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Paediatric age-dependent serum transferrin isoform distribution studied by HPLC
Torsten Arndt1, Sven Stanzel, Adrian C Sewell
1Bioscientia Institut fuer Medizinische Diagnostik GmbH, 55218 Ingelheim, Germany. torsten.arndt@bioscientia.de
Insights
Transferrin isoforms in children show age-dependent changes, with pentasialotransferrin decreasing with age. Asialo- and monosialotransferrin are considered abnormal in pediatric serum.
Area of Science:
- Biochemistry
- Clinical Chemistry
- Pediatric Medicine
Background:
- Human serum transferrin exists in various isoforms based on glycosylation levels, ranging from asialo- to octasialotransferrin.
- Understanding age-dependent variations in transferrin isoform distribution is crucial for accurate clinical interpretation.
Purpose of the Study:
- To investigate age-dependent differences in transferrin isoform distribution in pediatric patients.
- To establish reference ranges for transferrin isoforms in children.
Main Methods:
- Serum samples from 126 pediatric patients across seven age groups were analyzed using High-Performance Liquid Chromatography (HPLC).
- Statistical analysis, including calculation of means, medians, and percentiles, was performed for each transferrin isoform to identify significant age-related differences.
Main Results:
- Carbohydrate-deficient transferrin (CDT), corresponding to disialotransferrin, showed no significant age-related differences.
- Trisialotransferrin and tetrasialotransferrin also exhibited no statistically significant age-dependent variations.
- Pentasialotransferrin demonstrated a statistically significant decrease with increasing age in pediatric serum.
Conclusions:
- Age-independent decision limits for disialotransferrin (95th percentile: 1.1%) and trisialotransferrin (95th percentile: 5.3%) are proposed for differentiating normal from elevated levels in children.
- The detection of asialotransferrin and monosialotransferrin in pediatric serum should be considered indicative of an abnormal condition.
Background:
Human serum transferrin shows different transferrin isoforms with e.g. a varying amount of glycosylation, resulting in asialo-, mono-, di-, up to octasialotransferrin. We wanted to examine whether there are age-dependent differences in this transferrin isoform distribution.
Methods:
Serum samples from a total of 126 paediatric patients (mean/median/minimum/maximum: 6.8/6.0/0.5/14 years) grouped in seven age groups (<2 years, 3-4 years, up to 13-14 years) were analyzed on an HPLC (Recipe Chemicals & Instruments GmbH, Munich, Germany). Means, medians and percentiles were computed for each transferrin isoform and tested for statistically significant differences between the age groups.
Results:
CDT corresponded to disialotransferrin (since asialo- and monosialotransferrins were not detectable) and did not show statistically significant differences between the 7 age groups. The latter is also true for trisialo- and tetrasialotransferrin whereas pentasialotransferrin shows a statistically significant decrease with age.
Conclusions:
We suggest that age-independent decision limits, e.g. the 95% percentiles for disialotransferrin (1.1%) and trisialotransferrin (5.3%), can be used for the differentiation between normal and increased fractions of these isoforms until paediatric reference ranges have been established. The presence of asialo- and monosialotransferrin in paediatric serum should be considered as abnormal.
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