Isolating the white matter circuitry of the dorsal language stream: Connectome‐Symptom Mapping in stroke induced aphasia

The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R...

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Published inHuman brain mapping Vol. 42; no. 17; pp. 5689 - 5702
Main Authors Baboyan, Vatche, Basilakos, Alexandra, Yourganov, Grigori, Rorden, Chris, Bonilha, Leonardo, Fridriksson, Julius, Hickok, Gregory
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.12.2021
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Online AccessGet full text
ISSN1065-9471
1097-0193
1097-0193
DOI10.1002/hbm.25647

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Abstract The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke‐induced cases of aphasia presenting with varying left‐hemisphere lesions and repetition impairment, sPLS‐R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held‐out set of 21 subjects. A set of 10 short‐ and long‐range parieto‐temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short‐range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long‐range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and—notably—in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held‐out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus. The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits and effectively localize the white matter circuitry of the dorsal language stream.
AbstractList The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke‐induced cases of aphasia presenting with varying left‐hemisphere lesions and repetition impairment, sPLS‐R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held‐out set of 21 subjects. A set of 10 short‐ and long‐range parieto‐temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short‐range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long‐range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and—notably—in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held‐out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus.
The application of ℓ1-regularized machine learning models to high-dimensional connectomes offers a promising methodology to assess clinical-anatomical correlations in humans. Here, we integrate the connectome-based lesion-symptom mapping framework with sparse partial least squares regression (sPLS-R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke-induced cases of aphasia presenting with varying left-hemisphere lesions and repetition impairment, sPLS-R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held-out set of 21 subjects. A set of 10 short- and long-range parieto-temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short-range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long-range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and-notably-in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held-out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus.The application of ℓ1-regularized machine learning models to high-dimensional connectomes offers a promising methodology to assess clinical-anatomical correlations in humans. Here, we integrate the connectome-based lesion-symptom mapping framework with sparse partial least squares regression (sPLS-R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke-induced cases of aphasia presenting with varying left-hemisphere lesions and repetition impairment, sPLS-R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held-out set of 21 subjects. A set of 10 short- and long-range parieto-temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short-range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long-range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and-notably-in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held-out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus.
The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke‐induced cases of aphasia presenting with varying left‐hemisphere lesions and repetition impairment, sPLS‐R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held‐out set of 21 subjects. A set of 10 short‐ and long‐range parieto‐temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short‐range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long‐range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and—notably—in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held‐out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus. The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits and effectively localize the white matter circuitry of the dorsal language stream.
The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits. By mapping over 2,500 connections of the structural connectome in a cohort of 71 stroke‐induced cases of aphasia presenting with varying left‐hemisphere lesions and repetition impairment, sPLS‐R was trained on 50 subjects to algorithmically identify connectomic features on the basis of their predictive value. The highest ranking features were subsequently used to generate a parsimonious predictive model for speech repetition whose predictions were evaluated on a held‐out set of 21 subjects. A set of 10 short‐ and long‐range parieto‐temporal connections were identified, collectively delineating the broader circuitry of the dorsal white matter network of the language system. The strongest contributing feature was a short‐range connection in the supramarginal gyrus, approximating the cortical localization of area Spt, with parallel long‐range pathways interconnecting posterior nodes in supramarginal and superior temporal cortex with anterior nodes in both ventral and—notably—in dorsal premotor cortex, respectively. The collective disruption of these pathways indexed repetition performance in the held‐out set of participants, suggesting that these impairments might be characterized as a parietotemporal disconnection syndrome impacting cortical area Spt and its associated white matter circuits of the frontal lobe as opposed to being purely a disconnection of the arcuate fasciculus. The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical correlations in humans. Here, we integrate the connectome‐based lesion‐symptom mapping framework with sparse partial least squares regression (sPLS‐R) to isolate elements of the connectome associated with speech repetition deficits and effectively localize the white matter circuitry of the dorsal language stream.
Author Bonilha, Leonardo
Hickok, Gregory
Baboyan, Vatche
Basilakos, Alexandra
Fridriksson, Julius
Yourganov, Grigori
Rorden, Chris
AuthorAffiliation 1 Department of Cognitive Science University of California Irvine California USA
4 Department of Neurology Medical University of South Carolina Columbia South Carolina USA
2 Department of Communication Sciences and Disorders University of South Carolina Columbia South Carolina USA
3 Department of Psychology University of South Carolina Columbia South Carolina USA
AuthorAffiliation_xml – name: 2 Department of Communication Sciences and Disorders University of South Carolina Columbia South Carolina USA
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– name: 4 Department of Neurology Medical University of South Carolina Columbia South Carolina USA
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/34469044$$D View this record in MEDLINE/PubMed
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Copyright 2021 The Authors. published by Wiley Periodicals LLC.
2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
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Issue 17
Keywords aphasia
connectomics
arcuate fasciculus
speech repetition
conduction aphasia
superior longitudinal fasciculus
partial least squares
area spt
dorsal premotor cortex
Language English
License Attribution
2021 The Authors. Human Brain Mapping published by Wiley Periodicals LLC.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Notes Funding information
National Institute on Deafness and Other Communication Disorders, Grant/Award Number: P50 DC014664; National Science Foundation, Grant/Award Number: DGE‐1321846; National Institutes of Health
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Funding information National Institute on Deafness and Other Communication Disorders, Grant/Award Number: P50 DC014664; National Science Foundation, Grant/Award Number: DGE‐1321846; National Institutes of Health
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  year: 2021
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  day: 01
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PublicationTitle Human brain mapping
PublicationTitleAlternate Hum Brain Mapp
PublicationYear 2021
Publisher John Wiley & Sons, Inc
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Snippet The application of ℓ1‐regularized machine learning models to high‐dimensional connectomes offers a promising methodology to assess clinical‐anatomical...
The application of ℓ1-regularized machine learning models to high-dimensional connectomes offers a promising methodology to assess clinical-anatomical...
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SubjectTerms Aged
Aphasia
Aphasia - diagnostic imaging
Aphasia - etiology
Aphasia - pathology
Aphasia - physiopathology
arcuate fasciculus
area spt
Cerebral Cortex - diagnostic imaging
Cerebral Cortex - pathology
Cerebrum
Circuits
conduction aphasia
connectomics
Cortex (premotor)
dorsal premotor cortex
Female
Frontal lobe
Hemispheric laterality
Humans
Information processing
Language
Learning algorithms
Least squares method
Lesions
Localization
Machine learning
Magnetic Resonance Imaging
Male
Mapping
Medical imaging
Middle Aged
Natural language generation
Nerve Net - diagnostic imaging
Nerve Net - pathology
Nervous system diseases
Nodes
partial least squares
Phonology
Prediction models
Predictions
Repetition
Speech
speech repetition
Stroke
Stroke - complications
Stroke - diagnostic imaging
Stroke - pathology
Substantia alba
superior longitudinal fasciculus
Temporal cortex
White Matter - diagnostic imaging
White Matter - pathology
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Title Isolating the white matter circuitry of the dorsal language stream: Connectome‐Symptom Mapping in stroke induced aphasia
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