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Reference intervals for serum cystatin C in neonates and children 30 days to 18 years old
Tengyi Cai1, Vasiliki Karlaftis1, Stephen Hearps1
1Murdoch Children's Research Institute, Parkville, Australia.
Insights
This study established continuous paediatric reference intervals for serum cystatin C (CysC) in children. These new reference intervals account for age, blood group, and gender, improving kidney function assessment.
Area of Science:
- Clinical Biochemistry
- Paediatric Nephrology
Background:
- Serum cystatin C (CysC) offers superior accuracy and sensitivity for assessing kidney function compared to creatinine.
- Accurate and sensitive biomarkers are crucial for early detection and management of kidney disease in children.
Purpose of the Study:
- To establish continuous paediatric reference intervals (RIs) for serum CysC.
- To facilitate the clinical application of serum CysC as a reliable biomarker for paediatric kidney function.
Main Methods:
- Serum CysC levels were measured in healthy term neonates and children (30 days to 18 years).
- Immunoturbidimetric methods were employed for serum CysC quantification.
- Fractional polynomial and quantile regression models were utilized to generate continuous RIs.
Main Results:
- A total of 378 samples (equal male/female distribution) were analyzed.
- No outliers were detected in the serum CysC data.
- Continuous RIs were successfully generated and presented as equations and graphical scatterplots.
Conclusions:
- Continuous paediatric reference intervals for serum CysC were successfully established.
- The generated RIs demonstrate dynamic, age-based changes in serum CysC levels.
- Significant blood group and gender-specific differences were identified for serum CysC.
Background:
Serum cystatin C (CysC) is a promising biomarker of kidney function, which has higher accuracy and sensitivity when compared with creatinine. To better utilize serum CysC in clinical practice, this study aimed to establish continuous paediatric reference intervals (RIs) for serum CysC.
Methods:
The study subjects consisted of healthy term neonates and children aged 30 days to 18 years. Venous blood samples were collected and serum CysC levels were measured using the immunoturbidimetric measurement principle. Fractional polynomial regression model and quantile regression was applied in the statistical analysis to generate continuous RIs.
Results:
A total of 378 samples with equal numbers of males and females were analysed for serum CysC. No outliers were found in this analysis. The continuous RIs are presented as equations and graphical scatterplots.
Conclusions:
This study established continuous paediatric reference intervals (RIs) for serum CysC in healthy term neonates and children. The continuous RIs generated from this study show age-based dynamic changes as well as blood group and gender-specific differences for serum CysC. Graphical abstract.
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