Systemic sclerosis: Characterizing candidate retinal and choroidal imaging features using optical coherence tomography

OBJECTIVES: Systemic sclerosis is a complex autoimmune disease characterized by vasculopathy and fibrosis, capable of affecting virtually any organ system, including the eyes. Optical coherence tomography is a non - invasive imaging technique that enables high-resolution cross-sectional visualization of ocular structures. This study aimed to characterize candidate retinal imaging features in systemic sclerosis patients using Optical Coherence Tomography. METHODS: A total of 41 systemic sclerosis patients (10 males, 31 females; mean age: 58.7 ± 11.7 years) and 38 age-matched healthy controls (9 males, 29 females; 61.6 ± 12.8 years) were included. After all participants underwent a comprehensive ophthalmologic assessment, including best-corrected visual acuity, intraocular pressure measurement, slit-lamp biomicroscopy, fundus examination, and optical coherence tomography was applied. RESULTS: The mean best-corrected visual acuity among systemic sclerosis patients was 0.95. The central retinal thickness was slightly reduced in systemic sclerosis patients (241.7 µm) compared to controls (254.9 µm), though the difference was not statistically significant. Subfoveal choroidal thickness showed no significant difference (289.9 µm vs. 285.4 µm in controls). Notably, optical coherence tomography revealed previously unreported fundus abnormalities in systemic sclerosis patients: drusen-like deposits in 19 patients (46.3%), wide-based foveal pit in 26 patients (63%), and epiretinal membrane in 9 patients (21%), all of which occurred significantly more often than in the control group (p < 0.01). CONCLUSION: Systemic sclerosis is associated with a high prevalence of underrecognized retinal findings, like foveal contour abnormalities and drusen-like deposits. While these candidate imaging features require longitudinal validation, they likely reflect the systemic microvascular and fibrotic burden of the disease.

Authors

Institutions

Publication Details

Journal
PLoS ONE
Published
2026-04-21
DOI
https://doi.org/10.1371/journal.pone.0346705
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Systemic sclerosis: Characterizing candidate retinal and choroidal imaging features using optical coherence tomography

Szilárd Burcsár, Attila Balog, Lilla Smeller, Edit Tóth‐Molnár et al.
PLoS ONE
Ocular Diseases and Behçet’s Syndrome
article

Systemic sclerosis: Characterizing candidate retinal and choroidal imaging features using optical coherence tomography

Szilárd Burcsár, Attila Balog, Lilla Smeller, Edit Tóth‐Molnár, Nicolette Sohár, Dominika Ördögh, László Szalay
article en

Abstract

OBJECTIVES: Systemic sclerosis is a complex autoimmune disease characterized by vasculopathy and fibrosis, capable of affecting virtually any organ system, including the eyes. Optical coherence tomography is a non - invasive imaging technique that enables high-resolution cross-sectional visualization of ocular structures. This study aimed to characterize candidate retinal imaging features in systemic sclerosis patients using Optical Coherence Tomography. METHODS: A total of 41 systemic sclerosis patients (10 males, 31 females; mean age: 58.7 ± 11.7 years) and 38 age-matched healthy controls (9 males, 29 females; 61.6 ± 12.8 years) were included. After all participants underwent a comprehensive ophthalmologic assessment, including best-corrected visual acuity, intraocular pressure measurement, slit-lamp biomicroscopy, fundus examination, and optical coherence tomography was applied. RESULTS: The mean best-corrected visual acuity among systemic sclerosis patients was 0.95. The central retinal thickness was slightly reduced in systemic sclerosis patients (241.7 µm) compared to controls (254.9 µm), though the difference was not statistically significant. Subfoveal choroidal thickness showed no significant difference (289.9 µm vs. 285.4 µm in controls). Notably, optical coherence tomography revealed previously unreported fundus abnormalities in systemic sclerosis patients: drusen-like deposits in 19 patients (46.3%), wide-based foveal pit in 26 patients (63%), and epiretinal membrane in 9 patients (21%), all of which occurred significantly more often than in the control group (p < 0.01). CONCLUSION: Systemic sclerosis is associated with a high prevalence of underrecognized retinal findings, like foveal contour abnormalities and drusen-like deposits. While these candidate imaging features require longitudinal validation, they likely reflect the systemic microvascular and fibrotic burden of the disease.

PLoS ONEVol. 21(4)
University of Szeged (HU)
Good health and well-being
Openalex Percentile: Top 12%
Ocular Diseases and Behçet’s Syndrome
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.