Multimodal assessment of nigrosomal degeneration in Parkinson's disease
Jason Langley, Daniel E. Huddleston, Bruce Crosson, David Song,, Stewart A. Factor, and Xiaoping Hu

TL;DR
This study combines neuromelanin-sensitive and T2*-weighted imaging to assess nigrosomal degeneration in Parkinson's disease, identifying specific regions with reduced neuromelanin and increased iron that correlate with nigrosome-1.
Contribution
It introduces a multimodal imaging approach to accurately localize nigrosome-1 and differentiate it from other nigrosomes in Parkinson's disease.
Findings
qVBM clusters show reduced neuromelanin contrast in PD
Cluster-1 aligns with nigrosome-1 location in T2* images
Increased R2* indicates iron accumulation in PD regions
Abstract
Background: Approximately forty percent of all dopaminergic neurons in SNpc are located in five dense neuronal clusters, named nigrosomes. T2- or T2*-weighted images are used to delineate the largest nigrosome, named nigrosome-1. In these images, nigrosome-1 is a hyperintense region in the caudal and dorsal portion of the T2- or T2*-weighted substantia nigra. In PD, nigrosome-1 experiences iron accumulation, which leads to a reduction in T2-weighted hyperintensity. Here, we examine neuromelanin-depletion and iron deposition in regions of interest (ROIs) derived from quantitative-voxel based morphometry (qVBM) on neuromelanin-sensitive images and compare the ROIs with nigrosome-1 identified in T2*-weighted images. Methods: Neuromelanin-sensitive and multi-echo gradient echo imaging data were obtained. R2* was calculated from multi-echo gradient echo imaging data. qVBM analysis was…
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