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Polymorphism within the tumor necrosis factor α (TNF) promoter region in patients with ankylosing spondylitis

1999; Elsevier BV; Volume: 60; Issue: 2 Linguagem: Inglês

10.1016/s0198-8859(98)00099-8

1879-1166

Eric L. Kaijzel, Brigitta M. N. Brinkman, M V van Krugten, Louise Smith, T. Huizinga, Georges M. G. M. Verjans, Ferdinand C. Breedveld, Cornelis L. Verweij,

Systemic Lupus Erythematosus Research

In addition to HLA-B27, other genetic factors are thought to be involved in the pathogenesis of ankylosing spondylitis (AS). Because of the location of the TNF gene in the vicinity of the HLA-B locus, and the prominent role in inflammation of its product, we investigated the association between AS and two G to A transition polymorphisms located at position -238 and -376 in the promoter region of the TNF gene. The distribution of the TNF alleles was determined in 86 HLA-B27+ AS patients and 163 healthy controls. From the 86 AS patients, 33 suffered from acute anterior uveitis (AAU). No significant difference for the TNF-376 polymorphism in AS and healthy controls was observed. The frequency of the TNF-238A allele in HLA-B27+AS patients was significantly decreased compared to random controls (p = 0.021). However, the frequency of the TNF-238A allele in HLA-B27+ AS patients was not significantly different from that observed in HLA-B27+ healthy individuals (p = 0.6). Assessment of association showed that the TNF-238G allele is in linkage disequilibrium with the HLA-B27 allele (Δ = 0.053; P = 0.008). Therefore, we conclude that the association between TNF-238G and AS is secondary to the HLA-B27 gene and that TNF-238 and TNF-376 alleles are not likely to be involved in the susceptibility to AS.