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Renal injury in children with a solitary functioning kidney--the KIMONO study
Rik Westland1, Michiel F Schreuder, Arend Bökenkamp
1Department of Paediatric Nephrology, VU University Medical Centre, Amsterdam, The Netherlands. jae.vwijk@vumc.nl
Insights
Children with a solitary functioning kidney (SFK) face early renal injury, including hypertension and albuminuria. This risk is higher with congenital anomalies of the kidney and urinary tract (CAKUT), necessitating close clinical follow-up.
Area of Science:
- Pediatric Nephrology
- Renal Physiology
- Urology
Background:
- Children with a solitary functioning kidney (SFK) are at increased risk for hypertension, albuminuria, and chronic kidney disease.
- This risk may stem from glomerular hyperfiltration and congenital anomalies of the kidney and urinary tract (CAKUT).
Purpose of the Study:
- To assess renal injury markers in children with SFK.
- To investigate the impact of CAKUT on renal health in these children.
- To evaluate the long-term risk of chronic kidney disease.
Main Methods:
- Retrospective study of 206 children with SFK, categorized by origin (primary/congenital vs. secondary).
- Stratification of data based on ipsilateral CAKUT presence.
- Longitudinal modeling using generalized estimating equations for blood pressure, albuminuria, and glomerular filtration rate.
Main Results:
- Renal injury (hypertension, albuminuria, or renoprotective medication) was found in 32% of children with SFK.
- Children with ipsilateral CAKUT showed significantly higher rates of renal injury (48.3% vs. 24.6%).
- Longitudinal models indicated a decline in glomerular filtration rate starting from puberty.
Conclusions:
- Renal injury is prevalent in children with SFK even at a young age.
- The presence of ipsilateral CAKUT exacerbates renal injury.
- Children with SFK face an elevated risk of chronic kidney disease in adulthood, highlighting the need for ongoing clinical monitoring.
Background:
Children with a solitary functioning kidney (SFK) have an increased risk of developing hypertension, albuminuria and chronic kidney disease in later life. This renal injury is hypothesized to be caused by glomerular hyperfiltration that follows renal mass reduction in animal studies. Furthermore, children with an SFK show a high incidence of congenital anomalies of the kidney and urinary tract (CAKUT), which could further compromise renal function.
Methods:
A retrospective study of renal injury markers was performed in 206 children, divided into groups based on the origin of SFK [primary (congenital) SFK (n = 116) and secondary SFK (n = 90)]. Data on ipsilateral CAKUT were stratified separately. For blood pressure, albuminuria and glomerular filtration rate, longitudinal models were additionally developed using generalized estimated equation analysis.
Results:
Renal injury, defined as the presence of hypertension and/or albuminuria and/or the use of renoprotective medication, was present in 32% of all children with an SFK at a mean age of 9.5 (SD 5.6) years. Children with ipsilateral CAKUT had higher proportions of renal injury (48.3 versus 24.6%, P < 0.05). Furthermore, longitudinal models showed a decrease in glomerular filtration rate in both groups from the beginning of puberty onwards.
Conclusions:
This large cohort study demonstrates that renal injury is present in children with an SFK at a young age, whereas our longitudinal models show an increased risk for chronic kidney disease in adulthood. Renal injury is even more pronounced in the presence of ipsilateral CAKUT. Therefore, we underline that clinical follow-up of all children with an SFK is needed.
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