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Increased urinary podocytes following indomethacin suggests drug-induced glomerular injury
Alison L Kent1, Linda Brown, Margaret Broom
1Department of Neonatology, Canberra Hospital, PO Box 11, Woden, 2606, ACT, Australia. alison.kent@act.gov.au
Insights
Preterm infants exposed to indomethacin showed increased urinary podocytes and albumin, indicating glomerular injury. Further research is needed to understand long-term renal effects in these vulnerable infants.
Area of Science:
- Neonatal research
- Pediatric nephrology
- Renal development
Background:
- Glomerulogenesis continues post-birth in preterm infants, making them susceptible to renal insults.
- Urinary podocytes serve as a biomarker for glomerular injury.
- Medications like gentamicin and indomethacin may impact developing kidneys.
Purpose of the Study:
- To investigate podocyte excretion in preterm and term infants.
- To determine if gentamicin and indomethacin exposure increases urinary podocyte excretion.
Main Methods:
- Urine samples collected daily from preterm infants (<33 weeks gestation) on gentamicin or indomethacin.
- Urine samples collected for 3 days from preterm and term control infants.
- Quantification of urinary podocytes and casts compared between groups.
Main Results:
- Forty-two neonates participated.
- Both preterm and term controls excreted minimal podocytes (<2).
- Preterm infants receiving indomethacin showed significantly higher podocyte and albumin excretion (p=0.02).
Conclusions:
- Elevated urinary podocytes and albumin in preterm infants on indomethacin suggest glomerular injury.
- The long-term consequences of this early glomerular injury on renal development and adult function remain unknown.
Background:
Preterm infants are delivered while glomerulogenesis is ongoing and may be exposed to insults, including medications that may affect renal development. Podocytes detected in the urine are an indicator of glomerular injury. The aims of this study were to determine whether preterm and term infants excrete podocytes in their urine and whether exposure to gentamicin and indomethacin increase podocyte excretion in their urine.
Methods:
Preterm infants <33 weeks gestation had urine collected each day while receiving either gentamicin or indomethacin. Preterm and term control infants had urine collected for 3 days. The number of casts and podocytes present in the urine of infants receiving indomethacin and gentamicin were compared with preterm and term control infants.
Results:
Forty-two neonates were included in the study. Podocytes were present in small numbers (< 2) in the urine of both preterm and term control neonates. The number of podocytes in the preterm group receiving indomethacin was significantly higher than in all other groups (p=0.02) ,as was urinary albumin (p=0.02).
Conclusions:
Increased number of podocytes in preterm neonates receiving indomethacin and higher excretion of albumin suggest glomerular injury is occurring. It is unknown whether injury to glomeruli during glomerulogenesis in preterm neonates has long-term sequelae for renal development and function into adulthood.
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