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Uveitis: Autoimmunity… and beyond.

Authors :: Bertrand PJ
Jamilloux Y
Ecochard R
Richard-Colmant G
Gerfaud-Valentin M
Guillaud M
Denis P
Kodjikian L
Sève P
Source :: Autoimmunity reviews [Autoimmun Rev] 2019 Sep; Vol. 18 (9), pp. 102351. Date of Electronic Publication: 2019 Jul 16.
Publication Year :: 2019
Abstract: Objective: Uveitis is the most common ophthalmological finding in the practice of rheumatology and clinical immunology. The condition is frequently idiopathic but about 60 causes of uveitis have been described. Our aim was to analyze the clinical patterns and etiologies of uveitis in a tertiary referral center.<br />Methods: The records of 912 consecutive patients referred to the department of internal medicine (Lyon University Hospital, Lyon, France) for the diagnostic work-up of uveitis were examined. Demographic, clinical, anatomical, and etiological features of uveitis were analyzed.<br />Results: The mean age at onset was 48.8 years; 59.8% of the patients were women and 78.2% were Caucasians. Anterior uveitis was the most common type of uveitis (40.6%), followed by panuveitis (31.7%), posterior (18.75%) and intermediate uveitis (9%). 46.9% of the patients had idiopathic uveitis. The most common etiologies were systemic diseases (37.3%), such as sarcoidosis (17.1%), HLA-B27-related uveitis and/or spondyloarthritis (12.5%), and tuberculosis (7.5%).<br />Conclusion: We describe one of the largest cohorts of consecutive uveitis patients referred to a department of internal medicine. The high percentage of uveitis associated with underlying (systemic) diseases highlights the need for a multidisciplinary approach, in order to reduce the diagnostic delay.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)