Skip to main content
. 2019 Nov 9;24:102059. doi: 10.1016/j.nicl.2019.102059

Table. 3.

Nuclear medicine studies in PD-FOG.

Authors (Year) Participants (years) (mean age ± SD) Technique Outcome measures Imaging findings Clinical correlation
PET
Bartels et al. (2006) 10 PD-FOG (NA) 7 PD-nFOG (NA) 18 [F]-DOPA and 18 [F]-FDG Striatal dopamine and glucose metabolism Reduced uptake of FDOPA in putamen and caudate, bilaterally; increased uptake of FDG in putamen, bilaterally; reduced uptake of FDG in caudate, bilaterally, and right parietal regions No correlation
Lyoo et al. (2007) 10 PD-FOG (61.3±9.8) 18 [F]-FDG Glucose metabolism before and after STN-DBS for clinical-radiological correlations FOG improvement associated with increased metabolic activity in parieto-temporo-occipital areas after STN-DBS FOG improvement positively correlated with metabolic activity in parieto-temporo-occipital areas after STN-DBS
Bohnen et al. (2014) 20 PD-FOG (66±6) 123 PD-nFOG (65±8) 11[C]-DTBZ, 11[C]-PMP, 11[C]-PIB Dopaminergic and cholinergic activity, amyloid deposition Reduced striatal dopaminergic activity; Reduced neocortical cholinergic innervation; Increased neocortical β‐amyloid deposition Not performed
Maillet et al. (2015) 8 PD-FOG (12.3 ± 3.8) [H2150] Regional cerebral blood flow during motor imagery of gait in ON state of therapy compared to Off state of therapy Levodopa increased activation in motor regions, putamen, thalamus and cerebellum, while reduced premotor‐parietal and brainstem activation compared to OFF state of therapy Not performed
Tard et al. (2015) 11 PD-FOG (61±5) 11 PD-nFOG (62±3) 18[F]-FDG Glucose metabolism after performing a gait trajectory involving FOG triggers Increased metabolic activity in the paracentral lobule, Globus pallidus and left posterior parietal cortex; reduced metabolic activity in the left dorsolateral prefrontal cortex FOG occurrence positively correlated with metabolic activity in cerebellum, paracentral lobule and frontal eye field; negatively correlated with activity in orbitofrontal area, premotor cortex, SMA and temporal lobe.
Ono et al. (2016) 40 PD patients (69±8; 11 PD-nFOG) 11 HS (64±7) 6-18[F]-FMT AADC activity Reduced FMT uptake in putamen, caudate and LC in PD patients than HS Severity of FOG negatively correlated with FMT uptake in LC
Gallardo et al. (2018) 9 PD-FOG (NA) 8 PD-nFOG (NA) 18[F]-FDG Glucose metabolism Frontal and predominantly right-sided hypometabolism Not performed
Mitchell et al. (2019) 9 PD-FOG (68±6) 9 PD-nFOG (65±5) 18[F]-FDG Glucose metabolism during steering of gait compared to straight walking Changes in cortico-thalamic circuit and hyperdirect pathway (reduced activation of parietal regions; reduced deactivation of prefrontal regions and thalamus; increased activation of supplementary motor area) during staring of gait Activity in right dorsolateral prefrontal cortex negatively correlated with stride length during steering of gait
Bohnen et al. (2019) 15 PD-FOG (73±10) 79 PD-nFOG (67±7) 18[F]-FEOBV VAChT expression Reduced VAChT expression in bilateral striatum (mostly right caudate), temporal and mesiofrontal limbic regions. No correlation
SPECT
Matsui et al. (2005) 24 PD-FOG (66±8) 31 PD-nFOG (70±7) 123[I]‐IMP Brain perfusion Decreased perfusion in orbitofrontal cortex, bilaterally FOG severity negatively correlated with perfusion rate in the orbitofrontal cortex
Imamura et al. (2012) 21 PD-FOG (71±8) 34 PD-nFOG (69±10) 123[I]‐IMP Regional cerebral blood flow Increased perfusion in frontal lobe (bilateral BA 10, 11 and left BA 32) FOG severity positively correlated with perfusion increase in BA 10, 11, 32
Djaldetti et al. (2018) 15 PD-FOG (63±11) 26 PD-nFOG (61±9) 123[I]-FP-CIT DAT uptake Reduced DAT uptake in putamen and striatum Inverse association between DAT uptake in putamen and striatum and FOG
Kim et al. (2018) 390 PD patients (NA) (PPMI database) 123[I]-Ioflupane DAT uptake Reduced DAT uptake in caudate and putamen Inverse association between DAT uptake in caudate and putamen and FOG

PD-FOG: patients with Parkinson's disease and Freezing of Gait; PD-nFOG: patients with Parkinson's disease without Freezing of Gait; 18[F] DOPA: 18 [F]-6-fluoro-levodopa; 18[F] FDG: 18[F]-fluordesoxy-glucose; STN: subthalamic nucleus; DBS: Deep brain stimulation; 11[C] DTBZ: 11[C] Dihydrotetrabenazine; 11[C] PMP: 11[C]methyl4piperidyl propionate; 11[C] PIB: 11[C]-Pittsburgh compound B; On state of therapy: after Levodopa intake; Off state of therapy: after Levodopa withdrawal; HS: Healthy Subjects; 6-18[F] FMT: 6-18[F]Fluoro-l-m-tyrosine; AADC: Aromatic l-amino acid decarboxylase; LC: locus coeruleus; 18[F] FEOBV: 18[F]-fluoroethoxybenzovesamicol; VAChT: Vesicular acetylcholine transporter; 123[I]‐IMP: N-isopropyl-p-123[I]iodoamphetamine; BA: Brodmann Area; 123[I]-FP-CIT: 123[I]-2-b-carbomethoxy-3b-(4-iodophenyl)-N-(3-fluoropropyl) nortropane; DAT: Dopamine Transporter; PPMI: Parkinson's Progression Markers Initiative.

*NA: not available