4.7 Article

Lack of association of HLA-B*51 with a severe disease course in Behcet's disease

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RHEUMATOLOGY
卷 40, 期 6, 页码 668-672

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OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/40.6.668

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Behcet's disease; HLA-B51; uveitis; homozygosity; disease severity

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Objective. To investigate the previously reported association of HLA-B51 with the manifestations and severity of BehCet's disease (BD). Methods. The study group consisted of 148 consecutive ED patients (89 male, 59 female) with a minimum disease duration of 5 yr followed up at an out-patient ED clinic in a tertiary referral centre. Tire patients were classified into three severity groups (mild, moderate, severe) using a modified form of the ED total activity index. HLA-B alleles were determined by DNA amplification using the polymerase chain reaction and sequential hybridization with sequence-specific oligonucleotide probes. Results. The frequencies of genital ulceration [odds ratio (OR) = 3.1, 95% confidence interval (CI) 1.3-7.5], skin findings (erythema nodosum, folliculitis or acne-like lesions) (OR = 4.4, 95% CI 1.1-17.7), a positive skin pathergy test (OR = 3.4, 95% CI 1.1-10.9) and eye disease (OR = 1.8, 95% CI 0.9-3.7) were all higher in B*51-positive patients. By contrast, no significant association was observed between B*51 positivity and a severe disease course, and B*51 homozygosity did not exhibit a prominent association with the severity of ED. Male sex was found to be the strongest determinant of the severity of ED by logistic regression analysis (OR = 4.7, 95% CI 1.9-11.2). Conclusion. HLA-B*51 does not exhibit a strong association with a more severe disease course in ED. The involvement of other genetic and/or environmental factors seems to be required and to be more important than B*51 for the progression of ED.

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