Patients with neuromyelitis optica (NMO) have shown structural and functional impairments in the visual cortex. We aimed to characterize subregional grey matter volume (GMV) and resting-state functional connectivity (rsFC) changes in the visual cortex in NMO. Thirty-seven NMO patients and forty-two controls underwent structural and functional MRI scans. The GMV and rsFC of each visual subregion were compared between the groups. Compared with controls, NMO patients had GMV reductions in the bilateral V1, V2, V3d, VP, and LO and in the left V3A. In canonical visual pathways, the relatively low-level subregions showed more significant GMV reductions than did the high-level ones. Regardless of GMV correction, NMO patients showed reduced rsFC in the bilateral LO and V4v and in the left V2. The GMVs of the bilateral V1 and LO and of the left V2 and V3d were negatively correlated with clinical disability in NMO patients; these correlation coefficients were associated with hierarchical positions in the visual pathways. These findings suggest that in NMO, the low-level visual subregions have more severe structural damage; structural damage is not the only factor affecting rsFC alterations of visual subregions; GMV reduction in the low-level visual subregions has the highest predictive value for clinical disability.Neuromyelitis optica (NMO) is characterized by optic nerve damage that may result in structural and functional alterations of the posterior visual pathways via Wallerian degeneration 1-4 . For example, NMO patients have shown reduced grey matter volume (GMV) 2,5 and altered spontaneous brain activity 6,7 in the visual cortex and impaired integrity in the optic radiation [3][4][5][8][9][10][11][12][13][14] .The visual cortex is a heterogeneous region and has been subdivided into distinct areas; a visual area is defined as a swath of cortex that has similar function, architectonics, connections and topography 15 . However, the structural and functional damage of the visual cortex in NMO at the subregional level remains largely unknown. Investigating the structural and functional damage of the visual subregions in NMO is clinically important because doing so can improve our understanding of the neural mechanisms underlying the visual cortex impairment in NMO by answering the following questions: (1) whether the structural damage in the visual subregions is associated with the hierarchical positions in the visual pathways in NMO; (2) whether the structurally impaired visual subregions are also functionally impaired in NMO; and (3) which measure and which visual subregion can better predict clinical disability in NMO patients.To answer these questions, we performed an exploratory study by collecting structural MRI and resting-state functional MRI data from 37 NMO patients and 42 healthy controls. Using the GMV as a measure of structural damage and the resting-state functional connectivity (rsFC) as a measure of functional damage, we compared the GMV and rsFC differences in each visual subregion between the groups.
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