Department of Epidemiology and Statistics, Bengbu Medical College at Bengbu, Anhui, China.
PLoS Genet. 2010 Sep 23;6(9):e1001131. doi: 10.1371/journal.pgen.1001131.
Although great progress in genome-wide association studies (GWAS) has been made, the significant SNP associations identified by GWAS account for only a few percent of the genetic variance, leading many to question where and how we can find the missing heritability. There is increasing interest in genome-wide interaction analysis as a possible source of finding heritability unexplained by current GWAS. However, the existing statistics for testing interaction have low power for genome-wide interaction analysis. To meet challenges raised by genome-wide interactional analysis, we have developed a novel statistic for testing interaction between two loci (either linked or unlinked). The null distribution and the type I error rates of the new statistic for testing interaction are validated using simulations. Extensive power studies show that the developed statistic has much higher power to detect interaction than classical logistic regression. The results identified 44 and 211 pairs of SNPs showing significant evidence of interactions with FDR<0.001 and 0.001<FDR<0.003, respectively, which were seen in two independent studies of psoriasis. These included five interacting pairs of SNPs in genes LST1/NCR3, CXCR5/BCL9L, and GLS2, some of which were located in the target sites of miR-324-3p, miR-433, and miR-382, as well as 15 pairs of interacting SNPs that had nonsynonymous substitutions. Our results demonstrated that genome-wide interaction analysis is a valuable tool for finding remaining missing heritability unexplained by the current GWAS, and the developed novel statistic is able to search significant interaction between SNPs across the genome. Real data analysis showed that the results of genome-wide interaction analysis can be replicated in two independent studies.
尽管全基因组关联研究(GWAS)取得了重大进展,但 GWAS 确定的显著 SNP 关联仅占遗传变异的少数几个百分点,这使得许多人质疑我们在哪里以及如何找到缺失的遗传力。人们对全基因组相互作用分析越来越感兴趣,认为这可能是发现当前 GWAS 无法解释的遗传力的一种来源。然而,用于检测相互作用的现有统计数据在全基因组相互作用分析中功效较低。为了应对全基因组相互作用分析带来的挑战,我们开发了一种用于检测两个基因座(连锁或非连锁)之间相互作用的新统计方法。使用模拟验证了新的交互测试统计量的零分布和Ⅰ型错误率。广泛的功效研究表明,与经典的逻辑回归相比,开发的统计方法检测相互作用的功效要高得多。研究结果确定了 44 对和 211 对 SNP,它们与 FDR<0.001 和 0.001<FDR<0.003 之间存在显著的相互作用证据,这些 SNP 分别来自银屑病的两项独立研究。其中包括 LST1/NCR3、CXCR5/BCL9L 基因中 5 对相互作用的 SNP,其中一些 SNP 位于 miR-324-3p、miR-433 和 miR-382 的靶位点,以及 15 对具有非同义取代的相互作用 SNP。我们的研究结果表明,全基因组相互作用分析是发现当前 GWAS 无法解释的剩余遗传力缺失的一种有价值的工具,开发的新统计方法能够在整个基因组中搜索 SNP 之间的显著相互作用。真实数据分析表明,全基因组相互作用分析的结果可以在两项独立研究中得到复制。