Racial and ethnic differences in cardiometabolic predictors of white matter hyperintensities burden among males: The
Cellas A Hayes1, Raymond Jones2,3, Roland J Thorpe4,5
1Department of Epidemiology and Population Health, Stanford University School of Medicine, Palo Alto, CA, USA.
Insights
Cardiometabolic risk factors significantly impact white-matter hyperintensities (WMH) differently across racial and ethnic groups in males. Hispanic males show the highest vulnerability, highlighting the need for tailored interventions to reduce Alzheimer's disease risk.
Area of Science:
- Neuroscience
- Cardiology
- Public Health
Background:
- Cardiometabolic conditions accelerate white-matter hyperintensities (WMH), a marker of vascular injury linked to Alzheimer's disease risk.
- Understanding how these relationships vary by race and ethnicity in males is crucial for targeted health strategies.
Purpose of the Study:
- To investigate race and ethnicity-specific associations between cardiometabolic risk factors, blood pressure, and WMH volume in Non-Hispanic White (NHW), Non-Hispanic Black (NHB), and Hispanic males.
- To quantify the impact of various cardiometabolic exposures on brain health across diverse male populations.
Main Methods:
- Analysis of 1378 males from the Healthy Aging Brain Study-Health Disparities.
- Regression models used to assess five binary exposures (hypertension, diabetes, dyslipidemia, obesity, tobacco dependence) and four continuous blood pressure metrics against WMH volume, stratified by race.
Main Results:
- Hispanic males demonstrated the broadest vulnerability, with hypertension, diabetes, and tobacco dependence significantly predicting higher WMH.
- Elevated blood pressure metrics (systolic, diastolic, pulse, mean arterial pressure) were associated with increased WMH in Hispanic males, an effect not observed in NHW or NHB males.
- A composite cardiometabolic score showed the strongest association with WMH in Hispanic males.
Conclusions:
- Cardiometabolic and hemodynamic drivers of WMH exhibit significant racial and ethnic variations in males.
- Hispanic males present a more pervasive risk profile for WMH, while NHB males show selective associations and NHW males have limited links.
- Tailored vascular-risk interventions are essential to mitigate WMH-related pathways to Alzheimer's disease in diverse male populations.
Abstract:
Background: Cardiometabolic conditions accelerate white-matter hyperintensity (WMH) accumulation-a vascular injury marker linked to increased Alzheimer's disease risk-yet how these relationships vary by race and ethnicity in males is poorly understood. Objective: To quantify racial ethnic-specific associations between cardiometabolic risk factors, blood-pressure indices, and WMH volume in Non-Hispanic White (NHW), Non-Hispanic Black (NHB), and Hispanic males. Methods: We analyzed 1378 males (558 NHW, 375 NHB, 445 Hispanic) from the Healthy Aging Brain Study-Health Disparities. Five binary exposures (hypertension, diabetes, dyslipidemia, obesity, tobacco dependence), four continuous blood-pressure metrics (systolic, diastolic, pulse, mean arterial pressure), and a principal-component cardiometabolic score were regressed on log-transformed, intracranial volume-adjusted WMH volume in race-stratified models. Results: Hispanic males exhibited the broadest vulnerability: hypertension, diabetes, and tobacco dependence each predicted higher WMH (β range 0.60-0.77, p ≤ 0.002), and the composite score had the strongest association (β = 0.26, 0.13-0.39, p < 0.001). Additionally, every 10-mm Hg rise in systolic, diastolic, pulse, or mean arterial pressure further increased WMH in Hispanic males (e.g., systolic β = 0.18, 0.11-0.26), an effect absent in NHW and NHB males. Conclusions: Cardiometabolic and hemodynamic drivers of WMH differ markedly across racial and ethnic groups of males, with Hispanic males showing the most pervasive risk profile, NHB males selective associations, and NHW males limited links. Tailored vascular-risk interventions may be essential to curb WMH-related pathways to Alzheimer's disease in racially and ethnically diverse male populations.
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