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Serum and urine cystatin C levels in children with post-pyelonephritic renal scarring: a pilot study
Hüray Islekel1, Alper Soylu, Zekiye Altun
1Department of Biochemistry, Dokuz Eylül University School of Medicine, Izmir, Turkey.
Insights
Serum and urine cystatin C levels did not differ in children with or without renal scarring after acute pyelonephritis. However, urine cystatin C correlated with markers of tubular damage, suggesting its utility in assessing kidney function.
Area of Science:
- Pediatric Nephrology
- Renal Imaging
- Biomarker Discovery
Background:
- Acute pyelonephritis in children can lead to renal scarring, potentially causing long-term kidney damage.
- Early detection and monitoring of renal damage are crucial for managing pediatric kidney disease.
- Traditional markers of renal damage may not always be sensitive enough to detect subtle changes.
Purpose of the Study:
- To investigate the impact of unilateral renal scarring post-pyelonephritis on serum cystatin C (S(CysC)) and urine cystatin C (U(CysC)).
- To evaluate the correlation of cystatin C levels with other established markers of renal damage in pediatric patients.
- To determine the diagnostic utility of cystatin C in identifying renal scarring after acute pyelonephritis.
Main Methods:
- Children with DMSA-confirmed pyelonephritis were categorized into groups with (scar [+]) and without (scar [-]) unilateral renal scarring.
- The scar [+] group was further divided based on differential DMSA uptake (Delta(DMSA) <= 10% and > 10%).
- Serum creatinine, S(CysC), U(CysC)/Cr, urine NAG, microalbumin, protein, FE(Na), and TPR were measured in all participants.
Main Results:
- Neither S(CysC) nor U(CysC) showed significant differences between groups with and without renal scarring.
- S(CysC) levels did not increase in children with post-pyelonephritic scarring.
- U(CysC)/Cr demonstrated a significant correlation with urine microalbumin, NAG, and FE(Na) in the scar [+] group.
Conclusions:
- Serum and urine cystatin C are not significantly altered by unilateral renal scarring following pediatric pyelonephritis.
- Elevated S(CysC) levels may correlate with increased differential DMSA uptake, warranting further investigation.
- Urine cystatin C, particularly its ratio to creatinine, shows promise as a biomarker reflecting tubular dysfunction in children with renal scarring.
Aim:
We aimed to investigate in children with a history of acute pyelonephritis the influence of unilateral post-pyelonephritic renal scarring detected by DMSA scan on serum (S(CysC)) and urine cystatin C (U(CysC)) as well as upon other traditional markers of renal damage.
Methods:
Children with DMSA proven pyelonephritis (n = 28) were grouped as either scar [+] (n = 19, unilateral renal scarring) or scar [-] (no scarring, n = 9). The scar [+] group was further divided into scar-1 (differential DMSA uptake, Delta(DMSA) = 10%; n = 8) and scar-2 (Delta(DMSA) > 10%, n = 11) subgroups. S(CysC), serum creatinine, urine NAG, microalbumin, protein, fractional sodium excretion (FE(Na)), tubular phosphate reabsorption (TPR), and U(CysC/Cr) were evaluated in all patients.
Results:
Neither S(CysC) nor U(CysC) were affected by age, height, and weight. scar [+] versus scar [-] groups and scar-1 versus scar-2 subgroups were not different with regard to all studied parameters. S(CysC) did not increase in children with post-pyelonephritic unilateral renal scarring. However, 11 children with slightly increased (>0.95 mg/l) S(CysC) levels in scar [+] group tended to have higher Delta(DMSA), albeit not significantly. Furthermore, U(CysC/Cr) correlated well with urine microalbumin, NAG, and FE(Na) in all children and the scar [+] group (P < 0.05).
Conclusion:
S(CysC) and U(CysC) did not differ among pediatric patients with and without unilateral post-pyelonephritic renal scarring. However, Delta(DMSA) uptake between the two kidneys tended to be raised in children with S(CysC) levels higher than the reference ranges. Additionally, U(CysC/Cr) exhibits parallelism with tubular functions.
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