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Urinary biomarker as a predictor of urolithiasis in children: a systematic review and meta-analysis
Derryl Texaga1, Saskia Ratna Desita2, Nadira Muthi Tsania3
1Rantauprapat Regional General Hospital, Labuhanbatu.
Insights
Urinary citrate, oxalate, and calcium levels can help predict pediatric urolithiasis risk. Low citrate, high oxalate, and high calcium are key indicators of stone formation in children.
Area of Science:
- Pediatric Nephrology
- Urology
- Biomarker Discovery
Background:
- Pediatric urolithiasis poses long-term risks to kidney function and quality of life.
- Previous studies on urinary biomarkers for pediatric urolithiasis risk have yielded inconsistent results.
- This meta-analysis evaluates the diagnostic potential of urinary risk factors in children.
Purpose of the Study:
- To assess the diagnostic value of urinary citrate/creatinine (Cit/Cr), oxalate/creatinine (Ox/Cr), calcium/creatinine (Ca/Cr), phosphorus/creatinine (P/Cr), magnesium/creatinine (Mg/Cr), and urea/creatinine (Ur/Cr) ratios in pediatric urolithiasis.
- To identify reliable urinary biomarkers for predicting urolithiasis risk in children.
Main Methods:
- Systematic review and meta-analysis adhering to PRISMA 2020 guidelines.
- Inclusion of six studies (1 cohort, 5 case-control) with 2,060 pediatric patients.
- Analysis of urinary risk factors and calculation of Standard Mean Differences (SMD) with heterogeneity assessment.
Main Results:
- Significant differences observed in Cit/Cr, Ca/Cr, Ox/Cr, and Mg/Cr ratios between children with and without urolithiasis.
- Hypocitraturia (Cit/Cr), hyperoxaluria (Ox/Cr), hypercalciuria (Ca/Cr), and hypomagnesuria (Mg/Cr) are significantly associated with pediatric urolithiasis.
- No significant associations found for P/Cr and Ur/Cr ratios.
Conclusions:
- Cit/Cr, Ox/Cr, and Ca/Cr ratios show promise as urinary biomarkers for pediatric urolithiasis risk.
- Hypocitraturia, hyperoxaluria, and hypercalciuria are key metabolic abnormalities linked to urinary stone formation in children.
- Further research with standardized methods is needed to confirm findings and guide clinical practice.
Introduction:
Urolithiasis in children has become a clinical concern because of its longterm impact on kidney function and quality of life. In previous studies, the role of urinary biomarkers in predicting the risk of urolithiasis in children was still unclear due to inconsistent findings. This meta-analysis aimed to evaluate the diagnostic potential of various urinary risk factors in children with urolithiasis.
Methods:
A systematic review and meta-analysis was performed based on PRISMA 2020 guidelines, registered in PROSPERO (CRD42025644893). A total of six studies (1 cohort and 5 case-control) involving 2,060 pediatric patients (817 with urolithiasis; 1,243 controls) were analyzed. Urinary risk factors - including citrate/creatinine (Cit/Cr), oxalate/creatinine (Ox/Cr), calcium/creatinine (Ca/Cr), phosphorus/creatinine (P/Cr), magnesium/ creatinine (Mg/Cr), and urea/creatinine (Ur/Cr) - were examined. Standard Mean Differences (SMD) were calculated, and heterogeneity was assessed using the I² statistic.
Results:
Significant differences were obtained in the Cit/Cr, Ca/Cr, Ox/Cr, and Mg/Cr ratios between children with urolithiasis and controls. Hypocitraturia (Cit/Cr SMD: -0.60, 95% CI: -0.90 to -0.30, p = 0.0001), hyperoxaluria (Ox/Cr SMD: 0.76, 95% CI: 0.37-1.16, p = 0.0001), hypercalciuria (Ca/Cr SMD: 0.55, 95% CI: 0.10-1.01, p = 0.02), and hypomagnesuria (SMD -0.13 (95% CI: -0.24 to -0.01), p = 0.03) were significantly associated with the formation of stones in the urinary tract. On the contrary, there were no significant relationships for P/Cr and Ur/Cr ratios.
Conclusions:
This meta-analysis highlights Cit/Cr, Ox/Cr, and Ca/Cr ratios as potential urinary biomarkers to identify the risk of urolithiasis in pediatric patients. Hypocitraturia, hyperoxaluria, and hypercalciuria are the main metabolic abnormalities that contribute to urinary tract stone formation. Future studies with standardized methodology are essential to confirm these findings and guide clinical management strategies.
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