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Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry

This cross-sectional study compared the retinal morphology between patients with progressive supranuclear palsy (PSP) and healthy controls. (The retinal nerve fiber layer (RNFL) around the optic disc and the retina in the macular area of 22 PSP patients and 151 controls were investigated by spectral...

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Autores principales: Stemplewitz, Birthe, Kromer, Robert, Vettorazzi, Eik, Hidding, Ute, Frings, Andreas, Buhmann, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509679/
https://www.ncbi.nlm.nih.gov/pubmed/28706282
http://dx.doi.org/10.1038/s41598-017-05575-8
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author Stemplewitz, Birthe
Kromer, Robert
Vettorazzi, Eik
Hidding, Ute
Frings, Andreas
Buhmann, Carsten
author_facet Stemplewitz, Birthe
Kromer, Robert
Vettorazzi, Eik
Hidding, Ute
Frings, Andreas
Buhmann, Carsten
author_sort Stemplewitz, Birthe
collection PubMed
description This cross-sectional study compared the retinal morphology between patients with progressive supranuclear palsy (PSP) and healthy controls. (The retinal nerve fiber layer (RNFL) around the optic disc and the retina in the macular area of 22 PSP patients and 151 controls were investigated by spectral domain optical coherence tomography (SD-OCT). Additionally, the RNFL and the nerve fiber index (NFI) were measured by scanning laser polarimetry (SLP). Results of RNFL measurements with SD-OCT and SLP were compared to assess diagnostic discriminatory power. Applying OCT, PSP patients showed a smaller RNFL thickness in the inferior nasal and inferior temporal areas. The macular volume and the thickness of the majority of macular sectors were reduced compared to controls. SLP data showed a thinner RNFL thickness and an increase in the NFI in PSP patients. Sensitivity and specificity to discriminate PSP patients from controls were higher applying SLP than SD-OCT. Retinal changes did not correlate with disease duration or severity in any OCT or SLP measurement. PSP seems to be associated with reduced thickness and volume of the macula and reduction of the RNFL, independent of disease duration or severity. Retinal imaging with SD-OCT and SLP might become an additional tool in PSP diagnosis.
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spelling pubmed-55096792017-07-14 Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry Stemplewitz, Birthe Kromer, Robert Vettorazzi, Eik Hidding, Ute Frings, Andreas Buhmann, Carsten Sci Rep Article This cross-sectional study compared the retinal morphology between patients with progressive supranuclear palsy (PSP) and healthy controls. (The retinal nerve fiber layer (RNFL) around the optic disc and the retina in the macular area of 22 PSP patients and 151 controls were investigated by spectral domain optical coherence tomography (SD-OCT). Additionally, the RNFL and the nerve fiber index (NFI) were measured by scanning laser polarimetry (SLP). Results of RNFL measurements with SD-OCT and SLP were compared to assess diagnostic discriminatory power. Applying OCT, PSP patients showed a smaller RNFL thickness in the inferior nasal and inferior temporal areas. The macular volume and the thickness of the majority of macular sectors were reduced compared to controls. SLP data showed a thinner RNFL thickness and an increase in the NFI in PSP patients. Sensitivity and specificity to discriminate PSP patients from controls were higher applying SLP than SD-OCT. Retinal changes did not correlate with disease duration or severity in any OCT or SLP measurement. PSP seems to be associated with reduced thickness and volume of the macula and reduction of the RNFL, independent of disease duration or severity. Retinal imaging with SD-OCT and SLP might become an additional tool in PSP diagnosis. Nature Publishing Group UK 2017-07-13 /pmc/articles/PMC5509679/ /pubmed/28706282 http://dx.doi.org/10.1038/s41598-017-05575-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stemplewitz, Birthe
Kromer, Robert
Vettorazzi, Eik
Hidding, Ute
Frings, Andreas
Buhmann, Carsten
Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title_full Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title_fullStr Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title_full_unstemmed Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title_short Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
title_sort retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509679/
https://www.ncbi.nlm.nih.gov/pubmed/28706282
http://dx.doi.org/10.1038/s41598-017-05575-8
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