Explorer Alzheimer ' s disease susceptibility genes APOE and TOMM 40 , and brain white matter integrity in the Lothian Birth Cohort 1936

Abstract

Apolipoprotein E (APOE) ε genotype has previously been significantly associated with cognitive, brain imaging, and Alzheimer’s disease-related phenotypes (e.g., age of onset). In the TOMM40 gene, the rs10524523 (“523”) variable length poly-T repeat polymorphism has more recently been associated with similar ph/enotypes, although the allelic directions of these associations have varied between initial reports. Using diffusion magnetic resonance imaging tractography, the present study aimed to investigate whether there are independent effects of apolipoprotein E (APOE) and TOMM40 genotypes on human brain white matter integrity in a community-dwelling sample of older adults, the Lothian Birth Cohort 1936 (mean age1⁄4 72.70 years, standard deviation1⁄4 0.74, N approximately1⁄4 640e650; formost analyses). Some nominally significant effects were observed (i.e., covariate-adjusted differences between genotype groups at p < 0.05). For APOE, deleterious effects of ε4 “risk” allele presence (vs. absence) were found in the right ventral cingulum and left inferior longitudinal fasciculus. To test for biologically independent effects of the TOMM40 523 repeat, participants were stratified into APOE genotype subgroups, so that any significant effects could not be attributed to APOE variation. In participants with the APOE ε3/ε4 genotype, effects of TOMM40 523 status were found in the left uncinate fasciculus, left rostral cingulum, left ventral cingulum, and a general factor of white matter integrity. In all 4 of these tractography measures, carriers of the TOMM40523 “short” allele showed lowerwhitematter integritywhen comparedwith carriers of the “long” and “very-long” alleles. Most of these effects survived correction for childhood intelligence test scores and vascular disease history, though only the effect of TOMM40 523 on the left ventral cingulum integrity survived correction for false discovery rate. The effects of APOE in this older population are more specific and restricted compared with those reported in previous studies, and the effects of TOMM40 on white matter integrity appear to be novel, although replication is required in large independent samples. 2014 The Authors. Published by Elsevier Inc. All rights reserved.

2 Figures and Tables

Cite this paper

@inproceedings{Lyall2017ExplorerA, title={Explorer Alzheimer ' s disease susceptibility genes APOE and TOMM 40 , and brain white matter integrity in the Lothian Birth Cohort 1936}, author={Donald M. Lyall and Sarah Harris and Mark E. Bastin and Susana Mu{\~n}oz Maniega and Catherine M. Murray and Michael W Lutz and Ann M Saunders and A. D. Roses and Maria del C. Vald{\'e}s Hern{\'a}ndez and Natalie A. Royle and John M. Starr and David. J. Porteous and Joanna M. Wardlaw and Ian J. Deary}, year={2017} }