Clinical Focus ›› 2026, Vol. 41 ›› Issue (4): 328-334.doi: 10.3969/j.issn.1004-583X.2026.04.007

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Development and validation of an early nomogram prediction model for gestational diabetes mellitus based on routine biomarkers

Ren Jiayina(), Chen Chunqinb, Liu Fashenga, Shen Huib   

  1. a. Department of Clinical Laboratory; b. Department of Obstetrics and Gynecology, Dongguan Renkang Hospital,Dongguan 523952,China
  • Received:2026-03-11 Online:2026-04-20 Published:2026-04-24
  • Contact: Ren Jiayin,Email: 249746621@qq.com

Abstract:

Objective To develop and validate a nomogram prediction model for gestational diabetes mellitus (GDM) based on routine antenatal examination indicators, providing a quantitative tool for early risk stratification. Methods A retrospective cohort study was conducted. A total of 4, 547 singleton pregnant women who underwent antenatal examinations at Dongguan Renkang Hospital from September 2018 to December 2024 were included and randomly assigned in a 7∶3 ratio to a development cohort (3, 183 cases) and an internal validation cohort (1, 364 cases). Variables were selected using the least absolute shrinkage and selection operator (LASSO) regression, and a multivariate logistic regression model was constructed to generate the nomogram. Model discrimination, calibration, and potential clinical utility were evaluated using the area under the receiver operating characteristic (ROC) curve (AUC), calibration curves, and decision curve analysis (DCA), respectively. Results Multivariate logistic regression analysis showed that age (OR=1.08, 95%CI: 1.06-1.09), pre-pregnancy body mass index (OR=1.05, 95%CI: 1.02-1.08), uric acid (OR=1.00, 95%CI: 1.00-1.01), glycated hemoglobin (OR=3.53, 95%CI: 2.79-4.45), and fasting plasma glucose (OR=2.44, 95%CI: 1.99-3.00) were independent predictors of GDM (pre-pregnancy body mass index, P=0.002; all others P<0.01). The AUC of the prediction model was 0.723 (95%CI: 0.703-0.742) in the development cohort and 0.720(95%CI: 0.690-0.750) in the internal validation cohort, indicating moderate discrimination. The calibration curves showed good agreement between predicted probability and observed risk. DCA indicated that within a threshold probability range of 0.10-0.80, the model provided potential net clinical benefit compared with strategies of screening all or screening none. Conclusion The nomogram model developed in this study, based on routine indicators in early pregnancy, showed moderate predictive performance for GDM risk and may serve as a preliminary tool for early risk stratification. However, further improvement is needed, and its generalizability and clinical utility should be confirmed through multicenter external validation and prospective intervention trials.

Key words: diabetes mellitus, gestational, nomogram, early prediction, risk factors, receiver operating characteristic, decision curve analysis

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