INTERLEUKIN-10 (IL-10) PROMOTER POLYMORPHISM AT POSITION -1082 IN BULGARIAN PATIENTS WITH MULTIPLE SCLEROSIS

被引:2
|
作者
Grigorov, Boncho G. [1 ]
Trenova, Anastasiya G. [2 ]
Slavov, Georgi S. [2 ]
Miteva, Lyuba D. [1 ]
Stanilova, Spaska A. [1 ]
机构
[1] Trakia Univ, Fac Med, Dept Mol Biol Immunol & Med Genet, 11 Armeiska St, Stara Zagora 6000, Bulgaria
[2] Med Univ Plovdiv, Fac Med, Dept Neurol, 15A,V Aprilov St, Plovdiv 4000, Bulgaria
来源
关键词
rs1800896; disease onset; RRMS; SNP; cytokine; IL10; GENE; ASSOCIATION;
D O I
10.7546/CRABS.2019.01.11
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The role of promoter polymorphism within IL10 (rs1800896) in multiple sclerosis (MS) is not well established. The aim of this study was to investigate the association between -1082A/G polymorphism in interleukin-10 and genetic predisposition to MS development and onset of disease in Bulgarian patients. A group of 159 patients with relapsing remitting MS (RRMS) and 221 age-sex-matched controls were genotyped by amplification refractory mutation system (ARMS)-PCR. Our results demonstrated statistically significant elevation of the AA-genotype frequency in RRMS cases, compared to controls (38.4% vs. 28.5% with OR = 1.561, 95% CI = 0.989 divided by 2.464, P = 0.043). In addition, AA-genotype was overrepresented in cases with late-onset of disease than controls (44% vs. 28.5% with OR = 1.971, 95% CI = 1.107 divided by 3.508, P = 0.013). We also found that the carrying of AG-genotype was associated with a 1.8 fold increase of risk for early-onset of RRMS. In conclusion, our present results indicate that AA-genotype of -1082 G/A SNP in IL10 (rs1800896) might be accepted as a risk factor for RRMS susceptibility in Bulgarian patients and could be associated with manifestation of disease after the age of 30 years.
引用
收藏
页码:84 / 91
页数:8
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