Paul C. Lauterbur Research Center for Biomedical Imaging, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong, China; Key Laboratory of Health Informatics, Chinese Academy of Sciences, Shenzhen, Guangdong, China.
Paul C. Lauterbur Research Center for Biomedical Imaging, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, Guangdong, China; Department of Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, Guangdong, China.
Neuroimage Clin. 2022;33:102890. doi: 10.1016/j.nicl.2021.102890. Epub 2021 Nov 27.
Chemical exchange saturation transfer (CEST) MRI, versatile for detecting endogenous mobile proteins and tissue pH, has proved valuable in tumor imaging. However, CEST MRI scans are often performed under non-equilibrium conditions, which confound tissue characterization. This study proposed a quasi-steady-state (QUASS) CEST MRI algorithm to standardize fast and accurate tumor imaging at 3 T. The CEST signal evolution was modeled by longitudinal relaxation rate during relaxation delay (Td) and spinlock relaxation during RF saturation time (Ts), from which the QUASS CEST effect is derived. Numerical simulation and human MR imaging experiments (7 healthy volunteers and 19 tumor patients) were conducted at 3 T to compare the CEST measurements obtained under two representative experimental conditions. In addition, amide proton transfer (APT), combined magnetization transfer (MT) and nuclear overhauser enhancement (NOE) effects, and direct water saturation were isolated using a 3-pool Lorentzian fitting in white matter and gray matter of healthy volunteers and for patients in the contralateral normal-appearing white matter and tumor regions. Finally, the student's t-test was performed between conventional and QUASS CEST measurements. The routine APT and combined MT & NOE measures significantly varied with Ts and Td (P < .001) and were significantly smaller than the corresponding QUASS indices (P < .001). In contrast, the results from the QUASS reconstruction showed little dependence on the scan protocol (P > .05), indicating the accuracy and robustness of QUASS CEST MRI for tumor imaging. To summarize, the QUASS CEST reconstruction algorithm enables fast and accurate tumor CEST imaging at 3 T, promising to expedite and standardize clinical CEST MRI.
化学交换饱和传递(CEST)MRI 技术在检测内源性可移动蛋白质和组织 pH 值方面具有广泛的应用,已被证明在肿瘤成像中具有重要价值。然而,CEST MRI 扫描通常在非平衡条件下进行,这会混淆组织特征。本研究提出了一种准稳态(QUASS)CEST MRI 算法,用于在 3T 下进行快速准确的肿瘤成像标准化。CEST 信号的演化通过弛豫延迟(Td)期间的纵向弛豫率和射频饱和时间(Ts)期间的自旋锁定弛豫进行建模,由此得出 QUASS CEST 效应。在 3T 下进行了数值模拟和人体磁共振成像实验(7 名健康志愿者和 19 名肿瘤患者),以比较在两种代表性实验条件下获得的 CEST 测量值。此外,在健康志愿者的白质和灰质中,以及在肿瘤患者对侧正常外观的白质和肿瘤区域中,使用 3 池洛伦兹拟合来分离酰胺质子转移(APT)、联合磁化转移(MT)和核奥弗豪瑟增强(NOE)效应以及直接水饱和。最后,对常规和 QUASS CEST 测量值进行了学生 t 检验。常规 APT 和联合 MT & NOE 测量值随 Ts 和 Td 显著变化(P<.001),并且显著小于相应的 QUASS 指数(P<.001)。相比之下,QUASS 重建的结果对扫描方案的依赖性较小(P>.05),这表明 QUASS CEST MRI 用于肿瘤成像的准确性和稳健性。总之,QUASS CEST 重建算法能够在 3T 下快速准确地进行肿瘤 CEST 成像,有望加快和标准化临床 CEST MRI。