4.5 Article

Retinal thinning in progressive supranuclear palsy: differences with healthy controls and correlation with clinical variables

期刊

NEUROLOGICAL SCIENCES
卷 43, 期 8, 页码 4803-4809

出版社

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-022-06061-4

关键词

Progressive supranuclear palsy; Retina; Progression; Diagnosis; Optical coherence tomography

资金

  1. University of Salerno [FARB2019]

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This study describes retinal layer thickness in patients with progressive supranuclear palsy (PSP) compared to healthy controls using spectral-domain optical coherence tomography (SD-OCT). The results show significant thinning of certain retinal layers in PSP patients compared to controls. The study also finds a significant correlation between retinal layer thickness and visuospatial abilities.
Background Available evidence reports conflicting data on retinal thickness in progressive supranuclear palsy (PSP). In studies including healthy controls, PSP showed either the thinning of the retinal nerve fiber layer, macular ganglion cell, inner nuclear, or outer retina layer. Objectives The goals of the present study were to describe retinal layer thickness in a large cohort of PSP compared to healthy controls and in PSP phenotypes using spectral-domain optical coherence tomography (SD-OCT). The additional objective was to verify the relationship between retinal layers thickness and clinical variables in PSP. Methods Using a cross-sectional design, we examined retinal structure in 27 PSP patients and 27 controls using standard SD-OCT. Motor and cognitive impairment in PSP was rated with the PSP rating scale and the Montreal Cognitive Assessment battery (MoCA), respectively. Eyes with poor image quality or confounding diseases were excluded. SD-OCT measures of PSP and controls were compared with parametric testing, and correlations between retinal layer thicknesses and disease severity were evaluated. Results PSP showed significant thinning of the inner retinal layer (IRL), ganglion cell layer (GCL), inner plexiform layer (IPL), and the outer plexiform layer (OPL) compared to healthy controls. PSP phenotypes showed similar retinal layer thicknesses. Retinal layer thickness correlated with MoCA visuospatial subscore (p<0.001). Conclusions We demonstrated PSP patients disclosed thinner IRL, GCL, IPL, and OPL compared to healthy controls. Furthermore, we found a significant correlation between visuospatial abilities and retinal layers suggesting the existence of a mutual relationship between posterior cognitive function and retinal structure.

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