Human Genetics, Genome Institute of Singapore, 60 Biopolis Street, Singapore.
BMC Med Genet. 2012 Jan 13;13:5. doi: 10.1186/1471-2350-13-5.
There is reason to expect strong genetic influences on the risk of developing active pulmonary tuberculosis (TB) among latently infected individuals. Many of the genome wide linkage and association studies (GWAS) to date have been conducted on African populations. In order to identify additional targets in genetically dissimilar populations, and to enhance our understanding of this disease, we performed a multi-stage GWAS in a Southeast Asian cohort from Indonesia.
In stage 1, we used the Affymetrix 100 K SNP GeneChip marker set to genotype 259 Indonesian samples. After quality control filtering, 108 cases and 115 controls were analyzed for association of 95,207 SNPs. In stage 2, we attempted validation of 2,453 SNPs with promising associations from the first stage, in 1,189 individuals from the same Indonesian cohort, and finally in stage 3 we selected 251 SNPs from this stage to test TB association in an independent Caucasian cohort (n = 3,760) from Russia.
Our study suggests evidence of association (P = 0.0004-0.0067) for 8 independent loci (nominal significance P < 0.05), which are located within or near the following genes involved in immune signaling: JAG1, DYNLRB2, EBF1, TMEFF2, CCL17, HAUS6, PENK and TXNDC4.
Mechanisms of immune defense suggested by some of the identified genes exhibit biological plausibility and may suggest novel pathways involved in the host containment of infection with TB.
有理由预期潜伏性感染个体发生活动性肺结核(TB)的风险存在强烈的遗传影响。迄今为止,许多全基因组连锁和关联研究(GWAS)都是在非洲人群中进行的。为了在遗传上不同的人群中确定其他靶点,并增强我们对这种疾病的理解,我们在印度尼西亚的东南亚队列中进行了多阶段 GWAS。
在第 1 阶段,我们使用 Affymetrix 100 K SNP GeneChip 标记集对 259 名印度尼西亚样本进行基因分型。经过质量控制过滤后,对 108 例病例和 115 例对照进行了 95207 个 SNP 的关联分析。在第 2 阶段,我们试图在来自同一印度尼西亚队列的 1189 名个体中验证第 1 阶段中具有有希望关联的 2453 个 SNP,最后在第 3 阶段,我们从该阶段选择了 251 个 SNP 来测试在一个独立的高加索人群(n=3760)中与 TB 的关联来自俄罗斯。
我们的研究表明,8 个独立的基因座(名义显著性 P < 0.05)存在关联的证据(P=0.0004-0.0067),这些基因座位于或靠近参与免疫信号的以下基因内或附近:JAG1、DYNLRB2、EBF1、TMEFF2、CCL17、HAUS6、PENK 和 TXNDC4。
一些确定的基因所暗示的免疫防御机制具有生物学合理性,可能提示与宿主控制 TB 感染有关的新途径。