The Research Base of TCM Syndrom, Fujian University of Traditional Chinese Medicine, Huatuo Road No.1, Fuzhou 350108, PR China.
Arthritis Res Ther. 2011 Jan 31;13(1):R11. doi: 10.1186/ar3232.
Cytochrome P-450 2E1 (CYP2E1) is an important member of the CYP superfamily, which is involved in the metabolism and activation of many low molecular weight toxic compounds. We tried to investigate the possible association of CYP2E1 tag single nucleotide polymorphisms (SNPs) with susceptibility to systemic lupus erythematosus (SLE) in a Chinese Han population.
The coding and flanking regions of the CYP2E1 gene were scanned for polymorphisms and tag SNPs were selected. A two-stage case-control study was performed to genotype a total of 876 SLE patients and 680 geographically matched healthy controls (265 cases and 288 controls in stage I and 611 cases and 392 controls in stage II). SLE associations of alleles, genotypes and haplotypes were tested by age and sex adjusted logistic regression. The gene transcription quantitation was carried out for peripheral blood mononuclear cell (PBMC) samples from 120 healthy controls.
Tag SNP rs2480256 was found significantly associated with SLE in both stages of the study. The "A" allele was associated with slightly higher risk (odds ratio (OR) = 1.165, 95% confidence interval (CI) 1.073 to 1.265, P = 2.75E-4) and "A/A" genotype carriers were with even higher SLE risk (OR = 1.464 95% CI 1.259 to 1.702, P = 7.48E-7). When combined with another tag SNP rs8192772, we identified haplotype "rs8192772-rs2480256/TA" over presented in SLE patients (OR 1.407, 95% CI 1.182 to 1.675, P = 0.0001) and haplotype "TG" over presented in the controls (OR 0.771, 95% CI 0.667 to 0.890, P = 0.0004). The gene transcription quantitation analysis further proved the dominant effect of rs2480256 as the "A/A" genotype showed highest transcription.
Our results suggest the involvement of CYP2E1 as a susceptibility gene for SLE in the Chinese population.
细胞色素 P-450 2E1(CYP2E1)是细胞色素 P450 超家族的重要成员,参与许多低分子量有毒化合物的代谢和激活。我们试图在中国汉族人群中研究 CYP2E1 标签单核苷酸多态性(SNP)与系统性红斑狼疮(SLE)易感性的可能关联。
扫描 CYP2E1 基因的编码和侧翼区域以寻找多态性,并选择标签 SNP。进行了两阶段病例对照研究,对总共 876 例 SLE 患者和 680 名地理匹配的健康对照者(I 期 265 例和 288 例,II 期 611 例和 392 例)进行基因分型。通过年龄和性别调整的逻辑回归检验等位基因、基因型和单倍型与 SLE 的关联。对 120 名健康对照者的外周血单核细胞(PBMC)样本进行基因转录定量。
在研究的两个阶段,发现标签 SNP rs2480256 与 SLE 显著相关。“A”等位基因与稍高的风险相关(比值比(OR)=1.165,95%置信区间(CI)1.073 至 1.265,P=2.75E-4),“A/A”基因型携带者的 SLE 风险甚至更高(OR=1.464,95%CI 1.259 至 1.702,P=7.48E-7)。当与另一个标签 SNP rs8192772 结合时,我们鉴定出 SLE 患者中出现频率较高的单体型“rs8192772-rs2480256/TA”(OR=1.407,95%CI 1.182 至 1.675,P=0.0001)和对照组中出现频率较高的单体型“TG”(OR=0.771,95%CI 0.667 至 0.890,P=0.0004)。基因转录定量分析进一步证明了 rs2480256 的显性作用,因为“AA”基因型表现出最高的转录。
我们的结果表明 CYP2E1 作为 SLE 的易感基因在中国人群中发挥作用。