Yun Bo Ra, El-Sohemy Ahmed, Cornelis Marilyn C, Bae Sang-Cheol
Department of Internal Medicine, Division of Rheumatology, and the Hospital for Rheumatic Diseases, Hanyang University, Seoul, Korea.
J Rheumatol. 2005 Jun;32(6):992-7.
To determine the effects of genetic polymorphisms of glutathione S-transferase (GST) M1, GSTT1, and GSTP on risk and severity of rheumatoid arthritis (RA) in a Korean population.
A total of 258 patients with RA and 400 disease-free controls were enrolled. GST genotypes were determined by RFLP-PCR. HLA-DRB 1 typing and further subtyping of all alleles was performed using sequence-specific oligonucleotide probe hybridization after PCR. Severity of RA among cases was assessed by Steinbrocker anatomical stage. Risk was assessed by calculating the age and sex adjusted odds ratio (OR) and 95% confidence intervals (CI).
The OR for risk of RA with the GSTM1-null genotype was 1.40 (95% CI 1.02- 1.92, p = 0.04), and 1.86 (95% CI 1.12- 3.09, p = 0.005) among individuals without the shared epitope (SE). Among patients with RA, the OR for risk of severe RA for the GSTM1-null genotype was 2.45 (95% CI 1.04- 5.77, p = 0.02). No association was observed between the GSTT1 or GSTP1 genotypes and either risk or severity of RA.
These results suggest that the deletion polymorphism of GSTM1 is associated with increased susceptibility for RA, particularly among individuals who are not carriers of the HLA-DRB 1 SE.
确定谷胱甘肽S-转移酶(GST)M1、GSTT1和GSTP的基因多态性对韩国人群类风湿关节炎(RA)风险及严重程度的影响。
共纳入258例RA患者和400例无病对照。通过限制性片段长度多态性聚合酶链反应(RFLP-PCR)确定GST基因型。PCR后,使用序列特异性寡核苷酸探针杂交进行HLA-DRB1分型及所有等位基因的进一步亚型分析。采用斯坦布鲁克(Steinbrocker)解剖分期评估病例中RA的严重程度。通过计算年龄和性别校正比值比(OR)及95%置信区间(CI)评估风险。
GSTM1基因缺失型个体患RA的OR为1.40(95%CI 1.02 - 1.92,p = 0.04),在无共享表位(SE)的个体中为1.86(95%CI 1.12 - 3.09,p = 0.005)。在RA患者中,GSTM1基因缺失型患严重RA的OR为2.45(95%CI 1.04 - 5.77,p = 0.02)。未观察到GSTT1或GSTP1基因型与RA风险或严重程度之间存在关联。
这些结果表明,GSTM1的缺失多态性与RA易感性增加相关,尤其是在非HLA-DRB1 SE携带者中。