Systematic review defines uveitis causes in China, highlighting autoimmune conditions as prevalent.
Purpose Define the etiologic profile of uveitis in ChinaMaterials and Methods Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA)-guided systematic review of studies from PubMed, Scopus, PubMed Central, Web of Science, and the China National Knowledge Infrastructure (CNKI) (January 2005–January 2025). Eligible cross-sectional and cohort studies reporting etiologies were included. Proportions with 95% confidence intervals (CIs) were pooled, and heterogeneity was assessed with I2.Results Of 2,273 records, 10 studies met criteria (2005–2025; sample sizes 144–15373). Pooled proportions: idiopathic uveitis 41.75% (95% CI 36.88–46.78%); Vogt-Koyanagi-Harada (VKH) syndrome 14.12% (95% CI 10.56–18.63%); Behçet’s disease 7.7% (95% CI 5.2–11.27%); and Ankylosing spondylitis 5.75% (95% CI 3.65–8.96%). Infectious causes were less frequent: herpetic uveitis 2.22% (95% CI 1.47–3.34%), acute retinal necrosis (ARN) 0.94% (95% CI 0.39–2.25%), and syphilis 1.03% (95% CI 0.59–1.79%), although rates varied significantly across centers.Conclusion Uveitis in China is largely idiopathic (~41.75%), with a predominance of autoimmune etiologies, specifically Vogt-Koyanagi-Harada (VKH) syndrome and Behçet’s disease. These findings reflect a distinct epidemiological profile.
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