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ORIGINAL RESEARCH article

Front. Med.

Sec. Ophthalmology

Volume 12 - 2025 | doi: 10.3389/fmed.2025.1545415

This article is part of the Research Topic Advances in Ocular Autoimmune Diseases View all articles

Analysis of Central Corneal Thickness in Systemic Lupus Erythematosus

Provisionally accepted
Juan David Saldaña-Garrido Juan David Saldaña-Garrido 1,2*Mario Cantó Cerdán Mario Cantó Cerdán 3Vicente Francisco Gil-Guillén Vicente Francisco Gil-Guillén 2,4María Luisa Alfaro-Beltrá María Luisa Alfaro-Beltrá 1Francisca Sivera Francisca Sivera 2,5
  • 1 Ophthalmology Department, General University Hospital of Elda, Alicante, Spain
  • 2 Clinical Medicine Department, School of Medicine, Miguel Hernández University of Elche, Elche, Valencian Community, Spain
  • 3 Vissum Miranza, Alicante, Spain
  • 4 Investigations Department, General University Hospital of Elda, Alicante, Spain
  • 5 Rheumatology Department, General University Hospital of Elda, Alicante, Spain

The final, formatted version of the article will be published soon.

    Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with ocular involvement in up to 30% of cases. The cornea, due to its type I collagen composition, is particularly susceptible to thinning due to immune-complex deposition. A reduced central corneal thickness (CCT) is clinically relevant in glaucoma, where a thinner CCT increases glaucoma risk and in refractive surgery planning. Previous studies on CCT in SLE are limited due to methodological heterogeneity, technology use, inclusion criteria, and sample size, resulting in conflicting findings. This study aims to evaluate and compare the mean CCT values between patients with SLE and healthy controls.Materials and methods: This cross-sectional study assessed mean CCT in 71 participants, 36 patients with SLE and 35 age-and sex-matched healthy controls, recruited from ophthalmology consultations. Participants with other risk factors for corneal thinning were excluded. A pilot study estimated a sample size of 34 participants per group. One randomly selected eye per participant was included, after confirming concordance using the Kappa index. CCT was measured using Zeiss HD Cirrus 5000 optical coherence tomography. Correlation analysis was conducted using Spearman's Rho coefficient while a Loess regression was performed to visualize both linear and non-linear trends. Multivariate linear regression was employed to assess the relationship between CCT, SLE and other variables.Results: Patients in the SLE group exhibited significantly thicker CCT than controls (536.44±39.91 µm vs. 517.57±29.62 µm, p=0.014). Intraocular pressure (IOP) was similar between groups (14.31±3.12 mmHg vs 14.54±2.36 mmHg, p=0.898). CCT positively correlated with length of hydroxychloroquine (HCQ) use (R: 0.357; p=0.041) showing a trend towards an increase with prolonged usage, peaking around 100 months. Multivariate regression confirmed the association between SLE and higher CCT, potentially due to HCQ use.Discussion: We established an association between CCT and the presence of SLE, with SLE patients exhibiting significantly higher CCT values, potentially due to hydroxychloroquine use. These findings have important implications for IOP assessment, glaucoma risk evaluation, and refractive surgery planning in SLE patients and those undergoing treatment with HCQ. Further prospective studies are warranted to validate these observations and explore the underlying mechanisms.

    Keywords: systemic lupus erythematosus, central corneal thickness, Pachymetry, Optical Coherence Tomography, Glaucoma, Hydroxychloroquine

    Received: 14 Dec 2024; Accepted: 11 Feb 2025.

    Copyright: © 2025 Saldaña-Garrido, Cantó Cerdán, Gil-Guillén, Alfaro-Beltrá and Sivera. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Juan David Saldaña-Garrido, Ophthalmology Department, General University Hospital of Elda, Alicante, Spain

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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