Milicic A, Lindheimer F, Laval S, Rudwaleit M, Ackerman H, Wordsworth P, Hohler T, Brown M A
Nuffield Orthopaedic Centre, Windmill Rd, Headington, OX3 7LD, UK.
Genes Immun. 2000 Oct;1(7):418-22. doi: 10.1038/sj.gene.6363701.
The objective of this study was to investigate TNF promoter region polymorphisms for association with susceptibility to ankylosing spondylitis (AS). The TNF -238 and -308 polymorphisms were genotyped in 306 English AS cases and 204 ethnically matched healthy B27-positive controls, and 96 southern German AS cases, 58 B27-positive and 251 B27-negative ethnically matched controls. Additionally, the TNF -376 polymorphism was genotyped in the southern German cases and controls. In the southern German AS patients a significant reduction in TNF -308.2 alleles was seen, compared with B27 positive controls (odds ratio 0.4, P = 0.03, 95% confidence interval 0.2-0.9), but no difference in allele frequencies was observed at TNF -238. Significant association between AS and both TNF -238 and TNF -308 was excluded in the English cases. These results confirm previous observations in the southern German population of association between TNF promoter region polymorphisms and AS, but the lack of association in the English population suggests that these polymorphisms themselves are unlikely to be directly involved. More likely, a second, non-HLA-B, MHC locus is involved in susceptibility to AS in these two populations.
本研究的目的是调查肿瘤坏死因子(TNF)启动子区域多态性与强直性脊柱炎(AS)易感性之间的关联。对306例英国AS患者以及204例种族匹配的健康B27阳性对照进行了TNF -238和 -308多态性基因分型,同时对96例德国南部AS患者、58例B27阳性和251例种族匹配的B27阴性对照进行了基因分型。此外,还对德国南部的患者和对照进行了TNF -376多态性基因分型。在德国南部的AS患者中,与B27阳性对照相比,TNF -308.2等位基因显著减少(优势比0.4,P = 0.03,95%置信区间0.2 - 0.9),但在TNF -238处未观察到等位基因频率的差异。在英国患者中排除了AS与TNF -238和TNF -308之间的显著关联。这些结果证实了先前在德国南部人群中观察到的TNF启动子区域多态性与AS之间的关联,但英国人群中缺乏关联表明这些多态性本身不太可能直接起作用。更有可能的是,在这两个人群中,第二个非HLA - B的主要组织相容性复合体(MHC)位点与AS易感性有关。