Abstract

The aim of this study was to compare the performance of a deep-learning convolutional neural network (Faster R-CNN) model to detect imaging findings suggestive of idiopathic Parkinson’s disease (PD) based on [18F]FP-CIT PET maximum intensity projection (MIP) images versus that of nuclear medicine (NM) physicians. The anteroposterior MIP images of the [18F]FP-CIT PET scan of 527 patients were classified as having PD (139 images) or non-PD (388 images) patterns according to the final diagnosis. Non-PD patterns were classified as overall-normal (ONL, 365 images) and vascular parkinsonism with definite defects or prominently decreased dopamine transporter binding (dVP, 23 images) patterns. Faster R-CNN was trained on 120 PD, 320 ONL, and 16 dVP pattern images and tested on the 19 PD, 45 ONL, and seven dVP patterns images. The performance of the Faster R-CNN and three NM physicians was assessed using receiver operating characteristics curve analysis. The difference in performance was assessed using Cochran’s Q test, and the inter-rater reliability was calculated. Faster R-CNN showed high accuracy in differentiating PD from non-PD patterns and also from dVP patterns, with results comparable to those of NM physicians. There were no significant differences in the area under the curve and performance. The inter-rater reliability among Faster R-CNN and NM physicians showed substantial to almost perfect agreement. The deep-learning model accurately differentiated PD from non-PD patterns on MIP images of [18F]FP-CIT PET, and its performance was comparable to that of NM physicians.

Highlights

  • Based on the clinical diagnosis, maximum intensity projection (MIP) images of the [18 F]FP-CIT positron emission tomography (PET) of 139 subjects were classified as having Parkinson’s disease (PD) patterns and 388 as having non-PD patterns (Figure 1)

  • The non-PD patterns were further classified as 365 ONL and 23 dVP patterns

  • We evaluated the performance of the Faster R-CNN in distinguishing PD from other patterns in parkinsonism using one anteroposterior MIP image of each patient’s [18 F]FP-CIT PET

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Summary

Introduction

Parkinsonism is an umbrella term for a symptom complex that includes tremor at rest, bradykinesia, rigidity, and postural instability [1]. The underlying causes of parkinsonism are diverse, idiopathic Parkinson’s disease (PD) is by far the most common cause, followed by atypical parkinsonism (APD). The differential diagnosis of parkinsonism further includes essential tremor, vascular parkinsonism (VP), drug-induced parkinsonism, and other disorders [2]. Despite recent advances in neuroimaging and genetic analysis, this differential diagnosis remains primarily based on clinical assessment. All the mentioned conditions show a considerable overlap of their clinical features in the early stage, leading to frequent changes in the diagnosis of patients with parkinsonism during the first years [3,4]

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