4.5 Article

The role of the temporal pole in temporal lobe epilepsy: A diffusion kurtosis imaging study

期刊

NEUROIMAGE-CLINICAL
卷 36, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2022.103201

关键词

Temporal lobe epilepsy; Temporal pole; Diffusion kurtosis imaging; Automated fiber-tract quantification; Tract-based cortical analysis

资金

  1. Canadian Institutes of Health Research (CIHR) Foundation [333550]
  2. Natural Sciences and Engineering Research Council (NSERC) Discovery [RGPIN-2015-06639]
  3. Canada Research Chairs [950-231964]
  4. Canada Foundation for Innovation (CFI) John R. Evans Leaders Fund [37427]
  5. Canada First Research Excellence Fund, Brain Canada
  6. Ontario Brain Institute Epilepsy Program (EpLink)
  7. BrainsCAN postdoctoral fellowship

向作者/读者索取更多资源

This study evaluated the use of diffusion kurtosis imaging (DKI) to detect microstructural abnormalities in the temporal pole and its cortex in temporal lobe epilepsy (TLE) patients. The DKI measurements showed significant differences between lesional TLE patients and controls, particularly in the most temporopolar segment of the white matter bundles. There were also correlations between DKI measurements and disease duration in the temporopolar cortex. DKI has the potential to detect subtle microstructural alterations in the temporopolar cortex of TLE patients, which could improve our understanding of seizure generation and aid in surgical planning.
This study aimed to evaluate the use of diffusion kurtosis imaging (DKI) to detect microstructural abnormalities within the temporal pole (TP) and its temporopolar cortex in temporal lobe epilepsy (TLE) patients. DKI quantitative maps were obtained from fourteen lesional TLE and ten non-lesional TLE patients, along with twenty-three healthy controls. Data collected included mean (MK); radial (RK) and axial kurtosis (AK); mean diffusivity (MD) and axonal water fraction (AWF). Automated fiber quantification (AFQ) was used to quantify DKI measurements along the inferior longitudinal (ILF) and uncinate fasciculus (Unc). ILF and Unc tract profiles were compared between groups and tested for correlation with disease duration. To characterize temporopolar cortex microstructure, DKI maps were sampled at varying depths from superficial white matter (WM) towards the pial surface. Patients were separated according to the temporal lobe ipsilateral to seizure onset and their AFQ results were used as input for statistical analyses. Significant differences were observed between lesional TLE and controls, towards the most temporopolar segment of ILF and Unc proximal to the TP within the ipsilateral temporal lobe in left TLE patients for MK, RK, AWF and MD. No significant changes were observed with DKI maps in the non-lesional TLE group. DKI measurements correlated with disease duration, mostly towards the temporopolar segments of the WM bundles. Stronger differences in MK, RK and AWF within the temporopolar cortex were observed in the lesional TLE and noticeable differences (except for MD) in non-lesional TLE groups compared to controls. This study demonstrates that DKI has potential to detect subtle microstructural alterations within the temporopolar segments of the ILF and Unc and the connected temporopolar cortex in TLE patients including non-lesional TLE subjects. This could aid our understanding of the extrahippocampal areas, more specifically the temporal pole role in seizure generation in TLE and might inform surgical planning, leading to better seizure outcomes.

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