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Comparison of Renal Stones and Nephrocalcinosis in Children: Findings From Two Tertiary Centers in Saudi Arabia
Khalid A Alhasan1,2, Mohamed A Shalaby3,4, Amr S Albanna5
1Pediatrics Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Insights
Pediatric renal stones and nephrocalcinosis are increasing. Nephrocalcinosis presents earlier and has worse outcomes than renal stones in children, often leading to chronic kidney disease.
Area of Science:
- Pediatric Nephrology
- Urology
- Pediatric Kidney Disease
Background:
- Incidence of pediatric renal stones (nephrolithiasis/urolithiasis) and nephrocalcinosis is rising.
- These conditions are uncommon but increasingly diagnosed in children.
Purpose of the Study:
- Compare clinical presentation, etiology, and outcomes of childhood nephrolithiasis/urolithiasis versus nephrocalcinosis.
- Identify risk factors and disease trajectories in pediatric kidney stone and calcification disorders.
Main Methods:
- Multicenter retrospective study of 144 children (93 with renal stones, 51 with nephrocalcinosis).
- Analysis of clinical data, including age at presentation, consanguinity, congenital anomalies of the kidneys and urinary tract (CAKUT), symptoms, and underlying causes.
- Comparison of clinical outcomes, including progression to chronic kidney disease (CKD) and end-stage kidney disease (ESKD).
Main Results:
- Children with nephrocalcinosis presented younger (54 months) than those with renal stones (72 months).
- Metabolic disorders (hyperoxaluria, cystinuria) were primary causes of renal stones, while familial hypomagnesemia and distal renal tubular acidosis were common in nephrocalcinosis.
- Nephrocalcinosis was associated with worse outcomes, including persistent calcification, higher rates of CKD (stage II-IV), and ESKD compared to renal stones.
Conclusions:
- Nephrocalcinosis in children has a younger age of onset and poorer prognosis than nephrolithiasis.
- Congenital anomalies of the kidneys and urinary tract (CAKUT) are significant in pediatric renal stone cases.
- Nephrocalcinosis poses a greater risk for long-term kidney damage and disease progression in pediatric patients.
Abstract:
Background: Renal stones (nephrolithiasis and urolithiasis) and nephrocalcinosis are uncommon in children; however, their incidences in pediatric populations have been increasing. Patients and Methods: This multicenter retrospective study compared the clinical presentation, etiology, and outcomes of childhood nephrolithiasis or urolithiasis with those of nephrocalcinosis. Results: The study included 144 children: 93 with renal stones and 51 with nephrocalcinosis. The mean age at presentation was 72 months and 54 months for children with renal stones and nephrocalcinosis, respectively. A history of consanguinity was found in 65% and 76% of the cases of renal stones and nephrocalcinosis, respectively. Congenital anomalies of the kidneys and urinary tract (CAKUT) were present in 28 and 9.8% of the patients with renal stones and nephrocalcinosis, respectively. The most common symptoms of renal stones were flank pain (29%), hematuria (15%), and dysuria (11%). Urinary tract infection was the primary presentation in the nephrocalcinosis group (18%), followed by failure to thrive (16%), polyuria (12%), and dehydration (12%). The majority of renal stone cases were caused by metabolic disorders, including hyperoxaluria (18%), cystinuria (18%), hypercalciuria (12%), and hyperuricosuria (2%). In contrast, the most common underlying disorders in cases of nephrocalcinosis were familial hypomagnesemia, hypercalciuria, nephrocalcinosis (35%), distal renal tubular acidosis (23%), and Bartter syndrome (6%). Clinical outcomes were significantly better in children with nephrolithiasis/urolithiasis than in those with nephrocalcinosis, who showed radiological evidence of worsening/persistent calcinosis and progressed more frequently to chronic kidney disease (stage II-IV) and end-stage kidney disease. Conclusion: The average age at presentation for children with renal stones was greater than that for those presenting with nephrocalcinosis. More than 25% of the children with renal stones were found to have CAKUT. Nephrocalcinosis was associated with worse clinical outcomes related to kidney function and disease resolution than nephrolithiasis.
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