This study reinforces the independent effect of APOE ε4 on longitudinal brain atrophy, and provides no evidence this varies by APOE ε4 genotype.
Abstract
The associations of modifiable daily lifestyle variables (e.g., smoking, diet, alcohol intake, sedentary behavior, and physical activity) with structural brain atrophy, and interaction with apolipoprotein E (APOE) ε4 genetic risk, remain unclear.
The association between CVH and MCI and dementia was stronger among individuals with low or moderate genetic risk and appeared attenuated among those with high genetic risk.
Xiu Wu, Y. Zu, You Lu et al.· Diabetes Care· 0 citations
BAG is a reliable non-invasive marker of structural brain health sensitive to AD pathology and to modifiable AD risk and supports its relevance for early risk stratification and prevention-oriented research.
E. Kuhn, G. Antopoulos, L. Kleineidam et al.· medRxiv· 0 citations
Attenuated associations in older-old adults may reflect survivor bias, while stronger associations in APOE ε4 carriers are consistent with gene-environment interactions, which are consistent with gene-environment interactions.
Yang Kong, Xian Li, Rui-Qian Guan et al.· Alzheimer Disease and Associ...· 0 citations
Background The association between apolipoprotein E (APOE) ε4 and cerebral small vessel disease (CSVD) remains incompletely understood, with inconsistent evidence across imaging phenotypes and limited investigation into gene–environment interactions. Method This cross-sectional study included 728 patients with chronic...
Feng Liu, Yulan Gou· Frontiers in Neurology· 0 citations
This study demonstrates that structural brain ageing among cognitively normal adults follows highly heterogeneous trajectories, spanning from marked decline to near-complete resistance, and Modifiable lifestyle and vascular risk factors were associated with faster atrophy, supporting opportunities for risk stratificati...
Shohei Fujita, Susumu Mori, Kengo Onda et al.· Brain Communications· 0 citations
In this Indian cohort, APOE ε4 homozygosity reflects increased susceptibility and familial aggregation of AD but does not confer a more severe or distinct phenotype, suggesting ancestry- specific expression of APOE ε4 gene-dose effects.
Pratibha Vinod, C. Arampady, Somdatta Sen et al.· Neurodegenerative Disease Ma...· 0 citations
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