Associations of cardiometabolic polygenic risk scores with cardiovascular disease in African Americans
Related Experiment Video
Updated: Jul 16, 2025

Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
Published on: September 20, 2024
Workalemahu Tsegaselassie1, Ying Jian2, Gebremeskel G Berhanu3
1University of Utah Health.
Insights
Higher polygenic risk scores (PRS) for hemoglobin A1c (HbA1c) and systolic blood pressure (SBP) are linked to increased cardiovascular disease (CVD) risk in African Americans. These genetic scores may aid in early CVD prevention and management strategies.
Area of Science:
- Genetics
- Cardiology
- Public Health
Background:
- Cardiovascular disease (CVD) disproportionately affects African Americans, yet genomic studies often underrepresent this population, potentially exacerbating health disparities.
- Investigating genetic contributions to CVD risk is crucial for developing targeted prevention strategies.
Approach:
- Utilized the Jackson Heart Study cohort of African American adults (40-79 years old) without prior coronary heart disease or stroke.
- Derived genome-wide polygenic risk scores (PRS) for multiple cardiometabolic factors using UK Biobank data.
- Assessed associations between PRS and predicted 10-year atherosclerotic cardiovascular disease (ASCVD) risk, adjusting for covariates.
Key Points:
- Higher PRS for hemoglobin A1c (HbA1c) were associated with a 1.42 percentage-point increase in predicted 10-year ASCVD risk and increased odds of high ASCVD risk.
- Elevated PRS for systolic blood pressure (SBP) were linked to higher odds of meeting the ≥10% predicted 10-year ASCVD risk threshold.
- These findings highlight the role of specific genetic predispositions in CVD risk within the African American population.
Conclusions:
- Polygenic risk scores for HbA1c and SBP demonstrate significant associations with CVD risk in African Americans.
- PRS can potentially enhance the stratification of individuals for early CVD prevention and clinical management based on genetic risk factors.
Background:
Cardiovascular disease (CVD) is a complex disease, and genetic factors contribute individually or cumulatively to CVD risk. While African American women and men are disproportionately affected by CVD, their lack of representation in genomic investigations may widen disparities in health. We investigated the associations of cardiometabolic polygenic risk scores (PRSs) with CVD risk in African Americans.
Methods:
We used the Jackson Heart Study, a prospective cohort study of CVD in African American adults and the predicted atherosclerotic cardiovascular disease (ASCVD) 10-year risk. We included 40-79 years old adults without a history of coronary heart disease (CHD) or stroke at baseline. We derived genome-wide PRSs for systolic blood pressure (SBP), diastolic blood pressure (DBP), total cholesterol, LDL cholesterol, hemoglobin A1c (HbA1c), triglycerides, and C-reactive protein (CRP) separately for each of the participants, using African-origin UK Biobank participants' genome-wide association summary statistics. We estimated the associations between PRSs and 10-year predicted ASCVD risk adjusting for age, sex, study visit date, and genetic ancestry using linear and logistic regression models.
Results:
Participants (n=2,077) were 63% female and 66% never-smokers. They had mean (SD) 56 (10) years of age, 127.8 (16.3) mmHg SBP, 76.3 (8.7) mmHg DBP, 200.4 (40.2) mg/dL total cholesterol, 51.7 (14.7) mg/dL HDL cholesterol, 127.2 (36.7) mg/dL LDL cholesterol, 6.0 (1.3) mmol/mol HbA1c, 108.9 (81.7) mg/dL triglycerides and 0.53 (1.1) CRP. Their median (interquartile range) predicted 10-year predicted ASCVD risk was 8.0 (4.0-15.0). Participants in the >75th percentile for HbA1c PRS had 1.42 percentage-point greater predicted 10-year ASCVD risk (1.42 [95% CI: 0.58-2.26]) and higher odds of ≥10% predicted 10-year ASCVD risk (OR: 1.46 [95% CI: 1.03-2.07]) compared with those in the <25th percentile for HbA1c PRS. Participants in the >75th percentile for SBP PRS had higher odds of ≥10% predicted 10-year ASCVD risk (OR: 1.52 [95% CI: 1.07-2.15]) compared with those in the <25th percentile for SBP PRS.
Conclusion:
Among 40-79 years old African Americans without CHD and stroke, higher PRSs for HbA1c and SBP were associated with CVD risk. PRSs may help stratify individuals based on their clinical risk factors for CVD early prevention and clinical management.
More Related Videos
06:04Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
09:38Generalized Psychophysiological Interaction PPI Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease
Published on: November 14, 2017
Related Concept Videos
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
Coronary Artery Disease I: Introduction
Polygenic Traits
Imaging Studies for Cardiovascular System VI: Calcium -Scoring CT
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy