Abstract

Introduction Brain SPECT with 99mTc-TRODAT-1 (SPECT-TRODAT) may be a useful tool in the differential diagnosis of Parkinsonism. Objective To compare results of SPECT-TRODAT with clinical findings in patients with Parkinsonism. Methods We evaluated 153 outpatients. SPECT-TRODAT results were visually analyzed into normal, abnormal, symmetric, and asymmetric, and according to the degree of impairment into mild, moderate, marked, and severe (1–4). Results A direct relationship was found between motor scores severity (MDS-UPDRS-III) and SPECT-TRODAT-reduced binding in general, in the group of patients with synucleinopathies (rho = 0.258, p=0.005), especially in patients with Parkinson's disease (rho = 0.204, p=0.049). Changes in SPECT-TRODAT had high correspondence with symmetry in all Parkinsonism. When comparing groups to the correspondence predominantly bilateral or unilateral impairment in SPECT, there was a difference between patients with SNP (p=0.041) and between this group and patients with secondary Parkinsonism (SP) (p < 0.0001). It was handy in differentiating drug-induced Parkinsonism from synucleinopathies. In the group of drug-induced Parkinsonism, younger people were the ones who showed the most significant reductions in radiotracer uptake. In this group, nonmotor signs resulted in examinations with more significant reductions in radiotracer uptake. When the scans without alterations and those that did not correspond to the symmetry were considered negative, SPECT-TRODAT's accuracy and specificity to differentiate PD from other forms of Parkinsonism were low. There was an inverse correlation between the severity of the SPECT-TRODAT result and the absence of nonmotor signs in patients with drug-induced Parkinsonism. Conclusion The authors concluded that the SPECT with 99mTc-TRODAT-1 was mainly useful in differentiating between synucleinopathies and secondary Parkinsonism.

Highlights

  • Brain SPECT with 99mTc-TRODAT-1 (SPECT-TRODAT) may be a useful tool in the differential diagnosis of Parkinsonism

  • We included patients examined by the same neurologist specialized in movement disorders (GF), who had presented for at least three consultations and had their medical records complete. e diagnostic criteria should correspond to one of the following disorders: Parkinson’s disease (PD) [6], multiple system atrophy (MSA) [16], cortico-basal degeneration (CBD) [17], Lewy body dementia (LBD) [18], progressive supranuclear palsy (PSP) [19], vascular Parkinsonism (VP) [20], or drug-induced Parkinsonism (DIP) [21]. e patients must have performed their SPECTTRODAT in the same imaging laboratory (CMN Unit of CETAC Group, in Curitiba) and reports provided by the same nuclear physician (RMF)

  • Imaging with DAT/SPECT is increasingly present in evaluations of neurological patients functioning as highly specific and reliable imaging biomarkers in diagnosing and following neurodegenerative diseases, including PD, other SNPs, VP, and DIP [7–15, 28–35]

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Summary

Introduction

Brain SPECT with 99mTc-TRODAT-1 (SPECT-TRODAT) may be a useful tool in the differential diagnosis of Parkinsonism. When comparing groups to the correspondence predominantly bilateral or unilateral impairment in SPECT, there was a difference between patients with SNP (p 0.041) and between this group and patients with secondary Parkinsonism (SP) (p < 0.0001). It was handy in differentiating drug-induced Parkinsonism from synucleinopathies. Ere was an inverse correlation between the severity of the SPECT-TRODAT result and the absence of nonmotor signs in patients with drug-induced Parkinsonism. A Brazilian study that evaluated 1528 patients showed PD as the most common diagnosis representing 74.7% of the patients with Parkinsonism, followed by drug-induced Parkinsonism (DIP) in 7.9%, vascular Parkinsonism (VP) in 3.9%, other neurodegenerative diseases in 10%, and rare sporadic causes divided into genetic, infectious, and other, which totaled 3.5% [3].

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