Key result
Higher LE8 adherence is linked to ~124 days younger brain white matter per 10-point increase in non-APOE4 carriers.
Why the study?
The impact of Life's Essential 8 on brain ageing and its interactions with dementia genetic risk factors like APOE4 remain unclear.
Does higher adherence to Life's Essential 8 reduce white matter brain aging in adults?
Cross-Sectional (n=18,817)
Yes
Does higher adherence to Life's Essential 8 reduce white matter brain aging in adults?
Adherence to the AHA's Life's Essential 8 cardiovascular health metrics is associated with delayed white matter brain aging, providing broad benefits across different genetic risk profiles.
Answers are grounded in this paper and cite their sources.
Should not yet change practice; extends observational data on LE8 and brain aging to genetic subgroups.
BACKGROUND: The American Heart Association introduced Life's Essential 8 (LE8) to promote cardiovascular health and longevity. However, its impact on brain ageing and interactions with genetic risk factors of dementia, such as APOE4, remains unclear. This study investigates the relationship between LE8 and white matter brain ageing and evaluates the moderating effects of the APOE4 allele. METHODS: This cross-sectional study utilized data from the UK Biobank, including genetic, neuroimaging, and health-related data from touchscreen questionnaires, physical examinations, and biological samples. Participants were non-pregnant whites with LE8 variables, diffusion tensor imaging (DTI) data, and APOE4 genetic information available, excluding those with extreme white matter hyperintensities. Regional fractional anisotropy measures from DTI data were used to predict white matter brain age via random forest regression. The white matter brain age gap (BAG) was calculated by subtracting chronological age from predicted brain age. FINDINGS: The analysis included 18,817 participants (9430 women and 9387 men; mean age 55.45 years [SD: 7.46]). Higher LE8 scores were associated with a lower white matter BAG, indicating delayed brain ageing. The effect was more pronounced in non-APOE4 carriers (124 days younger per 10-point increase, 95% CI: 102-146 days; p < 0.001) compared to APOE4 carriers (84 days younger per 10-point increase, 95% CI: 47-120 days; p < 0.001). Potential interaction between APOE4 and LE8 on brain ageing was observed for some age and sex groups but with only borderline significance, further investigation in larger and more targeted studies is needed to validate the finding. INTERPRETATION: Adherence to LE8 is associated with delayed brain ageing, with genetic factors such as APOE4 potentially moderating this effect in specific age and sex groups. The overall benefit from a healthier lifestyle in individuals' brain ageing across genetic, sex, and age groups underscore the importance and broad applicability of behavioural lifestyle interventions in promoting brain health.
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Feng et al. (2025) conducted a cross-sectional in Brain aging (n=18,817). Life's Essential 8 (LE8) score vs. Lower LE8 score was evaluated on White matter brain age gap (BAG) (124 days younger per 10-point increase (in non-APOE4 carriers), 95% CI 102-146, p=<0.001). Higher adherence to Life's Essential 8 was associated with delayed white matter brain aging, with the protective effect being more pronounced in non-APOE4 carriers (124 days younger per 10-point increase) compared to APOE4 carriers.
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