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Table 1 Common magnetic resonance imaging findings in Parkinson’s disease and atypical parkinsonian syndromes

From: Imaging biomarkers in Parkinson’s disease and Parkinsonian syndromes: current and emerging concepts

Neuropathology

Disorders

MRI signs

Structural/volumetric MRI findings

Diffusion Tensor MRI findings

Proton MRS findings

Synucleinopathies

PD

1. Swallow tail sign

2. Loss of nigrosome-1

↓ in frontal lobe, hippocampus, anterior cingulate and superior temporal gyri, and olfactory bulb and tract volumes vs. HC [12, 13, 17]

↓ in orbitofrontal, ventrolateral, prefrontal and occipitoparietal cortex vs. HC [15]

or ↓ in caudate, putamen and brainstem volumes vs. HC [1416]

↑ R2* transverse relaxation rate in SN vs. HC [19, 25]

DTI may be normal in early-PD vs. HC [73].

↓ FA in SN and anterior olfactory structures; and ↑ in olfactory bulb and tracts vs. HC [6972].

↑ in primarily in corpus callosum, putamen, midbrain, cerebellum and cerebellar peduncles may distinguish atypical PS from PD [74].

↓ in NAA and NAA/Cr levels in LN, temporoparietal and posterior cingulate cortex, and in pre-SMA vs. HC [8891]

PDD/DLB (LBD)

 

↓ in temporal, occipital, frontal and parietal cortices in PDD vs. HC [12, 27].

↓ in temporal, occipital and parietal cortices may be seen in DLB vs. PDD [33]

↓ in occipital and entorhinal cortices in PDD vs. PD [12, 35].

↓ in thalamic, amygdala and nucleus accumbens volumes, and ↑ in rate of temporal, occipital, parietal and SMA cortical thinning in PD-MCI vs. PD-non-MCI [39, 40]

↑ WM abnormalities in corpus callosum, dorsal striatum, frontal, parietal and occipital regions, as well as in amygdala and inferior longitudinal fasciculus in DLB with less temporal involvement vs. HC [84, 85].

↓ FA in parietal lobe (precuneus) in DLB vs. AD [86].

↓ in NAA/Cr values in the posterior cingulate gyrus and medial temporal lobe structures in DLB and PDD, although to a lesser degree than in AD [98, 99].

MSA

1. Putaminal rim sign

2. Hot-cross-bun sign

3. MCP sign

↓ in putamen, MCP, cerebellum, pons and striatal volumes in MSA-P and MSA-C vs. HC [6, 16].

↓ in putaminal, cerebellar and pontine volumes in MSA vs. PD [16, 44, 45]

↓ in primary and SMA, prefrontal and insular cortices, striatum and midbrain in MSA-P vs. PD and HC [49]

↑ cortical thinning in parahippocampal and lingual cortex in MSA-demented vs. MSA-non-demented [50]

↑ putaminal in MSA-P vs. PD, MSA-C and HC [74, 75].

↓ FA and ↑ ADC in MSA-P in putamen, cerebellum and pons vs. PD and HC [76].

↓ FA in MCP, inferior cerebellar peduncle, and ventral pons in MSA-C vs. HC [79].

↓ FA and ↑ in MCP and pons vs. HC [77, 80].

↑ ADC in cerebellum and MCP in MSA-C vs. MSA-P and HC [80]; ↓ FA in MCP vs. PSP and HC [77, 78]

↓ in NAA/Cr ratio in putamen and pontine base in MSA vs. PD and HC [96].

Tauopathies

PSP

1. Hummingbird sign

2. Morning glory sign

↓ in prefrontal, frontal, insular, premotor, SMA, hippocampus and parahippocampal regions; ↓ WM in pulvinar, thalamus, colliculus, mesencephalon and frontotemporal regions; ↓ in midbrain, pons, thalamus and striatum, vs. HC [57, 58].

↓ in midbrain and SCP volumes vs. PD, MSA-P, CBS and HC [54, 55, 59, 61, 62]

↓ in brainstem, midbrain and frontal cortex vs. HC [56]

↓ midbrain atrophy and ↑ cortical/subcortical atrophy in PSP with dementia [61]

or ADC in decussation of SCP, thalamus, cingulum, motor and SMA; ↓ FA in the frontal inferior frontooccipital fasciculus, superior longitudinal fasciculus, arcuate fasciculus, posterior thalamic radiations, internal capsule, orbitofrontal WM, anterior cingulum, motor area vs. HC [58, 78, 81, 82]

↑ ADC in putamen and pons in MSA-P vs. MSA-C and HC [80]

in midbrain and SCP vs. atypical PS group [74].

↑ ADC in putamen, globus pallidus and caudate nucleus vs. PD [83].

↓ in NAA/Cr ratio in LN, brainstem, centrum semiovale, frontal and precentral cortex vs. HC [93, 94].

Relatively greater ↓ in NAA/Cr ratio in putamen and frontal cortex vs. PD [86, 88, 95].

CBD/CBS

 

↑ global brain atrophy in CBD vs. PSP [66]

↓ in bilateral frontal cortex (including SMA), dorsolateral prefrontal cortex, pre/post-central gyri, striatum, and brainstem in CBD vs. HC [68]

↓ in frontal and insula cortex with scarce WM atrophy in CBD-dementia; moderate ↓ in GM/WM of these regions in CBD with early extrapyramidal manifestations [61]

↓ in prefrontal cortex and parietal lobe, respectively, in CBD-FTD and CBD-AD [11]

↓ FA in the long frontoparietal connecting tracts, intraparietal associative fibers, corpus callosum and sensorimotor projections of cortical hand areas, in CBS vs. HC [65].

↓ FA and ↑ D in posterior truncus of corpus callosum may differentiate CBS from PD [73].

↓ in NAA and NAA/Cr levels contralaterally in frontoparietal cortex, LN, centrum semiovale and putamen, in CBS vs. HC [94, 95, 97].

Greater ↓ in NAA and NAA/Cr levels in frontal cortex and putamen with marked putaminal asymmetry, in CBS vs. PD, MSA and vascular parkinsonism [95]

  1. Legend: normal; ↓ decrease; ↑ increase
  2. Abbreviations: AD, Alzheimer’s disease; ADC, apparent diffusion coefficient; CBD, pathologically-proven corticobasal degeneration; CBS, clinically-diagnosed corticobasal syndrome; D̄, mean diffusivity; DLB, dementia with Lewy bodies; DTI, diffusion-tensor imaging; FA, fractional anisotropy; FTD, frontotemporal degeneration; HC, healthy controls; LBD, Lewy body spectrum disorders; LN, lentiform nucleus; MCI, mild cognitive impairment; MCP, middle cerebellar peduncle; MRS, magnetic resonance spectroscopy; MSA, multiple system atrophy; MSA-P, MSA-parkinsonian type; MSA-C, MSA-cerebellar type; NAA, N-acetyl aspartate; NAA/Cr, NAA-to-creatine ratio; PD, Parkinson’s disease; PDD, Parkinson’s disease dementia; PS, parkinsonian syndromes; PSP, progressive supranuclear palsy; SCP, superior cerebellar peduncle; SMA, supplementary motor area; SN, substantia nigra; WM, white matter