Epidemiology, Institute of Public Health, University of Southern Denmark, Odense C, Denmark.
Aging Cell. 2013 Aug;12(4):690-4. doi: 10.1111/acel.12092. Epub 2013 May 15.
Genetic interactions or epistasis could make a substantial contribution to variation in human complex traits including longevity. However, detecting epistatic interactions in high dimensional datasets is difficult due to various reasons including multiple testing of correlated tests. We introduce a novel permutation strategy to the case-only analysis of gene-by-gene interaction using multiple SNPs. The method is applied to genes coding for Forkhead box O transcription factors which recently have been associated with human longevity across different populations hypothesizing that epistatic interaction in the regulation and expression of the FOXO gene family could contribute to the human longevity phenotype. Genotype data were collected from 1088 individuals from the Danish 1905 birth cohort aged over 92-93 years with 12 SNPs in the FOXO1a and 15 SNPs in the FOXO3a genes. Our analysis detected a joint effect between rs9486902 in FOXO3a and rs2701858 in FOXO1a that highly significantly contributes to human longevity (OR = 3.23, 95% CI: 2.93-3.53) which is consistent in both males and females. Our results were compared with published studies, and importance of our novel method and findings was discussed.
遗传相互作用或上位性可能对人类复杂特征(包括长寿)的变异性做出重大贡献。然而,由于多种原因,包括相关测试的多次测试,在高维数据集中检测上位性相互作用是困难的。我们为使用多个 SNP 的基因-基因相互作用的仅病例分析引入了一种新的置换策略。该方法应用于编码叉头框 O 转录因子的基因,这些基因最近在不同人群中与人类长寿相关,假设 FOXO 基因家族的调控和表达中的上位性相互作用可能有助于人类长寿表型。基因型数据来自丹麦 1905 年出生队列的 1088 名年龄在 92-93 岁以上的个体,FOXO1a 基因中有 12 个 SNP,FOXO3a 基因中有 15 个 SNP。我们的分析检测到 FOXO3a 中的 rs9486902 和 FOXO1a 中的 rs2701858 之间的联合效应,该效应高度显著地影响人类的长寿(OR=3.23,95%CI:2.93-3.53),在男性和女性中均一致。我们的结果与已发表的研究进行了比较,并讨论了我们新方法和发现的重要性。