Abstract 4359477: Evaluation of PREVENT Equations for Estimating Cardiovascular Disease Risk in Individual Asian American and Native Hawaiian and Pacific Islander Groups

M Michael Au (Kaiser Permanente Bernard J. Tyson School of Medicine, 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) M Mengnan Zhou (KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States) S Soonie Choi (Kaiser Permanente, Pasadena, California, United States) H Hui Zhou (Department of Chemistry and Materials) T Teresa Harrison (KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States) M Matthew Mefford (Kaiser Permanente, Pasadena, California, United States) M Mingsum Lee (Kaiser Permanente, Los Angeles, California, United States) E Eugene Yang N Nilay Shah (Northwestern University, Chicago, Illinois, United States) K Kristi Reynolds (Kaiser Permanente Southern California, Pasadena, California, United States) J Jaejin An (Kaiser Permanente, Pasadena, California, United States)

Abstract

Background: The race-free Predicting Risk of cardiovascular disease (CVD) EVENTS (PREVENT) equations estimate 10-year risk for total CVD. However, their accuracy in individual Asian or Native Hawaiian and Pacific Islander (NHPI) ethnic groups remain unknown. Research Question: What is the risk prediction accuracy of the PREVENT Base and Full Equations in Asian and NHPI ethnic groups? Methods: A retrospective cohort study was conducted among adults aged 30-79 years without a history of CVD who self-reported as non-Hispanic (NH) White, NH Asian, or NH NHPI and were actively enrolled as members of Kaiser Permanente Southern California on September 30 th , 2009, with follow-up through 2019. Asian participants were further disaggregated into ethnic groups. Ten-year risk for total CVD was estimated using the PREVENT Base and Full (Base plus hemoglobin A1c, urine albumin-creatinine ratio, and social deprivation index) equations. Model discrimination was evaluated using Harrell’s C-index, and calibration assessed using predicted-to-observed event ratios. Results: Among 542,848 adults (424,277 NH White; 110,855 NH Asian; 7,716 NH NHPI), 31,556 CVD events occurred over 10 years. Harrell’s C-index for the PREVENT Base equation was 0.764 (95% CI = 0.761–0.767) in NH White, 0.773 (95% CI = 0.765–0.779) in NH Asian, and 0.757 (95% CI = 0.733–0.780) in NH NHPI adults ( Table ). PREVENT Full equation showed similar C-indexes. Among Asian ethnic groups, PREVENT Base and Full equation discrimination was highest in Chinese (0.810) adults and lowest in Vietnamese (0.735) adults. The PREVENT Base and Full equations underestimated total CVD risk in NH White (mean calibration 0.63–0.84) and NH NHPI (mean calibration 0.74–0.86) adults. In contrast, the PREVENT Base equation overestimated total CVD risk in overall NH Asian adults (mean calibration 1.18) and most disaggregated Asian ethnic groups (mean calibration 1.04-1.39), while the PREVENT Full equation underestimated total CVD risk in overall NH Asian (mean calibration 0.96) and generally well calibrated or underestimated total CVD risk in disaggregated Asian ethnic groups (mean calibration 0.83–1.07). Conclusions: Despite the overall strong discrimination of the PREVENT Base and Full equations in predicting total CVD over 10 years, calibration varied across disaggregated Asian and NHPI ethnic groups, highlighting the importance of accounting for population heterogeneity in CVD risk assessment.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (12)

M

Michael Au

Kaiser Permanente Bernard J. Tyson School of Medicine, 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

M

Mengnan Zhou

KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States

S

Soonie Choi

Kaiser Permanente, Pasadena, California, United States

H

Hui Zhou

Department of Chemistry and Materials

T

Teresa Harrison

KAISER PERMANENTE SOUTHERN CA, Pasadena, California, United States

M

Matthew Mefford

Kaiser Permanente, Pasadena, California, United States

M

Mingsum Lee

Kaiser Permanente, Los Angeles, California, United States

E

Eugene Yang

N

Nilay Shah

Northwestern University, Chicago, Illinois, United States

K

Kristi Reynolds

Kaiser Permanente Southern California, Pasadena, California, United States

J

Jaejin An

Kaiser Permanente, Pasadena, California, United States