National Institute of Rheumatology and Physiotherapy, Budapest, Hungary.
J Rheumatol. 2010 Feb;37(2):379-84. doi: 10.3899/jrheum.090806. Epub 2009 Dec 23.
Associations have been found between ankylosing spondylitis (AS) and polymorphisms in the aminopeptidase regulator of TNFR1 shedding (ARTS1) gene. We studied the association of 5 polymorphisms within the ARTS1 gene with AS in Hungarian patients. We also investigated the prevalence of HLA-B27 subtypes in the Hungarian population.
A case-control study including 297 patients with AS and 200 sex and ethnically matched healthy controls was performed. Patients and controls were genotyped for rs27044, rs17482078, rs10050860, rs30187, and rs2287987 single-nucleotide polymorphisms using real-time polymerase chain reaction (PCR) allelic discrimination. HLA-B27 subtypes were determined with PCR sequence-specific primer (PCR-SSP) technique.
We observed a significant increase in the minor allele frequency of rs27044 (p = 0.001) in the AS group compared to controls. The minor allele frequencies of rs10050860 (p = 0.006) and rs2287987 (p = 0.002) showed a significant decrease in AS patients compared to controls. Haplotype analysis revealed association of 2 ARTS1 haplotypes with AS in the Hungarian population. We found that HLA-B2705 was the predominant subtype in Hungarians with AS. Carriage of the G allele of rs27044 was significantly associated with the HLA-B2705 subtype (p = 0.009) in AS patients.
We confirmed reported associations of ARTS1 gene polymorphisms with AS in a Hungarian cohort study. We found HLA-B*2705 as the predominant subtype in Hungarian AS patients in accord with other studies on Caucasian populations. Our results suggest that the ARTS1 gene variants together with HLA-B27 strongly contribute to disease susceptibility in patients with AS.
已经发现,在氨基肽酶调节肿瘤坏死因子受体 1 脱落(ARTS1)基因的多态性与强直性脊柱炎(AS)之间存在关联。我们研究了 ARTS1 基因内的 5 个多态性与匈牙利患者 AS 的关联。我们还调查了匈牙利人群中 HLA-B27 亚型的患病率。
进行了一项病例对照研究,包括 297 例 AS 患者和 200 名性别和种族匹配的健康对照者。使用实时聚合酶链反应(PCR)等位基因鉴别法对 rs27044、rs17482078、rs10050860、rs30187 和 rs2287987 单核苷酸多态性进行基因分型。使用聚合酶链反应序列特异性引物(PCR-SSP)技术确定 HLA-B27 亚型。
与对照组相比,AS 组中 rs27044 的次要等位基因频率明显增加(p = 0.001)。与对照组相比,AS 患者的 rs10050860(p = 0.006)和 rs2287987(p = 0.002)的次要等位基因频率明显降低。在匈牙利人群中,ARTS1 单倍型分析显示与 AS 相关的 2 个 ARTS1 单倍型。我们发现,HLA-B2705 是匈牙利 AS 患者的主要亚型。在 AS 患者中,rs27044 的 G 等位基因的携带与 HLA-B2705 亚型显著相关(p = 0.009)。
我们在匈牙利队列研究中证实了报告的 ARTS1 基因多态性与 AS 之间的关联。我们发现 HLA-B*2705 是匈牙利 AS 患者的主要亚型,与其他关于白种人群的研究一致。我们的结果表明,ARTS1 基因变异与 HLA-B27 一起强烈导致 AS 患者的疾病易感性。