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Updated: May 24, 2026

Immunoglobulin G N-Glycan Analysis by Ultra-Performance Liquid Chromatography
Published on: January 18, 2020
Changes in plasma and IgG N-glycome during childhood and adolescence
Maja Pucic1, Ana Muzinic, Mislav Novokmet
1Genos Ltd, Glycobiology Laboratory, Zagreb, Croatia.
Insights
The glycome in children remains largely unexplored. This study reveals significant age-related changes in children's plasma and IgG N-glycans, differing from adult patterns.
Area of Science:
- Biochemistry
- Immunology
- Pediatrics
Background:
- Protein glycosylation is crucial for physiological and pathological processes.
- Glycans hold potential as diagnostic markers and therapeutic targets.
- The glycome of pediatric populations is understudied.
Purpose of the Study:
- To analyze N-linked plasma and IgG glycomes in children and adolescents.
- To identify age- and sex-dependent glycan changes in this demographic.
- To compare pediatric glycan patterns with those of adults.
Main Methods:
- Analysis of N-linked plasma and IgG glycomes.
- Study cohort: 170 children and adolescents aged 6–18 years.
- Statistical analysis to identify associations between glycans, age, and sex.
Main Results:
- Significant biological variability and numerous age-associated glycan changes were observed.
- Younger children showed higher proportions of large complex glycan structures.
- Age-dependent increases in disialylated biantennary structures and digalactosylated glycans were noted, with decreases in core fucosylation and agalactosylated glycans.
- Observed pediatric glycan changes differ in direction and intensity from adult patterns.
- Sex differences in glycan profiles were minimal in children, becoming more apparent during puberty.
Conclusions:
- The glycome undergoes distinct age-related transformations during childhood and adolescence.
- Pediatric glycan profiles exhibit unique characteristics compared to adults.
- These findings are critical for developing and evaluating glycan-based diagnostics and therapeutics in children.
Abstract:
Despite the importance of protein glycosylation in all physiological and pathological processes and their potential as diagnostic markers and drug targets, the glycome of children is still unexplored. We analyzed N-linked plasma and IgG glycomes in 170 children and adolescents between 6 and 18 years of age. The results showed large biological variability at the population level as well as a large number of associations between different glycans and age. The plasma N-glycome of younger children was found to contain a larger proportion of large complex glycan structures (r = -0.71 for tetrasialylated glycans; r = -0.41 for trisialylated glycans) as well as an increase in disialylated biantennary structures (r = 0.55) with age. Core fucosylation and the level of agalactosylated plasma and IgG glycans decreased while digalactosylated glycans increased with age. This pattern of age-dependent changes in children differs from changes reported in adult population in both, direction and the intensity of changes. Also, sex differences are much smaller in children than in adults and are present mainly during puberty. These important observations should be accounted for when glycan-based diagnostic tests or therapeutics are being developed or evaluated.
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