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Beta-trace protein--a marker of kidney function in children: "Original research communication-clinical investigation"
Arend Bökenkamp1, Ingo Franke, Michael Schlieber
1Children's Hospital, Bonn University Medical Center, Bonn, Germany. Bokenkamp@VUmc.nl
Insights
Serum beta-trace protein (beta-TP) shows potential as a kidney function marker in children. Its pediatric reference interval was established and compared to cystatin C and beta(2)-microglobulin.
Area of Science:
- Pediatric Nephrology
- Clinical Chemistry
- Biomarker Discovery
Background:
- Accurate assessment of glomerular filtration rate (GFR) is crucial in pediatric kidney disease.
- Established low-molecular-weight (LMW) markers like cystatin C (CysC) and beta(2)-microglobulin (beta(2)-M) have limitations.
- Beta-trace protein (beta-TP) is an endogenous LMW protein with potential as a GFR marker.
Purpose of the Study:
- To establish the pediatric reference interval for serum beta-trace protein (beta-TP).
- To compare the performance of beta-TP against established GFR markers, CysC and beta(2)-M, in children.
- To evaluate beta-TP's utility as an endogenous marker for GFR in pediatric populations.
Main Methods:
- Serum samples from 106 healthy children (age >2 years) were used to determine non-parametric reference intervals for beta-TP, CysC, and beta(2)-M.
- Immunonephelometry was employed for the quantitative measurement of all three LMW markers.
- The relative increase in marker concentrations was analyzed in 107 samples from 96 pediatric patients across the full spectrum of GFR.
Main Results:
- The established reference range for serum beta-TP in children over 2 years old was 0.43-1.04 mg/L.
- Beta-TP demonstrated a comparable rise to beta(2)-M as GFR decreased.
- While CysC showed a less pronounced increase in the lowest GFR group ( <30 mL/min/1.73 m(2)), beta-TP and beta(2)-M exhibited significant elevations (p=0.043 and p=0.027, respectively).
Conclusions:
- Serum beta-trace protein (beta-TP) is a reliable endogenous marker for assessing GFR in children.
- Beta-TP exhibits comparable performance to beta(2)-microglobulin and potentially offers advantages over cystatin C in severely impaired GFR.
- Further validation supports beta-TP's role in pediatric nephrology for GFR estimation.
Objectives:
To determine the pediatric reference interval for serum beta-trace protein (beta-TP) and to compare beta-TP with established LMW markers of GFR, i.e., cystatin C (CysC) and beta(2)-microglobulin (beta(2)-M).
Design And Methods:
All three LMW markers were measured immunonephelometrically. In 106 children above the age of 2 years without evidence of kidney disease, non-parametric reference intervals were calculated. The relative rise of the GFR marker concentrations above the upper reference was studied in 107 samples from 96 patients covering the entire GFR range.
Results:
Above 2 years, the reference range of beta-TP was constant at 0.43-1.04 mg/L. With decreasing Schwartz-GFR, there was a comparable rise in beta-TP and beta(2)-M, while CysC rose less in the group with GFR below 30 mL/min/1.73 m(2) (278+/-49% [CysC] versus 336+/-65% [beta-TP] and 342+/-76% [beta(2)-M]; p=0.043 and 0.027, respectively).
Conclusions:
These data confirm the potential of ss-TP as an endogenous GFR marker in children.
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