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Temporal lobe epilepsy lateralization using retrospective cerebral blood volume MRI

Authors :
Xinyang Feng
Marla J. Hamberger
Hannah C. Sigmon
Jia Guo
Scott A. Small
Frank A. Provenzano
Source :
NeuroImage: Clinical, Vol 19, Iss , Pp 911-917 (2018)
Publication Year :
2018
Publisher :
Elsevier, 2018.

Abstract

Steady-state cerebral blood volume (CBV) is tightly coupled to regional cerebral metabolism, and CBV imaging is a variant of MRI that has proven useful in mapping brain dysfunction. CBV derived from exogenous contrast-enhanced MRI can generate sub-millimeter functional maps. Higher resolution helps to more accurately interrogate smaller cortical regions, such as functionally distinct regions of the hippocampus. Many MRIs have fortuitously adequate sequences required for CBV mapping. However, these scans vary substantially in acquisition parameters. Here, we determined whether previously acquired contrast-enhanced MRI scans ordered in patients with unilateral temporal lobe epilepsy can be used to generate hippocampal CBV. We used intrinsic reference regions to correct for intensity scaling on a research CBV dataset to identify white matter as a robust marker for scaling correction. Next, we tested the technique on a sample of unilateral focal epilepsy patients using clinical MRI scans. We find evidence suggestive of significant hypometabolism in the ipsilateral-hippocampus of unilateral TLE subjects. We also highlight the subiculum as a potential driver of this effect. This study introduces a technique that allows CBV maps to be generated retrospectively from clinical scans, potentially with broad application for mapping dysfunction throughout the brain. Keywords: Cerebral hemodynamics, Cortical mapping, Epilepsy, Hippocampus, MRI

Details

Language :
English
ISSN :
22131582
Volume :
19
Issue :
911-917
Database :
Directory of Open Access Journals
Journal :
NeuroImage: Clinical
Publication Type :
Academic Journal
Accession number :
edsdoj.77953026bee4ef1a69b474857c5fef7
Document Type :
article
Full Text :
https://doi.org/10.1016/j.nicl.2018.05.012