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Longitudinal patterns of urine biomarkers in infants across gestational ages
Authors:Marissa J. DeFreitas  Wacharee Seeherunvong  Chryso P. Katsoufis  Satish RamachandraRao  Shahnaz Duara  Salih Yasin  Gaston Zilleruelo  Maria M. Rodriguez  Carolyn L. Abitbol
Affiliation:1.Division of Pediatric Nephrology,University of Miami/ Holtz Children’s Hospital,Miami,USA;2.O’Brien Center for AKI Research,UC San Diego School of Medicine,San Diego,USA;3.Division of Neonatology,University of Miami/Holtz Children’s Hospital,Miami,USA;4.Division of Perinatology and Obstetrics,University of Miami/Holtz Children’s Hospital,Miami,USA;5.Division of Pediatric Pathology,University of Miami/Holtz Children’s Hospital,Miami,USA
Abstract:

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 m2 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.
Keywords:
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