Evidence map›Paper›PMID 40392288›Full record

ArticleNeuroradiology2025

Disrupted static and dynamic Large-scale brain functional network connectivity in the differentiation of myelin oligodendrocyte glycoprotein Antibody-Seropositive from seronegative optic neuritis.

Wentao Wang, Xilan Liu, Yan Sha, Ximing Wang, Ping Lu

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Article in Neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Wentao WangZhongshan Hospital, Shanghai, China.
Xilan LiuShanghai Children's Medical Center, Shanghai, China.
Yan ShaEye & ENT Hospital of Fudan University, Shanghai, China.
Ximing WangFirst Affiliated Hospital of Soochow University, Suzhou, China.
Ping LuSuzhou Municipal Hospital, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China. Luping1521132@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe ability to distinguish myelin oligodendrocyte glycoprotein antibody-seropositive optic neuritis (MOG-ON) from seronegative-ON is critical in clinical practice. We investigate potential neural mechanisms and differentiation biomarkers via large-scale functional network connectivity (FNC) using resting-state functional magnetic resonance imaging (RS-fMRI).

methodsRS-fMRI-based independent component analysis (ICA) was performed in 79 subjects, including 23 with MOG-ON, 30 with seronegative-ON and 26 healthy controls (HCs). The resting-state networks (RSNs) extracted from the ICA were used to investigate static FNC (sFNC) changes within and between groups. In addition, 5 dynamic FNC (dFNC) states were identified using k-means cluster analysis, and several state-related properties were calculated. Receiver operating characteristic (ROC) curve analysis was also performed to determine its value in differential diagnosis.

resultsIn the sFNC analysis, the patient groups showed decreased intranetwork functional connectivity (FC) within several RSNs compared to the HC group. The MOG-ON group presented significantly altered intranetwork FC in the medial visual network (mVN) and posterior default mode network (pDMN) compared with the seronegative-ON group. Compared with the HCs, the patient groups also presented abnormal internetwork FC between RSNs. In the dFNC analysis, the patient groups presented altered fractional occupancy and dwell times in states 1 and 5 compared with HCs, and the changes in state-related metrics were also distinct between the MOG-ON and seronegative-ON groups. In terms of ROC curve analysis, optimal diagnostic performance was achieved by combining static and dynamic approaches.

conclusionsAbnormal large-scale static and dynamic brain functional networks may help to better understand the neural mechanisms of MOG-ON and seronegative-ON and their differentiation.

Indexed as

AutoantibodiesMagnetic Resonance ImagingMyelin-Oligodendrocyte GlycoproteinOptic NeuritisAdultBiomarkersCase-Control StudiesDiagnosis, DifferentialFemaleHumansMaleMiddle AgedAutoantibodiesBiomarkersMyelin-Oligodendrocyte GlycoproteinFunctional network connectivityIndependent component analysisMyelin oligodendrocyte glycoproteinOptic neuritis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.