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Urinary endothelin-1 in children with acute renal failure of tubular origin
1Department of Pediatrics, National Taiwan University Hospital, Taipei.
Insights
Urinary endothelin-1 (ET-1) levels change with age in children and are altered in acute renal failure (ARF). Renal production, not filtration, appears to be the primary source of urinary ET-1 in humans.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Biochemistry
Background:
- Endothelin-1 (ET-1) is a potent vasoconstrictor with implications in renal function.
- Urinary ET-1 excretion patterns and its origin in children, particularly during acute renal failure (ARF), are not well understood.
Purpose of the Study:
- To characterize developmental changes in urinary ET-1 concentrations in healthy children.
- To investigate the changes in urinary and plasma ET-1 in children with ARF.
- To explore the source of urinary ET-1 in humans.
Main Methods:
- Measured urinary endothelin-1 to creatinine ratio (ET-1/Cr) in 70 healthy children and 12 children with ARF.
- Correlated urinary ET-1/Cr with daily urinary ET-1 and plasma ET-1 levels.
- Monitored ET-1 levels during the course of ARF relative to serum creatinine peaks.
Main Results:
- Urinary ET-1/Cr was highest in infancy among healthy children.
- Children with ARF showed elevated plasma ET-1 and a positive correlation between urinary ET-1/Cr and total urinary ET-1.
- Urinary ET-1/Cr decreased during peak serum creatinine in ARF, while plasma ET-1 declined post-peak.
Conclusions:
- Urinary ET-1 concentrations exhibit developmental changes in children.
- ARF alters both plasma and urinary ET-1 levels.
- Results suggest renal production is the main source of urinary ET-1, rather than glomerular filtration.
Abstract:
To understand the changes of urinary endothelin-1 (ET-1) concentrations in acute renal failure (ARF) and to investigate the origin of human urinary ET-1, we studied urinary ET-1 excretion in 70 normal children and 12 children with ARF caused by tubular dysfunction. Urinary ET-1 excretion was expressed as a ratio of urinary ET-1 to urinary creatinine (ET-1/Cr). Among healthy children, the highest urinary ET-1/Cr values were found during infancy. In patients with ARF, there was a positive correlation between urinary ET-1/Cr values and daily total urinary ET-1 (r = 0.42, n = 26, p < 0.05). Plasma ET-1 concentrations were elevated in children with ARF during the period of peak serum creatinine concentration. During the course of ARF, the lowest urinary ET-1/Cr value occurred during the period of peak serum creatinine, whereas the plasma ET-1 concentration declined after the peak. These results provide insight into the developmental changes of urinary ET-1 values in normal children, and illustrate the pattern of changes in plasma and urinary ET-1 concentrations during the course of ARF in children. The results suggest that renal production, rather than clearance from the circulation by glomerular filtration, may be the source of urinary ET-1.
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