Altered functional connectivity of resting-state networks and the correlation with clinical characteristics in intermittent exotropia adult patients: a resting-state magnetic resonance imaging study.


Journal

BMC ophthalmology
ISSN: 1471-2415
Titre abrégé: BMC Ophthalmol
Pays: England
ID NLM: 100967802

Informations de publication

Date de publication:
19 Sep 2024
Historique:
received: 25 02 2024
accepted: 05 09 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 19 9 2024
Statut: epublish

Résumé

The pathogenesis of intermittent exotropia (IXT) remains unclear. The study aims to investigate alterations of resting-state networks (RSNs) in IXT adult patients using resting-state functional magnetic resonance imaging (rs-fMRI) data to explore the potential neural mechanisms. Twenty-six IXT adult patients and 22 age-, sex-, handedness-, and education-matched healthy controls (HCs) underwent fMRI scanning and ophthalmological examinations. Brain areas with significant functional connectivity (FC) differences between the IXT and HC groups were selected as regions of interest (ROI) and mean z-scores were calculated to control for individual differences. Compared with HCs, IXT patients exhibited altered FC in various brain regions within RSNs involved in binocular fusion, stereopsis, ocular movement, emotional processes and social cognition, including the default mode network (DMN), the dorsal attention network (DAN), the visual network (VN), the sensorimotor network (SMN), the executive control network (ECN), the frontoparietal network (FPN) and the auditory network (AN). The degree of exodeviation was positively correlated with FC value of left middle occipital gyrus (MOG) within the VN. Correspondingly, we found a negative correlation between the degree of exodeviation and the FC value of left angular gyrus (AG) within FPN (P < 0.05). The FNC analysis between different RSNs also provides evidence on visual-motor cortical plasticity. IXT patients showed widespread changes of brain activity within RSNs related to binocular fusion, stereopsis, oculomotor control, emotional processes, and social cognition. These findings extend our current understanding of the neuropathological mechanisms of IXT. Beginning date of the trial: 2021-09-01. Date of registration:2021-07-18. Trial registration number: ChiCTR 2,100,048,852. Trial registration site: http://www.chictr.org.cn/index.aspx .

Sections du résumé

BACKGROUND BACKGROUND
The pathogenesis of intermittent exotropia (IXT) remains unclear. The study aims to investigate alterations of resting-state networks (RSNs) in IXT adult patients using resting-state functional magnetic resonance imaging (rs-fMRI) data to explore the potential neural mechanisms.
METHODS METHODS
Twenty-six IXT adult patients and 22 age-, sex-, handedness-, and education-matched healthy controls (HCs) underwent fMRI scanning and ophthalmological examinations. Brain areas with significant functional connectivity (FC) differences between the IXT and HC groups were selected as regions of interest (ROI) and mean z-scores were calculated to control for individual differences.
RESULTS RESULTS
Compared with HCs, IXT patients exhibited altered FC in various brain regions within RSNs involved in binocular fusion, stereopsis, ocular movement, emotional processes and social cognition, including the default mode network (DMN), the dorsal attention network (DAN), the visual network (VN), the sensorimotor network (SMN), the executive control network (ECN), the frontoparietal network (FPN) and the auditory network (AN). The degree of exodeviation was positively correlated with FC value of left middle occipital gyrus (MOG) within the VN. Correspondingly, we found a negative correlation between the degree of exodeviation and the FC value of left angular gyrus (AG) within FPN (P < 0.05). The FNC analysis between different RSNs also provides evidence on visual-motor cortical plasticity.
CONCLUSIONS CONCLUSIONS
IXT patients showed widespread changes of brain activity within RSNs related to binocular fusion, stereopsis, oculomotor control, emotional processes, and social cognition. These findings extend our current understanding of the neuropathological mechanisms of IXT.
TRIAL REGISTRATION BACKGROUND
Beginning date of the trial: 2021-09-01. Date of registration:2021-07-18. Trial registration number: ChiCTR 2,100,048,852. Trial registration site: http://www.chictr.org.cn/index.aspx .

Identifiants

pubmed: 39300474
doi: 10.1186/s12886-024-03672-7
pii: 10.1186/s12886-024-03672-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

411

Subventions

Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998
Organisme : National Natural Science Foundation of China
ID : 82070998

Informations de copyright

© 2024. The Author(s).

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Auteurs

Huixin Li (H)

Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing Tongren Eye Center, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China.

Wei Li (W)

Department of Radiology, Beijing Tongren Hospital, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China.

Jie Hong (J)

Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing Tongren Eye Center, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China.

Jiawen Liu (J)

Department of Quantitative Theory and Methods, Emory University, Atlanta, GA, USA.

Jie Hao (J)

Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing Tongren Eye Center, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China.

Wei Dai (W)

Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing Tongren Eye Center, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China.

Zhaohui Liu (Z)

Department of Radiology, Beijing Tongren Hospital, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China. lzhtrhos@163.com.

Jing Fu (J)

Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing Tongren Eye Center, Capital Medical University, Dong Jiao Min Xiang Street 1#, Dongcheng District, Beijing, China. fu_jing@126.com.

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