Journal
FRONTIERS IN HUMAN NEUROSCIENCE
Volume 16, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fnhum.2022.943618
Keywords
glaucoma; optic neuritis; traumatic optic neuropathy; resting-state fMRI; visual cortex; dorsal visual stream; ventral visual stream; LGN
Categories
Funding
- United States Department of Defense CDMRP Vision Research Program [W81XWH1910853]
- U.S. Department of Defense (DOD) [W81XWH1910853] Funding Source: U.S. Department of Defense (DOD)
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This article reviews the application of resting-state functional magnetic resonance imaging (RS-fMRI) in the field of optic neuropathies. The studies show that there are changes in brain activity and functional connectivity in patients with optic neuropathies, and these changes vary across different types of diseases. Additionally, RS-fMRI studies of optic neuropathies demonstrate recovery of brain activity in certain areas.
Optic neuropathy refers to disease of the optic nerve and can result in loss of visual acuity and/or visual field defects. Combining findings from multiple fMRI modalities can offer valuable information for characterizing and managing optic neuropathies. In this article, we review a subset of resting-state functional magnetic resonance imaging (RS-fMRI) studies of optic neuropathies. We consider glaucoma, acute optic neuritis (ON), discuss traumatic optic neuropathy (TON), and explore consistency between findings from RS and visually driven fMRI studies. Consistent with visually driven studies, glaucoma studies at rest also indicated reduced activation in the visual cortex and dorsal visual stream. RS-fMRI further reported varying levels of functional connectivity in the ventral stream depending on disease severity. ON patients show alterations within the visual cortex in both fMRI techniques. Particularly, higher-than-normal RS activity is observed in the acute phase and decreases as the disease progresses. A similar pattern is observed in the visual cortex of TON-like, open globe injury (OGI), patients. Additionally, visually driven and RS-fMRI studies of ON patients show recovery of brain activity in the visual cortex. RS-fMRI suggests recovery of signals in higher-tier visual areas MT and LOC as well. Finally, RS-fMRI has not yet been applied to TON, although reviewing OGI studies suggests that it is feasible. Future RS-fMRI studies of optic neuropathies could prioritize studying the fine scale RS activity of brain areas that visually driven studies have identified. We suggest that a more systematic longitudinal comparison of optic neuropathies with advanced fMRI would provide improved diagnostic and prognostic information.
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