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July 01, 2014; 83 (1) Article

Automated detection of cortical dysplasia type II in MRI-negative epilepsy

Seok-Jun Hong, Hosung Kim, Dewi Schrader, Neda Bernasconi, Boris C. Bernhardt, Andrea Bernasconi
First published June 4, 2014, DOI: https://doi.org/10.1212/WNL.0000000000000543
Seok-Jun Hong
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Hosung Kim
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Dewi Schrader
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Neda Bernasconi
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Boris C. Bernhardt
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Andrea Bernasconi
From the NeuroImaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Center, McGill University, Montreal Neurological Institute and Hospital, Canada.
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Citation
Automated detection of cortical dysplasia type II in MRI-negative epilepsy
Seok-Jun Hong, Hosung Kim, Dewi Schrader, Neda Bernasconi, Boris C. Bernhardt, Andrea Bernasconi
Neurology Jul 2014, 83 (1) 48-55; DOI: 10.1212/WNL.0000000000000543

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Abstract

Objective: To detect automatically focal cortical dysplasia (FCD) type II in patients with extratemporal epilepsy initially diagnosed as MRI-negative on routine inspection of 1.5 and 3.0T scans.

Methods: We implemented an automated classifier relying on surface-based features of FCD morphology and intensity, taking advantage of their covariance. The method was tested on 19 patients (15 with histologically confirmed FCD) scanned at 3.0T, and cross-validated using a leave-one-out strategy. We assessed specificity in 24 healthy controls and 11 disease controls with temporal lobe epilepsy. Cross-dataset classification performance was evaluated in 20 healthy controls and 14 patients with histologically verified FCD examined at 1.5T.

Results: Sensitivity was 74%, with 100% specificity (i.e., no lesions detected in healthy or disease controls). In 50% of cases, a single cluster colocalized with the FCD lesion, while in the remaining cases a median of 1 extralesional cluster was found. Applying the classifier (trained on 3.0T data) to the 1.5T dataset yielded comparable performance (sensitivity 71%, specificity 95%).

Conclusion: In patients initially diagnosed as MRI-negative, our fully automated multivariate approach offered a substantial gain in sensitivity over standard radiologic assessment. The proposed method showed generalizability across cohorts, scanners, and field strengths. Machine learning may assist presurgical decision-making by facilitating hypothesis formulation about the epileptogenic zone.

Classification of evidence: This study provides Class II evidence that automated machine learning of MRI patterns accurately identifies FCD among patients with extratemporal epilepsy initially diagnosed as MRI-negative.

GLOSSARY

FCD=
focal cortical dysplasia;
GM=
gray matter;
LDA=
linear discriminant analysis;
MNI=
Montreal Neurological Institute;
RI=
relative intensity;
SEEG=
stereotactic implanted depth electrodes;
TE=
echo time;
TLE=
temporal lobe epilepsy;
TR=
repetition time;
WM=
white matter

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Received August 22, 2013.
  • Accepted in final form February 5, 2014.
  • © 2014 American Academy of Neurology
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