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A study examining the bias of albumin and albumin/creatinine ratio measurements in urine

  • Beryl E. Jacobson , David W. Seccombe EMAIL logo , Alex Katayev and Adeera Levin
Published/Copyright: March 28, 2015

Abstract

Background: The objective of the study was to examine the bias of albumin and albumin/creatinine (ACR) measurements in urine.

Methods: Pools of normal human urine were augmented with purified human serum albumin to generate a series of 12 samples covering the clinical range of interest for the measurement of ACR. Albumin and creatinine concentrations in these samples were analyzed three times on each of 3 days by 24 accredited laboratories in Canada and the USA. Reference values (RV) for albumin measurements were assigned by a liquid chromatography-tandem mass spectrometry (LC-MS/MS) comparative method and gravimetrically. Ten random urine samples (check samples) were analyzed as singlets and albumin and ACR values reported according to the routine practices of each laboratory.

Results: Augmented urine pools were shown to be commutable. Gravimetrically assigned target values were corrected for the presence of endogenous albumin using the LC-MS/MS comparative method. There was excellent agreement between the RVs as assigned by these two methods. All laboratory medians demonstrated a negative bias for the measurement of albumin in urine over the concentration range examined. The magnitude of this bias tended to decrease with increasing albumin concentrations. At baseline, only 10% of the patient ACR values met a performance limit of RV ±15%. This increased to 84% and 86% following post-analytical correction for albumin and creatinine calibration bias, respectively.

Conclusions: International organizations should take a leading role in the standardization of albumin measurements in urine. In the interim, accuracy based urine quality control samples may be used by clinical laboratories for monitoring the accuracy of their urinary albumin measurements.


Corresponding author: David W. Seccombe, Department of Pathology and Laboratory Medicine, University of British Columbia, c/o 307-2083 Alma Street, Vancouver BC V6R 4N6, Canada, Phone: +1 604 336 3695, E-mail: ; and Canadian External Quality Assessment Laboratory (CEQAL), Vancouver, BC, Canada

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Received: 2014-11-10
Accepted: 2015-2-27
Published Online: 2015-3-28
Published in Print: 2015-10-1

©2015 by De Gruyter

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