Evidence map›Paper›PMID 42327444›Full record

ArticleCJC open2026

Initial Cardiovascular Disease Risk Assessment in Nonclinical Settings: Framingham-Simplified Model Predictive Performance in a Canadian Cohort.

Jacquecin Garçon, Mathilde Lavigne-Robichaud, Alain Milot, Denis Talbot, Mahée Gilbert-Ouimet, Chantal Brisson, Clermont E Dionne, Xavier Trudel

Abstract read
In one paragraph

Article in CJC open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Jacquecin GarçonDepartment of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada.
Mathilde Lavigne-RobichaudPopulation Health and Optimal Health Practices Research Program, CHU de Québec-Université Laval Research Center, Québec, Québec, Canada.
Alain MilotPopulation Health and Optimal Health Practices Research Program, CHU de Québec-Université Laval Research Center, Québec, Québec, Canada.
Denis TalbotDepartment of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada.
Mahée Gilbert-OuimetPopulation Health and Optimal Health Practices Research Program, CHU de Québec-Université Laval Research Center, Québec, Québec, Canada.
Chantal BrissonDepartment of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada.
Clermont E DionneDepartment of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada.
Xavier TrudelDepartment of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Framingham risk model is recommended for estimating 10-year cardiovascular disease (CVD) risk in Canada. Its simplified version (Framingham-SP) replaces lipids with body mass index, eliminating the need for laboratory testing. The predictive performance of the Framingham-SP in Canada is unknown. This external validation study assessed the discrimination and calibration of the Framingham-SP model in a prospective cohort from Quebec, Canada. Methods: The study sample included 3692 women and 3671 men free of CVD at baseline (1999-2001; follow-up until 2011). Incident CVD events were identified using medico-administrative databases. Multiple imputation was used to handle missing data. Discrimination was assessed using C-statistics. Calibration was evaluated using calibration-in-the-large, absolute difference, and discordance. Results: Over the 10-year follow-up, 211 CVD events occurred among women and 453 occurred among men. For women, the predicted 10-year CVD risk was 4.07% (95% confidence interval [CI]: 3.94-4.20), and the observed risk was 5.72% (95% CI: 5.01-6.51). The C-statistic was 0.72 (95% CI: 0.68-0.76). For men, the predicted risk was 11.73% (95% CI: 11.44-12.02), and the observed risk was 12.34% (95% CI: 11.32-13.44). The C-statistic was 0.72 (95% CI: 0.69-0.74). Overall, calibration was lower among women, particularly those in intermediate and high predicted risk categories. Conclusions: The Framingham-SP model demonstrated acceptable predictive performance in this Canadian cohort. Its simplified format may help support preliminary CVD risk assessment and lifestyle counselling, including in nonclinical settings, while remaining complementary to guideline-based clinical evaluation. Recalibration may improve performance among high-risk women.

Indexed as

cardiovascular diseasecohort study, nonclinical settingsexternal validation studyFramingham, non-laboratory basedrisk prediction

Identifiers

PMID42327444
PMCPMC13282532

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LicenceCC BY-NC-ND
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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.