Evaluation of a high-performance liquid chromatography method for urinary oxalate determination and investigation regarding the pediatric reference interval of spot urinary oxalate to creatinine ratio for screening of primary hyperoxaluria

• Main Authors: Cheng, L. (Author), Guan, Q. (Author), Li, H. (Author), Luo, X. (Author), Shen, Y. (Author)
• Format: Article
• Language: English
• Published: John Wiley and Sons Inc 2021
• Subjects: adolescent; Adolescent; Article; calibration; Calibration; child; Child; Child, Preschool; childhood; Chromatography, High Pressure Liquid; controlled study; creatinine; Creatinine; diagnostic accuracy; diagnostic test accuracy study; female; Female; high performance liquid chromatography; high-performance liquid chromatography; human; Humans; Hyperoxaluria, Primary; infant; Infant; Infant, Newborn; kidney disease; limit of detection; Limit of Detection; limit of quantitation; major clinical study; male; Male; newborn; oxalate; Oxalates; oxalic acid; oxalosis 1; preschool child; primary hyperoxaluria; procedures; reference value; Reference Values; renal system parameters; sensitivity and specificity; spot urinary oxalate to creatinine ratio; spot urine; urinalysis; Urinalysis; urine; urine level; urine sampling
• Online Access: View Fulltext in Publisher

 Background: Urinary oxalate can provide important clues for the screening and monitoring of children with primary hyperoxaluria (PH), which is a potentially life-threatening condition. However, little effort has been devoted to improve the oxalate assay in recent years. We have proposed a reliable and cost-effective high-performance liquid chromatography (HPLC) method for urinary oxalate determination. Methods: Urine specimens were centrifuged after one-step derivatization, and the supernatants were subjected to HPLC analysis. Results: The method was validated with consistent linearity from 0.0625 to 2.0 mmol/L with coefficients of variation ≤7.73%, good recovery, low carryover, satisfactory sample stability, and analytical specificity. The lower limit of quantification and the limit of detection were 0.03130 and 0.0156 mmol/L, respectively. Imprecision values were ≤2.92% and ≤16.6% for externally and internally produced controls, respectively. The pediatric reference interval of spot urinary oxalate to creatinine ratios was established together with its application in screening of PH in patients with renal diseases, revealing its successful deployment in our laboratory. Conclusions: This reliable HPLC method could serve as a significant tool to determine urinary oxalate levels for screening and monitoring of children with PH in routine clinical laboratories. © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.