From the Departments of Radiology (A.S.K., K.A.P., M.A.M., J.D.K., F.A.G., T.M.), Psychiatry (J.T.O.), and Clinical Neurosciences (J.B.R.), University of Cambridge, Hills Road, Cambridge CB2 0QQ, England; and Departments of Radiology (O.I.V., F.A.G., T.M.) and Neurology (J.B.R.), Cambridge University Hospitals NHS Foundation Trust, Cambridge, England.
Radiology. 2024 Jul;312(1):e232407. doi: 10.1148/radiol.232407.
Background Impaired glucose metabolism is characteristic of several types of dementia, preceding cognitive symptoms and structural brain changes. Reduced glucose uptake in specific brain regions, detected using fluorine 18 (F) fluorodeoxyglucose (FDG) PET, is a valuable diagnostic marker in Alzheimer disease (AD). However, the use of F-FDG PET in clinical practice may be limited by equipment availability and high cost. Purpose To test the feasibility of using MRI-based deuterium (H) metabolic imaging (DMI) at a clinical magnetic field strength (3 T) to detect and localize changes in the concentration of glucose and its metabolites in the brains of patients with a clinical diagnosis of AD. Materials and Methods Participants were recruited for this prospective case-control pilot study between March 2021 and February 2023. DMI was performed at 3 T using a custom birdcage head coil following oral administration of deuterium-labeled glucose (0.75 g/kg). Unlocalized whole-brain MR spectroscopy (MRS) and three-dimensional MR spectroscopic imaging (MRSI) (voxel size, 3.2 cm cubic) were performed. Ratios of H-glucose, H-glutamate and H-glutamine (H-Glx), and H-lactate spectroscopic peak signals to H-water peak signal were calculated for the whole-brain MR spectra and for individual MRSI voxels. Results A total of 19 participants, including 10 participants with AD (mean age, 68 years ± 5 [SD]; eight males) and nine cognitively healthy control participants (mean age, 70 years ± 6; six males) were evaluated. Whole-brain spectra demonstrated a reduced ratio of H-Glx to H-glucose peak signals in participants with AD compared with control participants (0.41 ± 0.09 vs 0.58 ± 0.20, respectively; = .04), suggesting an impairment of oxidative glucose metabolism in AD. However, there was no evidence of localization of these changes to the expected regions of metabolic impairment at MRSI, presumably due to insufficient spatial resolution. Conclusion DMI at 3 T demonstrated impairment of oxidative glucose metabolism in the brains of patients with AD but no evidence of regional signal differences. © RSNA, 2024
背景 葡萄糖代谢受损是几种类型痴呆症的特征,先于认知症状和结构脑变化。使用氟 18(F)氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)检测到特定脑区葡萄糖摄取减少是阿尔茨海默病(AD)的有价值的诊断标志物。然而,FDG-PET 在临床实践中的使用可能受到设备可用性和高成本的限制。目的 测试在临床磁场强度(3 T)下使用基于磁共振成像的氘(H)代谢成像(DMI)检测和定位 AD 临床诊断患者脑内葡萄糖及其代谢物浓度变化的可行性。
材料与方法 这项前瞻性病例对照初步研究于 2021 年 3 月至 2023 年 2 月期间招募参与者。参与者口服氘标记葡萄糖(0.75 g/kg)后,在定制鸟笼头线圈下于 3 T 进行 DMI。进行非局部化全脑磁共振波谱(MRS)和三维磁共振波谱成像(MRSI)(体素大小 3.2 cm 立方)。计算全脑 MR 光谱和各个 MRSI 体素的 H-葡萄糖、H-谷氨酸和 H-谷氨酰胺(H-Glx)以及 H-乳酸光谱峰信号与 H-水峰信号的比值。
结果 共评估了 19 名参与者,包括 10 名 AD 患者(平均年龄 68 岁±5[标准差];8 名男性)和 9 名认知健康对照参与者(平均年龄 70 岁±6;6 名男性)。AD 患者的全脑光谱显示 H-Glx 与 H-葡萄糖峰信号的比值低于对照组(分别为 0.41±0.09 比 0.58±0.20;P=.04),提示 AD 患者的氧化葡萄糖代谢受损。然而,在 MRSI 上,没有证据表明这些变化定位于预期的代谢受损区域,推测是由于空间分辨率不足。
结论 3 T 下的 DMI 显示 AD 患者脑内氧化葡萄糖代谢受损,但没有证据表明存在区域信号差异。