either 10% formalin in phosphate buffered saline (PBS) or in 50% glycerol in PBS. Imaging protocol was set at TE=30 ms, TR=1.5 s, matrix size=265 x 512, NEX=128, slice thickness=1 mm and in-plane resolution=0.1 mm for total sample size 2.5 cm. Soon after imaging done, carotid artery tissues were cut into 5-mm segments and processed for histological section for successive 5-micrometer slices. To compare morphology of 5 mum thin CEA section with that of 1 mm MR slices, registration was obtained between histologic sections and MR slices. Contrast and magnetic resonance relaxation characteristics were analyzed.
Total carotid artery area computed by MR imaging was correlated with areas determined from histologic sections (r(2)=0.989, p=0.0001). For the lumen area, the correlation between MR images and histologic area was (r(2)=0.942, p=0.0001). Relaxation times and T(2) parametric images of different plaque components were determinant for contrast resolution. Scan parameters were optimized for fibrous cap and atheroma. Scan parameters were characteristic for comparison at 1.5T and 9.4T MR imagers.
The observed correlation validated MR microimaging to assess morphological features of carotid artery plaques and contrast resolution highlighted the potential of in vivo MR imaging as non-invasive MRI marker to monitor carotid artery plaque morphometry and plaque composition.
为评估颈动脉粥样硬化斑块磁共振(MR)显微成像作为磁共振成像(MRI)标志物的潜在作用,在9.4T布鲁克动物成像仪上以优化参数采集经颈动脉内膜切除术(CEA)切除的闭塞组织的离体MR图像,并进行相应的组织病理学分析。
为进行成像,将长度为2 - 6厘米、宽度为0.5 - 1.5厘米的CEA组织转移至15毫升共聚物实验室培养管中,管内含有磷酸盐缓冲盐水(PBS)中的10%福尔马林或PBS中的50%甘油。成像方案设置为TE = 30毫秒,TR = 1.5秒,矩阵大小 = 265×512,激励次数(NEX)= 128,层厚 = 1毫米,面内分辨率 = 0.1毫米,总样本大小为2.5厘米。成像完成后,立即将颈动脉组织切成5毫米的片段,并处理成连续5微米切片的组织学切片。为比较5微米厚的CEA切片与1毫米MR切片的形态,在组织学切片和MR切片之间进行配准。分析对比度和磁共振弛豫特性。
通过MR成像计算的总颈动脉面积与组织学切片确定的面积相关(r² = 0.989,p = 0.0001)。对于管腔面积,MR图像与组织学面积之间的相关性为(r² = 0.942,p = 0.0001)。不同斑块成分的弛豫时间和T₂参数图像对于对比度分辨率具有决定性作用。针对纤维帽和动脉粥样硬化优化了扫描参数。扫描参数在1.5T和9.4T MR成像仪上具有比较特征。
观察到的相关性验证了MR显微成像可用于评估颈动脉斑块的形态特征,对比度分辨率突出了活体MR成像作为无创MRI标志物监测颈动脉斑块形态测量和斑块成分的潜力。