# Increased O-GlcNAcylation in Leukocytes from Overweight Pediatric Subjects: A Pilot Study

**Authors:** Alessia Remigante, Sara Spinelli, Gianluca Rizzo, Daniele Caruso, Angela Marino, Elisabetta Straface, Silvia Dossena, Rossana Morabito

PMC · DOI: 10.3390/ijms26125665 · International Journal of Molecular Sciences · 2025-06-13

## TL;DR

This study found higher O-GlcNAcylation in blood cells of overweight children, suggesting it could be a new early marker for future diabetes risk.

## Contribution

The study identifies elevated O-GlcNAcylation in leukocytes of overweight children as a potential novel biomarker for early metabolic risk detection.

## Key findings

- Leukocyte O-GlcNAcylation was higher in overweight children compared to normal-weight children.
- O-GlcNAcylation levels correlated with BMI, LDL-cholesterol, triglycerides, and CRP.
- The findings suggest O-GlcNAcylation may serve as an early biomarker for metabolic abnormalities.

## Abstract

Type II diabetes mellitus (T2D) is a metabolic disorder. Childhood overweight or obesity raises the risk for developing T2D later in life. Early identification of at-risk individuals is fundamental for disease prevention and patient management. The scope of this pilot study was to explore whether leukocyte protein O-GlcNAc modification is elevated in an overweight pediatric cohort. Eight overweight and eight normal-weight children aged 3–13 years were recruited at the Papardo General Hospital (Messina, Italy). Physical exams, complete blood tests, and determination of leukocyte protein O-GlcNAcylation were carried out. Protein O-GlcNAcylation was higher in leucocytes from overweight children compared to normal-weight children, and was significantly correlated with BMI, metabolic markers (LDL-cholesterol/triglycerides), and the inflammatory marker CRP. This study suggests that leukocyte protein O-GlcNAcylation may represent a novel biomarker for the early detection of metabolic abnormalities that may lead to the development of pre-diabetes or T2D later in life.

## Linked entities

- **Diseases:** Type II diabetes mellitus (MONDO:0005148), pre-diabetes (MONDO:0006920)

## Full-text entities

- **Genes:** OGT (O-linked N-acetylglucosamine (GlcNAc) transferase) [NCBI Gene 8473] {aka HINCUT-1, HRNT1, MRX106, O-GLCNAC, OGT1, XLID106}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** inflammatory (MESH:D007249), metabolic abnormalities (MESH:D008659), T2D (MESH:D003924), Overweight (MESH:D050177), obesity (MESH:D009765), pre (MESH:D058246), diabetes (MESH:D003920)
- **Chemicals:** triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12193343/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12193343/full.md

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Source: https://tomesphere.com/paper/PMC12193343