Evidence map›Paper›PMID 40461349›Full record

ArticleThe Lancet. Digital health2025

Refined selection of individuals for preventive cardiovascular disease treatment with a transformer-based risk model.

Shishir Rao, Yikuan Li, Mohammad Mamouei, Gholamreza Salimi-Khorshidi, Malgorzata Wamil, Milad Nazarzadeh, Christopher Yau, Gary S Collins, Rod Jackson, Andrew Vickers and 2 more

Abstract read
In one paragraph

Article in The Lancet. Digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Automotive Health 2.0: Steering Toward Proactive Preventive Care.Mayo Clinic proceedings. Digital health · 2026
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
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

12 authors.

Shishir RaoDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Yikuan LiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Mohammad MamoueiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Gholamreza Salimi-KhorshidiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Malgorzata WamilDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Milad NazarzadehDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK.
Christopher YauNuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK; Health Data Research UK, London, UK.
Gary S CollinsCentre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology, and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Rod JacksonSchool of Population Health, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Andrew VickersMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Goodarz DanaeiDepartment of Global Health and Population and Department of Epidemiology, Harvard TH Chan School of Public Health, Boston, MA, USA.
Kazem RahimiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK; Nuffield Department of Women's & Reproductive Health, University of Oxford, Oxford, UK. Electronic address: kazem.rahimi@wrh.ox.ac.uk.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundAlthough statistical models have been commonly used to identify patients at risk of cardiovascular disease for preventive therapy, these models tend to over-recommend therapy. Moreover, in populations with pre-existing diseases, the current approach is to indiscriminately treat all, as modelling in this context is currently inadequate. This study aimed to develop and validate the Transformer-based Risk assessment survival (TRisk) model, a novel deep learning model, for predicting 10-year risk of cardiovascular disease in both the primary prevention population and individuals with diabetes.

methodsAn open cohort of 3 million adults aged 25-84 years was identified using linked electronic health records from 291 general practices, for model development, and 98 general practices, for validation, across England from 1998 to 2015. Comparison against the QRISK3 score and a deep learning derivation of it was done. Additional analyses compared discriminatory performance in other age groups, by sex, and across categories of socioeconomic status.

findingsTRisk showed superior discrimination (C index in the primary prevention population 0·910; 95% CI 0·906-0·913). TRisk's performance was found to be less sensitive to population age range than the benchmark models and outperformed other models also in analyses stratified by age, sex, or socioeconomic status. All models were overall well calibrated. In decision curve analyses, TRisk showed a greater net benefit than benchmark models across the range of relevant thresholds. At the widely recommended 10% risk threshold and the higher 15% threshold, TRisk reduced both the total number of patients classified at high risk (by 20·6% and 34·6%, respectively) and the number of false negatives as compared with recommended strategies. TRisk similarly outperformed other models in patients with diabetes. Compared with the widely recommended treat-all policy approach for patients with diabetes, TRisk at a 10% risk threshold would lead to deselection of 24·3% of individuals, with a small fraction of false negatives (0·2% of the cohort).

interpretationTRisk enabled a more targeted selection of individuals at risk of cardiovascular disease in both the primary prevention population and cohorts with diabetes, compared with benchmark approaches. Incorporation of TRisk into routine care could potentially reduce the number of treatment-eligible patients by approximately one-third while preventing at least as many events as with currently adopted approaches.

fundingNone.

Indexed as

Cardiovascular DiseasesDeep LearningPrimary PreventionAdultAgedAged, 80 and overEnglandFemaleHumansMaleMiddle AgedRisk Assessment

Identifiers

PMID40461349
PMCPMC12935155

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Registered trials

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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.