Abstract

ObjectivesTo provide an automated classification method for degenerative parkinsonian syndromes (PS) based on semiquantitative 123I-FP-CIT SPECT striatal indices and support-vector-machine (SVM) analysis.Methods123I-FP-CIT SPECT was performed at a single-center level on 370 individuals with PS, including 280 patients with Parkinson’s disease (PD), 21 with multiple system atrophy-parkinsonian type (MSA-P), 41 with progressive supranuclear palsy (PSP) and 28 with corticobasal syndrome (CBS) (mean age 70.3 years, 47% female, mean disease duration at scan 1.4 year), as well as 208 age- and gender-matched control subjects. Striatal volumes-of-interest (VOIs) uptake, VOIs asymmetry indices (AIs) and caudate/putamen (C/P) ratio were used as input for SVM individual classification using fivefold cross-validation.ResultsUnivariate analyses showed significantly lower VOIs uptake, higher striatal AI and C/P ratio for each PS in comparison to controls (all p < 0.001). Among PS, higher degree of striatal impairment was observed in MSA-P and PSP, while CBS showed moderate uptake reduction and higher AI. Binary SVM classification showed 92.9% accuracy in distinguishing PS from controls. Classification based on each binary combination of PS ranged 62.9–83.7% accuracy with the most satisfactory results when separating CBS from the other PS. Sensitivity and specificity values were high and balanced ranging from 60 to 80% for all analyses with > 70% accuracy. Overall, striatal AI and C/P ratio on the more affected side had the highest weighting factors.ConclusionSemiquantitative 123I-FP-CIT SPECT striatal evaluation combined with SVM represents a promising approach to disentangle PD from non-degenerative conditions and from atypical PS at the early stage.

Highlights

  • Parkinson Disease (PD) is the most common neurodegenerative movement disorder in the general population and accounts for 65% of all parkinsonian syndromes (PS) [1]

  • 1363 subjects were scanned in our institution with the same SPECT acquisition protocol during the 13-year study period, among which 370 participants presented with a degenerative PS and fulfilled inclusion criteria: 280 PD, 21 multiple system atrophy-parkinsonian type (MSA-P), 41 progressive supranuclear palsy (PSP) and 28 corticobasal syndrome (CBS) subjects

  • Head-to-head comparisons showed that PD subjects exhibited significantly higher mean uptake in the S, C and P compared to multiple system atrophy (MSA)-P and PSP and lower P uptake compared to CBS (p < 0.005)

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Summary

Introduction

Parkinson Disease (PD) is the most common neurodegenerative movement disorder in the general population and accounts for 65% of all parkinsonian syndromes (PS) [1]. It is characterized by progressive akinesia in association with rest tremor and muscular rigidity as well as an excellent response to levodopa therapy [2]. Compared to PD, APS are characterized by additional clinical features besides parkinsonism (cerebellar or pyramidal signs, postural instability or apraxia), a moderate or transient response to levodopa and a worse prognosis with a mean life expectancy of 7–10 years from disease onset [4, 5]. Only a few of the proposed biomarkers have proved robust enough to be included in the new MDS criteria for PD—olfactory loss and cardiac sympathetic denervation as supportive criteria, and a normal presynaptic dopaminergic system as exclusion criterion [2]

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