Interplay between stress-related genes may influence Alzheimer's disease development: The results of genetic interaction analyses of human data.

Journal Article (Journal Article)

Emerging evidence from experimental and clinical research suggests that stress-related genes may play key roles in AD development. The fact that genome-wide association studies were not able to detect a contribution of such genes to AD indicates the possibility that these genes may influence AD non-linearly, through interactions of their products. In this paper, we selected two stress-related genes (GCN2/EIF2AK4 and APP) based on recent findings from experimental studies which suggest that the interplay between these genes might influence AD in humans. To test this hypothesis, we evaluated the effects of interactions between SNPs in these two genes on AD occurrence, using the Health and Retirement Study data on white indidividuals. We found several interacting SNP-pairs whose associations with AD remained statistically significant after correction for multiple testing. These findings emphasize the importance of nonlinear mechanisms of polygenic AD regulation that cannot be detected in traditional association studies. To estimate collective effects of multiple interacting SNP-pairs on AD, we constructed a new composite index, called Interaction Polygenic Risk Score, and showed that its association with AD is highly statistically significant. These results open a new avenue in the analyses of mechanisms of complex multigenic AD regulation.

Full Text

Duke Authors

Cited Authors

  • Yashin, AI; Wu, D; Arbeev, K; Bagley, O; Akushevich, I; Duan, M; Yashkin, A; Ukraintseva, S

Published Date

  • June 2021

Published In

Volume / Issue

  • 196 /

Start / End Page

  • 111477 -

PubMed ID

  • 33798591

Pubmed Central ID

  • PMC8173104

Electronic International Standard Serial Number (EISSN)

  • 1872-6216

International Standard Serial Number (ISSN)

  • 0047-6374

Digital Object Identifier (DOI)

  • 10.1016/j.mad.2021.111477

Language

  • eng