Evidence for Non‐additive Influence of Single Nucleotide Polymorphisms within the Apolipoprotein E Gene

• Published in: Annals of Human Genetics
• Main Authors: Hamon, S. C., Stengard, J. H., Clark, A. G., Salomaa, V., Boerwinkle, E., Sing, C. F.
• Format: Article in Journal/Newspaper
• Language: English
• Published: Wiley 2004
• Subjects: karelia*
• Online Access: http://dx.doi.org/10.1046/j.1529-8817.2003.00112.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1529-8817.2003.00112.x; https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1529-8817.2003.00112.x

Summary We analyzed 13 single nucleotide polymorphisms (SNPs) within the apolipoprotein E ( APOE ) gene, to identify pairs of SNPs that interact in a non‐additive manner to influence genotypic mean levels of the ApoE protein in blood. An overparameterized general linear model of two‐SNP genotype means was applied to data from 456 female and 398 male unrelated European Americans from Rochester, MN, USA. We found statistically significant evidence for non‐additivity between SNPs within the male sample, but not within the female sample. We observed nine pairs of SNPs with evidence of non‐additivity at the α= 0.05 level of statistical significance within the male sample, when approximately three were expected by chance. Five of the nine pairs involved three SNPs (560, 624 and 1163) that did not have a statistically significant influence when considered separately in a single‐site analysis. Three of the nine pairs involving four SNPs (832, 1998, 3937 and 4951) showed significant evidence for non‐additivity in at least one of two other male samples from Jackson, MS, USA and North Karelia, Finland. Although all four of these SNPs had a statistically significant influence in Rochester when considered separately, only SNP 3937 gave a significant result in the other male samples. The four SNPs are located in the promoter, intronic and exonic regions, and 3' to the polyadenylation signal in the APOE gene. Our study suggests that analyses that only consider SNPs located in exons and ignore contexts such as those indexed by gender and population, and disregard non‐additivity of SNP effects, may inappropriately model the contribution of a gene to the genetic architecture of a trait that has a complex multifactorial etiology.