Literature DB >> 26037845

Cortical feature analysis and machine learning improves detection of "MRI-negative" focal cortical dysplasia.

Bilal Ahmed1, Carla E Brodley1, Karen E Blackmon2, Ruben Kuzniecky2, Gilad Barash1, Chad Carlson2, Brian T Quinn2, Werner Doyle2, Jacqueline French2, Orrin Devinsky2, Thomas Thesen3.   

Abstract

Focal cortical dysplasia (FCD) is the most common cause of pediatric epilepsy and the third most common lesion in adults with treatment-resistant epilepsy. Advances in MRI have revolutionized the diagnosis of FCD, resulting in higher success rates for resective epilepsy surgery. However, many patients with histologically confirmed FCD have normal presurgical MRI studies ('MRI-negative'), making presurgical diagnosis difficult. The purpose of this study was to test whether a novel MRI postprocessing method successfully detects histopathologically verified FCD in a sample of patients without visually appreciable lesions. We applied an automated quantitative morphometry approach which computed five surface-based MRI features and combined them in a machine learning model to classify lesional and nonlesional vertices. Accuracy was defined by classifying contiguous vertices as "lesional" when they fell within the surgical resection region. Our multivariate method correctly detected the lesion in 6 of 7 MRI-positive patients, which is comparable with the detection rates that have been reported in univariate vertex-based morphometry studies. More significantly, in patients that were MRI-negative, machine learning correctly identified 14 out of 24 FCD lesions (58%). This was achieved after separating abnormal thickness and thinness into distinct classifiers, as well as separating sulcal and gyral regions. Results demonstrate that MRI-negative images contain sufficient information to aid in the in vivo detection of visually elusive FCD lesions.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Epilepsy; Focal cortical dysplasia; Machine learning; Structural MRI

Mesh:

Year:  2015        PMID: 26037845      PMCID: PMC4500682          DOI: 10.1016/j.yebeh.2015.04.055

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  48 in total

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