Evidence map›Paper›PMID 41907110›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2026

Machine Learning-Derived Predictive Risk Score for Prediabetes and Type 2 Diabetes Development in Parous Women.

Amélie Taschereau, Jenna Wong, Soren Harnois-Leblanc, Marie A Brunet, Myriam Doyon, Mélina Arguin, Sheryl L Rifas-Shiman, Emily Oken, Patrice Perron, Pierre-Étienne Jacques and 2 more

Abstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 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.

Amélie TaschereauDépartement de Biologie, Université de Sherbrooke, Sherbrooke, QC, Canada.ORCID 0000-0001-8046-1322
Jenna WongDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.
Soren Harnois-LeblancDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.
Marie A BrunetDepartment of Pediatrics, Université de Sherbrooke, Sherbrooke, QC, Canada.ORCID 0000-0001-5973-3522
Myriam DoyonCentre de recherche du Centre hospitalier universitaire de Sherbrooke (CRCHUS), Sherbrooke, QC, J1H 5N3, Canada.
Mélina ArguinCentre de recherche du Centre hospitalier universitaire de Sherbrooke (CRCHUS), Sherbrooke, QC, J1H 5N3, Canada.
Sheryl L Rifas-ShimanDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.
Emily OkenDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.
Patrice PerronCentre de recherche du Centre hospitalier universitaire de Sherbrooke (CRCHUS), Sherbrooke, QC, J1H 5N3, Canada.
Pierre-Étienne JacquesDépartement de Biologie, Université de Sherbrooke, Sherbrooke, QC, Canada.
Luigi Bouchard *Centre de recherche du Centre hospitalier universitaire de Sherbrooke (CRCHUS), Sherbrooke, QC, J1H 5N3, Canada.
Marie-France Hivert *Department of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Pregnancy is a window of opportunity for closer links with clinical care, and to identify women at risk of chronic disease. Because of the elevated risk of type 2 diabetes (T2D) associated with gestational diabetes mellitus (GDM), most existing prediction models for post-delivery T2D focus on women with GDM, leaving many parous women without clear risk stratification. This study aimed to develop a prediction model for prediabetes or T2D risk in the general population of parous women, based on clinical pregnancy variables. Methods: We assessed prediabetes/T2D five years after delivery in the Genetics of Glucose Regulation in Gestation and Growth (Gen3G) cohort (N=403). Using a machine-learning approach, we developed a risk prediction model from which we derived a simple, clinically usable risk index: the Gestational 4-variable Prediabetes/type 2 diabetes (G4PD) index. The G4PD index was then validated in the Project Viva cohort at three years (n=562) and seventeen years (n=541) after delivery. Results: The G4PD index included gestational weight gain, pre-gestational body mass index, first-trimester maternal age, and a GDM variable reflecting hyperglycemia severity during pregnancy. In Gen3G, the model achieved a cross-validated estimate of the area under the receiver operating characteristic curve (ROC-AUC) of 0.696. The G4PD index achieved ROC-AUC of 0.682 in the 17-year Project Viva dataset, with similar results in the 3-year dataset. Beyond overall discrimination, the model effectively stratified women into clinically meaningful risk categories, with those in the lowest group (<2) exhibiting an expected risk of ~2% and ~15% at three and seventeen years after delivery, respectively, whereas those with the highest scores (≥7 or ≥5) expected substantially higher risks (~7% and ~37% at respective time points). Conclusion: The G4PD index, derived from clinical pregnancy variables, moderately predicts the risk of prediabetes/T2D over several years.

Indexed as

machine-learning algorithmprediabetesprediction modelpregnancyrisk stratificationtype 2 diabetes

Identifiers

PMID41907110
PMCPMC13024410

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.