The Effects of rs405509 on APOE ε4 Non-carriers in Non-demented Aging

There is evidence that the T allele of rs405509 located in the apolipoprotein E ( ) promotor region is a risk factor for Alzheimer's disease (AD). However, the effect of the T/T allele on brain function in non-demented aging is still unclear. We analyzed the effects of the rs405509 T/T allele o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Frontiers in neuroscience 2021-06, Vol.15, p.677823-677823
Hauptverfasser: Wu, Dongpeng, Zhao, Han, Gu, Huali, Han, Bin, Wang, Qingqing, Man, Xu, Zhao, Renliang, Liu, Xuejun, Sun, Jinping
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:There is evidence that the T allele of rs405509 located in the apolipoprotein E ( ) promotor region is a risk factor for Alzheimer's disease (AD). However, the effect of the T/T allele on brain function in non-demented aging is still unclear. We analyzed the effects of the rs405509 T/T allele on cognitive performances using multiple neuropsychological tests and local brain function using resting-state functional magnetic resonance imaging (rs-fMRI). Significant differences were found between T/T carriers and G allele carriers on general cognitive status, memory, and attention ( < 0.05). Rs-fMRI analyses demonstrated decreased amplitude of low frequency fluctuation (ALFF) in the right middle frontal gyrus, decreased percent amplitude of fluctuation (PerAF) in the right middle frontal gyrus, increased regional homogeneity (ReHo) in the right cerebellar tonsil and decreased ReHo in the right putamen, and decreased degree centrality (DC) in the left middle frontal gyrus ( < 0.05, corrected). Furthermore, significant correlations were found between cognitive performance and these neuroimaging changes ( < 0.05). These findings suggest that T/T allele may serve as an independent risk factor that can influence brain function in different regions in non-demented aging.
ISSN:1662-4548
1662-453X
1662-453X
DOI:10.3389/fnins.2021.677823