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Reference ranges for serum β-trace protein in neonates and children younger than 1 year of age
Insights
This study establishes β-trace protein (BTP) reference ranges for infants, showing levels are highest at birth and decrease with age. BTP may be a useful marker for kidney function in newborns.
Area of Science:
- Pediatric Nephrology
- Biomarker Discovery
- Clinical Chemistry
Background:
- Glomerular filtration rate (GFR) assessment in infants is crucial for diagnosing kidney disease.
- β-trace protein (BTP) is a potential endogenous marker for GFR, but reference ranges in young children are lacking.
- Establishing BTP reference ranges in infants is essential for its clinical application.
Purpose of the Study:
- To determine the reference range of serum β-trace protein (BTP) in healthy children under one year of age.
- To investigate the developmental changes in BTP concentrations during the first year of life.
- To evaluate BTP as a potential alternative marker for GFR estimation in neonates and infants.
Main Methods:
- Serum samples were collected from 95 healthy children aged less than 12 months.
- Serum BTP was measured using a latex assay on a nephelometer.
- Serum creatinine and cystatin C were measured to confirm normal renal function.
Main Results:
- The 50th centile BTP reference concentration for children under one year was 0.82 mg/L (5th-95th centiles: 0.27-1.38 mg/L).
- BTP concentrations were highest in neonates and showed a steady decline with increasing age (Spearman's correlation: -0.415, p=0.002).
- No significant gender differences in BTP levels were observed.
Conclusions:
- This study provides the first reference range for serum BTP in infants up to one year of age.
- The observed postnatal decline in BTP is limited, suggesting its potential as a reliable GFR marker in newborns.
- BTP may offer a valuable alternative to current creatinine-based GFR estimation methods in the pediatric population.
Background:
β-Trace protein (BTP) has been proposed as an alternative endogenous marker of glomerular filtration rate. Data on BTP reference ranges in young children are scarce. We therefore aim to establish reference ranges and examine the developmental course of serum BTP in basically healthy children younger than 1 year of age.
Methods:
Single blood samples were taken from healthy children (born at gestational age ≥37 weeks) <12 months of age. Serum BTP was measured using the N latex B-trace protein assay (Siemens Diagnostics, Deerfield, IL, USA) on an Immage® 800 Rate Nephelometer (Beckman Coulter Inc. Brea, CA, USA). Serum creatinine and cystatin C were additionally determined and compared to reference values to confirm a normal renal function.
Results:
From June 2010 to January 2014, 95 blood samples were collected from 95 children {67.4% male; median age 120 days [inter quartile range 57-166]}. BTP was normally distributed (mean concentration 0.84±standard deviation 0.35 mg/L). Considering all children, the 50th centile BTP reference concentration was 0.82 mg/L (5th-95th centiles; 0.27-1.38). BTP concentrations were the highest in neonates and steadily declined with increasing age (Spearman's rank correlation was -0.415, p=0.002). No gender differences were found.
Conclusions:
Our data provide a BTP reference range for the first year of life. Seeing the biological pattern of BTP, with only a limited postnatal decline, this marker might offer a promising alternative to serum creatinine-based methods for estimating glomerular filtration rate in newborns.
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