Evidence map›Paper›PMID 41445760›Full record

ArticleFrontiers in digital health2025

Uncovering bias and variability in how large language models attribute cardiovascular risk.

Justine Tin Nok Chan, Ray Kin Kwek

Abstract read
In one paragraph

Article in Frontiers in digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Justine Tin Nok ChanSchool of Clinical Medicine, University of Cambridge, Cambridge, United Kingdom.
Ray Kin KwekLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large language models (LLMs) are used increasingly in medicine, but their decision-making in cardiovascular risk attribution remains underexplored. This pilot study examined how an LLM apportioned relative cardiovascular risk across different demographic and clinical domains. A structured prompt set across six domains was developed, across general cardiovascular risk, body mass index (BMI), diabetes, depression, smoking, and hyperlipidaemia, and submitted in triplicate to ChatGPT 4.0 mini. For each domain, a neutral prompt assessed the LLM's risk attribution, while paired comparative prompts examined whether including the domain changed the LLM's decision of the higher-risk demographic group. The LLM attributed higher cardiovascular risk to men than women, and to Black rather than white patients, across most neutral prompts. In comparative prompts, the LLM's decision between sex changed in two of six domains: when depression was included, risk attribution was equal between men and women. It changed from females being at higher risk than males in scenarios without smoking, but changed to males being at higher risk than females when smoking was present. In contrast, race-based decisions of relative risk were stable across domains, as the LLM consistently judged Black patients to be higher-risk. Agreement across repeated runs was strong (ICC of 0.949, 95% CI: 0.819-0.992,

Indexed as

artificial intelligencebiascardiovascular riskgender equalitylarge language model

Identifiers

PMID41445760
PMCPMC12722456

What OpenQuestion holds

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LicenceCC BY
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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.