Evidence map›Paper›PMID 39854547›Full record

ArticlePloS one2025

Assessing cardiovascular disease risk and social determinants of health: A comparative analysis of five risk estimation instruments using data from the Eastern Caribbean Health Outcomes Research Network.

Jeremy I Schwartz, Christina Howitt, Sumitha Raman, Sanya Nair, Saria Hassan, Carol Oladele, Ian R Hambleton, Daniel F Sarpong, Oswald P Adams, Rohan G Maharaj and 3 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Jeremy I SchwartzEquity Research and Innovation Center, Section of General Internal Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.ORCID 0000-0003-0139-2600
Christina HowittGeorge Alleyne Chronic Disease Research Centre, Caribbean Institute for Health Research, The University of the West Indies, Barbados.
Sumitha RamanDivision of General Internal Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, United States of America.
Sanya NairYale University, New Haven, Connecticut, United States of America.
Saria HassanDivision of General Internal Medicine, Emory Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Carol OladeleEquity Research and Innovation Center, Section of General Internal Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.
Ian R HambletonGeorge Alleyne Chronic Disease Research Centre, Caribbean Institute for Health Research, The University of the West Indies, Barbados.
Daniel F SarpongSection of General Internal Medicine and Office of Health Equity Research, Yale School of Medicine, New Haven, Connecticut, United States of America.
Oswald P AdamsDepartment of Family Medicine, Faculty of Medical Sciences, University of the West Indies Cave Hill, Cave Hill, Barbados.
Rohan G MaharajDepartment of Paraclinical Sciences, University of the West Indies, Saint Augustine, Trinidad and Tobago.ORCID 0000-0001-8319-8187
Cruz M NazarioDepartment of Biostatistics and Epidemiology, Graduate School of Public Health, University of Puerto Rico at Medical Sciences Campus, San Juan, Puerto Rico.
Maxine NunezSchool of Nursing, University of the Virgin Islands, St. Thomas, US Virgin Islands.
Marcella Nunez-SmithEquity Research and Innovation Center, Section of General Internal Medicine, Yale School of Medicine, New Haven, Connecticut, United States of America.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale University Clinical and Translational Science Award ProgramUL1TR000142 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$31.8M
Yale Transdisciplinary Collaborative Center for Health Disparities Research (YALE-TCC)U54MD010711 · NIMHD · YALE UNIVERSITY · PI NUNEZ-SMITH, MARCELLA · 2016 to 2021
$14.4M
Eastern Caribbean Health Outcomes Research Network (ECHORNU24MD006938 · NIMHD · YALE UNIVERSITY · PI NUNEZ-SMITH, MARCELLA · 2011 to 2016
$5.7M
A Plan to Reduce Non-Communicable Disease-Related Morbidity and Mortality After Natural DisastersK23HL152368 · NHLBI · EMORY UNIVERSITY · PI HASSAN, SARIA · 2020 to 2024
$860k
NCATS NIH HHS UL1 TR000142NCATS NIH HHS UL1 TR001863NHLBI NIH HHS K23 HL152368NIMHD NIH HHS U24 MD006938NIMHD NIH HHS U54 MD010711
6 · The paper itself

Abstract

backgroundAccurate assessment of cardiovascular disease (CVD) risk is crucial for effective prevention and resource allocation. However, few CVD risk estimation tools consider social determinants of health (SDoH), despite their known impact on CVD risk. We aimed to estimate 10-year CVD risk in the Eastern Caribbean Health Outcomes Research Network Cohort Study (ECS) across multiple risk estimation instruments and assess the association between SDoH and CVD risk.

methodsFive widely used CVD risk estimation tools (Framingham and WHO laboratory, both laboratory and non-laboratory-based, and ASCVD) were applied using data from ECS participants aged 40-74 without a history of CVD. SDoH variables included educational attainment, occupational status, household food security, and perceived social status. Multivariable logistic regression models were used to compare differences in the association between selected SDoH and high CVD risk according to the five instruments.

findingsAmong 1,777 adult participants, estimated 10-year CVD risk varied substantially across tools. Framingham non-lab and ASCVD demonstrated strong agreement in categorizing participants as high risk. Framingham non-lab categorized the greatest percentage as high risk, followed by Framingham lab, ASCVD, WHO lab, and WHO non-lab. Fifteen times more people were classified as high risk by Framingham non-lab compared with WHO non-lab (31% vs 2%). Mean estimated 10-year risk in the sample was over 2.5 times higher using Framingham non-lab vs WHO non-lab (17.3% vs 6.6%). We found associations between food insecurity, those with the lowest level compared to the highest level of education, and non-professional occupation and increased estimated CVD risk.

interpretationOur findings highlight significant discrepancies in CVD risk estimation across tools and underscore the potential impact of incorporating SDoH into risk assessment. Further research is needed to validate and refine existing risk tools, particularly in ethnically diverse populations and resource-constrained settings, and to develop race- and ethnicity-free risk estimation models that consider SDoH.

Indexed as

Cardiovascular DiseasesSocial Determinants of HealthAdultAgedCaribbean RegionCohort StudiesFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedRisk AssessmentRisk Factors

Identifiers

PMID39854547
PMCPMC11760610

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.