Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin
Language English Country England, Great Britain Media print
Document type Clinical Trial, Comparative Study, Journal Article
PubMed
18613859
DOI
10.1111/j.1365-2710.2008.00932.x
PII: JCP932
Knihovny.cz E-resources
- MeSH
- Acetylglucosaminidase urine MeSH
- Amikacin administration & dosage pharmacokinetics pharmacology MeSH
- Anti-Bacterial Agents administration & dosage pharmacokinetics pharmacology MeSH
- Biomarkers blood MeSH
- Time Factors MeSH
- Cystatin C MeSH
- Cystatins blood MeSH
- Cystic Fibrosis blood drug therapy MeSH
- Child MeSH
- Adult MeSH
- Glomerular Filtration Rate * MeSH
- Infusions, Intravenous MeSH
- Creatinine blood urine MeSH
- Kidney drug effects pathology MeSH
- Humans MeSH
- Adolescent MeSH
- Drug Monitoring MeSH
- Child, Preschool MeSH
- ROC Curve MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Comparative Study MeSH
- Names of Substances
- Acetylglucosaminidase MeSH
- Amikacin MeSH
- Anti-Bacterial Agents MeSH
- Biomarkers MeSH
- CST3 protein, human MeSH Browser
- Cystatin C MeSH
- Cystatins MeSH
- Creatinine MeSH
BACKGROUND AND OBJECTIVE: Monitoring of renal function in cystic fibrosis (CF) patients is essential. The dosage regimen of amikacin is regularly modified according to the patient's glomerular filtration rate (GFR). The aim of the study was to evaluate the use of cystatin C (CyC) for monitoring amikacin therapy along with other markers of renal tubular and glomerular function, and damage [N-acetyl-beta-d glucosaminidase (NAG), creatinine level and creatinine clearance]. METHODS: We compared the GFR, estimated from the serum concentrations of creatinine (Cockcroft-Gault formula) and CyC (Grubb's formula). Seventy-one patients (mean age 12 years; range 4-28 years) with CF were treated by intermittent intravenous infusion of amikacin. Tubular nephrotoxicity was investigated by measurement of urine NAG/urine creatinine ratio (U-NAG/U-creatinine). Concentrations of all markers were measured before starting amikacin therapy and at days 3, 5, 7, 10 and 12. Fluorescence polarization analysis, turbidimetry, enzymatic phototometric creatinine deaminase method and fluorimetry were used for determination of serum amikacin, serum CyC, creatinine and urine NAG activity. Receiver operating characteristic (ROC) analysis was performed to assess the influence of GFR estimated from serum creatinine and serum CyC for the prediction of amikacin clearance during aminoglycoside therapy. RESULTS: Significant differences in the rate of U-NAG/U-creatinine were noted before and after treatment with amikacin (P < 0.001). Serum creatinine levels and creatinine clearance at the end of amikacin therapy (12th day) did not show any significant differences in comparison with the levels measured before the start of therapy (0th day). At days 5, 7, 10 and 12, serum CyC levels showed a significant elevation (P < 0.001), and CyC clearance showed a significant decrease (P < 0.001) in comparison with the levels measured at day 0. The ratio of amikacin clearance/creatinine clearance decreased with therapy whereas the amikacin clearance/CyC and amikacin clearance/CyC clearance increased. CONCLUSION: We showed that the rate of U-NAG/U-creatinine is a suitable marker for monitoring tubular nephrotoxicity in CF patients. Serum creatinine and estimated creatinine clearance are modest predictors of GFR in CF patients. CyC appears to be a better marker of GFR than serum creatinine concentration or creatinine clearance in our study. Serum CyC levels and CyC clearance showed greater ability to predict amikacin clearance during therapy than creatinine clearance.
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