# The Role of Inflammatory Factors in the Pathogenesis of Gestational Diabetes Mellitus and May Be Potential Biomarkers for Its Diagnosis and Prognosis

**Authors:** Yuanyuan Guo, Xian Zheng, Jingru Jiao, Hongli Wu, Yan An

PMC · DOI: 10.1155/humu/4623346 · Human Mutation · 2025-11-17

## TL;DR

This study explores how inflammatory factors and genetic variations may help diagnose and predict outcomes for gestational diabetes in Han women from northern China.

## Contribution

The study identifies specific cytokine gene polymorphisms and inflammatory markers as potential biomarkers for gestational diabetes in a specific population.

## Key findings

- Elevated levels of IL-1, IL-6, IL-10, and TNF-α were found in gestational diabetes mellitus (GDM) patients.
- Certain gene polymorphisms, such as IL-1β −511 C/T and IL-6 −174 G/C, are strongly linked to increased GDM risk.
- ACC haplotypes of IL-10 are associated with a lower risk of GDM in Han women from northern China.

## Abstract

The biomarkers associated with gestational diabetes mellitus (GDM) remain incompletely understood. This article is aimed at investigating whether inflammatory factors may contribute as risk factors for GDM.

The study included 160 adult patients with GDM, who were enrolled as the experimental group. Additionally, 280 healthy individuals from the same time period were selected as the control group. Cytokine expression levels were measured using a flow cytometer with fluorescence, while gene polymorphisms were analyzed through the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The cytokines examined included interleukin-1 (IL-1), interleukin-6 (IL-6), interleukin-10 (IL-10), tumor necrosis factor-alpha (TNF-α), and interferon-gamma (IFN-γ).

Significantly higher expression levels of IL-1, IL-6, IL-10, and TNF-α were detected in GDM patients (p < 0.05). Additionally, the study identified specific polymorphisms—IL-1β −511 C/T, IL-10 −1082 G/A, IL-6 −174 G/C, and TNF-α −308 G/A—that were significantly associated with an increased risk of GDM (p < 0.05). IL-6, TNF-α, and IL-1β levels significantly differed among genotypes of IL-6 −174 G/C, TNFA −308 G/A, and IL-1B −511 C/T, respectively (p < 0.01), with risk-associated alleles linked to higher cytokine expression. No significant differences were observed for IL-10 −1082 G/A or IFN-γ +874 A/T. These results suggest that select polymorphisms may regulate cytokine levels relevant to GDM inflammation.

Elevated plasma levels of IL-1, IL-6, IL-10, and TNF-α have been observed in patients with GDM. Furthermore, polymorphisms such as IL-1β −511 C/T, IL-6 −174 G/C, IL-10 −1082 G/A, IFN-γ +874 A/T, and TNF-α −308 G/A show a strong correlation with an increased risk of GDM in the Han women from northern China (specifically, Hebei Province). Pregnant women with ACC haplotypes of IL-10 have a lower risk of GDM. Cytokine gene polymorphisms in IL-6, TNF-α, and IL-1B are associated with altered inflammatory profiles in GDM, suggesting a genetic contribution to disease-related immune dysregulation. Our study suggests that these factors hold potential as biomarkers for the diagnosis and clinical prognosis of GDM in Han women from northern China (Hebei Province).

## Linked entities

- **Genes:** IL1A (interleukin 1 alpha) [NCBI Gene 3552], IL6 (interleukin 6) [NCBI Gene 3569], IL10 (interleukin 10) [NCBI Gene 3586], TNF (tumor necrosis factor) [NCBI Gene 7124], IFNG (interferon gamma) [NCBI Gene 3458], IL1B (interleukin 1 beta) [NCBI Gene 3553]
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** immune dysregulation (OMIM:614878), GDM (MESH:D016640), Inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** -511 C/T, +874 A/T, -308 G/A, -174 G/C, -1082 G/A

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12643721/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12643721/full.md

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Source: https://tomesphere.com/paper/PMC12643721