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(123)I-FP-CIT SPECT validation of nigro-putaminal MRI tractography in dementia with Lewy bodies

BACKGROUND: Assessment of nigrostriatal degeneration is a key element to discriminate between dementia with Lewy bodies (DLB) and Alzheimer disease (AD), and it is often evaluated using ioflupane ((123)I-FP-CIT) single-photon emission computed tomography (SPECT). Given the limited availability of (1...

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Detalles Bibliográficos
Autores principales: Pardini, Matteo, Nobili, Flavio, Arnaldi, Dario, Morbelli, Silvia, Bauckneht, Matteo, Rissotto, Roberto, Serrati, Carlo, Serafini, Gianluca, Lapucci, Caterina, Ghio, Lucio, Amore, Mario, Massucco, Davide, Sassos, Davide, Bonzano, Laura, Mancardi, Giovanni Luigi, Roccatagliata, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196565/
https://www.ncbi.nlm.nih.gov/pubmed/32363488
http://dx.doi.org/10.1186/s41747-020-00153-6
Descripción
Sumario:BACKGROUND: Assessment of nigrostriatal degeneration is a key element to discriminate between dementia with Lewy bodies (DLB) and Alzheimer disease (AD), and it is often evaluated using ioflupane ((123)I-FP-CIT) single-photon emission computed tomography (SPECT). Given the limited availability of (123)I-FP-CIT SPECT, we evaluated if a mask-based approach to nigroputaminal magnetic resonance imaging (MRI) diffusion-weighted tractography could be able to capture microstructural changes reflecting nigroputaminal degeneration in DLB. METHODS: A nigroputaminal bundle mask was delineated on 12 healthy volunteers (HV) and applied to MRI diffusion-weighted data of 18 subjects with DLB, 21 subjects with AD and another group of 12 HV. The correlation between nigroputaminal fractional anisotropy (FA) values and (123)I-FP-CIT SPECT findings was investigated. Shapiro-Wilk, ANOVA, ANCOVA, and parametric correlation statistics as well as receiver operating characteristic (ROC) analysis were used. RESULTS: DLB patients showed a higher nigroputaminal FA values compared with both AD and HV-controls groups (p = 0.001 for both comparisons), while no difference was observed between HV-controls and AD groups (p = 0.450); at ROC analysis, the area under the curve for the discriminating DLB and AD subjects was 0.820; FA values correlated with (123)I-FP-CIT values (on the left, r = -0.670; on the right, r = -720). No significant differences were observed for the FA of the corticospinal tract across the three groups (p = 0.740). CONCLUSIONS: In DLB, nigroputaminal degeneration could be reliably assessed on MRI diffusion scans using a mask of nigroputaminal bundle trajectory. Nigroputaminal FA in DLB patients correlated with (123)I-FP-CIT values data may allow to differentiate these patients from AD patients and HV-controls.