Abstract

PurposeWe aimed to evaluate the diagnostic performances of quantitative indices obtained from dopamine transporter (DAT) single-photon emission computed tomography (SPECT) and 123I-metaiodobenzylguanidine (MIBG) scintigraphy for Parkinsonian syndromes (PS) using the classification and regression tree (CART) analysis.MethodsWe retrospectively enrolled 216 patients with or without PS, including 80 without PS (NPS) and 136 with PS [90 Parkinson’s disease (PD), 21 dementia with Lewy bodies (DLB), 16 progressive supranuclear palsy (PSP), and 9 multiple system atrophy (MSA). The striatal binding ratio (SBR), putamen-to-caudate ratio (PCR), and asymmetry index (AI) were calculated using DAT SPECT. The heart-to-mediastinum uptake ratio (H/M) based on the early (H/M [Early]) and delayed (H/M [Delay]) images and cardiac washout rate (WR) were calculated from MIBG scintigraphy. The CART analysis was used to establish a diagnostic decision tree model for differentiating PS based on these quantitative indices.ResultsThe sensitivity, specificity, positive predictive value, negative predictive value, and accuracy were 87.5, 96.3, 93.3, 92.9, and 93.1 for NPS; 91.1, 78.6, 75.2, 92.5, and 83.8 for PD; 57.1, 95.9, 60.0, 95.4, and 92.1 for DLB; and 50.0, 98.0, 66.7, 96.1, and 94.4 for PSP, respectively. The PCR, WR, H/M (Delay), and SBR indices played important roles in the optimal decision tree model, and their feature importance was 0.61, 0.22, 0.11, and 0.05, respectively.ConclusionThe quantitative indices showed high diagnostic performances in differentiating NPS, PD, DLB, and PSP, but not MSA. Our findings provide useful guidance on how to apply these quantitative indices in clinical practice.

Highlights

  • This article is part of the Topical Collection on Neurology - Movement disorders.Atypical parkinsonian syndromes (APS) are characterized by a more rapid progression and poorer prognosis than typical Parkinson’s disease (PD)

  • This study investigated the diagnostic performances of quantitative indices obtained from dopamine transporter (DAT) single-photon emission computed tomography (SPECT) and MIBG scintigraphy for Parkinsonian syndromes (PS) using the classification and regression tree (CART) analysis

  • The findings demonstrated that patients with NPS, PD, dementia with Lewy bodies (DLB), and progressive supranuclear palsy (PSP) could be differentiated using the optimal decision tree model with encouraging diagnostic performances

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Summary

Introduction

This article is part of the Topical Collection on Neurology - Movement disorders. Atypical parkinsonian syndromes (APS) are characterized by a more rapid progression and poorer prognosis than typical Parkinson’s disease (PD). Clinicopathologic studies have indicated that patients with APS are underdiagnosed; the clinical diagnostic accuracy is not optimal [1]. For more accurate diagnosis and appropriate treatment of different types of APS, proper utilization of dopamine transporter (DAT) single-photon emission computed tomography (SPECT) and 123I-metaiodobenzylguanidine (MIBG) scintigraphy would be valuable. Quantitative assessments are effective in interpreting DAT SPECT and MIBG scintigraphy, thereby leading to reduced inter-observer disagreement and more accurate diagnoses for Parkinsonian syndromes (PS) [2, 3]. The striatal binding ratio (SBR), putamen-to-caudate ratio (PCR), and asymmetry

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