Comparison of Two Strategies of Analysis of Urinary Protein Composition for the Diagnosis and Follow‐Up of Renal Diseases

Proteinuria analysis is necessary to detect the early stages of kidney disease before the estimated glomerular filtration rate deteriorates and to monitor the progression of treated kidney disease. Electrophoresis is often the first orientation test, although this test is time-consuming and its interpretation may be subjective. Two types of electrophoresis gel for urinary proteins are available: (1) high-resolution (HR) agarose gel and (2) agarose gel combined with immunological detection of specific urinary proteins after their electrophoretic migration (UP). As the former is known to provide the best results for the quantification of monoclonal protein and the latter for its characterization, we only investigated methods for determining the type of kidney damage in our study. Therefore, the aim of our study was to compare two strategies for proteinuria typing: UP gel to HR gel with quantification of specific proteins (albumin, eventually transferrin, α1-microglobulin, eventually β2-microglobulin, immunoglobulin G (IgG), and α2-macroglobulin if blood is present), and HR gel allowing the visualization of RBP, β2-microglobulin, and transferrin. The two methods were comparable in detecting abnormal excretion of tubular markers (α1-microglobulin and β2-microglobulin), nonselective glomerular markers such as IgG, and post-renal marker (α2-macroglobulin). The results differed for albumin, whose limit of detection was 25 times lower than the limit of quantification by immunoassay, leading to false positives and no differentiation between low and high excretion of albuminuria. In conclusion on UP gel, when proteinuria typing is prescribed without investigating monoclonal protein, we recommend carrying out immunoassays for specific proteins (e.g., albumin, α1-microglobulin, eventually β2-microglobulin, and IgG). In a context of associated monoclonal protein investigation, tubular and glomerular damage markers (excluding albumin) can be interpreted on a UP gel. If blood is present, α2-macroglobulin must be measured using immunoassays to determine the post-renal origin of proteinuria using the ratio α2-macroglobulin/albumin.

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Journal
Electrophoresis
Published
2025-09-20
DOI
https://doi.org/10.1002/elps.70037
Primary Topic
Renal Diseases and Glomerulopathies
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article

Comparison of Two Strategies of Analysis of Urinary Protein Composition for the Diagnosis and Follow‐Up of Renal Diseases

Joris Guyon, Lila Rami Arab, Laurence Piéroni, Sylvie Caspar‐Bauguil et al.
Electrophoresis
Renal Diseases and Glomerulopathies
article

Comparison of Two Strategies of Analysis of Urinary Protein Composition for the Diagnosis and Follow‐Up of Renal Diseases

Joris Guyon, Lila Rami Arab, Laurence Piéroni, Sylvie Caspar‐Bauguil, Annie M. Bérard, Hien V. Pham, Jeanne Malaubier, Marie‐Laure Curutchet‐Burtin, Rémi Segues
article en

Abstract

Proteinuria analysis is necessary to detect the early stages of kidney disease before the estimated glomerular filtration rate deteriorates and to monitor the progression of treated kidney disease. Electrophoresis is often the first orientation test, although this test is time-consuming and its interpretation may be subjective. Two types of electrophoresis gel for urinary proteins are available: (1) high-resolution (HR) agarose gel and (2) agarose gel combined with immunological detection of specific urinary proteins after their electrophoretic migration (UP). As the former is known to provide the best results for the quantification of monoclonal protein and the latter for its characterization, we only investigated methods for determining the type of kidney damage in our study. Therefore, the aim of our study was to compare two strategies for proteinuria typing: UP gel to HR gel with quantification of specific proteins (albumin, eventually transferrin, α1-microglobulin, eventually β2-microglobulin, immunoglobulin G (IgG), and α2-macroglobulin if blood is present), and HR gel allowing the visualization of RBP, β2-microglobulin, and transferrin. The two methods were comparable in detecting abnormal excretion of tubular markers (α1-microglobulin and β2-microglobulin), nonselective glomerular markers such as IgG, and post-renal marker (α2-macroglobulin). The results differed for albumin, whose limit of detection was 25 times lower than the limit of quantification by immunoassay, leading to false positives and no differentiation between low and high excretion of albuminuria. In conclusion on UP gel, when proteinuria typing is prescribed without investigating monoclonal protein, we recommend carrying out immunoassays for specific proteins (e.g., albumin, α1-microglobulin, eventually β2-microglobulin, and IgG). In a context of associated monoclonal protein investigation, tubular and glomerular damage markers (excluding albumin) can be interpreted on a UP gel. If blood is present, α2-macroglobulin must be measured using immunoassays to determine the post-renal origin of proteinuria using the ratio α2-macroglobulin/albumin.

ElectrophoresisVol. 46(23)
Université Toulouse III - Paul Sabatier (FR), Université de Bordeaux (FR), Inserm (FR), Centre Hospitalier Universitaire de Grenoble (FR), Centre Hospitalier Universitaire de Toulouse (FR), Département de Chimie Moléculaire (FR), Technologie Médicale (France) (FR), Bordeaux Population Health (FR), Centre Hospitalier de la Côte Basque (FR), BoRdeaux Institute of onCology (FR)
Openalex Percentile: Top 73%
Renal Diseases and Glomerulopathies
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