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Kidney Function and Size in Children With Down Syndrome: A Cross-Sectional Study
Flavia Padoan1, Rossella Stifano1, Milena Brugnara1
1Pediatric Unit, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.
Insights
Children with Down syndrome (DS) have a high risk of kidney problems. Early kidney evaluations are crucial for detecting chronic kidney disease (CKD) in DS patients, especially adolescents.
Area of Science:
- Nephrology
- Pediatrics
- Genetics
Background:
- Down syndrome (DS) is linked to significant congenital anomalies, including renal and urinary tract issues.
- Renal anomalies in DS occur 4-5 times more frequently than in the general population.
- Current DS management guidelines do not mandate routine kidney evaluations, despite risk factors for chronic kidney disease (CKD).
Purpose of the Study:
- To analyze kidney size and function in children with Down syndrome.
- To highlight the need for early kidney assessments in DS patients.
- To underscore the importance of monitoring renal health, particularly in adolescents with DS.
Main Methods:
- Cross-sectional study design.
- Analysis of kidney size and function in 54 children with Down syndrome.
- Assessment of estimated glomerular filtration rate (eGFR), prevalence of renal hypoplasia, and body mass index (BMI).
Main Results:
- 25% of DS patients exhibited renal hypoplasia.
- 26% of DS patients had an eGFR below 90 mL/min/1.73 m².
- 55.5% of DS adolescents showed eGFR values below 90 mL/min/1.73 m²; 29.6% were overweight and 7.4% obese.
Conclusions:
- Early kidney assessments are necessary to detect early renal decline in DS.
- Close monitoring for CKD is vital in DS patients, with a particular focus on adolescents.
- Further research is needed to identify prognostic factors for CKD risk and renal replacement therapies in DS.
Abstract:
Down syndrome (DS) is associated with a high prevalence of congenital heart, gastrointestinal, and endocrine anomalies, as well as a heightened risk for kidney and urinary tract abnormalities. The renal anomalies occur in up to 3.2% of DS cases at birth-four to five times higher than in the general population. Despite this, current DS management guidelines lack routine kidney evaluations, even though risk factors like neonatal acute kidney injury, renal hypoplasia and obesity may predispose DS children to chronic kidney disease (CKD). In a cross-sectional study, we analysed kidney size and function in 54 DS children. Results revealed that 25% of patients exhibited renal hypoplasia, 26% had an estimated glomerular filtration rate (eGFR) below 90 mL/min/1.73 m2 Among adolescents, 55.5% showed eGFR values below 90 mL/min/1.73 m2 Additionally, 29.6% of the cohorts were overweight and 7.4% obese. There is a need for early kidney assessments in DS patients to detect initial renal decline and underscore the importance of close monitoring, particularly in adolescents. Further studies are needed to identify specific prognostic factors to better assess CKD risk in DS children, and limited research exists on renal replacement therapies for this population.
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