{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,10]],"date-time":"2026-05-10T17:36:03Z","timestamp":1778434563612,"version":"3.51.4"},"reference-count":29,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2019,2,21]],"date-time":"2019-02-21T00:00:00Z","timestamp":1550707200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100010878","name":"AbbVie Biotherapeutics","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100010878","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Transplantation"],"published-print":{"date-parts":[[2019,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>We investigated circulating levels of individual soluble urokinase plasminogen activation receptor (su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content>) forms to determine if specific circulating fragments of su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">III<\/jats:styled-content>) and (I) can better serve as clinical biomarkers for focal segmental glomerulosclerosis (<jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content>) and the risk of recurrence after transplantation.<\/jats:p><\/jats:sec><jats:sec><jats:title>Materials and Methods<\/jats:title><jats:p>Serum levels of intact su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> and its cleaved forms were measured with two assays, <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">TR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">FIA<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> levels in healthy controls were significantly lower than those who had glomerular diseases but were not significantly different between <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> patients and glomerular controls. Intact su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> (I\u2010<jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">III<\/jats:styled-content>) levels were noted to be elevated in glomerular diseases including <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content>. u<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> fragment (I) levels measured with the <jats:styled-content style=\"fixed-case\">TR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">FIA<\/jats:styled-content> 4 assay were significantly higher in <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> (695.4\u00a0+\u00a091.29\u00a0pMol\/L) than glomerular controls (239.1\u00a0+\u00a040.45\u00a0pMol\/L, <jats:italic>P<\/jats:italic>\u00a0=\u00a00.001). However, su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content>(I) levels were not significantly different between recurrent <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> and nonrecurrent <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> patients.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Our analysis of su<jats:styled-content style=\"fixed-case\">PAR<\/jats:styled-content> using the <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content> assay used in all previous studies does not appear to be a useful marker for <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> nor serve as a predictor for its recurrence after transplantation. The <jats:styled-content style=\"fixed-case\">TR<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">FIA<\/jats:styled-content> assay results suggest that <jats:styled-content style=\"fixed-case\">uPAR<\/jats:styled-content>(I) is a potential biomarker for <jats:styled-content style=\"fixed-case\">FSGS<\/jats:styled-content> but not of its recurrence.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ctr.13487","type":"journal-article","created":{"date-parts":[[2019,1,28]],"date-time":"2019-01-28T22:10:02Z","timestamp":1548713402000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Identifying a potential biomarker for primary focal segmental glomerulosclerosis and its association with recurrence after 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