Topography of Dopamine Transporter Availability in the Cerebellar Variant of Multiple System Atrophy.

Mov Disord Clin Pract 2017 May-Jun;4(3):389-396. Epub 2016 Nov 2.

Department of Neurology Medical University of Innsbruck Innsbruck Austria.

Background: Voxel-wise comparison of [I]-2β-carbomethoxy-3beta-(4-iodophenyl)tropane ([I]β-CIT) radioligand distribution measured by single-photon emission computed tomography (SPECT) revealed distinct patterns of reduced dopamine transporter (DAT) availability in the Parkinson's variant of MSA (MSA-P). The aim of this study was to identify the monoamine transporter distribution pattern in patients with the cerebellar variant of MSA (MSA-C). Additionally, monoamine transporter availability was investigated in a small cohort of patients with sporadic adult-onset ataxia (SAOA).

Methods: [I]β-CIT SPECT was performed in patients with MSA-C (n = 12), MSA-P (n = 14), SAOA (n = 5), and controls (n = 15) matched for age. Parametric images of [I]β-CIT binding potential (BP) were generated and analyzed by statistical parametric mapping (SPM) and region of interest (ROI) analysis.

Results: SPM localized significant reductions of [I]β-CIT BP in the striatum, midbrain, and pons in MSA-C compared to controls. When compared with MSA-P, the striatal DAT decline was significantly less affected in MSA-C. ROI analysis revealed reductions of striatal and midbrain [I]β-CIT binding in MSA-C compared to SAOA, whereas no significant difference was apparent between the SAOA and control groups.

Conclusions: Midbrain and pontine monoaminergic transporter binding was severely impaired in MSA-C, matching the underlying pathological features. Striatal DAT availability was relatively less affected in MSA-C compared to MSA-P, reflecting measureable, but less-profound, degeneration of the nigrostriatal dopaminergic projections. Preliminary results of reduced striatal and midbrain [I]β-CIT binding in MSA-C, compared to SAOA, suggest that the potential of DAT-SPECT as a surrogate marker in the diagnostic workup of patients with adult-onset cerebellar ataxia should be further investigated.

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http://dx.doi.org/10.1002/mdc3.12446DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174450PMC
November 2016
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