Open AccessEffects of APOE promoter polymorphism on the topological organization of brain structural connectome in nondemented elderly
Author(s) -
Shu Ni,
Li Xin,
Ma Chao,
Zhang Junying,
Chen Kewei,
Liang Ying,
Chen Yaojing,
Zhang Zhanjun
Publication year - 2015
Publication title -
human brain mapping
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.005
H-Index - 191
eISSN - 1097-0193
pISSN - 1065-9471
DOI - 10.1002/hbm.22954
Subject(s) - apolipoprotein e , neuroscience , connectome , allele , white matter , tractography , psychology , cognition , human connectome project , genotype , biology , genetics , disease , medicine , gene , functional connectivity , magnetic resonance imaging , radiology
The polymorphism of the Apolipoprotein E (APOE) promoter rs405509 can regulate the transcriptional activity of the APOE gene and is related to Alzheimer's disease (AD). However, its effects on cognitive performance and the underlying brain mechanisms remain unknown. Here, we performed a battery of neuropsychological tests in a large sample (837 subjects) of nondemented elderly Chinese people, and explored the related brain mechanisms via the construction of diffusion MRI‐based structural connectome and graph analysis from a subset (84 subjects) of the sample. Cognitively, the rs405509 risk allele (TT) carriers showed decreased attention and execution functions compared with noncarriers (GG/GT). Regarding the topological alterations of the brain connectome, the risk allele group exhibited reduced global and local efficiency of white matter structural networks, mainly in the left anterior and posterior cingulate cortices (PCC). Importantly, the efficiency of the left PCC is correlated with the impaired attention function and mediates the impacts of the rs405509 genotype on attention. These results demonstrated that the rs405509 polymorphism affects attention function in nondemented elderly people, possibly by modulating brain structural connectivity of the PCC. This polymorphism may help us to understand the neural mechanisms of cognitive aging and to serve as a potential marker assessing the risk of AD. Hum Brain Mapp 36:4847–4858, 2015 . © 2015 Wiley Periodicals, Inc .