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Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging
To explore the functional changes of the frontal eye field (FEF) and relevant brain regions and its role in the pathogenesis of intermittent exotropia (IXT) children via functional magnetic resonance imaging (fMRI). Twenty‐four IXT children (mean age, 11.83 ± 1.93 years) and 28 normal control (NC) s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502682/ https://www.ncbi.nlm.nih.gov/pubmed/37539805 http://dx.doi.org/10.1002/hbm.26427 |
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author | Zhang, Weijia Fei, Nanxi Wang, Yachen Yang, Bingbing Liu, Zhihan Cheng, Luyao Li, Junfa Xian, Junfang Fu, Tao |
author_facet | Zhang, Weijia Fei, Nanxi Wang, Yachen Yang, Bingbing Liu, Zhihan Cheng, Luyao Li, Junfa Xian, Junfang Fu, Tao |
author_sort | Zhang, Weijia |
collection | PubMed |
description | To explore the functional changes of the frontal eye field (FEF) and relevant brain regions and its role in the pathogenesis of intermittent exotropia (IXT) children via functional magnetic resonance imaging (fMRI). Twenty‐four IXT children (mean age, 11.83 ± 1.93 years) and 28 normal control (NC) subjects (mean age, 11.11 ± 1.50 years) were recruited. During fMRI scans, the IXT children and NCs were provided with static visual stimuli (to evoke sensory fusion) and dynamic visual stimuli (to evoke motor fusion and vergence eye movements) with binocular disparity. Brain activation in the relevant brain regions and clinical characteristics were evaluated. Group differences of brain activation and brain‐behavior correlations were investigated. For dynamic and static visual disparity relative to no visual disparity, reduced brain activation in the right FEF and right inferior occipital gyrus (IOG), and increased brain activation in the left middle temporal gyrus complex (MT+) were found in the IXT children compared with NCs. Significant positive correlations between the fusional vergence amplitude and the brain activation values were found in the right FEF, right IPL, and left cerebellum in the NC group. Positive correlations between brain activation values and Newcastle Control Scores (NCS) were found in the left MT+ in the IXT group. For dynamic visual disparity relative to static visual disparity, reduced brain activation in the right middle occipital gyrus, left cerebellum, and bilateral IPL was found in the IXT children compared with NCs. Significant positive correlations between brain activation values and the fusional vergence amplitude were found in the right FEF and right cerebellum in the NC group. Negative correlations between brain activation values and NCS were found in the right middle occipital gyrus, right cerebellum, left IPL, and right FEF in the IXT group. These results suggest that the reduced brain activation in the right FEF, left IPL, and cerebellum may play an important role in the pathogenesis of IXT by influencing fusional vergence function. While the increased brain activation in the left MT+ may compensate for this dysfunction in IXT children. |
format | Online Article Text |
id | pubmed-10502682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105026822023-09-16 Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging Zhang, Weijia Fei, Nanxi Wang, Yachen Yang, Bingbing Liu, Zhihan Cheng, Luyao Li, Junfa Xian, Junfang Fu, Tao Hum Brain Mapp Research Articles To explore the functional changes of the frontal eye field (FEF) and relevant brain regions and its role in the pathogenesis of intermittent exotropia (IXT) children via functional magnetic resonance imaging (fMRI). Twenty‐four IXT children (mean age, 11.83 ± 1.93 years) and 28 normal control (NC) subjects (mean age, 11.11 ± 1.50 years) were recruited. During fMRI scans, the IXT children and NCs were provided with static visual stimuli (to evoke sensory fusion) and dynamic visual stimuli (to evoke motor fusion and vergence eye movements) with binocular disparity. Brain activation in the relevant brain regions and clinical characteristics were evaluated. Group differences of brain activation and brain‐behavior correlations were investigated. For dynamic and static visual disparity relative to no visual disparity, reduced brain activation in the right FEF and right inferior occipital gyrus (IOG), and increased brain activation in the left middle temporal gyrus complex (MT+) were found in the IXT children compared with NCs. Significant positive correlations between the fusional vergence amplitude and the brain activation values were found in the right FEF, right IPL, and left cerebellum in the NC group. Positive correlations between brain activation values and Newcastle Control Scores (NCS) were found in the left MT+ in the IXT group. For dynamic visual disparity relative to static visual disparity, reduced brain activation in the right middle occipital gyrus, left cerebellum, and bilateral IPL was found in the IXT children compared with NCs. Significant positive correlations between brain activation values and the fusional vergence amplitude were found in the right FEF and right cerebellum in the NC group. Negative correlations between brain activation values and NCS were found in the right middle occipital gyrus, right cerebellum, left IPL, and right FEF in the IXT group. These results suggest that the reduced brain activation in the right FEF, left IPL, and cerebellum may play an important role in the pathogenesis of IXT by influencing fusional vergence function. While the increased brain activation in the left MT+ may compensate for this dysfunction in IXT children. John Wiley & Sons, Inc. 2023-08-04 /pmc/articles/PMC10502682/ /pubmed/37539805 http://dx.doi.org/10.1002/hbm.26427 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Zhang, Weijia Fei, Nanxi Wang, Yachen Yang, Bingbing Liu, Zhihan Cheng, Luyao Li, Junfa Xian, Junfang Fu, Tao Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title | Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title_full | Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title_fullStr | Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title_full_unstemmed | Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title_short | Functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
title_sort | functional changes in fusional vergence‐related brain areas and correlation with clinical features in intermittent exotropia using functional magnetic resonance imaging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502682/ https://www.ncbi.nlm.nih.gov/pubmed/37539805 http://dx.doi.org/10.1002/hbm.26427 |
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