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Cardiovascular Health at Midlife and Alzheimer Disease Biomarkers
Christina S Dintica1, Xiaqing Jiang1, Leslie M Shaw2
1Department of Psychiatry and Behavioral Sciences, University of California San Francisco, San Francisco, CA, USA.
Insights
Poor cardiovascular health in midlife is linked to early Alzheimer's disease (AD) biomarkers. This includes amyloid burden and brain changes, highlighting the importance of heart health for cognitive function.
Area of Science:
- Neuroscience
- Cardiovascular Health
- Aging Research
Background:
- Cardiovascular health is linked to cognitive decline and Alzheimer's disease (AD) risk, primarily studied in older adults.
- Research has focused less on midlife vascular and lifestyle factors' impact on early AD biomarkers.
Purpose of the Study:
- To investigate the association between midlife cardiovascular health and early AD plasma and imaging biomarkers.
- To determine if vascular and lifestyle factors in early midlife predict AD pathology in late midlife.
Main Methods:
- Utilized data from 1,406 participants in the Coronary Artery Risk Development in Young Adults (CARDIA) study.
- Assessed cardiovascular health using the American Heart Association's "life's essential 8" (LE8) guidelines in early midlife.
- Measured AD biomarkers including plasma phosphorylated tau 217 (ptau-217), amyloid beta 42/40 ratio (Aβ42/40), and brain atrophy patterns (SPARE-AD) in late midlife using linear regression.
Main Results:
- Poor and intermediate cardiovascular health (LE8 scores) were associated with a lower Aβ42/40 ratio compared to ideal LE8.
- No significant association was found between LE8 group and ptau-217 levels.
- Poor cardiovascular health was linked to a higher SPARE-AD atrophy pattern, indicating greater AD-like brain changes.
Conclusions:
- Suboptimal cardiovascular health in midlife, assessed by AHA LE8, is associated with less favorable early Alzheimer's disease biomarker profiles.
- Findings suggest that poor cardiovascular health may contribute to increased amyloid burden and structural brain changes indicative of AD.
- Midlife cardiovascular health is a critical factor influencing AD pathology development.
Background:
Cardiovascular health factors are associated with cognitive decline and risk of dementia, including Alzheimer disease (AD); however, this has been mostly studied in late life. We investigated whether vascular and lifestyle factors are associated with AD plasma and imaging biomarkers in midlife.
Methods:
We investigated 1,406 participants from the Coronary Artery Risk Development in Young Adults (CARDIA) study with information on vascular and lifestyle factors framed from the American Heart Association (AHA) "life's essential 8" (LE8) guidelines for cardiovascular health at early midlife (mean age 45.0 ± SD 3.6) and AD biomarkers in late midlife (mean age 60 ± SD 3.5). LE8 was calculated and categorized into poor (0-49), intermediate (50-79), and ideal (80-100) cardiovascular health, based on 8 components including smoking, diet, body mass index (BMI), sleep, fasting glucose, blood pressure, cholesterol, and physical activity. We assessed the AD plasma biomarkers phosphorylated tau 217 (ptau-217) and amyloid beta 42/40 ratio (Aβ42/40) and the Spatial Pattern of Abnormality for Recognition of Early AD (SPARE-AD), an algorithm that characterizes AD-like brain atrophy on brain MRI. We used linear regression to examine the association between LE8 and log transformed and standardized AD biomarker measures adjusting for age, sex, race, education, and kidney function.
Results:
Compared to ideal LE8, intermediate (67.9% of participants) and poor (12.6%) LE8 was associated with lower Αβ42/40 (adjusted mean difference: -2.37, 95% CI: -2.38 to -2.36 and -2.38, 95% CI: -2.40 to -2.36, respectively). There was no association between the LE8 group and ptau-217 level. Moreover, compared to ideal LE8 participants, those with poor LE8 had higher SPARE-AD atrophy pattern (adjusted mean difference: -0.71, 95% CI: -0.81 to -0.62).
Conclusion:
These findings indicate that poor cardiovascular health in midlife, as defined by the AHA LE8, is linked to less favorable early AD biomarker profiles, particularly reflecting greater amyloid burden and structural brain changes.
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