Teixeira Vitor Hugo, Jacq Laurent, Lasbleiz Sandra, Hilliquin Pascal, Oliveira Catarina Resende, Cornelis François, Petit-Teixeira Elisabeth
GenHotel-EA3886, Evry-Paris VII Universities, Evry-Genopole, France.
J Rheumatol. 2008 Oct;35(10):1912-8. Epub 2008 Sep 1.
To study the possible role of the caspase 7 (CASP7) gene in susceptibility to rheumatoid arthritis (RA) in a European Caucasian population.
CASP7 rs2227309 single nucleotide polymorphism (SNP) was genotyped in 197 French RA trio families and in 252 European RA families available for replication using Taqman allelic discrimination assay. Relative quantification of caspase 7 isoforms alpha and beta mRNA expression was performed from whole blood in 25 unrelated patients with RA and in 15 healthy controls by real-time quantitative reverse transcription-polymerase chain reaction. The genetic analyses for association and linkage were performed using the comparison of allelic frequencies, the transmission disequilibrium test, and the genotype relative risk.
We observed, in the first sample, a significant association of rs2227309-AA genotype with RA [p=0.03, odds ratio (OR) 2.11 (95% CI 1.0-4.6)]. The second sample did not show any significant association of the AA genotype with RA [p=0.6, OR 0.87 (95% CI 0.4-1.8)]. When the 2 samples were combined, no significant association of the AA genotype [p=0.3, OR 1.32 (95% CI 0.8-2.2)] was observed. CASP7 isoforms alpha and beta mRNA were expressed in patients with RA at lower level than in healthy controls (-89%, p=0.003 and -47%, p=0.01; respectively).
CASP7 rs2227309 SNP was not associated with RA in a European Caucasian population. Nevertheless, CASP7 isoforms alpha and beta could have an involvement in the apoptosis process in RA.
研究半胱天冬酶7(CASP7)基因在欧洲白种人群类风湿关节炎(RA)易感性中可能发挥的作用。
采用Taqman等位基因鉴别分析方法,对197个法国RA三联家庭以及252个可用于重复研究的欧洲RA家庭中的CASP7 rs2227309单核苷酸多态性(SNP)进行基因分型。通过实时定量逆转录-聚合酶链反应,对25例无亲缘关系的RA患者及15名健康对照者全血中的半胱天冬酶7亚型α和β mRNA表达进行相对定量分析。采用等位基因频率比较、传递不平衡检验及基因型相对风险等方法进行关联和连锁的遗传分析。
在第一个样本中,我们观察到rs2227309-AA基因型与RA存在显著关联[p = 0.03,优势比(OR)2.11(95%可信区间1.0 - 4.6)]。第二个样本未显示AA基因型与RA有任何显著关联[p = 0.6,OR 0.87(95%可信区间0.4 - 1.8)]。当将两个样本合并时,未观察到AA基因型有显著关联[p = 0.3,OR 1.32(95%可信区间0.8 - 2.2)]。RA患者中半胱天冬酶7亚型α和β mRNA的表达水平低于健康对照者(分别为-89%,p = 0.003和-47%,p = 0.01)。
在欧洲白种人群中,CASP7 rs2227309 SNP与RA无关联。然而,半胱天冬酶7亚型α和β可能参与了RA的凋亡过程。