Predictive factors for risk of chronic evolution in Vogt–Koyanagi–Harada disease at 1 month after pulse steroid therapy
In this study, we aimed to identify factors for risk of chronic evolution in Vogt–Koyanagi–Harada (VKH) disease at 1 month following pulse steroid therapy. This was a retrospective clinical cohort, single center study. A total of 121 eyes from 61 treatment-naïve patients with acute VKH disease, who underwent pulse steroid therapy and had follow-up for over 12 months were evaluated. Patients were categorized into SGF and non-SGF groups according to fundus outcomes at 12 months after treatment. Anterior chamber morphology was assessed using Pentacam ® , while axial length and lens thickness were measured with the IOLMaster 700. Multivariable analysis demonstrated that lower best-corrected visual acuity (BCVA) ( p < 0.001) and increased corneal thickness ( p = 0.016) at 1 month were significantly associated with the development of SGF. Receiver operating characteristic curve analysis determined optimal cut-off values for predicting SGF as a logarithmic BCVA greater than −0.040 and a corneal thickness exceeding 574.500 µm. The corresponding Youden index values were 0.291 for BCVA and 0.244 for corneal thickness. Elevated logarithmic BCVA values and increased corneal thickness at 1 month after treatment were identified as risk factors for the subsequent SGF development. Applying higher cut-off values for these factors may facilitate more targeted therapeutic strategies in patients with VKH disease.
Authors
- Shigeki Machida (ORCID: https://orcid.org/0000-0001-8671-2399)
- Masaaki Sakamoto (ORCID: https://orcid.org/0000-0001-9832-5791)
- Shinichiro Imaizumi
- Tetsuya Muto (ORCID: https://orcid.org/0000-0003-1690-9254)
- Shoichiro Kusuda
- Tetsuju Sekiryu
Institutions
- Fukushima Medical University (JP)
- Dokkyo Medical University Saitama Medical Center (JP)
Publication Details
- Journal
- PLoS ONE
- Published
- 2026-11-11
- DOI
- https://doi.org/10.1371/journal.pone.0362558
- Primary Topic
- Ocular Diseases and Behçet’s Syndrome
- Type
- article
- Field-Weighted Citation Impact
- 0.00