Partners MS Center (T.S., K.O.C., R.C., S.C., S.T., H.L.W., R.B.), Laboratory for Neuroimaging Research, Ann Romney Center for Neurological Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School; Division of Nuclear Medicine and Molecular Imaging (S.D., M.K., M.D.), Department of Radiology, Brigham and Women's Hospital, Harvard Medical School; Functional Neuroimaging Laboratory (H.P., D.S., E.S.), Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School; Department of Medicine (S.H.) and Department of Radiology (E.S., R.B.), Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Neurol Neuroimmunol Neuroinflamm. 2019 Jul 1;6(5):e587. doi: 10.1212/NXI.0000000000000587. eCollection 2019 Sep.
To determine the value of [F-18]PBR06-PET for assessment of microglial activation in the cerebral gray matter in patients with MS.
Twelve patients with MS (7 relapsing-remitting and 5 secondary progressive [SP]) and 5 healthy controls (HCs) had standardized uptake value (SUV) PET maps coregistered to 3T MRI and segmented into cortical and subcortical gray matter regions. SUV ratios (SUVRs) were global brain normalized. Voxel-by-voxel analysis was performed using statistical parametric mapping (SPM). Normalized brain parenchymal volumes (BPVs) were determined from MRI using SIENAX.
Cortical SUVRs were higher in the hippocampus, amygdala, midcingulate, posterior cingulate, and rolandic operculum and lower in the medial-superior frontal gyrus and cuneus in the MS vs HC group (all < 0.05). Subcortical gray matter SUVR was higher in SPMS vs RRMS (+10.8%, = 0.002) and HC (+11.3%, = 0.055) groups. In the MS group, subcortical gray matter SUVR correlated with the Expanded Disability Status Scale (EDSS) score (r = 0.75, = 0.005) and timed 25-foot walk (T25FW) (r = 0.70, = 0.01). Thalamic SUVRs increased with increasing EDSS scores (r = 0.83, = 0.0008) and T25FW (r = 0.65, = 0.02) and with decreasing BPV (r = -0.63, = 0.03). Putaminal SUVRs increased with increasing EDSS scores (0.71, = 0.009) and with decreasing BPV (r = -0.67, = 0.01). On SPM analysis, peak correlations of thalamic voxels with BPV were seen in the pulvinar and with the EDSS score and T25FW in the dorsomedial thalamic nuclei.
This study suggests that [F-18]PBR06-PET detects widespread abnormal microglial activation in the cerebral gray matter in MS. Increased translocator protein binding in subcortical gray matter regions is associated with brain atrophy and may link to progressive MS.
评估 [F-18]PBR06-PET 在多发性硬化症(MS)患者大脑灰质中微胶质激活的价值。
12 名 MS 患者(7 名复发缓解型,5 名继发进展型[SP])和 5 名健康对照者(HCs)进行了标准摄取值(SUV)PET 图谱与 3T MRI 的配准,并分为皮质和皮质下灰质区。对大脑进行全局脑标准化后计算 SUV 比值(SUVRs)。采用统计参数映射(SPM)进行体素分析。使用 SIENAX 从 MRI 中确定正常脑组织体积(BPVs)。
与 HC 组相比,MS 患者的海马体、杏仁核、中扣带回、后扣带回和 Rolandic 脑回的皮质 SUVRs 较高,而额内侧上回和楔前叶的 SUVRs 较低(均<0.05)。SPMS 患者的皮质下灰质 SUVR 高于 RRMS(+10.8%, = 0.002)和 HC(+11.3%, = 0.055)。在 MS 组中,皮质下灰质 SUVR 与扩展残疾状况量表(EDSS)评分(r = 0.75, = 0.005)和 25 英尺步行测试(T25FW)(r = 0.70, = 0.01)呈正相关。丘脑 SUVRs 随着 EDSS 评分(r = 0.83, = 0.0008)和 T25FW(r = 0.65, = 0.02)的升高而增加,与 BPV(r = -0.63, = 0.03)的降低而增加。壳核 SUVRs 随着 EDSS 评分(0.71, = 0.009)的升高和 BPV(r = -0.67, = 0.01)的降低而增加。SPM 分析显示,丘脑与 BPV 之间的峰值相关性出现在 Pulvinar 和背内侧丘脑核的 EDSS 评分和 T25FW 中。
本研究表明,[F-18]PBR06-PET 可检测多发性硬化症患者大脑灰质中广泛的异常小胶质细胞激活。皮质下灰质区转位蛋白结合增加与脑萎缩有关,可能与进展性多发性硬化症有关。