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Screening for proteinuria in Japanese schoolchildren: a new approach
M J Pugia1, M Murakami, J A Lott
1Diagnostics Business Group, Bayer Corporation, Elkhart, IN, USA.
Insights
This study enhanced a school screening for kidney disorders by adding albumin and creatinine tests. The improved urinalysis effectively identified more cases of nephritis, diabetes mellitus, and other urinary tract abnormalities in students.
Area of Science:
- Pediatric Nephrology
- Diagnostic Screening
- Public Health
Background:
- Japanese school children undergo annual screening for proteinuria, hematuria, and glucosuria.
- Existing screening protocols aim to detect potential renal disorders early.
Purpose of the Study:
- To evaluate the utility of adding urine dipstick tests for albumin and creatinine to the existing Japanese school screening protocol.
- To assess the impact of these additions on identifying various urinary tract abnormalities and diabetes mellitus.
Main Methods:
- Implemented urine dipstick tests for albumin, creatinine, blood, glucose, and protein.
- Used sulfosalicylic acid precipitation test to confirm trace protein results.
- Analyzed data from 23,121 students participating in the enhanced screening.
Main Results:
- Identified seven cases of likely nephritis, one confirmed nephritis, and one nephrotic syndrome.
- Detected 170 instances of persistent unexplained hematuria and 19 of persistent unexplained proteinuria.
- Found 14 urinary tract infections and 20 likely cases of diabetes mellitus.
Conclusions:
- Dipstick testing for albumin, protein, creatinine, glucose, and occult blood is valuable in a multilevel screening scheme.
- Assaying albumin enhances screening sensitivity for renal disorders.
- The albumin-to-creatinine ratio mitigates errors from urine concentration variations.
Abstract:
By governmental mandate, Japanese school children are screened annually for proteinuria, hematuria, and glucosuria to identify children with possible renal disorders. We added urine dipstick tests for albumin and creatinine to the Japanese screening protocol, and used their dipstick results for blood, glucose and protein. The sulfosalicylic acid precipitation test was used to confirm "trace" positive protein dipsticks. The Japanese and our screening protocol have in common the same data for glucosuria and proteinuria. Their scheme has an algorithm for repeat testing of children with abnormal results, and further testing and medical evaluation for those showing persistently abnormal values. Out of the 23,121 students, we found seven with likely nephritis, one with confirmed nephritis, one with nephrotic syndrome, 170 with persistent unexplained hematuria, 19 with persistent unexplained proteinuria, 14 cases of urinary tract infection, and 20 cases of likely diabetes mellitus. We conclude that dipstick testing for albumin, protein, creatinine, glucose and occult blood has significant value in a multilevel testing scheme for identifying children with urinary tract abnormalities or diabetes. The assay of albumin increases the sensitivity of the screening, and dividing the albumin by the creatinine concentration reduces the potential errors arising from concentrated or dilute urines.
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