Evidence mapPaperPMID 42424585Full record

SynthesisJournal of medical Internet research2026

Performance of AI in Predicting the Progression of Gestational Diabetes to Type 2 Diabetes: Systematic Review and Meta-Analysis.

Alaa Abd-Alrazaq, Shahira Padinharepattel Mohamed, Mohannad Alajlani, Aliya Tabassum, José Manuel Ordóñez-Mena, Shehel Yoosuf, Mais Alkhateeb, Arfan Ahmed, Mohammed Bashir, Junaid Qadir and 2 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Journal of medical Internet research, 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

12 authors.

Alaa Abd-AlrazaqAI Center for Precision Health, Weill Cornell Medicine-Qatar, Qatar Foundation, A031, Doha, Doha, 000, Qatar, 974 453456653.ORCID http://orcid.org/0000-0001-7695-4626
Shahira Padinharepattel MohamedDivision of Information and Computing Technology, College of Science and Engineering, Hamad Bin Khalifa University, Qatar Foundation, Doha, Qatar.ORCID http://orcid.org/0009-0001-4316-8861
Mohannad AlajlaniInstitute of Digital Healthcare, WMG, University of Warwick, Warwick, England, United Kingdom.ORCID http://orcid.org/0000-0002-5691-7120
Aliya TabassumComputer Science and Engineering Department, College of Engineering, Qatar University, Doha, Qatar.ORCID http://orcid.org/0000-0002-9384-7053
José Manuel Ordóñez-MenaNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.ORCID http://orcid.org/0000-0002-8965-104X
Shehel YoosufAI Center for Precision Health, Weill Cornell Medicine-Qatar, Qatar Foundation, A031, Doha, Doha, 000, Qatar, 974 453456653.ORCID http://orcid.org/0000-0001-9524-8575
Mais AlkhateebAI Center for Precision Health, Weill Cornell Medicine-Qatar, Qatar Foundation, A031, Doha, Doha, 000, Qatar, 974 453456653.ORCID http://orcid.org/0009-0006-7644-8604
Arfan AhmedAI Center for Precision Health, Weill Cornell Medicine-Qatar, Qatar Foundation, A031, Doha, Doha, 000, Qatar, 974 453456653.ORCID http://orcid.org/0000-0002-4025-5767
Mohammed BashirQatar Metabolic Institute, Hamad Medical Corporation, Doha, Qatar.ORCID http://orcid.org/0000-0003-3096-2641
Junaid QadirComputer Science and Engineering Department, College of Engineering, Qatar University, Doha, Qatar.ORCID http://orcid.org/0000-0001-9466-2475
Ali AlSanousiClinical Information Systems Department, Hamad Medical Corporation, Doha, Qatar.ORCID http://orcid.org/0000-0003-3822-3798
Javaid SheikhAI Center for Precision Health, Weill Cornell Medicine-Qatar, Qatar Foundation, A031, Doha, Doha, 000, Qatar, 974 453456653.ORCID http://orcid.org/0000-0002-5762-4186

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gestational diabetes mellitus (GDM) significantly increases the risk of developing type 2 diabetes mellitus (T2DM) post partum, with up to half of affected women progressing within a decade. Early identification of high-risk individuals is critical for implementing preventive interventions. Artificial intelligence (AI) offers enhanced predictive capabilities that can substantially enhance the prevention of postpartum diabetes. Objective: This systematic review and meta-analysis aimed to evaluate the performance of AI models in predicting the progression from GDM to T2DM or prediabetes. Methods: A total of 7 databases (MEDLINE, Embase, Scopus, Web of Science, IEEE Xplore, ACM Digital Library, and Google Scholar) were systematically searched from inception through September 12, 2025, supplemented by backward and forward reference screening and biweekly alerts to capture newly published studies. This review included peer-reviewed English-language studies that applied AI algorithms to predict T2DM or prediabetes among women with previous GDM. Eligible studies focused on human participants; reported performance metrics (eg, accuracy, sensitivity, and specificity); and excluded non-AI models, animal studies, reviews, protocols, abstracts, and non-English publications. Moreover, 2 reviewers independently conducted study selection, data extraction, and risk of bias assessment using the PROBAST (Prediction Model Risk of Bias Assessment Tool)+AI tool. Pooled estimates were computed using random-effects meta-analysis models. Results: In total, 10 studies met the inclusion criteria, of which 8 were eligible for meta-analysis. The reviewed studies spanned from 2011 to 2025 and were conducted across 7 countries, predominantly in the United States (3/10, 30%). Most publications were journal articles (9/10, 90%), and retrospective designs (6/10, 60%) were slightly more common than prospective designs (4/10, 40%). AI models demonstrated high predictive performance for T2DM, with pooled accuracy of 0.85 (95% CI 0.79-0.90; prediction interval [PI] 0.64-0.98), sensitivity of 0.89 (95% CI 0.81-0.95; PI 0.63-1.00), specificity of 0.88 (95% CI 0.81-0.93; PI 0.67-0.99), F1-score of 0.80 (95% CI 0.75-0.85; PI 0.68-0.93), and area under the curve of 0.86 (95% CI 0.77-0.91; PI 0.54-0.97). However, AI performance for prediabetes prediction was modest (area under the curve=0.69, 95% CI 0.60-0.77). Subgroup analyses showed that random forest, decision tree, logistic regression, and naïve Bayes models performed comparably. Fasting plasma glucose and BMI were the most identified significant predictors in the included studies. Conclusions: AI models show potential in predicting T2DM after GDM. However, evidence remains limited by small sample sizes, high heterogeneity, lack of external validation, and high risk of bias. Our findings have important implications for digital health, supporting the integration of AI-driven risk prediction into electronic health record systems and postpartum care pathways to enable early identification, targeted prevention, and improved long-term outcomes. Future research should use large, diverse cohorts, integrate multidimensional data, adopt standardized reporting frameworks, and encourage open-access data sharing.

Indexed as

Artificial IntelligenceDiabetes, GestationalDiabetes Mellitus, Type 2Disease ProgressionFemaleHumansPrediabetic StatePrediction AlgorithmsPredictive Learning ModelsPregnancyartificial intelligencediabetes mellitusgestational diabetesmachine learningmeta-analysisprediabetessystematic review

Identifiers

PMID42424585
PMCPMC13349230

What Socratic 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 Socratic graph.