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The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy

OBJECTIVE: The distributed white matter network underlying language leads to difficulties in extracting clinically meaningful summaries of neural alterations leading to language impairment. Here we determine the predictive ability of the structural connectome (SC), compared with global measures of w...

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Autores principales: Kaestner, Erik, Balachandra, Akshara R., Bahrami, Naeim, Reyes, Anny, Lalani, Sanam J., Macari, Anna Christina, Voets, Natalie L., Drane, Daniel L., Paul, Brianna M., Bonilha, Leonardo, McDonald, Carrie R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953962/
https://www.ncbi.nlm.nih.gov/pubmed/31927128
http://dx.doi.org/10.1016/j.nicl.2019.102125
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author Kaestner, Erik
Balachandra, Akshara R.
Bahrami, Naeim
Reyes, Anny
Lalani, Sanam J.
Macari, Anna Christina
Voets, Natalie L.
Drane, Daniel L.
Paul, Brianna M.
Bonilha, Leonardo
McDonald, Carrie R.
author_facet Kaestner, Erik
Balachandra, Akshara R.
Bahrami, Naeim
Reyes, Anny
Lalani, Sanam J.
Macari, Anna Christina
Voets, Natalie L.
Drane, Daniel L.
Paul, Brianna M.
Bonilha, Leonardo
McDonald, Carrie R.
author_sort Kaestner, Erik
collection PubMed
description OBJECTIVE: The distributed white matter network underlying language leads to difficulties in extracting clinically meaningful summaries of neural alterations leading to language impairment. Here we determine the predictive ability of the structural connectome (SC), compared with global measures of white matter tract microstructure and clinical data, to discriminate language impaired patients with temporal lobe epilepsy (TLE) from TLE patients without language impairment. METHODS: T1- and diffusion-MRI, clinical variables (CVs), and neuropsychological measures of naming and verbal fluency were available for 82 TLE patients. Prediction of language impairment was performed using a robust tree-based classifier (XGBoost) for three models: (1) a CV-model which included demographic and epilepsy-related clinical features, (2) an atlas-based tract-model, including four frontotemporal white matter association tracts implicated in language (i.e., the bilateral arcuate fasciculus, inferior frontal occipital fasciculus, inferior longitudinal fasciculus, and uncinate fasciculus), and (3) a SC-model based on diffusion MRI. For the association tracts, mean fractional anisotropy was calculated as a measure of white matter microstructure for each tract using a diffusion tensor atlas (i.e., AtlasTrack). The SC-model used measurement of cortical-cortical connections arising from a temporal lobe subnetwork derived using probabilistic tractography. Dimensionality reduction of the SC was performed with principal components analysis (PCA). Each model was trained on 49 patients from one epilepsy center and tested on 33 patients from a different center (i.e., an independent dataset). Randomization was performed to test the stability of the results. RESULTS: The SC-model yielded a greater area under the curve (AUC; .73) and accuracy (79%) compared to both the tract-model (AUC: .54, p < .001; accuracy: 70%, p < .001) and the CV-model (AUC: .59, p < .001; accuracy: 64%, p < .001). Within the SC-model, lateral temporal connections had the highest importance to model performance, including connections similar to language association tracts such as links between the superior temporal gyrus to pars opercularis. However, in addition to these connections many additional connections that were widely distributed, bilateral and interhemispheric in nature were identified as contributing to SC-model performance. CONCLUSION: The SC revealed a white matter network contributing to language impairment that was widely distributed, bilateral, and lateral temporal in nature. The distributed network underlying language may be why the SC-model has an advantage in identifying sub-components of the complex fiber networks most relevant for aspects of language performance.
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spelling pubmed-69539622020-01-14 The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy Kaestner, Erik Balachandra, Akshara R. Bahrami, Naeim Reyes, Anny Lalani, Sanam J. Macari, Anna Christina Voets, Natalie L. Drane, Daniel L. Paul, Brianna M. Bonilha, Leonardo McDonald, Carrie R. Neuroimage Clin Regular Article OBJECTIVE: The distributed white matter network underlying language leads to difficulties in extracting clinically meaningful summaries of neural alterations leading to language impairment. Here we determine the predictive ability of the structural connectome (SC), compared with global measures of white matter tract microstructure and clinical data, to discriminate language impaired patients with temporal lobe epilepsy (TLE) from TLE patients without language impairment. METHODS: T1- and diffusion-MRI, clinical variables (CVs), and neuropsychological measures of naming and verbal fluency were available for 82 TLE patients. Prediction of language impairment was performed using a robust tree-based classifier (XGBoost) for three models: (1) a CV-model which included demographic and epilepsy-related clinical features, (2) an atlas-based tract-model, including four frontotemporal white matter association tracts implicated in language (i.e., the bilateral arcuate fasciculus, inferior frontal occipital fasciculus, inferior longitudinal fasciculus, and uncinate fasciculus), and (3) a SC-model based on diffusion MRI. For the association tracts, mean fractional anisotropy was calculated as a measure of white matter microstructure for each tract using a diffusion tensor atlas (i.e., AtlasTrack). The SC-model used measurement of cortical-cortical connections arising from a temporal lobe subnetwork derived using probabilistic tractography. Dimensionality reduction of the SC was performed with principal components analysis (PCA). Each model was trained on 49 patients from one epilepsy center and tested on 33 patients from a different center (i.e., an independent dataset). Randomization was performed to test the stability of the results. RESULTS: The SC-model yielded a greater area under the curve (AUC; .73) and accuracy (79%) compared to both the tract-model (AUC: .54, p < .001; accuracy: 70%, p < .001) and the CV-model (AUC: .59, p < .001; accuracy: 64%, p < .001). Within the SC-model, lateral temporal connections had the highest importance to model performance, including connections similar to language association tracts such as links between the superior temporal gyrus to pars opercularis. However, in addition to these connections many additional connections that were widely distributed, bilateral and interhemispheric in nature were identified as contributing to SC-model performance. CONCLUSION: The SC revealed a white matter network contributing to language impairment that was widely distributed, bilateral, and lateral temporal in nature. The distributed network underlying language may be why the SC-model has an advantage in identifying sub-components of the complex fiber networks most relevant for aspects of language performance. Elsevier 2019-12-13 /pmc/articles/PMC6953962/ /pubmed/31927128 http://dx.doi.org/10.1016/j.nicl.2019.102125 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Kaestner, Erik
Balachandra, Akshara R.
Bahrami, Naeim
Reyes, Anny
Lalani, Sanam J.
Macari, Anna Christina
Voets, Natalie L.
Drane, Daniel L.
Paul, Brianna M.
Bonilha, Leonardo
McDonald, Carrie R.
The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title_full The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title_fullStr The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title_full_unstemmed The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title_short The white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
title_sort white matter connectome as an individualized biomarker of language impairment in temporal lobe epilepsy
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953962/
https://www.ncbi.nlm.nih.gov/pubmed/31927128
http://dx.doi.org/10.1016/j.nicl.2019.102125
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