Jacq Laurent, Garnier Sophie, Dieudé Philippe, Michou Laëtitia, Pierlot Céline, Migliorini Paola, Balsa Alejandro, Westhovens René, Barrera Pilar, Alves Helena, Vaz Carlos, Fernandes Manuela, Pascual-Salcedo Dora, Bombardieri Stefano, Dequeker Jan, Radstake Timothy R, Van Riel Piet, van de Putte Leo, Lopes-Vaz Antonio, Glikmans Elodie, Barbet Sandra, Lasbleiz Sandra, Lemaire Isabelle, Quillet Patrick, Hilliquin Pascal, Teixeira Vitor Hugo, Petit-Teixeira Elisabeth, Mbarek Hamdi, Prum Bernard, Bardin Thomas, Cornélis François
GenHotel-EA3886, Evry-Paris VII Universities, 91057 Evry-Genopole cedex, France.
Arthritis Res Ther. 2007;9(4):R63. doi: 10.1186/ar2221.
The integrin alpha(v)beta3, whose alpha(v) subunit is encoded by the ITGAV gene, plays a key role in angiogenesis. Hyperangiogenesis is involved in rheumatoid arthritis (RA) and the ITGAV gene is located in 2q31, one of the suggested RA susceptibility loci. Our aim was to test the ITGAV gene for association and linkage to RA in a family-based study from the European Caucasian population. Two single nucleotide polymorphisms were genotyped by PCR-restriction fragment length polymorphism in 100 French Caucasian RA trio families (one RA patient and both parents), 100 other French families and 265 European families available for replication. The genetic analyses for association and linkage were performed using the comparison of allelic frequencies (affected family-based controls), the transmission disequilibrium test, and the genotype relative risk.We observed a significant RA association for the C allele of rs3738919 in the first sample (affected family-based controls, RA index cases 66.5% versus controls 56.7%; P = 0.04). The second sample showed the same trend, and the third sample again showed a significant RA association. When all sets were combined, the association was confirmed (affected family-based controls, RA index cases 64.6% versus controls 58.1%; P = 0.005). The rs3738919-C allele was also linked to RA (transmission disequilibrium test, 56.5% versus 50% of transmission; P = 0.009) and the C-allele-containing genotype was more frequent in RA index cases than in controls (RA index cases 372 versus controls 339; P = 0.002, odds ratio = 1.94, 95% confidence interval = 1.3-2.9). The rs3738919-C allele of the ITGAV gene is associated with RA in the European Caucasian population, suggesting ITGAV as a new minor RA susceptibility gene.
整合素α(v)β3,其α(v)亚基由ITGAV基因编码,在血管生成中起关键作用。血管生成过度与类风湿性关节炎(RA)有关,且ITGAV基因位于2q31,这是一个提示的RA易感位点之一。我们的目的是在一项来自欧洲白种人群体的基于家系的研究中,检测ITGAV基因与RA的关联和连锁关系。通过聚合酶链反应-限制性片段长度多态性对两个单核苷酸多态性进行基因分型,样本包括100个法国白种人RA三联体家庭(一名RA患者及其父母双方)、100个其他法国家庭以及265个可用于重复验证的欧洲家庭。使用等位基因频率比较(基于患病家系的对照)、传递不平衡检验和基因型相对风险进行关联和连锁的遗传分析。我们在第一个样本中观察到rs3738919的C等位基因与RA存在显著关联(基于患病家系的对照,RA指数病例为66.5%,对照为56.7%;P = 0.04)。第二个样本呈现相同趋势,第三个样本再次显示出与RA的显著关联。当所有数据集合并时,该关联得到确认(基于患病家系的对照,RA指数病例为64.6%,对照为58.1%;P = 0.005)。rs3738919 - C等位基因也与RA连锁(传递不平衡检验,传递率为56.5%对50%;P = 0.009),且含C等位基因的基因型在RA指数病例中比在对照中更常见(RA指数病例372例,对照339例;P = 0.002,优势比 = 1.94,95%置信区间 = 1.3 - 2.9)。ITGAV基因的rs3738919 - C等位基因在欧洲白种人群体中与RA相关,提示ITGAV是一个新的RA小易感基因。