Evidence map›Paper›PMID 42119064›Full record

ReviewJMIR AI2026

Methodological Approaches to and Reported Performance of Applications of Automated Machine Learning in Diabetes Risk Prediction: Rapid Review.

Alexandre Castonguay, Sandrine Hegg-Deloye, Arthur Chatton, Amélie Goyette

Abstract readReview
In one paragraph

Review in JMIR AI, 2026. 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

4 authors.

Alexandre CastonguayFaculté des sciences infirmières, Université de Montréal, Pavillon Marguerite d'Youville, 2375, Chemin de la Côte-Sainte-Catherine, Montréal, QC, H3T 1A8, Canada, 1 4182626594.ORCID http://orcid.org/0000-0002-7102-9893
Sandrine Hegg-DeloyeFaculté des sciences infirmières, Université de Montréal, Pavillon Marguerite d'Youville, 2375, Chemin de la Côte-Sainte-Catherine, Montréal, QC, H3T 1A8, Canada, 1 4182626594.ORCID http://orcid.org/0000-0001-6209-2252
Arthur ChattonDépartement de médecine sociale et préventive, Université de Montréal, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-0018-5899
Amélie GoyetteCentre de recherche Azrieli, CHU Sainte-Justine, Montréal, QC, Canada.ORCID http://orcid.org/0009-0008-2461-3764

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Type 2 diabetes (T2D) is a complex, chronic condition that imposes a substantial burden on health care systems. Prevention and early detection are critical to mitigating its impact. Automated machine learning (AutoML) models have the potential to predict individual risk and guide personalized interventions. However, their clinical deployment remains limited due to the retrospective nature of most datasets, a lack of external validation, and heterogeneity in variable selection. Objective: This study aimed to map AutoML approaches applied to T2D risk prediction, with a specific focus on their ability to integrate clinical, behavioral, environmental, and genomic data. Methods: A PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)-guided rapid review was conducted across 6 databases (PubMed, Scopus, Web of Science, IEEE Xplore, Google Scholar, and Embase) to identify empirical studies (published between 2015 and 2025) that used AutoML tools for T2D prediction based on at least 2 data types (eg, clinical, behavioral, environmental, and genomic). Screening, data extraction, and synthesis were performed systematically by 2 independent reviewers, with arbitration by ChatGPT acting as an artificial intelligence-based third reviewer. Results: In total, 13 studies met the inclusion criteria. Methodological diversity ranged from conventional machine learning with manual feature selection to partially or fully automated pipelines using tools such as the Tree-Based Pipeline Optimization Tool, H2O AutoML, or Azure Machine Learning. Reported performance varied (area under the curve=0.74-0.99); however, external validation was uncommon. Behavioral and environmental data were only partially integrated, and no study incorporated genomic data despite its recognized potential. Most studies lacked transparency and reproducibility, with no public code or pipeline sharing. Conclusions: AutoML holds significant promise for improving T2D risk prediction through automation and model explainability. However, to support clinical adoption and generalizability, future AutoML pipelines must be developed using prospective, multicenter datasets; integrate diverse, harmonized data types, including genomics; and adhere to open science principles of transparency, reproducibility, and interpretability.

Indexed as

AIartificial intelligenceautomated machine learningAutoMLexplainable artificial intelligencemachine learning validationmultimodal data integrationtype 2 diabetes risk prediction

Identifiers

PMID42119064
PMCPMC13167060

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.