Evidence map›Paper›PMID 40669956›Full record

ArticleJournal of the American College of Cardiology2025

AHA PREVENT Equations and Cardiovascular Disease Risk in Diverse Health Care Populations.

So Mi Jemma Cho, Michael Levin, Robert Chen, Ryan Samarakoon, Renae Judy, Katherine Hartmann, Darina Postupaka, Victoria Viscosi, Eric Farber-Eger, Akl C Fahed and 7 more

Abstract read
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Article in Journal of the American College of Cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

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0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. The PREVENT Risk Equations and Cardiovascular Prevention in East Asia.Journal of atherosclerosis and thrombosis · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

So Mi Jemma ChoProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Integrative Research Center for Cerebrovascular and Cardiovascular Diseases, Seoul, Republic of Korea.
Michael LevinDivision of Cardiovascular Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.
Robert ChenDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA; Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA; Medical Scientist Training Program, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ryan SamarakoonVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Renae JudyDepartment of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Katherine HartmannDepartment of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Darina PostupakaProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Victoria ViscosiProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Eric Farber-EgerVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Akl C FahedProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Michael C HonigbergProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Chirag J PatelDepartment of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.
Whitney HornsbyProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Quinn S WellsVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Scott M DamrauerCorporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA; Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Ron DoDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA; Center for Genomic Data Analytics, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Pradeep NatarajanProgram in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: pnatarajan@mgh.harvard.edu.

Funding

MOUNT SINAI MEDICAL SCIENTIST TRAINING PROGRAMT32GM007280 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BARON, MARGARET H · 1985 to 2021
$22.8M
Using genetic variation to study biology of blood lipids & coronary heart diseaseR01HL127564 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Pradeep Natarajan, Gina Marie Peloso · 2015 to 2026
$7.3M
RESEARCH TRACK RADIOLOGY RESIDENCYT32EB004311 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI Terence P Gade, Misun Hwang · 2005 to 2026
$4.5M
Towards an integrated map of causal connections for common, complex diseasesR35GM124836 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ron Do · 2017 to 2026
$3.9M
Coronary plaque changes with statin and colchicine among people with high polygenic risk- a mechanistic pilot studyR01HL164629 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Akl C Fahed, Michael TseYin Lu · 2023 to 2026
$3.3M
Integrating genomic and nongenomic risk for coronary artery diseaseK08HL161448 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Akl C Fahed · 2022 to 2026
$751k
Clonal hematopoiesis as a mediator of cardiovascular disease in women with premature menopauseK08HL166687 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HONIGBERG, MICHAEL · 2023 to 2025
$507k
Integration of novel contextual and genomic blood pressure measures to enhance cardiovascular disease prediction and management in young adultsK99HL177340 · NHLBI · BROAD INSTITUTE, INC. · PI So Mi Cho · 2025 to 2026
$331k
American Heart Association-American Stroke Association 24RGRSG1275749American Heart Association-American Stroke Association 940166BLRD VA IK2 BX006551NHLBI NIH HHS K08 HL161448NHLBI NIH HHS K08 HL166687NHLBI NIH HHS K99 HL177340NHLBI NIH HHS R01 HL127564NHLBI NIH HHS R01 HL164629NIBIB NIH HHS T32 EB004311NIGMS NIH HHS R35 GM124836NIGMS NIH HHS T32 GM007280
6 · The paper itself

Abstract

backgroundThe American Heart Association's Predicting Risk of cardiovascular Events (PREVENT) aims to improve cardiovascular risk prediction. Whether PREVENT suitably predicts 10-year incident atherosclerotic cardiovascular disease (ASCVD) in health care populations is unknown.

objectivesThis study sought to evaluate the calibration and discrimination of the PREVENT equations across integrated U.S. health care systems.

methodsWe retrospectively evaluated electronic health records of 270,320 patients (Mass General Brigham [MGB]: 136,654; Mount Sinai Health: 43,321; Penn Medicine: 56,889; Vanderbilt University Medical Center: 33,456) aged 30 to 79 years and without prior ASCVD from 2010 to 2014. We compared 10-year estimated ASCVD risk based on PREVENT and empirically observed first ASCVD event over a 10-year follow-up. Calibration was assessed based on Greenwood-Nam-d'Agostino test, discordance, and mean calibration. Discrimination was assessed with the use of the time-dependent Harrell's C-index.

resultsBased on PREVENT, the mean estimated 10-year ASCVD risk was 4.9% ± 4.7% in MGB (mean age 54 years, 42% female), 6.0% ± 5.6% in Mount Sinai (mean age 56 years, 54% female), 6.0% ± 5.2% in Penn (mean age 58 years, 55% female), and 4.8% ± 1.3% in Vanderbilt (mean age 60 years, 51% female). Although PREVENT underestimated the observed incidence rate in MGB (discordance: -71.0%), Mount Sinai (discordance: -36.2%), and Vanderbilt (discordance: -40.0%), it more closely mirrored the empirical rate in Penn (+1.3%). Overall, PREVENT yielded moderate discrimination C-index in MGB (0.70 [95% CI: 0.70-0.70]), Mount Sinai (0.74 [95% CI: 0.73-0.75]), Penn (0.69 [95% CI: 0.68-0.70]), and Vanderbilt (0.73 [95% CI: 0.72-0.74]). Nevertheless, calibration differed by sex, with greater underestimation among women in MGB (discordance: -80.7%) and Vanderbilt (discordance: -55.5%) but among men in Mount Sinai (discordance: -40.7%). The race and ethnicity-stratified predictive performance varied across health care systems. Compared with the pooled cohort equations, PREVENT demonstrated better overall calibration in Penn (+2.5% vs +93.6%) but worse in MGB (-70.0% vs -41.6%) and Mount Sinai (-36.4% vs 4.8%), notwithstanding comparable discrimination. The PREVENT predictive performance further differed with better discrimination among patients without diabetes mellitus or antihypertensives.

conclusionsThe PREVENT model moderately discriminated ASCVD incidence across 4 geographically distinct academic health care systems in the United States. However, calibration metrics varied widely across health care systems, sociodemographics, and underlying cardiometabolic comorbidities.

Indexed as

American Heart AssociationCardiovascular DiseasesAdultAgedFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk FactorsUnited Statescardiovascular diseaseepidemiologyprimary preventionrisk prediction

Identifiers

PMID40669956
PMCPMC12686678

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.