Multi-shell connectome DWI-based graph theory measures for the prediction of temporal lobe epilepsy and cognition

Author:

Garcia-Ramos Camille1,Adluru Nagesh23,Chu Daniel Y12,Nair Veena2,Adluru Anusha2,Nencka Andrew4,Maganti Rama1,Mathis Jedidiah5,Conant Lisa L5,Alexander Andrew L36,Prabhakaran Vivek2,Binder Jeffrey R5,Meyerand Mary E6,Hermann Bruce1,Struck Aaron F17

Affiliation:

1. University of Wisconsin-Madison Department of Neurology, , Medical Foundation Centennial Building, 1685 Highland Ave, Madison, WI 53705-2281 , United States

2. University of Wisconsin-Madison Department of Radiology, , 600 Highland Ave, Madison, WI 53792 , United States

3. Waisman Center, University of Wisconsin-Madison , 1500 Highland Ave, Madison, WI 53705 , United States

4. Medical College of Wisconsin Department of Radiology, , 9200 W. Wisconsin Ave. Milwaukee, WI 53226 , United States

5. Department of Neurology, Medical College of Wisconsin , 9200 W. Wisconsin Ave. Milwaukee, WI 53226 , United States

6. Department of Medical Physics, University of Wisconsin-Madison , 1111 Highland Ave, Rm 1005, Madison, WI 53705-2275 , United States

7. William S. Middleton VA Hospital , 2500 Overlook Terrace, Madison, WI 53705 , United States

Abstract

Abstract Temporal lobe epilepsy (TLE) is the most common epilepsy syndrome that empirically represents a network disorder, which makes graph theory (GT) a practical approach to understand it. Multi-shell diffusion-weighted imaging (DWI) was obtained from 89 TLE and 50 controls. GT measures extracted from harmonized DWI matrices were used as factors in a support vector machine (SVM) analysis to discriminate between groups, and in a k-means algorithm to find intrinsic structural phenotypes within TLE. SVM was able to predict group membership (mean accuracy = 0.70, area under the curve (AUC) = 0.747, Brier score (BS) = 0.264) using 10-fold cross-validation. In addition, k-means clustering identified 2 TLE clusters: 1 similar to controls, and 1 dissimilar. Clusters were significantly different in their distribution of cognitive phenotypes, with the Dissimilar cluster containing the majority of TLE with cognitive impairment (χ2 = 6.641, P = 0.036). In addition, cluster membership showed significant correlations between GT measures and clinical variables. Given that SVM classification seemed driven by the Dissimilar cluster, SVM analysis was repeated to classify Dissimilar versus Similar + Controls with a mean accuracy of 0.91 (AUC = 0.957, BS = 0.189). Altogether, the pattern of results shows that GT measures based on connectome DWI could be significant factors in the search for clinical and neurobehavioral biomarkers in TLE.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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