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肿瘤坏死因子α 5'侧翼区多态性与HLA - DRB1联合作用对类风湿关节炎患者放射学进展的影响

Combining effects of polymorphism of tumor necrosis factor alpha 5'-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis.

作者信息

Ichikawa Naomi, Kotake Shigeru, Hakoda Masayuki, Higami Kenshi, Kawasaki Aya, Furuya Takefumi, Nanke Yuki, Tsuchiya Naoyuki, Tokunaga Katsushi, Kamatani Naoyuki

机构信息

Institute of Rheumatology, Tokyo Women's Medical University, 10-22 Kawada-cho, Shinjuku-ku, Tokyo 162-0054, Japan.

出版信息

Mod Rheumatol. 2009;19(2):134-9. doi: 10.1007/s10165-008-0134-0. Epub 2008 Nov 12.

Abstract

We examined whether polymorphisms upstream of the TNF-alpha gene (TNFA) were associated with the radiological progression of rheumatoid arthritis (RA). One hundred and twenty-three patients with early RA (disease duration <1 year) were enrolled in a prospective follow-up study. The laboratory findings (ESR, CRP, and RF) were evaluated every 2 months for 2 years. Radiological progression in hands/wrists and feet was evaluated every 6 months for 2 years using Larsen's score. HLA-DRB1 genotype was determined by PCR-RFLP method. The genotypes for -1031, -863, and -857 single-nucleotide polymorphisms in the upstream 5'-flanking region of TNFA were determined by a PCR-preferential homoduplex formation assay in patients with RA and 265 healthy controls. Four TNFA alleles (U01, U02, U03, and U04) were identified. The frequency of individuals with U02 was significantly higher in patients than in controls (P = 0.0025). Radiographs of hands/wrists/feet were available for 72 patients after 1 year and for 73 patients after 2 years. When the HLA-DRB1 genotype was analyzed simultaneously, patients possessing U02 without an HLA-DRB1 shared epitope (SE) (U02+SE-) showed the lowest progression of Larsen's score (12 months). There was no difference in the level of ESR, CRP, or RF at the first visit among U02+SE+, U02+SE-, U02-SE+, and U02-SE- groups. The combination of the polymorphism of the TNFA upstream promoter region and HLA-DRB1 allele was associated with radiological progression in the early stage of RA.

摘要

我们研究了肿瘤坏死因子-α基因(TNFA)上游的多态性是否与类风湿关节炎(RA)的放射学进展相关。123例早期RA患者(病程<1年)被纳入一项前瞻性随访研究。在2年时间里,每2个月评估一次实验室检查结果(血沉、C反应蛋白和类风湿因子)。使用Larsen评分,每6个月评估一次双手/腕关节和足部的放射学进展情况,为期2年。通过聚合酶链反应-限制性片段长度多态性方法确定HLA-DRB1基因型。采用聚合酶链反应-优先同源双链体形成分析法,对RA患者和265名健康对照者TNFA基因5'-侧翼上游区域的-1031、-863和-857单核苷酸多态性进行基因分型。鉴定出4个TNFA等位基因(U01、U02、U03和U04)。患者中携带U02的个体频率显著高于对照组(P = 0.0025)。1年后72例患者、2年后73例患者有双手/腕关节/足部的X线片。同时分析HLA-DRB1基因型时,携带U02但无HLA-DRB1共享表位(SE)(U02+SE-)的患者Larsen评分进展最低(12个月)。U02+SE+、U02+SE-、U02-SE+和U02-SE-组在首次就诊时血沉、C反应蛋白或类风湿因子水平无差异。TNFA上游启动子区域多态性与HLA-DRB1等位基因的组合与RA早期的放射学进展相关。

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