Xie Sheng-Hui, Lang Rui, Li Bo, Zhao He, Wang Peng, He Jin-Long, Ma Xue-Ying, Wu Qiong, Wang Shao-Yu, Zhang Hua-Peng, Gao Yang, Wu Jian-Lin
Graduate School of Tianjin Medical University, Tianjin, China.
Department of Radiology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia, China.
Neuroradiology. 2023 Jan;65(1):55-64. doi: 10.1007/s00234-022-03000-0. Epub 2022 Jul 15.
To evaluate two advanced diffusion models, diffusion kurtosis imaging and the newly proposed mean apparent propagation factor-magnetic resonance imaging, in the grading of gliomas and the assessing of their proliferative activity.
Fifty-nine patients with clinically diagnosed and pathologically proven gliomas were enrolled in this retrospective study. All patients underwent DKI and MAP-MRI scans. Manually outline the ROI of the tumour parenchyma. After delineation, the imaging parameters were extracted using only the data from within the ROI including mean diffusion kurtosis (MK), return-to-origin probability (RTOP), Q-space inverse variance (QIV) and non-Gaussian index (NG), and the differences in each parameter in the classification of glioma were compared. Receiver operating characteristic (ROC) curve analysis was used to evaluate the diagnostic performance of these parameters.
MK, NG, RTOP and QIV were significantly different amongst the different grades of glioma. MK, NG and RTOP had excellent diagnostic value in differentiating high-grade from low-grade glioma, with largest areas under the curve (AUCs; 0.929, 0.933 and 0.819, respectively; P < 0.01). MK and NG had the largest AUCs (0.912 and 0.904) when differentiating grade II tumours from III tumours (P < 0.01) and large AUCs (0.791 and 0.786) when differentiating grade III from grade IV tumours. Correlation analysis of tumour proliferation activity showed that MK, NG and QIV were strongly correlated with the Ki-67 LI (P < 0.001).
MK, RTOP and NG can effectively represent the microstructure of these altered tumours. Multimodal diffusion-weighted imaging is valuable for the preoperative evaluation of glioma grade and tumour proliferative activity.
评估两种先进的扩散模型,即扩散峰度成像和新提出的平均表观传播因子磁共振成像,在胶质瘤分级及其增殖活性评估中的应用。
本回顾性研究纳入了59例临床诊断并经病理证实的胶质瘤患者。所有患者均接受了扩散峰度成像(DKI)和平均表观传播因子磁共振成像(MAP-MRI)扫描。手动勾勒肿瘤实质的感兴趣区(ROI)。勾勒完成后,仅使用ROI内的数据提取成像参数,包括平均扩散峰度(MK)、回波原点概率(RTOP)、Q空间逆方差(QIV)和非高斯指数(NG),并比较各参数在胶质瘤分级中的差异。采用受试者操作特征(ROC)曲线分析来评估这些参数的诊断性能。
不同级别胶质瘤的MK、NG、RTOP和QIV存在显著差异。MK、NG和RTOP在区分高级别与低级别胶质瘤方面具有出色的诊断价值,曲线下面积(AUC)最大(分别为0.929、0.933和0.819;P < 0.01)。在区分Ⅱ级肿瘤与Ⅲ级肿瘤时,MK和NG的AUC最大(分别为0.912和0.904;P < 0.01),在区分Ⅲ级与Ⅳ级肿瘤时,AUC也较大(分别为0.791和0.786)。肿瘤增殖活性的相关性分析表明,MK、NG和QIV与Ki-67标记指数(LI)密切相关(P < 0.001)。
MK、RTOP和NG能够有效反映这些病变肿瘤的微观结构。多模态扩散加权成像对胶质瘤分级及肿瘤增殖活性的术前评估具有重要价值。