Lily C Wong-Kisiel1, Diego F Tovar Quiroga2, Daniel L Kenney-Jung3, Robert J Witte4, Alexandra Santana-Almansa5, Gregory A Worrell6, Jeffrey Britton7, Benjamin H Brinkmann8. 1. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: wongkisiel.lily@mayo.edu. 2. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: df.tovar@gmail.com. 3. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: kenney-jung.daniel@mayo.edu. 4. Department of Radiology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: witte.robert@mayo.edu. 5. Center for Clinical and Translation Sciences, Mayo Clinic, 200 First St., SW, Rochester, MN, 59905, USA. Electronic address: alexandra.rsantana@gmail.com. 6. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: worrell.gregory@mayo.edu. 7. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: britton.jeffrey@mayo.edu. 8. Department of Neurology, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA; Department of Biomedical Engineering, Mayo Clinic, 200 First St., SW, Rochester, MN, 55905, USA. Electronic address: brinkmann.benjamin@mayo.edu.
Abstract
OBJECTIVE: Focal cortical dysplasia (FCD) is a common pathology in focal drug resistant epilepsy (DRE). Voxel based morphometric MRI analysis has been proposed as an adjunct to visual detection of FCD, which remains challenging given the subtle radiographic appearance of FCD. This study evaluates the diagnostic value of morphometric analysis program (MAP) in focal DRE with pathology-confirmed FCD. METHODS: Automated morphometric analysis program analysis generated z-score maps derived from T1 images, referenced to healthy adult or pediatric controls for each of 39 cases with pathology-confirmed FCD. MAP identified abnormal extension of gray matter into white matter (MAP-E) and blurring of the gray-white matter junction (MAP-J), independently of clinical data and other imaging modalities. MRI was visually reviewed by neuroradiologists as part of usual clinical care, and independently re-reviewed retrospectively by a neuroradiologist with >10-years' experience in epilepsy MRI. Sensitivity and specificity were calculated for MRI, MAP, scalp-EEG, PET and SISCOM compared to resection area (RA). RESULTS: In this cohort of 39 histologically proven FCD cases, the sensitivity and specificity of MAP-J [64% (95% CI 48%-77%) and 96% (95% CI 93%-0.98%)] and MAP-E [74% (95% CI 59%-86%) and 94% (95% CI 91%-97%)] were higher than qualitative MRI review, SISCOM, and FDG-PET. Initial MRI review detected FCD in 17, expert review identified 26. Among cases not detected by initial MRI review, MAP-J correctly identified FCD in 12 additional cases and MAP-E in 13 cases. Among cases not detected by expert MRI review, MAP-J correctly identified 6 and MAP-E 8 cases. Excellent surgical outcome was achieved in 76% of patients. SIGNIFICANCE: MAP showed favorable sensitivity compared to visual inspection and other non-invasive imaging modalities. MAP complements non-invasive imaging evaluation for detection of FCD in focal DRE patients.
OBJECTIVE: Focal cortical dysplasia (FCD) is a common pathology in focal drug resistant epilepsy (DRE). Voxel based morphometric MRI analysis has been proposed as an adjunct to visual detection of FCD, which remains challenging given the subtle radiographic appearance of FCD. This study evaluates the diagnostic value of morphometric analysis program (MAP) in focal DRE with pathology-confirmed FCD. METHODS: Automated morphometric analysis program analysis generated z-score maps derived from T1 images, referenced to healthy adult or pediatric controls for each of 39 cases with pathology-confirmed FCD. MAP identified abnormal extension of gray matter into white matter (MAP-E) and blurring of the gray-white matter junction (MAP-J), independently of clinical data and other imaging modalities. MRI was visually reviewed by neuroradiologists as part of usual clinical care, and independently re-reviewed retrospectively by a neuroradiologist with >10-years' experience in epilepsy MRI. Sensitivity and specificity were calculated for MRI, MAP, scalp-EEG, PET and SISCOM compared to resection area (RA). RESULTS: In this cohort of 39 histologically proven FCD cases, the sensitivity and specificity of MAP-J [64% (95% CI 48%-77%) and 96% (95% CI 93%-0.98%)] and MAP-E [74% (95% CI 59%-86%) and 94% (95% CI 91%-97%)] were higher than qualitative MRI review, SISCOM, and FDG-PET. Initial MRI review detected FCD in 17, expert review identified 26. Among cases not detected by initial MRI review, MAP-J correctly identified FCD in 12 additional cases and MAP-E in 13 cases. Among cases not detected by expert MRI review, MAP-J correctly identified 6 and MAP-E 8 cases. Excellent surgical outcome was achieved in 76% of patients. SIGNIFICANCE: MAP showed favorable sensitivity compared to visual inspection and other non-invasive imaging modalities. MAP complements non-invasive imaging evaluation for detection of FCD in focal DRE patients.
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