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谷胱甘肽S-转移酶的基因多态性与类风湿关节炎的疾病活动度

Genetic polymorphisms of glutathione S-transferases and disease activity of rheumatoid arthritis.

作者信息

Bohanec Grabar P, Logar D, Tomsic M, Rozman B, Dolzan V

机构信息

Institute of Biochemistry, Faculty of Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.

出版信息

Clin Exp Rheumatol. 2009 Mar-Apr;27(2):229-36.

Abstract

OBJECTIVES

Glutathione S-transferases (GST); GST-mu1 (GSTM1), GST-pi1 (GSTP1) and GST-theta1 (GSTT1) have peroxidase activity towards cytotoxic metabolites produced in inflammatory reactions, the main feature of rheumatoid arthritis (RA). Genetic polymorphisms in GSTM1, GSTP1 and GSTT1 modify the enzyme conjugation capacity and may be associated with the activity of RA.

METHODS

A genotyping approach was used to analyze GSTM1-0, GSTT1-0 and GSTP1 Ile105Val and Ala114Val polymorphisms in 213 RA patients. Disease activity was assessed by the disease activity score of 28 joint counts (DAS28) twice for each patient and mean DAS28 values were calculated.

RESULTS

The patients with GSTT1-0 genotype had a higher risk for developing high activity RA than the patients with GSTT1 genes present (p=0.028, OR=2.761, 95% CI=1.114-6.843). An interaction between the GSTT1 polymorphism and smoking was observed. In the group of smokers, the carriers of a homozygous deletion GSTT1 had an 8.5-fold higher risk for developing high disease activity than the patients with the GSTT1-1 genotype (p=0.004, OR=8.640, 95% CI=1.995-37.426). GSTM1 and GSTP1 polymorphisms were not associated with the disease activity.

CONCLUSION

Our results suggest that the presence of the GSTT1-0 genotype contributed to higher disease activity in RA patients. The risk for developing highly active RA was the highest in smokers with the GSTT1-0 genotype.

摘要

目的

谷胱甘肽S-转移酶(GST);GST-μ1(GSTM1)、GST-π1(GSTP1)和GST-θ1(GSTT1)对炎症反应中产生的细胞毒性代谢产物具有过氧化物酶活性,这是类风湿性关节炎(RA)的主要特征。GSTM1、GSTP1和GSTT1中的基因多态性会改变酶的结合能力,可能与RA的活动有关。

方法

采用基因分型方法分析213例RA患者的GSTM1-0、GSTT1-0以及GSTP1 Ile105Val和Ala114Val多态性。每位患者通过28个关节计数的疾病活动评分(DAS28)评估疾病活动度两次,并计算平均DAS28值。

结果

与存在GSTT1基因的患者相比,GSTT1-0基因型的患者发生高活动度RA的风险更高(p = 0.028,OR = )。观察到GSTT1多态性与吸烟之间存在相互作用。在吸烟组中,纯合缺失GSTT1的携带者发生高疾病活动度的风险比GSTT1-1基因型的患者高8.5倍(p = 0.004,OR = 8.640,95% CI = 1.995 - 37.426)。GSTM1和GSTP1多态性与疾病活动度无关。

结论

我们的结果表明,GSTT1-0基因型的存在导致RA患者疾病活动度更高。GSTT1-0基因型的吸烟者发生高活性RA的风险最高。

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