Yu S F, Cheng T T, Hsu Y H, Lai H M, Chen Y C, Chiu C K, Lin K M, Chang C, Chen C J, Kang H Y
Graduate Institute of Clinical Medical Sciences, Chang Gung University, 16F-4, No. 123-9, Ta-Pei Road, Niao-Sung Hsiang, 833, Kaohsiung Hsein, Taiwan.
Division of Rheumatology, Allergy and Immunology, Department of Internal Medicine, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, 123, Ta-Pei Road, Niao-Sung Hsiang, 833, Kaohsiung Hsein, Taiwan.
Clin Rheumatol. 2007 Dec;26(12):2051. doi: 10.1007/s10067-007-0616-z. Epub 2007 Apr 13.
We investigated the relationship between CAG and GGC repeat polymorphism of the androgen receptor (AR) gene and rheumatoid arthritis (RA) in female patients with different disease subtypes. This case-control study enrolled 215 women in three groups: RA patients refractory to standardized therapy (n = 51); RA patients at complete remission phase (n = 60); and healthy controls (n = 104). CAG and GGC repeat lengths were determined by automated fluorescence-based DNA fragment-sizing method. Demographic data, allele lengths, allele distribution, and zygosity status of CAG/GGC repeats were assessed for the three groups. Refractory RA patients tend to have a significantly younger onset age of RA and more elevated erythrocyte sedimentation rates than do remission RA patients. Mean and median values of CAG and GGC repeat lengths are similar in both RA and control patients. However, RA patients harboring any long CAG alleles with more than 23 repeats had an increased risk of a refractory course, whereas differences in risk were not observed between these patients and RA subtypes harboring any long GGC alleles with more than 16 repeats. In addition, the homozygous frequency of CAG but not GGC alleles was lower in refractory RA than in remission RA patients or in controls (p = 0.042). Neither CAG nor GGC repeat lengths had a significant relationship with rheumatoid factor reactivity. Our observations indicate that short CAG repeats of the AR gene with higher transactivation activity may have protective effects against refractory course of RA development and that homozygous frequency of CAG alleles may be involved in the disease remission subtype. In contrast, lack of association of GGC polymorphism and RA was also observed. Together, these data imply that CAG but not GGC alleles in the AR polymorphism may play an important role in modulating the disease pattern of RA among Taiwanese women.
我们研究了雄激素受体(AR)基因的CAG和GGC重复多态性与不同疾病亚型女性类风湿关节炎(RA)患者之间的关系。这项病例对照研究纳入了215名女性,分为三组:标准化治疗难治的RA患者(n = 51);完全缓解期的RA患者(n = 60);以及健康对照者(n = 104)。通过基于自动荧光的DNA片段大小测定法确定CAG和GGC重复长度。评估了三组的人口统计学数据、等位基因长度、等位基因分布以及CAG/GGC重复的纯合状态。难治性RA患者的RA发病年龄往往明显比缓解期RA患者更小,红细胞沉降率更高。RA患者和对照患者中CAG和GGC重复长度的平均值和中位数相似。然而,携带任何CAG重复次数超过23次的长CAG等位基因的RA患者出现难治病程的风险增加,而携带任何GGC重复次数超过16次的长GGC等位基因的患者与这些患者之间未观察到风险差异。此外,难治性RA患者中CAG等位基因的纯合频率低于缓解期RA患者或对照者(p = 0.042),而GGC等位基因并非如此。CAG和GGC重复长度与类风湿因子反应性均无显著关系。我们的观察结果表明,具有较高转录激活活性的AR基因的短CAG重复可能对RA发展的难治病程具有保护作用,并且CAG等位基因的纯合频率可能与疾病缓解亚型有关。相比之下,也观察到GGC多态性与RA缺乏关联。总之,这些数据表明AR多态性中的CAG而非GGC等位基因可能在调节台湾女性RA的疾病模式中起重要作用。