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Record W4415299893 · doi:10.1136/heartjnl-2025-bcs.202

7-006 The prognostic value of the american heart association prevent cardiovascular disease risk equations in cancer survivorship: a nhanes population-based study (2009–2018)

2025· article· W4415299893 on OpenAlexaff
Mustafa Hussein Ajlan Al-Jarshawi, Ofer Kobo, Dennis T. Ko, Harindra C. Wijeysundera, Mohd Azam, Victoria Silverwood, Ram Bajpai, Rodrigo Bagur

Bibliographic record

Venuenot available
Typearticle
Language
FieldMedicine
TopicChemotherapy-induced cardiotoxicity and mitigation
Canadian institutionsLondon Health Sciences CentreHealth Sciences CentreWestern UniversitySunnybrook Health Science Centre
Fundersnot available
KeywordsProportional hazards modelNational Health and Nutrition Examination SurveyCohortCancerRisk assessmentDiseaseRisk of mortalityBaseline (sea)Framingham Risk Score

Abstract

fetched live from OpenAlex

Background The PREVENT equations offer a contemporary tool for estimating long-term cardiovascular (CV) risk in the general population.1 2 However, their prognostic significance in cancer survivors remains unclear. This study evaluates the association of baseline CV risk, calculated by PREVENT equations, with all-cause and CV mortality in cancer survivors. Methods Using 10 years of data from the National Health and Nutrition Examination Survey (NHANES) (2009–2018), we analysed a cohort representing over 18 million U.S. cancer survivors to evaluate the association between baseline CV risk, as defined by the PREVENT equations, and long-term all-cause and CV mortality. A Cox proportional hazards model was used to evaluate the relationship with all-cause mortality, while competing risk analysis was applied for CV mortality using the Fine and Gray semiparametric proportional hazards model, accounting for the competing risk of non-CV mortality. Models were adjusted for family income, education level, and cancer site. All statistical analyses were based on weighted records. Results A total of 18,722,334 weighted records (2,792 unweighted) were analysed, recording 4,875,627 all-cause deaths (26%) and 1,025,053 CV deaths (5.5%) over a 118-month median follow-up. When compared to low-risk individuals, those at high CV risk had a nearly sixteenfold higher risk of all-cause mortality (aHR: 15.60, 95% CI: 8.45–28.82, p < 0.001) and a fourteenfold higher risk of CV mortality (sHR: 14.01, 95% CI: 3.37–58.26, p < 0.001) during up to a decade of follow-up. Each 5% increase in baseline CV risk was associated with higher risks of all-cause mortality (36%) and CV mortality (50%) (aHR: 1.36 [95% CI: 1.30–1.42], sHR: 1.50 [95% CI: 1.35–1.66], p < 0.001 for both). Conclusion This study highlights the usefulness of the PREVENT score across diverse cancer survivor populations in predicting all-cause and CV mortality outcomes regardless of cancer site. References Khan SS, Coresh J, Pencina MJ, Ndumele CE, Rangaswami J, Chow SL, et al. Novel prediction equations for absolute risk assessment of total cardiovascular disease incorporating cardiovascular-kidney-metabolic health: a scientific statement from the american heart association. Circulation [Internet]. 2023 Dec 12 [cited 2025 Mar 6];148(24):1982–2004. Available from: https://pubmed.ncbi.nlm.nih.gov/37947094/. Scheuermann B, Brown A, Colburn T, Hakeem H, Chen ,, Chow H, et al. External validation of the American heart association PREVENT cardiovascular disease risk equations key points + invited commentary + supplemental content. JAMA Netw Open. 2024;7(10):2438311.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.006
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.010
Threshold uncertainty score0.020

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.006
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0050.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.015
GPT teacher head0.289
Teacher spread0.274 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
Has abstractyes

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