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Initial diagnostic workup of parkinsonism: Dopamine transporter positron emission tomography versus susceptibility map-weighted imaging at 3T

Authors
Sung, Young HeeLee, JonghoNam, YoonhoShin, Hyeong-GeolNoh, YoungHwan, Kyung HoonLee, HaejunKim, Eung Yeop
Issue Date
May-2019
Publisher
ELSEVIER SCI LTD
Keywords
Parkinsonism; Nigrosomel; Susceptibility map-weighted imaging (SMWI); N-3-Fluoropropyl-2-beta-carbomethoxy-3-beta-(4-iodophenyl) nortropane (F-18-FP-CIT) positron emission tomography (PET)
Citation
PARKINSONISM & RELATED DISORDERS, v.62, pp.171 - 178
Journal Title
PARKINSONISM & RELATED DISORDERS
Volume
62
Start Page
171
End Page
178
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/1558
DOI
10.1016/j.parkreldis.2018.12.019
ISSN
1353-8020
Abstract
Background and Purpose: Evaluation of dorsal nigral hyperintensity on MRI can help detect nigrostriatal degeneration. We aimed to compare the diagnostic performance between susceptibility map-weighted imaging (SMWI) and N-3-fluoropropyl-2-beta-carbomethoxy-3-beta-(4-iodophenyl) nortropane (F-18-FP-CIT) positron emission tomography (PET) as an initial diagnostic tool of parkinsonism. Materials and methods: This local ethics committee-approved retrospective study enrolled 223 patients with parkinsonism and 15 healthy subjects (mean age, 69.7 years; 135 females) who underwent both SMWI at 3T and F-18-FP-CIT PET. The diagnostic performances of the two tests for nigrostriatal degeneration were compared by evaluating whether the 90% confidence interval (CI) of the difference between the two tests was within the equivalence margin by using the DTComPair package of R. The concordance rate was tested by Cohen's kappa. Results: The diagnostic sensitivities of SMWI and F-18-FP-CIT PET were 94.5% and 100% per SN and 100% and 100% per participant, respectively; their specificities were 95.3% and 86.7% per SN and 94.4% and 84.0% per participant, respectively. While the diagnostic sensitivity was comparable between the two tests for each SN and participant, the lower 90% CI of the differences in the specificity were -0.086 per SN and -0.104 per participant, indicating a higher diagnostic specificity of SMWI than that of F-18-FP-CIT PET. When excluding 20 participants with basal ganglia lesions, the two tests exhibited similar diagnostic performance and had excellent agreement (k = 0.899 per SN; k = 0.945 per participant). Conclusion: For patients with parkinsonism, SMWI and F-18-FP-CIT PET exhibit similar diagnostic performance.
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