Abstract 064: Fairness Heterogeneity of the PREVENT Equations in US Young Adults

A Abigail Gauen (Northwestern University, Chicago, Illinois, United States) L Lucia Petito (Northwestern University, Chicago, Illinois, United States) M Mengnan Zhou (KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States) H Hui Zhou (Department of Chemistry and Materials) J Jaejin An (Kaiser Permanente, Pasadena, California, United States) Y Yiyi Zhang (Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology) K Kristi Reynolds (Kaiser Permanente Southern California, Pasadena, California, United States) D Donald Lloyd-Jones (Framingham Center for Population and Prevention Science, Framingham, MA) N Norrina Allen (NORTHWESTERN UNIVERSITY, Chicago, Illinois, United States)

Abstract

Background: In 2023, the AHA published Predicting Risk of cardiovascular disease EVENTs (PREVENT), a new set of race-agnostic risk prediction equations that estimate 10-year risk of cardiovascular disease (CVD) in US adults ages 30-79 years. Equations include a base model and a model adding social deprivation index (SDI). Aim: To evaluate fairness of the base and SDI-enhanced PREVENT equations across race/ethnicity and sex groups in US young adults. Methods: We included adults aged 20-39 years enrolled between 2008-2009 without a history of CVD from Kaiser Permanente Southern California. From the eligible sample of 266,378, we randomly selected 50,000 young adults for computational efficiency. Primary outcome was incident CVD (defined as myocardial infarction, fatal coronary heart disease, fatal and nonfatal stroke, and heart failure) at 10 years. We estimated 10-year CVD risk using the PREVENT base and SDI-enhanced models. To assess race-sex specific model performance, we used Brier score, Harrell’s C, and mean calibration in each group. Overall algorithmic fairness was evaluated by (1) fair calibration, which measures whether agreement between predicted and observed risk is equally accurate across groups using Hosmer-Lemeshow goodness-of-fit and pairwise Wilcoxon signed-rank tests, and (2) concordance imparity, which measures the largest deviation of discriminative abilities across racial and ethnic groups by taking the difference between maximum and minimum Harrell’s C across groups. Results: We included 50,000 young adults who were mean (SD) age 31.7 (5.4) years, 61.3% female, and 51.1% Hispanic, who had 312 incident CVD events by 10 years. Performance metrics were similar in the base and SDI-enhanced equations. Models were under-calibrated in Black and White females and Asian and Black males, indicating observed risk was higher than predicted risk. Agreement between predicted and observed risk was not equally accurate across racial and ethnic groups in males or females (biased calibrated). Discriminative abilities also varied across groups, with Harrell’s C highest in Black males and lowest in Asian females. Concordance imparity was similar in the base and SDI-enhanced models (0.097 vs. 0.095). Conclusion: The PREVENT equations may not provide consistent risk predictions for young adults across race/ethnicity and sex groups, which could lead to unequal CVD prevention efforts. Addition of SDI to the PREVENT equations did not provide improvement in fairness.

Article Details

Journal Circulation
Volume / Issue Vol. 151, Issue Suppl_1
Published March 11, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (9)

A

Abigail Gauen

Northwestern University, Chicago, Illinois, United States

L

Lucia Petito

Northwestern University, Chicago, Illinois, United States

M

Mengnan Zhou

KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States

H

Hui Zhou

Department of Chemistry and Materials

J

Jaejin An

Kaiser Permanente, Pasadena, California, United States

Y

Yiyi Zhang

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology

K

Kristi Reynolds

Kaiser Permanente Southern California, Pasadena, California, United States

D

Donald Lloyd-Jones

Framingham Center for Population and Prevention Science, Framingham, MA

N

Norrina Allen

NORTHWESTERN UNIVERSITY, Chicago, Illinois, United States