Evidence map›Paper›PMID 41299655›Full record

ArticleBMC medical genomics2025

Advanced machine learning techniques for coronary artery disease risk prediction in early middle-aged adults.

Georgios Ntritsos, Erez Ornan, Eran Feldhay, Gil Chernin, Evangelos Evangelou

Abstract read
In one paragraph

Article in BMC medical genomics, 2025. 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

5 authors.

Georgios NtritsosDepartment of Economics, University of Ioannina, 45110, Ioannina, Greece. georgios@open-dna.com.
Erez OrnanOpenDNA LTD, Haifa, Israel.
Eran FeldhayOpenDNA LTD, Haifa, Israel.
Gil CherninFaculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Evangelos EvangelouOpenDNA LTD, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary artery disease (CAD) is the leading cause of death globally, with early risk prediction being vital for timely intervention. In this study we utilized advanced machine learning techniques, incorporating clinical, lifestyle, and Genetic factors with the aim to enhance the 10-year risk prediction of CAD in early middle-aged adults (40–55 years).

methodsFor developing the machine learning models, we used data from the UK Biobank, a large cohort of over 500,000 participants. Among participants aged 40 to 55, we identified 3,012 CAD cases and 155,176 controls, without any prior CAD diagnosis. More than 700 clinical and lifestyle variables were evaluated, alongside a polygenic risk score (PRS) derived from more than 560,000 genetic variants. Forward feature selection was performed, followed by the application of a stacking ensemble model combining Random Forest and Deep Learning Neural Networks as base learners with a Logistic Regression model serving as a meta-learner. The model’s performance for the 10-years prediction of CAD risk was evaluated using Area Under the Receiver Operating Characteristic Curve (AUC) and calibrated against the ACC/AHA guidelines.

resultsForward feature selection identified 22 CAD risk factors, including the PRS. The final model yielded an AUC of 0.81 in the training dataset and 0.80 in the testing dataset. At the 7.5% risk threshold, the model demonstrated higher sensitivity (0.511 vs. 0.346) and comparable specificity (0.863 vs. 0.866) compared to the ACC ASCVD model. The Net Reclassification Index (NRI) improved by 13.79%, emphasizing the model’s accuracy and alignment.

conclusionsOur findings highlight the potential of combining Genetic information with clinical and lifestyle factors through machine learning to improve CAD risk prediction in early middle-aged adults. The use of a stacking ensemble approach enabled modeling of complex relationships, yielding superior performance over standard risk models. This framework supports more precise and actionable 10-year risk stratification, reinforcing the value of PRSs when combined with traditional factors. Future research should validate these methods across diverse populations and clinical environments.

Indexed as

Coronary Artery DiseaseMachine LearningAdultClassification AlgorithmsFemaleGenetic Risk ScoreHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom ForestRisk AssessmentRisk FactorsCoronary artery disease (CAD)Machine learningPolygenic risk scores (PRS)Risk prediction

Identifiers

PMID41299655
PMCPMC12751634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 OpenQuestion graph.