Visual brain plasticity induced by central and peripheral visual field loss

被引:0
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作者
Nicolae Sanda
Leonardo Cerliani
Colas N. Authié
Norman Sabbah
José-Alain Sahel
Christophe Habas
Avinoam B. Safran
Michel Thiebaut de Schotten
机构
[1] Sorbonne Universités,Department of Clinical Neurosciences
[2] UPMC Université Paris 06,Frontlab, UPMC Univ Paris 06, Inserm, CNRS, Institut du cerveau et la moelle (ICM), Hôpital Pitié
[3] UMR S968,Salpêtrière
[4] Institut de la Vision,Brain Connectivity and Behaviour Group
[5] INSERM,Department of Psychiatry
[6] U968,Amsterdam Brain and Cognition
[7] Institut de la Vision,Centre de Neuroimagerie
[8] CNRS,Institute of Ophthalmology
[9] UMR 7210,Department of Ophthalmology, School of Medicine
[10] Institut de la Vision,Groupe d’Imagerie Neurofonctionnelle, Institut des Maladies Neurodégénératives, UMR 5293, CNRS
[11] Centre d’investigation clinique,undefined
[12] Centre Hospitalier National d’Ophtalmologie des Quinze-Vingts,undefined
[13] INSERM-DHOS CIC 1423,undefined
[14] Geneva University Hospital and Geneva University School of Medicine,undefined
[15] Boulevard de l’hôpital,undefined
[16] Sorbonne University,undefined
[17] Academic Medical Centre,undefined
[18] University of Amsterdam,undefined
[19] Centre Hospitalier National d’Ophtalmologie des Quinze-Vingts,undefined
[20] University College of London,undefined
[21] Fondation Ophtalmologique Adolphe de Rothschild,undefined
[22] University of Pittsburg,undefined
[23] CEA University of Bordeaux,undefined
来源
关键词
Visual plasticity; Cortical thickness; Resting-state cortical entropy; Central visual field loss; Peripheral visual field loss; Retinitis pigmentosa; Stargardt macular degeneration; Cytoarchitectonic areas;
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摘要
Disorders that specifically affect central and peripheral vision constitute invaluable models to study how the human brain adapts to visual deafferentation. We explored cortical changes after the loss of central or peripheral vision. Cortical thickness (CoTks) and resting-state cortical entropy (rs-CoEn), as a surrogate for neural and synaptic complexity, were extracted in 12 Stargardt macular dystrophy, 12 retinitis pigmentosa (tunnel vision stage), and 14 normally sighted subjects. When compared to controls, both groups with visual loss exhibited decreased CoTks in dorsal area V3d. Peripheral visual field loss also showed a specific CoTks decrease in early visual cortex and ventral area V4, while central visual field loss in dorsal area V3A. Only central visual field loss exhibited increased CoEn in LO-2 area and FG1. Current results revealed biomarkers of brain plasticity within the dorsal and the ventral visual streams following central and peripheral visual field defects.
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页码:3473 / 3485
页数:12
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