An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis

Abstract To investigate corneal microstructure of systemic sclerosis (SSc) patients using in vivo confocal microscopy (IVCM). 33 patients with SSc and 30 age-matched healthy subjects were recruited. All participants underwent comprehensive ophthalmic examination including IVCM (Heidelberg Retina Tom...

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Main Authors: Eszter Szalai, Gabriella Szucs, Szilvia Szamosi, Zsuzsa Aszalos, Ildiko Afra, Adam Kemeny-Beke
Format: Article
Language:English
Published: Nature Portfolio 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-90594-9
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author Eszter Szalai
Gabriella Szucs
Szilvia Szamosi
Zsuzsa Aszalos
Ildiko Afra
Adam Kemeny-Beke
author_facet Eszter Szalai
Gabriella Szucs
Szilvia Szamosi
Zsuzsa Aszalos
Ildiko Afra
Adam Kemeny-Beke
author_sort Eszter Szalai
collection DOAJ
description Abstract To investigate corneal microstructure of systemic sclerosis (SSc) patients using in vivo confocal microscopy (IVCM). 33 patients with SSc and 30 age-matched healthy subjects were recruited. All participants underwent comprehensive ophthalmic examination including IVCM (Heidelberg Retina Tomograph III, Heidelberg Engineering GmbH, Heidelberg, Germany) and ocular surface evaluation. Subbasal nerve plexus morphology was investigated using automated software analysis (ACCMetrics V3; University of Manchester, Manchester, UK). Keratocyte cell densities in the anterior stroma were significantly lower in patients with SSc compared to controls (P < 0.0001). In 7 SSc patients no keratocyte nuclei were identified in the anterior stroma and in most patients scattered hyperreflective punctate material were observed in the anterior stroma. Significantly lower subbasal nerve fiber parameters were found in patients with SSc compared to healthy subjects (P < 0.05). There were no significant correlations between the duration of SSc and any of the corneal cell density values. Tear break-up time values (4.82 ± 3.15 s) and Ocular Surface Disease Index scores (33.27 ± 30.11) were abnormal, Schirmer values (6.78 ± 5.82 mm) were borderline in SSc patients. In SSc, corneal morphological changes and accumulation of punctate material in the stroma was detected with confocal microscopy. Severe ocular surface disease was observed in SSc patients with significant impairment in subbasal nerve plexus morphology resembling peripheral neuropathy.
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spelling doaj.art-222dd37c6ba4438a9268730a36cc44c42022-12-21T22:54:51ZengNature PortfolioScientific Reports2045-23222021-05-011111710.1038/s41598-021-90594-9An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosisEszter Szalai0Gabriella Szucs1Szilvia Szamosi2Zsuzsa Aszalos3Ildiko Afra4Adam Kemeny-Beke5Department of Ophthalmology, University of PecsDepartment of Rheumatology, Institute of Medicine, Faculty of Medicine, University of DebrecenDepartment of Rheumatology, Institute of Medicine, Faculty of Medicine, University of DebrecenDepartment of Immunology, Institute of Medicine, Faculty of Medicine, University of DebrecenDepartment of Ophthalmology, Faculty of Medicine, University of DebrecenDepartment of Ophthalmology, Faculty of Medicine, University of DebrecenAbstract To investigate corneal microstructure of systemic sclerosis (SSc) patients using in vivo confocal microscopy (IVCM). 33 patients with SSc and 30 age-matched healthy subjects were recruited. All participants underwent comprehensive ophthalmic examination including IVCM (Heidelberg Retina Tomograph III, Heidelberg Engineering GmbH, Heidelberg, Germany) and ocular surface evaluation. Subbasal nerve plexus morphology was investigated using automated software analysis (ACCMetrics V3; University of Manchester, Manchester, UK). Keratocyte cell densities in the anterior stroma were significantly lower in patients with SSc compared to controls (P < 0.0001). In 7 SSc patients no keratocyte nuclei were identified in the anterior stroma and in most patients scattered hyperreflective punctate material were observed in the anterior stroma. Significantly lower subbasal nerve fiber parameters were found in patients with SSc compared to healthy subjects (P < 0.05). There were no significant correlations between the duration of SSc and any of the corneal cell density values. Tear break-up time values (4.82 ± 3.15 s) and Ocular Surface Disease Index scores (33.27 ± 30.11) were abnormal, Schirmer values (6.78 ± 5.82 mm) were borderline in SSc patients. In SSc, corneal morphological changes and accumulation of punctate material in the stroma was detected with confocal microscopy. Severe ocular surface disease was observed in SSc patients with significant impairment in subbasal nerve plexus morphology resembling peripheral neuropathy.https://doi.org/10.1038/s41598-021-90594-9
spellingShingle Eszter Szalai
Gabriella Szucs
Szilvia Szamosi
Zsuzsa Aszalos
Ildiko Afra
Adam Kemeny-Beke
An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
Scientific Reports
title An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
title_full An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
title_fullStr An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
title_full_unstemmed An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
title_short An in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
title_sort in vivo confocal microscopy study of corneal changes in patients with systemic sclerosis
url https://doi.org/10.1038/s41598-021-90594-9
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