Journal
FRONTIERS IN NEUROLOGY
Volume 12, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fneur.2021.636518
Keywords
idiopathic normal pressure hydrocephalus; diffusion spectrum imaging; corticospinal tract; quantitative anisotropy; diffusion magnetic resonance image
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Funding
- Basic Plan Program of Shenzhen, China [JCYJ20180228163333734]
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In this study, DSI was used to measure diffusion parameters of corticospinal tracts in iNPH patients compared to healthy controls. Results showed lower QA and ISO values, and higher MD, AD, and RD values in iNPH patients, with no significant differences in GFA and FA values. This quantitative evaluation using DSI could enhance understanding of the disease mechanism.
Purpose: The purpose of this study was to measure the diffusion spectrum imaging (DSI) parameters of corticospinal tracts (CSTs) and evaluate diffusional changes in CSTs in patients with idiopathic normal pressure hydrocephalus (iNPH) by DSI. Methods: Twenty-three iNPH patients and twenty-one healthy controls (HCs) were involved in this study. Brain DSI data for all participants were collected through the same MR scanning procedure. The diffusion parameters measured and analyzed included quantitative anisotropy (QA), the isotropic diffusion component (ISO), general fractional anisotropy (GFA), fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) of corticospinal tracts. Results: The QA and ISO values of corticospinal tracts in iNPH patients were significantly lower than those in HCs (P-LQA = 0.008, P-RQA = 0.016, P-LISO = 0.024, P-RISO = 0.016). The mean MD, AD, and RD values in iNPH patients were significantly higher than those in HCs (P-MD = 0.032, P-AD = 0.032, P-RD = 0.048,). No significant differences in GFA and FA values were noted between iNPH patients and HCs. Conclusion: Decreased QA and ISO values of corticospinal tracts were found in iNPH patients. Quantitative CST evaluation using DSI may lead to information that can improve the present understanding of the disease mechanism.
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