# A Novel Single-Test Approach for GDM Diagnosis: Identification and Prediction of High-Risk Postprandial Hyperglycemia

**Authors:** Hao Wu, Danqing Chen, Xue Li, Menglin Zhou, Qi Wu

PMC · DOI: 10.3390/metabo16010027 · 2025-12-25

## TL;DR

This study introduces a new method to predict high-risk post-meal blood sugar in pregnant women using fasting blood tests, potentially replacing the current time-consuming glucose test.

## Contribution

A novel fasting metabolite-based model for early prediction of postprandial hyperglycemia in gestational diabetes.

## Key findings

- Incorporating amino acids and traditional predictors improved prediction accuracy from 78.2% to 91.1%.
- A practical nomogram was developed for clinical risk assessment of postprandial hyperglycemia.
- The model may reduce reliance on the oral glucose tolerance test in clinical practice.

## Abstract

Background: Early prediction of gestational diabetes mellitus (GDM) remains a major clinical challenge, and the current oral glucose tolerance test (OGTT) is time-consuming and inconvenient for clinical routine. This study aimed to develop a novel predictive model for postprandial hyperglycemia GDM (pp-GDM) and postprandial glucose elevation using fasting serological and metabolic profiles. Method: We used High-Performance Liquid Chromatography-Mass Spectrometry (HPLC-MS) to analyze fasting plasma amino acid profiles at 24–28 weeks of gestation for 60 pp-GDM patients and 120 controls. Binary logistic regression model was constructed to identify potential biomarkers for pp-GDM prediction. Results: By incorporating amino acid indicators such as isoleucine, phenylalanine, threonine, and aspartate into the predictive model alongside traditional predictors (including BMI at sampling, fasting insulin, glycated hemoglobin, and uric acid), the overall predictive performance was significantly improved from 78.2% to 91.1%. A clinically practical nomogram for risk assessment was subsequently developed. Conclusions: This fasting metabolite-based model provides a reliable tool for early prediction of pp-GDM and postprandial hyperglycemia, which may reduce the need for OGTT and facilitate timely clinical decision making.

## Linked entities

- **Chemicals:** isoleucine (PubChem CID 791), phenylalanine (PubChem CID 994), threonine (PubChem CID 205), aspartate (PubChem CID 5960)
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** GDM (MESH:D016640), Postprandial Hyperglycemia (MESH:D006943)
- **Chemicals:** isoleucine (MESH:D007532), threonine (MESH:D013912), aspartate (MESH:D001224), phenylalanine (MESH:D010649), glucose (MESH:D005947), amino acid (MESH:D000596), uric acid (MESH:D014527)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844304/full.md

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Source: https://tomesphere.com/paper/PMC12844304