Genetic polymorphisms modifying oxidative stress are associated with disease activity in rheumatoid arthritis patients

被引:31
作者
Grabar, Petra Bohanec [1 ]
Logar, Dusan [2 ]
Tomsic, Matija [2 ]
Rozman, Blaz [2 ]
Dolzan, Vita [1 ]
机构
[1] Univ Ljubljana, Fac Med, Inst Biochem, Ljubljana 1000, Slovenia
[2] Univ Med Ctr Ljubljana, Dept Rheumatol, Ljubljana, Slovenia
关键词
Reactive oxygen species; rheumatoid arthritis; genetic polymorphism; disease activity; TUMOR-NECROSIS-FACTOR; MANGANESE SUPEROXIDE-DISMUTASE; FACTOR-ALPHA GENE; NITRIC-OXIDE; TNF-ALPHA; PROMOTER POLYMORPHISM; SHARED EPITOPE; SEVERITY; CATALASE; GENOTYPE;
D O I
10.3233/DMA-2009-0603
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Reactive oxygen and nitrogen species are involved in the pathology of rheumatoid arthritis (RA). Polymorphisms in genes coding for superoxide dismutases (SOD2 and SOD3), catalase (CAT), tumor necrosis factor-alpha (TNFA) and inducible NO synthase (NOS2A) may influence RA activity. We determined SOD2 Ala-9Val, SOD3 Arg213Gly, CAT C-262T, TNFA G-308A, TNFA C-857T and NOS2A (CCTTT)(n) polymorphisms in 327 RA patients. Carriers of CAT -262T and TNFA -308A allele had lower mean disease activity score of 28 joint count (DAS28) values than patients with CAT -262CC and TNFA -308GG genotypes (p = 0.014 and p = 0.046, respectively). Patients with the combination of CAT -262T and TNFA -308A allele had lower mean DAS28 values and a higher probability for low disease activity than non-carriers (p = 0.003, OR = 3.585, 95% CI = 1.538-8.357). Our results suggest that CAT and TNFA polymorphisms alone and in combination influence the activity of RA.
引用
收藏
页码:41 / 48
页数:8
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