# Genetic variants in HLA-DQA1/DQB1 genes modulate the risk of gestational diabetes mellitus in a southern Chinese population

**Authors:** Lijie Nie, Yan Sun, Ruiqi Li, Qiulian Liang, Guocun Deng, Xinyu He, Yifei Zeng, Hui Zheng, Xinhe Xiao, Xiaodong Ding, Jian Huang, Xiangyuan Yu

PMC · DOI: 10.3389/fendo.2025.1511561 · Frontiers in Endocrinology · 2025-07-23

## TL;DR

This study finds that genetic variations in HLA-DQA1/DQB1 genes are linked to a higher risk of gestational diabetes in southern Chinese women.

## Contribution

The study identifies specific SNPs and haplotypes in HLA-DQA1/DQB1 genes associated with gestational diabetes mellitus risk in a southern Chinese population.

## Key findings

- Individuals with 2–7 unfavorable genotypes had a 1.54-fold increased risk of GDM.
- The haplotypes ACGAGTA and ACGGATA were significantly associated with increased GDM risk.
- A 7-loci model was best for predicting GDM risk using multifactor dimensionality reduction.

## Abstract

Gestational diabetes mellitus (GDM) is an endocrine disorder that occurs easily in women during pregnancy. HLA-DQA1/DQB1 genes play a crucial role in the regulation of the human immune and endocrine systems, potentially influencing the pathogenesis of GDM.

To explore the associations between single nucleotide polymorphisms (SNPs) in HLA-DQA1/DQB1 genes and the risk of GDM.

Seven functional SNPs of HLA-DQA1/DQB1 genes were selected and genotyped in 523 GDM patients and 638 normal pregnant women. The odds ratio (OR) and its corresponding 95% confidence interval (CI) were utilized to assess the association between candidate SNPs and the risk of GDM. And then, false positive report probability (FPRP), multifactor dimensionality reduction (MDR) and haplotype analysis were employed to validate the statistically significant associations between studied SNPs and GDM risk.

Compared to those with 0–1 risk genotypes, individuals with 2–7 unfavorable genotypes presented an increased risk of GDM (adjusted OR = 1.54, 95% CI=1.04-2.28, P=0.033). A dose- accumulation effect was detected between the number of unfavorable genotypes and GDM risk (P
trend=0.024). Furthermore, stratified analysis revealed that the increased GDM risk was more likely to occur in individuals with higher blood pressure and TG, and lower HDL-c levels (P<0.05). Multifactor dimensionality reduction (MDR) analysis revealed that rs9274666 was the best single locus model, whereas the 7-loci model was the best multifactor interaction model for predicting GDM risk (χ²=134.28, P<0.0001). Finally, haplotype analysis revealed that the ACGAGTA and ACGGATA haplotypes were significantly associated with the increased GDM risk. HLA-DQA1/DQB1 SNPs can significantly alter individuals’ genetic susceptibility to GDM.

The genetic variations in the HLA-DQA1 and HLA-DQB1 genes may collectively contribute to the susceptibility to gestational diabetes mellitus. These findings suggest that these genetic markers could be useful for early prediction of GDM, and further validation in larger cohorts is warranted.

## Linked entities

- **Genes:** HLA-DQA1 (major histocompatibility complex, class II, DQ alpha 1) [NCBI Gene 3117], HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119]
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}, HLA-DQA1 (major histocompatibility complex, class II, DQ alpha 1) [NCBI Gene 3117] {aka CELIAC1, DQ-A1, DQA1, HLA-DQA, HLA-DQA1*}
- **Diseases:** GDM (MESH:D016640), endocrine disorder (MESH:D004700)
- **Chemicals:** TG (MESH:D013866)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs9274666

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12325038/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12325038/full.md

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Source: https://tomesphere.com/paper/PMC12325038