Holly D H Brown, Richard J W Vernon, Heidi A Baseler, Antony B Morland
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引用次数: 0
Abstract
Individuals with central visual deficits exhibit atrophy of the visual cortex in regions representing the central visual field and show little or no functional response there. Information in the central and peripheral visual field appear to be represented preferentially in extrastriate regions that are selective to faces and places, respectively. We recruited individuals with bilateral macular degeneration (age-related or juvenile) and age-matched sighted controls. We used resting state fMRI (RS-fMRI) to examine functional connectivity between striate (V1) and extrastriate face and place selective areas as it allows better comparison between those with unaffected vision and those with visual loss, whose stimulus related signals are already known to differ from those of controls. Selective deficits emerged in our central loss group, showing reduced functional connectivity between regions with foveal biases (central V1-face area) compared to sighted controls, whereas no such difference emerged in the peripheral biased regions (peripheral V1-place area). This result was evident regardless of whether eyes were closed or open and fixating, but was only significant in the right hemisphere, supporting the functional lateralisation of face processing. This pilot study provides some evidence for reduced functional connectivity between foveal-biased visual areas in central vision loss, suggesting that communication within the posterior visual pathway may be selectively affected in partial vision loss. Functional connectivity differences did not appear to be driven by changes in viewing condition. RS-fMRI is a valuable tool that allows us to explore functional brain changes without the need for retinal input.
期刊介绍:
Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.