| Literature DB >> 32394788 |
Xuan Vinh To1, Joseph Benetatos1, Neha Soni1, Dedao Liu2, Hyab Mehari Abraha3, Wenyi Yan2, Olga Panagiotopoulou3, Fatima A Nasrallah1,4.
Abstract
Although concussions can result in persistent neurological post-concussion symptoms, they are typically invisible on routine magnetic resonance imaging (MRI) scans. Our study aimed to investigate the use of ultra-high-field diffusion tensor imaging (UHF-DTI) in discerning severity-dependent microstructural changes in the mouse brain following a concussion. Twenty-three C57BL/6 mice were randomly allocated into three groups: the low concussive (LC, n = 9) injury group, the high concussive (HC, n = 6) injury group, and the sham control (SC, n = 7) group. Mice were perfused on day 2 post-injury, and the brains were scanned on a 16.4T MRI scanner with UHF-DTI and neurite orientation dispersion imaging (NODDI). Finite element analysis (FEA) was performed to determine the pattern and extent of the physical impact on the brain tissue. MRI findings were correlated with histopathological analysis in a subset of mice. In the LC group, increased fractional anisotropy (FA) and decreased orientation dispersion index (ODI) but limited neurite density index (NDI) changes were found in the gray matter, and minimal changes to white matter (WM) were observed. The HC group presented increased mean diffusivity (MD), decreased NDI, and decreased ODI in the WM and gray matter (GM); decreased FA was also found in a small area of the WM. WM changes were associated with WM degeneration and neuroinflammation. FEA showed varying region-dependent degrees of stress, in line with the different imaging findings. This study provides evidence that UHF-DTI combined with NODDI can detect concussions of variable intensities. This has significant implications for the diagnosis of concussion in humans.Entities:
Keywords: concussion; diffusion tensor imaging; finite element analysis; neurite orientation dispersion imaging; ultra-high-field magnetic resonance imaging
Mesh:
Year: 2020 PMID: 32394788 DOI: 10.1089/neu.2019.6944
Source DB: PubMed Journal: J Neurotrauma ISSN: 0897-7151 Impact factor: 5.269