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Updated: Mar 26, 2026

Transdermal Measurement of Glomerular Filtration Rate in Mechanically Ventilated Piglets
Published on: September 13, 2022
Longitudinal analysis of serum cystatin C for estimating the glomerular filtration rate in preterm infants
Toshinori Nakashima1,2, Hirosuke Inoue3, Junko Fujiyoshi3
1Department of Pediatrics, Kitakyushu Municipal Medical Center, Fukuoka, Japan. binki@nifty.com.
Insights
Serum cystatin C (Cys-C) levels decrease with age in premature infants, establishing it as a reliable marker for estimating glomerular filtration rate (eGFR) in this population. This study provides crucial reference values for Cys-C in preterm infants during their first year of life.
Area of Science:
- Pediatric Nephrology
- Biomarkers
- Infant Health
Background:
- Cystatin C (Cys-C) is a more sensitive renal function marker than creatinine (Cre).
- Limited data exists on serum Cys-C reference values for estimating glomerular filtration rates (eGFRs) in premature infants during their first year of life.
Purpose of the Study:
- To establish reference values for serum Cys-C in premature infants.
- To evaluate Cys-C as a marker for eGFR in preterm infants during the first year of life.
Main Methods:
- Prospective study of 261 preterm infants with uncomplicated clinical courses.
- Collected 481 blood samples at multiple time points (6-30 days, 3-5 months, 7-9 months, 12-14 months).
- Measured serum Cys-C and Cre levels; calculated eGFR using two published equations.
Main Results:
- Median serum Cys-C levels significantly decreased with age up to 12-14 months.
- Cys-C levels were independent of gestational age and gender.
- Cys-C-based eGFR significantly increased with age, unlike Cys-C + Cre-based eGFR.
Conclusions:
- Reference ranges for Cys-C in premature infants gradually decline over the first year.
- Cys-C is a more reliable marker than Cre for estimating GFR in preterm infants.
Background:
Cystatin C (Cys-C) is a more sensitive marker of renal function than creatinine (Cre) in pediatric and adult populations. However, the reference values of serum Cys-C for estimating glomerular filtration rates (eGFRs) in premature infants during the first year of life have not been sufficiently studied.
Methods:
In this prospective study, 481 blood samples were collected from 261 preterm infants with uncomplicated clinical courses during their first year of life. Infants were divided into three groups according to gestational age at birth: 27-30 weeks, 31-33 weeks, and 34-36 weeks. Serum Cys-C and Cre levels were measured at 6-30 days, 3-5 months, 7-9 months, and 12-14 months after birth and the eGFR was calculated using two previously published equations.
Results:
The median serum Cys-C levels were 1.776, 1.248, 1.037, and 0.960 mg/L at the first, second, third, and fourth measurement time-point, respectively, with the value significantly decreasing with age up to 12-14 months. Cys-C levels were independent of gestational age and gender. In contrast to Cys-C, serum Cre values declined rapidly up to 3-5 months, then remained constant up to 12-14 months. Using the Cys-C-based equation, the eGFR significantly increased with increasing age until approximately 1 year after birth; however, no such trend was noted using the equation based on Cys-C + Cre.
Conclusions:
Reference ranges for Cys-C in premature infants decline gradually over the first year after birth. Cys-C appears to be a more reliable marker than Cre for estimating GFR in preterm infants.
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