Department of Molecular Imaging and Diagnosis, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan (O.T.); Department of Clinical Radiology, Graduate School of Medical Science, Kyushu University, Fukuoka, Japan (O.T., T.Y., A.H., K.Y., K.K., H.H.); Philips Research, Hamburg, Germany (J.K.); Philips Electronics Japan, Tokyo, Japan (Y.S.); Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan (S.O.S., T.I.); Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan (N.H., M.M., K.Y.); Advanced Imaging Research Center, UT Southwestern Medical Center, Dallas, Texas (K.S., M.T.).
Neuro Oncol. 2014 Mar;16(3):441-8. doi: 10.1093/neuonc/not158. Epub 2013 Dec 4.
Amide proton transfer (APT) imaging is a novel molecular MRI technique to detect endogenous mobile proteins and peptides through chemical exchange saturation transfer. We prospectively assessed the usefulness of APT imaging in predicting the histological grade of adult diffuse gliomas.
Thirty-six consecutive patients with histopathologically proven diffuse glioma (48.1 ± 14.7 y old, 16 males and 20 females) were included in the study. APT MRI was conducted on a 3T clinical scanner and was obtained with 2 s saturation at 25 saturation frequency offsets ω = -6 to +6 ppm (step 0.5 ppm). δB0 maps were acquired separately for a point-by-point δB0 correction. APT signal intensity (SI) was defined as magnetization transfer asymmetry at 3.5 ppm: magnetization transfer ratio (MTR)asym = (S[-3.5 ppm] - S[+3.5 ppm])/S0. Regions of interest were carefully placed by 2 neuroradiologists in solid parts within brain tumors. The APT SI was compared with World Health Organization grade, Ki-67 labeling index (LI), and cell density.
The mean APT SI values were 2.1 ± 0.4% in grade II gliomas (n = 8), 3.2 ± 0.9% in grade III gliomas (n = 10), and 4.1 ± 1.0% in grade IV gliomas (n = 18). Significant differences in APT intensity were observed between grades II and III (P < .05) and grades III and IV (P < .05), as well as between grades II and IV (P < .001). There were positive correlations between APT SI and Ki-67 LI (P = .01, R = 0.43) and between APT SI and cell density (P < .05, R = 0.38). The gliomas with microscopic necrosis showed higher APT SI than those without necrosis (P < .001).
APT imaging can predict the histopathological grades of adult diffuse gliomas.
酰胺质子转移(APT)成像是一种新型的分子 MRI 技术,可通过化学交换饱和转移来检测内源性移动蛋白和肽。我们前瞻性评估了 APT 成像在预测成人弥漫性神经胶质瘤组织学分级中的作用。
本研究纳入了 36 例经组织病理学证实的弥漫性神经胶质瘤患者(48.1±14.7 岁,男性 16 例,女性 20 例)。APT MRI 在 3T 临床扫描仪上进行,采用 2s 饱和,25 个饱和频率偏移 ω = -6 至+6 ppm(步长 0.5 ppm)。分别采集 δB0 图谱以进行逐点 δB0 校正。APT 信号强度(SI)定义为 3.5 ppm 处的磁化转移不对称性:磁化转移比(MTR)不对称=(S[-3.5 ppm]-S[+3.5 ppm])/S0。两位神经放射科医生在脑肿瘤的实体部分仔细放置感兴趣区。APT SI 与世界卫生组织分级、Ki-67 标记指数(LI)和细胞密度进行比较。
2 级神经胶质瘤(n=8)的平均 APT SI 值为 2.1±0.4%,3 级神经胶质瘤(n=10)为 3.2±0.9%,4 级神经胶质瘤(n=18)为 4.1±1.0%。APT 强度在 2 级和 3 级(P<.05)、3 级和 4 级(P<.05)以及 2 级和 4 级(P<.001)之间存在显著差异。APT SI 与 Ki-67 LI 之间呈正相关(P=0.01,R=0.43),与细胞密度之间呈正相关(P<.05,R=0.38)。有镜下坏死的神经胶质瘤的 APT SI 高于无坏死的神经胶质瘤(P<.001)。
APT 成像可预测成人弥漫性神经胶质瘤的组织病理学分级。