Longitudinal patterns of urine biomarkers in infants across gestational ages
Marissa J DeFreitas1, Wacharee Seeherunvong2, Chryso P Katsoufis2
1Division of Pediatric Nephrology, University of Miami/ Holtz Children's Hospital, 1611 NW 12th Avenue (Annex 504), Miami, FL, 33136, USA. mdefreitas@med.miami.edu.
Insights
Urinary biomarkers like epidermal growth factor (EGF) and uromodulin (UMOD) change with gestational age in neonates. These developmental patterns help assess normal kidney development in infants.
Area of Science:
- Neonatal physiology
- Pediatric nephrology
- Biomarker research
Background:
- Urinary biomarkers may indicate acute kidney injury (AKI) but their developmental patterns in healthy neonates are poorly understood.
- Understanding these patterns is crucial for assessing kidney health in infants across a spectrum of gestational ages.
Purpose of the Study:
- To investigate the developmental trajectories of seven urinary biomarkers in healthy neonates from birth to three months of age.
- To characterize how these biomarkers change with advancing gestational age (GA) and post-natal development.
Main Methods:
- Urine samples were collected from 52 infants (24-41 weeks GA) from birth to 3 months.
- Assayed for albumin (ALB), beta-2-microglobulin (B2M), cystatin-C (CysC), epidermal growth factor (EGF), neutrophil-gelatinase-associated lipocalin (NGAL), osteopontin (OPN), and uromodulin (UMOD).
Main Results:
- Epidermal growth factor (EGF) and uromodulin (UMOD) increased with advancing GA and post-natal age.
- By 3 months, preterm infants' EGF and UMOD levels reached those of term infants.
- EGF and UMOD showed potential for distinguishing estimated glomerular filtration rate (GFR) <30 ml/min/1.73 m², while cystatin-C/creatinine and albumin/creatinine were significant functional markers.
Conclusions:
- Urinary biomarker levels significantly vary with gestational age in healthy neonates.
- These findings support the utility of urinary biomarkers for monitoring normal kidney development in infants.
- Specific biomarkers like EGF and UMOD can track kidney maturation and function in the neonatal period.
Background:
Urinary biomarkers may be indicators of acute kidney injury (AKI), although little is known of their developmental characteristics in healthy neonates across a full range of gestational age (GA). The purpose of this study was to examine patterns of urinary biomarkers across GA groups from birth to 3 months of age.
Methods:
Fifty-two infants ranging from 24 to 41 weeks' GA had urine assayed from birth through 3 months of age for 7 biomarkers including albumin (ALB), beta-2-microglobulin (B2M), cystatin-C (CysC), epidermal growth factor (EGF), neutrophil-gelatinase-associated lipocalin (NGAL), osteopontin (OPN), and uromodulin (UMOD).
Results:
Of the seven urinary biomarkers, EGF and UMOD increased while others decreased with advancing GA. By 3 months of age, EGF and UMOD had increased in preterm infants to levels similar to those of term infants. UMOD/ml and EGF/ml appeared to be predominantly developmental biomarkers distinguishing estimated glomerular filtration rate (GFR) <30 ml/min/1.73 m(2) with receiver operator characteristic area under the curve (ROC-AUC) of 0.82; p = 0.002. When factored by urine creatinine CysC/cr + ALB/cr were the most significant functional markers with AUC = 0.79; p = 0.004; sensitivity 96 %; specificity 58 %.
Conclusions:
Among healthy neonates, urinary biomarkers vary with GA. These data support the use of urinary biomarkers in the assessment of normal kidney development in the absence of injury.
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