{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T02:38:07Z","timestamp":1790735887292,"version":"4.1.0"},"reference-count":20,"publisher":"Wiley","issue":"23","license":[{"start":{"date-parts":[[2025,9,20]],"date-time":"2025-09-20T00:00:00Z","timestamp":1758326400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["analyticalsciencejournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Electrophoresis"],"published-print":{"date-parts":[[2025,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>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\u2010consuming and its interpretation may be subjective. Two types of electrophoresis gel for urinary proteins are available: (1) high\u2010resolution (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, \u03b11\u2010microglobulin, eventually \u03b22\u2010microglobulin, immunoglobulin G (IgG), and \u03b12\u2010macroglobulin if blood is present), and HR gel allowing the visualization of RBP, \u03b22\u2010microglobulin, and transferrin. The two methods were comparable in detecting abnormal excretion of tubular markers (\u03b11\u2010microglobulin and \u03b22\u2010microglobulin), nonselective glomerular markers such as IgG, and post\u2010renal marker (\u03b12\u2010macroglobulin). 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, \u03b11\u2010microglobulin, eventually \u03b22\u2010microglobulin, 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, \u03b12\u2010macroglobulin must be measured using immunoassays to determine the post\u2010renal origin of proteinuria using the ratio \u03b12\u2010macroglobulin\/albumin.<\/jats:p>","DOI":"10.1002\/elps.70037","type":"journal-article","created":{"date-parts":[[2025,9,20]],"date-time":"2025-09-20T10:09:22Z","timestamp":1758362962000},"page":"1673-1680","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Comparison of Two Strategies of Analysis of Urinary Protein Composition for the Diagnosis and Follow\u2010Up of Renal Diseases"],"prefix":"10.1002","volume":"46","author":[{"given":"Joris","family":"Guyon","sequence":"first","affiliation":[{"name":"University of Bordeaux, INSERM, BRIC, U1312  Bordeaux France"},{"name":"CHU De Bordeaux, Laboratoire de Biochimie, INSERM, U1312  Bordeaux 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