Evidence map›Paper›PMID 39392843›Full record

ArticlePloS one2024

Machine learning-based risk prediction for major adverse cardiovascular events in a Brazilian hospital: Development, external validation, and interpretability.

Gilson Yuuji Shimizu, Michael Schrempf, Elen Almeida Romão, Stefanie Jauk, Diether Kramer, Peter P Rainer, José Abrão Cardeal da Costa, João Mazzoncini de Azevedo-Marques, Sandro Scarpelini, Katia Mitiko Firmino Suzuki and 2 more

Abstract readValidation Study
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Leveraging artificial intelligence for cardiovascular risk: a primary care perspective.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

12 authors.

Gilson Yuuji ShimizuRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID 0000-0003-3711-5592
Michael SchrempfPredicting Health GmbH, Graz, Austria.
Elen Almeida RomãoRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Stefanie JaukSteiermärkische Krankenanstaltengesellschaft m. b. H., Graz, Austria.
Diether KramerSteiermärkische Krankenanstaltengesellschaft m. b. H., Graz, Austria.
Peter P RainerMedical University of Graz, Graz, Austria.
José Abrão Cardeal da CostaRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
João Mazzoncini de Azevedo-MarquesRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Sandro ScarpeliniRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Katia Mitiko Firmino SuzukiRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Hilton Vicente CésarRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Paulo Mazzoncini de Azevedo-MarquesRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID 0000-0002-7271-2774

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies of cardiovascular disease risk prediction by machine learning algorithms often do not assess their ability to generalize to other populations and few of them include an analysis of the interpretability of individual predictions. This manuscript addresses the development and validation, both internal and external, of predictive models for the assessment of risks of major adverse cardiovascular events (MACE). Global and local interpretability analyses of predictions were conducted towards improving MACE's model reliability and tailoring preventive interventions.

methodsThe models were trained and validated on a retrospective cohort with the use of data from Ribeirão Preto Medical School (RPMS), University of São Paulo, Brazil. Data from Beth Israel Deaconess Medical Center (BIDMC), USA, were used for external validation. A balanced sample of 6,000 MACE cases and 6,000 non-MACE cases from RPMS was created for training and internal validation and an additional one of 8,000 MACE cases and 8,000 non-MACE cases from BIDMC was employed for external validation. Eight machine learning algorithms, namely Penalized Logistic Regression, Random Forest, XGBoost, Decision Tree, Support Vector Machine, k-Nearest Neighbors, Naive Bayes, and Multi-Layer Perceptron were trained to predict a 5-year risk of major adverse cardiovascular events and their predictive performance was evaluated regarding accuracy, ROC curve (receiver operating characteristic), and AUC (area under the ROC curve). LIME and Shapley values were applied towards insights about model interpretability.

findingsRandom Forest showed the best predictive performance in both internal validation (AUC = 0.871 (0.859-0.882); Accuracy = 0.794 (0.782-0.808)) and external one (AUC = 0.786 (0.778-0.792); Accuracy = 0.710 (0.704-0.717)). Compared to LIME, Shapley values suggest more consistent explanations on exploratory analysis and importance of features.

conclusionsAmong the machine learning algorithms evaluated, Random Forest showed the best generalization ability, both internally and externally. Shapley values for local interpretability were more informative than LIME ones, which is in line with our exploratory analysis and global interpretation of the final model. Machine learning algorithms with good generalization and accompanied by interpretability analyses are recommended for assessments of individual risks of cardiovascular diseases and development of personalized preventive actions.

Indexed as

Cardiovascular DiseasesMachine LearningAgedAlgorithmsBrazilFemaleHospitalsHumansMaleMiddle AgedReproducibility of ResultsRetrospective StudiesRisk AssessmentRisk Factors

Identifiers

PMID39392843
PMCPMC11469522

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.