4.7 Article

Investigation of Hippocampal Substructures in Focal Temporal Lobe Epilepsy With and Without Hippocampal Sclerosis at 7T

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JOURNAL OF MAGNETIC RESONANCE IMAGING
卷 45, 期 5, 页码 1359-1370

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WILEY
DOI: 10.1002/jmri.25447

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  1. CIHR
  2. NSERC

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Purpose: To provide a more detailed investigation of hippocampal subfields using 7T magnetic resonance imaging (MRI) for the identification of hippocampal sclerosis in temporal lobe epilepsy (TLE). Materials and Methods: Patients (n = 13) with drug-resistant TLE previously identified by conventional imaging as having hippocampal sclerosis (HS) or not (nine without HS, four HS) and 20 age-matched healthy controls were scanned and compared using a 7T MRI protocol. Using a manual segmentation scheme to delineate hippocampal subfields, subfield-specific volume changes and apparent transverse relaxation rate (R-2*) were studied between the two groups. In addition, qualitative assessment at 7T and clinical outcomes were correlated with measured subfield changes. Results: Volumetry of the hippocampus at 7T in HS patients revealed significant ipsilateral subfield atrophy in CA1 (P= 0.001) and CA4 DG (P < 0.001). Volumetry also uncovered subfield atrophy in 33% of patients without HS, which had not been detected using conventional imaging. RZ was significantly lower in the CA4 DG subfields (P = 0.001) and the whole hippocampus (P = 0.029) of HS patients compared to controls but not significantly lower than the group without HS (P= 0.077, P= 0.109). No correlation was found between quantitative volumetry and qualitative assessment as well as surgical outcomes (Sub, P = 0.495, P = 0.567, P= 0.528; CA1, P= 0.104 L- 0.171, P = 0.273, P = 0.554; CA2+CA3, P = 0.517, P = 0.952, P = 0.130 t 0.256; CA4+DG, P= 0.052 7 0.173, P = 0.212, P = 0.124 t 0.204; Whole Hipp, P= 0.187, P = 0.132 0.197, P= 0.628). Conclusion: These preliminary findings indicate that hippocampal subfield volumetry assessed at 7T is capable of identifying characteristic patterns of hippocampal atrophy in HS patients; however, difficulty remains in using imaging to identify hippocampal pathologies in cases without HS.

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