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Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia
BACKGROUND: The complex crossing-fiber characteristics in the dual-stream system have been ignored by traditional diffusion tensor models regarding disconnections in post-stroke aphasia. It is valuable to identify microstructural damage of crossing-fiber pathways and reveal accurate fiber-specific l...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358698/ https://www.ncbi.nlm.nih.gov/pubmed/34371239 http://dx.doi.org/10.1016/j.nicl.2021.102774 |
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author | Zhang, Jie Zheng, Weihao Shang, Desheng Chen, Yating Zhong, Shuchang Ye, Jing Li, Lingling Yu, Yamei Zhang, Li Cheng, Ruidong He, Fangping Wu, Dan Ye, Xiangming Luo, Benyan |
author_facet | Zhang, Jie Zheng, Weihao Shang, Desheng Chen, Yating Zhong, Shuchang Ye, Jing Li, Lingling Yu, Yamei Zhang, Li Cheng, Ruidong He, Fangping Wu, Dan Ye, Xiangming Luo, Benyan |
author_sort | Zhang, Jie |
collection | PubMed |
description | BACKGROUND: The complex crossing-fiber characteristics in the dual-stream system have been ignored by traditional diffusion tensor models regarding disconnections in post-stroke aphasia. It is valuable to identify microstructural damage of crossing-fiber pathways and reveal accurate fiber-specific language mapping in patients with aphasia. METHODS: This cross-sectional study collected magnetic resonance imaging data from 29 participants with post-stroke aphasia in the subacute stage and from 33 age- and sex-matched healthy controls. Fixel-based analysis was performed to examine microstructural fiber density (FD) and bundle cross-section alterations of specific fiber populations in crossing-fiber regions. Group comparisons were performed, and relationships with language scores were assessed. RESULTS: The aphasic group exhibited significant fixel-wise FD reductions in the dual-stream tracts, including the left inferior fronto-occipital fasciculus (IFOF), arcuate fasciculus, and superior longitudinal fasciculus (SLF) III (family-wise-error-corrected p < 0.05). Voxel- and fixel-wise comparisons revealed mismatched distributions in regions with crossing-fiber nexuses. Fixel-wise correlation analyses revealed significant associations between comprehension impairment and reduced FD in the temporal and frontal segments of the left IFOF, and also mapped naming ability to the IFOF. Average features along the whole course of dominant tracts assessed with tract-wise analyses attributed word-level comprehension to the IFOF (r = 0.723, p < 0.001) and revealed a trend-level correlation between sentence-level comprehension and FD of the SLF III (r = 0.451, p = 0.021). The mean FD of the uncinate fasciculus (UF) and IFOF correlated with total and picture naming scores, and the IFOF also correlated with responsive naming subdomains (Bonferroni corrected p < 0.05). CONCLUSIONS: FD reductions of dual streams suggest that intra-axonal volume reduction constitutes the microstructural damage of white matter integrity in post-stroke aphasia. Fixel-based analysis provides a complementary method of language mapping that identifies fiber-specific tracts in the left hemisphere language network with greater specificity than voxel-based analysis. It precisely locates the precise segments of the IFOF for comprehension, yields fiber-specific evidence for the debated UF-naming association, and reveals dissociative subdomain associations with distinct tracts. |
format | Online Article Text |
id | pubmed-8358698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83586982021-08-15 Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia Zhang, Jie Zheng, Weihao Shang, Desheng Chen, Yating Zhong, Shuchang Ye, Jing Li, Lingling Yu, Yamei Zhang, Li Cheng, Ruidong He, Fangping Wu, Dan Ye, Xiangming Luo, Benyan Neuroimage Clin Regular Article BACKGROUND: The complex crossing-fiber characteristics in the dual-stream system have been ignored by traditional diffusion tensor models regarding disconnections in post-stroke aphasia. It is valuable to identify microstructural damage of crossing-fiber pathways and reveal accurate fiber-specific language mapping in patients with aphasia. METHODS: This cross-sectional study collected magnetic resonance imaging data from 29 participants with post-stroke aphasia in the subacute stage and from 33 age- and sex-matched healthy controls. Fixel-based analysis was performed to examine microstructural fiber density (FD) and bundle cross-section alterations of specific fiber populations in crossing-fiber regions. Group comparisons were performed, and relationships with language scores were assessed. RESULTS: The aphasic group exhibited significant fixel-wise FD reductions in the dual-stream tracts, including the left inferior fronto-occipital fasciculus (IFOF), arcuate fasciculus, and superior longitudinal fasciculus (SLF) III (family-wise-error-corrected p < 0.05). Voxel- and fixel-wise comparisons revealed mismatched distributions in regions with crossing-fiber nexuses. Fixel-wise correlation analyses revealed significant associations between comprehension impairment and reduced FD in the temporal and frontal segments of the left IFOF, and also mapped naming ability to the IFOF. Average features along the whole course of dominant tracts assessed with tract-wise analyses attributed word-level comprehension to the IFOF (r = 0.723, p < 0.001) and revealed a trend-level correlation between sentence-level comprehension and FD of the SLF III (r = 0.451, p = 0.021). The mean FD of the uncinate fasciculus (UF) and IFOF correlated with total and picture naming scores, and the IFOF also correlated with responsive naming subdomains (Bonferroni corrected p < 0.05). CONCLUSIONS: FD reductions of dual streams suggest that intra-axonal volume reduction constitutes the microstructural damage of white matter integrity in post-stroke aphasia. Fixel-based analysis provides a complementary method of language mapping that identifies fiber-specific tracts in the left hemisphere language network with greater specificity than voxel-based analysis. It precisely locates the precise segments of the IFOF for comprehension, yields fiber-specific evidence for the debated UF-naming association, and reveals dissociative subdomain associations with distinct tracts. Elsevier 2021-07-25 /pmc/articles/PMC8358698/ /pubmed/34371239 http://dx.doi.org/10.1016/j.nicl.2021.102774 Text en © 2021 The Authors https://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 Zhang, Jie Zheng, Weihao Shang, Desheng Chen, Yating Zhong, Shuchang Ye, Jing Li, Lingling Yu, Yamei Zhang, Li Cheng, Ruidong He, Fangping Wu, Dan Ye, Xiangming Luo, Benyan Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title | Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title_full | Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title_fullStr | Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title_full_unstemmed | Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title_short | Fixel-based evidence of microstructural damage in crossing pathways improves language mapping in Post-stroke aphasia |
title_sort | fixel-based evidence of microstructural damage in crossing pathways improves language mapping in post-stroke aphasia |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358698/ https://www.ncbi.nlm.nih.gov/pubmed/34371239 http://dx.doi.org/10.1016/j.nicl.2021.102774 |
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