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Association of Cardiovascular Risk Factors with Cerebral Perfusion in Whites and African Americans
Lindsay R Clark1,2,3, Megan Zuelsdorff1,4, Derek Norton5
1Wisconsin Alzheimer's Disease Research Center, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Insights
Midlife cardiovascular risk factors, like high diastolic blood pressure, are linked to reduced brain blood flow, a potential Alzheimer's disease (AD) risk. This association was observed across racial groups, emphasizing the need for inclusive neuroimaging research.
Area of Science:
- Neuroscience
- Cardiovascular Medicine
- Public Health
Background:
- Midlife cardiovascular risk factors are associated with an increased risk of Alzheimer's disease (AD).
- African Americans experience disproportionately high rates of cardiovascular disease and dementia but are underrepresented in AD research.
- There is a lack of research-based guidance for targeting vascular risk factors in diverse populations to mitigate AD risk.
Purpose of the Study:
- To investigate the relationships between specific cardiovascular risk factors and cerebral perfusion in White and African American adults.
- To examine how these relationships are influenced by race and APOE genotype in individuals at risk for AD.
Main Methods:
- Utilized pseudo-continuous arterial spin labeling MRI on 397 cognitively unimpaired adults (330 White, 67 African American).
- Employed multiple linear regression models to assess independent associations between cardiovascular risk factors and mean cerebral perfusion.
- Conducted interaction and stratified analyses to evaluate the moderating roles of APOE genotype and race.
Main Results:
- After FDR adjustment, diastolic blood pressure was significantly associated with reduced mean cerebral perfusion.
- No significant associations were found between perfusion and tobacco use, triglycerides, waist-to-hip ratio, or a composite risk score.
- Without FDR adjustment, obesity, cholesterol, and fasting glucose also showed relationships with perfusion. Race and APOE genotype did not moderate these associations.
Conclusions:
- Higher diastolic blood pressure was a stronger predictor of lower cerebral perfusion compared to other cardiovascular risk factors.
- The observed relationship between diastolic blood pressure and perfusion did not differ by race or genetic risk for AD.
- Findings underscore the importance of including underrepresented groups in neuroimaging studies and investigating modifiable risk factors for cerebrovascular health and AD risk in these populations.
Background:
Midlife cardiovascular risk factors increase risk for Alzheimer's disease (AD). Despite disproportionately high cardiovascular disease and dementia rates, African Americans are under-represented in studies of AD risk and research-based guidance on targeting vascular risk factors is lacking.
Objective:
This study investigated relationships between specific cardiovascular risk factors and cerebral perfusion in White and African American adults enriched for AD risk.
Methods:
Participants included 397 cognitively unimpaired White (n = 330) and African American (n = 67) adults enrolled in the Wisconsin Alzheimer's Disease Research Center who underwent pseudo-continuous arterial spin labeling MRI. Multiple linear regression models examined independent relationships between cardiovascular risk factors and mean cerebral perfusion. Subsequent interaction and stratified models assessed the role for APOE genotype and race.
Results:
When risk factor p-values were FDR-adjusted, diastolic blood pressure was significantly associated with mean perfusion. Tobacco use, triglycerides, waist-to-hip ratio, and a composite risk score were not associated with perfusion. Without FDR adjustment, a relationship was also observed between perfusion and obesity, cholesterol, and fasting glucose. Neither APOE genotype nor race moderated relationships between risk factors and perfusion.
Conclusion:
Higher diastolic blood pressure predicted lower perfusion more strongly than other cardiovascular risk factors. This relationship did not vary by racial group or genetic risk for AD, although the African American sample had greater vascular risk burden and lower perfusion rates. Our findings highlight the need to prioritize inclusion of underrepresented groups in neuroimaging studies and to continue exploring the link between modifiable risk factors, cerebrovascular health, and AD risk in underrepresented populations.
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