Reference ranges for 24-h urinary protein/creatinine ratio and urinary microalbumin/creatinine ratio in Chinese

Lele Ding1, Ying Ding2, Shanshan Xu3

  • 1Department of Pediatrics, Henan University of Chinese Medicine, Zhengzhou, China.

Insights

This study established reference ranges for 24-h urinary protein/creatinine ratio (24hUPCR) and urinary microalbumin/creatinine ratio (UMACR) in Chinese children. Results show these ratios vary with age, gender, and BMI, highlighting the need for age- and gender-specific pediatric cutoff values.

Area of Science:

  • Pediatric Nephrology
  • Clinical Chemistry
  • Biomarker Research

Background:

  • Urinary protein and albumin excretion are key indicators of kidney health in children.
  • Establishing accurate reference ranges for 24-h urinary protein/creatinine ratio (24hUPCR) and urinary microalbumin/creatinine ratio (UMACR) is crucial for diagnosing kidney disease in pediatric populations.
  • Existing reference ranges may not adequately account for demographic variations such as age, gender, and ethnicity.

Purpose of the Study:

  • To investigate the age and gender characteristics of 24hUPCR and UMACR in healthy Chinese children.
  • To identify related factors influencing these urinary markers.
  • To establish preliminary, age- and gender-specific reference ranges for 24hUPCR and UMACR in this population.

Main Methods:

  • A cohort of 200 healthy Chinese children aged 2-15 years was analyzed.
  • Subjects were stratified into twelve age groups.
  • Kruskal-Wallis ANOVA and Spearman correlation analyses were employed to assess relationships between urinary markers and various parameters, with 95% reference ranges calculated.

Main Results:

  • Both 24hUPCR and UMACR demonstrated significant correlations with age, height, weight, and BMI (p < 0.001).
  • Females exhibited higher levels of both markers compared to males (p < 0.01).
  • Critical age nodes for significant changes in 24hUPCR and UMACR were identified at 6 and 8 years, respectively. Preliminary reference ranges were established, with distinct values for males and females across different age brackets (e.g., 24hUPCR < 24.34 mg/mmol for males aged 2-6 years, < 17.60 mg/mmol for males aged 6-15 years).

Conclusions:

  • Pediatric 24hUPCR and UMACR levels are influenced by age, gender, anthropometric measurements, and ethnicity.
  • Developing precise pediatric cutoff values that incorporate age, gender, and ethnicity is essential for optimizing the sensitivity and specificity of these biomarkers in clinical practice.
  • The established reference ranges provide a foundation for improved pediatric kidney function assessment in the studied population.
Abstract

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