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Published on: June 23, 2015
[Study of renal function in infants diagnosed with renal pyelectasis in the first year of life]
J León González1, V García Nieto, A Hernández Rodríguez
1Unidad de Nefrología Pediátrica. Departamento de Pediatría. Hospital Nuestra Señora de la Candelaria. Santa Cruz de Tenerife.
Insights
Infants with pyelectasis show normal glomerular function but may have moderate tubular abnormalities, with some at risk for kidney stones later in life. Further research on renal pelvis dilatation is warranted.
Area of Science:
- Pediatric Nephrology
- Urology
- Developmental Biology
Context:
- Pyelectasis, or renal pelvis dilatation, is a common finding in infants.
- Understanding its long-term impact on kidney function is crucial for early intervention.
- Glomerular and tubular functions are key indicators of overall renal health.
Purpose:
- To assess glomerular and tubular function in infants diagnosed with pyelectasis.
- To identify potential risks for kidney stone formation in this population.
- To evaluate the reversibility of observed renal function abnormalities.
Summary:
- This study evaluated 14 infants with pyelectasis, measuring creatinine, urinary calcium, citrate, oxalate, N-acetyl-D-glucosaminidase (NAG), microalbumin, and urine osmolality.
- While glomerular function remained normal, 42.9% had abnormal urine osmolality, and 28.6% showed elevated albuminuria.
- Metabolic urinary anomalies, including hypercalciuria and hyperoxaluria, were present in 10 patients, suggesting a potential risk for lithiasis.
Impact:
- Reveals that infants with pyelectasis generally maintain normal glomerular function.
- Highlights the presence of moderate tubular dysfunction and metabolic urinary anomalies in some infants.
- Suggests pyelectasis may be an early indicator for future kidney stone risk, necessitating further investigation.
Objective:
To evaluate glomerular and tubular function in a group of infants diagnosed with pyelectasis.
Patients And Methods:
We studied 14 patients diagnosed with renal pelvis dilatation in-utero or during the first year of life. Creatinine concentrations, urinary excretion of calcium, citrate, oxalate, N-acetyl-D-glucosaminidase (NAG), microalbumin and maximum urine osmolality after administration of intranasal desmopressin were determined. The latter three variables were determined at diagnosis and at the end of follow-up.
Results:
In all patients creatinine levels were normal. In six patients (42.9%) maximum urine osmolality values were abnormal. In four patients NAG/creatinine concentrations were elevated and in another four patients (28.6%) albumin urinary excretion was elevated. These anomalies tended to return to normal but, at the end of the study, three patients (21.4%) showed increased albuminuria and one (7.1%) showed persistently defective renal concentrating capacity. Ten patients showed metabolic urinary anomalies, potentially leading to the formation of stones (isolated hypercalciuria in five [35,7%], hyperoxaluria in two and hypocitraturia in one, and hypercalciuria associated with hyperoxaluria in two).
Conclusions:
All patients showed normal glomerular function. Some patients presented increased albuminuria and moderate tubular function abnormalities, both of which tended to return to normal. Although studies with greater numbers of patients are needed, we propose that pyelectasis maybe a predictor of risk for lithiasis at later stages of life.
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