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Diffusion Measure Changes of Substantia Nigra Subregions and the Ventral Tegmental Area in Newly Diagnosed Parkinson’s Disease

Authors
심재혁백현만
Issue Date
Oct-2021
Publisher
한국뇌신경과학회
Keywords
Parkinson’s disease; Basal ganglia; MRI; Diffusion tractography
Citation
Experimental Neurobiology, v.30, no.5, pp.365 - 373
Journal Title
Experimental Neurobiology
Volume
30
Number
5
Start Page
365
End Page
373
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/82744
DOI
10.5607/en21025
ISSN
1226-2560
Abstract
Historically, studies have extensively examined the basal ganglia in Parkinson’s disease for specific characteristics that can be observed with medi cal imaging. One particular methodology used for detecting changes that occur in Parkinson’s disease brains is diffusion tensor imaging, which yields diffusion indices such as fractional anisotropy and radial diffusivity that have been shown to correlate with axonal damage. In this study, we compare the diffusion measures of basal ganglia structures (with substantia nigra divided into subregions, pars compacta, and pars reticula), as well as the diffusion measures of the diffusion tracts that pass through each pair of basal ganglia structures to see if significant differences in diffusion measures can be observed in structures or tracts in newly diagnosed Parkinson’s disease patients. Additionally, we include the ventral tegmental area, a structure connected to various basal ganglia structures affected by dopaminergic neuronal loss and have historically shown significant al terations in Parkinson’s disease, in our analysis. We found significant fractional anisotropy differences in the putamen, and in the diffusion tracts that pass through pairs of both substantia nigra subregions, subthalamic nucleus, parabrachial pigmental nucleus, ventral tegmental area. Addition ally, we found significant radial diffusivity differences in diffusion tracts that pass through the parabrachial nucleus, putamen, both substantia nigra subregions, and globus pallidus externa. We were able to find significant diffusion measure differences in structures and diffusion tracts, potentially due to compensatory mechanisms in response to dopaminergic neuronal loss that occurs in newly diagnosed Parkinson’s disease patients.
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