Author:
Amin Mariam Maged,Abdel Latif Osama M.
Abstract
AbstractBackgroundBehçet’s syndrome (BS) is a multi-systemic vasculitis characterized by recurrent oral ulcers, genital ulcers, ocular lesions, and other systemic manifestations. As there is no laboratory diagnostics of BS, the diagnosis is mainly clinical.ObjectiveTo investigate the utility of the autoantibody against tubulin-α-1c in diagnosis of BS and its clinical significance.MethodsSixty BS patients and sixty healthy controls were enrolled in this study. We assessed all patients by Behçet disease current activity form (BDCAF), routine laboratory investigations, and immunological markers (ANA, anti-DNA, ANCA). Anti-endothelial cell antibodies (AECA) and anti-tubulin-alpha-1c antibodies were performed for all participants.ResultsRegarding duration of illness, Birmingham Vasculitis Activity Score (BVAS), and BDCAF, the mean value was 4.77 ± 4.239, 19.80 ± 10.020, and 9.52 ± 5.476, respectively. On comparing laboratory investigations, there was only significant increase in anti-tubulin-alpha-1c antibody in BS patients compared to healthy controls. Regarding AECA, there was no any significant correlation except with CRP. Anti-tubulin-alpha-1c detected significant direct correlation with the presence of posterior uveitis, panuveitis, and venous thrombosis as well as BVAS, C4, and protein/creatinine ratio. Regarding diagnostic performance of both AECA and anti-tubulin-alpha-1c, the cutoff value of AECA for diagnosis was 27.250, with sensitivity and specificity of 93.3% and 96.7%, respectively. The cutoff value of the anti-tubulin-alpha-1c for diagnosis was 22.300, with sensitivity and specificity of 100% and 96.7% respectively.ConclusionAnti-tubulin-α-1c antibodies are of diagnostic value in BS and are indicative of activity with 100% sensitivity and 96.7% specificity.Key Points•There is lack of specific laboratory, radiological, or histological diagnostics for Behcet syndrome.•We aimed to evaluate the significance of tubulin-α-1c autoantibody in diagnosis of Behcet syndrome.•There is elevation of tubulin-α-1c autoantibody with sensitivity and specificity of 100% and 96.7%, respectively.
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Reference45 articles.
1. Hatemi G, Seyahi E, Fresko I, Talarico R, Hamuryudan V (2016) One year in review 2016: Behçet’s syndrome. Clin Exp Rheumatol 34(Suppl. 102):S10-22
2. Hatemi G, Seyahi E, Fresko I, Talarico R, Hamuryudan V (2017) One year in review 2017: Behçet’s syndrome. Clin Exp Rheumatol 35(Suppl. 108):S3-15
3. Colburn NT (2012) Review of rheumatology. Springer–Verlag London Limited. 417–430. https://doi.org/10.1007/978-1-84882-093-75
4. Gheita TA, El-Latif EA, El-Gazzar II, Samy N, Hammam N, A Abdel Noor R. et al (2019) Behçet’s disease in Egypt: a multicenter nationwide study on 1526 adult patients and review of the literature [published correction appears in Clin Rheumatol. 38(9):2565–2575
5. Sakane T, Takeno M, Suzuki N, Inaba G (1999) Behçet’s disease. N Engl J Med 341:1284–1291
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