BIOMARKERS OF RENAL INJURY RISK IN CHILDREN WITH PYELONEPHRITIS

T Sorokman1, S Sokolnyk1, O Popelyuk1

  • 1Bukovinian State Medical University, Department of Pediatrics and Medical Genetics; Department of human anatomy Mykola Turkevich; Department nursing of higher nursing education; Department of Pharmacology Chernivtsi, Ukraine.

Georgian Medical News
|September 12, 2018
PubMed

Insights

Pyelonephritis (PN) in infants with urinary anomalies is often linked to congenital issues. Organ-specific enzymes in urine and serum markers like Galectin-3 show promise for diagnosing kidney damage and fibrotic changes in children with PN.

Area of Science:

  • Pediatric Nephrology
  • Clinical Biochemistry
  • Urology

Background:

  • Pyelonephritis (PN) is a common cause of fever in children with urinary system anomalies.
  • Current diagnostic markers for PN in children are insufficient, necessitating research into novel biomarkers.
  • Congenital malformations frequently underlie PN in pediatric patients.

Purpose of the Study:

  • To investigate the utility of urinary organ-specific enzymes (neutral α-glucosidase, L-alanine aminopeptidase, γ-glutamyltranspeptidase) and serum markers (galectin-3, C-reactive protein) for diagnosing PN in infants.
  • To assess the correlation between these markers and the severity of PN, particularly in cases associated with vesicoureteral reflux (VUR).
  • To explore the potential of galectin-3 for early detection of renal parenchymal fibrosis in children with PN and VUR.

Main Methods:

  • A prospective study involving 75 infants under one year old with fever and urinary changes.
  • Measurement of urinary enzymes (NAG, AAP, GGTP) and serum markers (Gal-3, CRP) as indicators of proximal tubule damage.
  • Clinical and instrumental examinations to diagnose PN and assess VUR grades.

Main Results:

  • PN was diagnosed in the majority of hospitalized children, often associated with congenital urinary tract malformations.
  • Elevated urinary enzyme levels correlated with active PN, leukocyturia, and CRP levels.
  • Higher urinary enzyme levels were observed in the inactive phase of PN with VUR compared to PN without VUR.
  • Increased Gal-3 levels were associated with underlying VUR, inflammatory activity, and CRP, suggesting its role in diagnosing fibrotic changes.

Conclusions:

  • Urinary organ-specific enzymes and serum Gal-3 are valuable markers for assessing kidney damage in pediatric PN.
  • Gal-3 shows potential for early diagnosis of renal fibrosis in children with PN and VUR.
  • Congenital anomalies, especially VUR, are significant factors in pediatric PN and influence marker expression.

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