Evaluating nerve dysfunction in Behçet's disease: a study using corneal confocal microscopy and electromyography
INTERNATIONAL OPHTHALMOLOGY, vol.46, no.1, 2026 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 46 Issue: 1
- Publication Date: 2026
- Doi Number: 10.1007/s10792-026-03978-z
- Journal Name: INTERNATIONAL OPHTHALMOLOGY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, EMBASE, MEDLINE, Biomedical Reference Collection: Corporate Edition (EBSCO), Health Research Premium Collection (ProQuest), Pharma Collection (ProQuest)
- Acibadem Mehmet Ali Aydinlar University Affiliated: Yes
Abstract
Purpose: To evaluate peripheral nerves in Beh & ccedil;et's disease (BD) by monitoring the corneal nerves with in vivo corneal confocal microscopy (IVCCM) and measuring sympathetic skin response (SSR) and cutaneous silent period (CSP) with electromyography (EMG). Methods: This cross-sectional study included 90 participants: 60 BD patients, divided into Group 1 (n = 30) with uveitis and Group 2 (n = 30) without uveitis, and 30 healthy controls (Group 3). IVCCM assessed the subbasal nerve plexus (SNP), while EMG measured sensory and motor nerve conduction, CSP and SSR. SNP images were analyzed with ACCMetrics software, and dendritic cell (DC) densities were calculated using ImageJ software. In addition, patients under systemic medication were divided by subgroups and analysed separately. Results: No significant differences in SNP analysis or DC densities were observed across groups (p > 0.05). Patients treated with conventional agents (azathioprine) exhibited significantly lower total DC densities compared to those on colchicine and biological agents (p = 0.003, p = 0.0033). Group 2 demonstrated reduced SSR lower extremity amplitude compared to controls (p = 0.017); nevertheless, no significant differences in CSP durations or SSR latencies were found (p > 0.05). Conclusion: Evidence of small fiber neuropathy in BD was suggested by SSR amplitudes, reflecting autonomic nervous system involvement. The lack of significant differences in CSP and SSR latencies may indicate nerve regeneration due to controlled inflammation. Additionally, lower DC densities in patients on conventional treatments may highlight the mechanism of azathioprine at the in vivo level.