{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T22:23:45Z","timestamp":1792707825968,"version":"4.5.0"},"reference-count":29,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["CJASN"],"published-print":{"date-parts":[[2016,5]]},"abstract":"<jats:sec>\n                    <jats:title>Background and objectives<\/jats:title>\n                    <jats:p>Hypervolemia is a common feature of patients with CKD and associated with hypertension. Recent work has shown stimulation of sodium retention by urinary plasmin during nephrotic syndrome. However, it is unclear whether plasminuria plays a role in patients with stable CKD and non-nephrotic proteinuria.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, setting, participants, &amp; measurements<\/jats:title>\n                    <jats:p>\n                      In this cross-sectional study, we analyzed the fluid status of 171 patients with CKD consecutively presenting to our outpatient clinic from 2012 to 2013 using bioimpedance spectroscopy (Body Composition Monitor [BCM]; Fresenius Medical Care, Germany) and its associations to the urinary excretion of plasminogen and plasmin from a spot urine sample. Two\u2013electrode voltage clamp measurements were performed in\n                      <jats:italic toggle=\"yes\">Xenopus laevis<\/jats:italic>\n                      oocytes expressing human epithelial sodium channel to investigate whether plasmin in concentrations found in urine can activate the channel.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Overhydration &gt;5% and overhydration &gt;10% of the extracellular volume were found in 29% and 17% of the patients, respectively, and overhydration was associated with edema, hypertension, higher stages of CKD, and proteinuria. Proteinuria was the strongest independent predictor for overhydration (+0.58 L\/1.73 m\n                      <jats:sup>2<\/jats:sup>\n                      per 10-fold increase;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001). Urinary excretion of plasmin(ogen) quantified by ELISA correlated strongly with proteinuria (\n                      <jats:italic toggle=\"yes\">r<\/jats:italic>\n                      =0.87) and overhydration (\n                      <jats:italic toggle=\"yes\">r<\/jats:italic>\n                      =0.47). Using a chromogenic substrate, active plasmin was found in 44% of patients and correlated with proteinuria and overhydration. Estimated urinary plasmin concentrations were in a range sufficient to activate epithelial sodium channel currents\n                      <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                      . In multivariable analysis, urinary excretion of plasmin(ogen) was associated with overhydration similar to proteinuria.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Hypervolemia in patients with CKD is strongly associated with proteinuria, even in the non-nephrotic range. Protein-rich urine contains high amounts of plasminogen and active plasmin, rendering plasminuria as a possible link between proteinuria and hypervolemia.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2215\/cjn.12261115","type":"journal-article","created":{"date-parts":[[2016,3,1]],"date-time":"2016-03-01T22:24:55Z","timestamp":1456871095000},"page":"761-769","source":"Crossref","is-referenced-by-count":50,"title":["Association of Plasminuria with Overhydration in Patients with CKD"],"prefix":"10.2215","volume":"11","author":[{"given":"Anja","family":"Schork","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthias","family":"Woern","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hubert","family":"Kalbacher","sequence":"additional","affiliation":[{"name":"Interfacultary Institute of Biochemistry, University Tuebingen, Tuebingen, Germany; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wolfgang","family":"Voelter","sequence":"additional","affiliation":[{"name":"Interfacultary Institute of Biochemistry, University Tuebingen, Tuebingen, Germany; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Regina","family":"Nacken","sequence":"additional","affiliation":[{"name":"Institute of Cellular and Molecular Physiology, Friedrich Alexander University Erlangen-N\u00fcrnberg, Erlangen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marko","family":"Bertog","sequence":"additional","affiliation":[{"name":"Institute of Cellular and Molecular Physiology, Friedrich Alexander University Erlangen-N\u00fcrnberg, Erlangen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Silke","family":"Haerteis","sequence":"additional","affiliation":[{"name":"Institute of Cellular and Molecular Physiology, Friedrich Alexander University Erlangen-N\u00fcrnberg, Erlangen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christoph","family":"Korbmacher","sequence":"additional","affiliation":[{"name":"Institute of Cellular and Molecular Physiology, Friedrich Alexander University Erlangen-N\u00fcrnberg, Erlangen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nils","family":"Heyne","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andreas","family":"Peter","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hans-Ulrich","family":"H\u00e4ring","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ferruh","family":"Artunc","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, Division of Endocrinology, Diabetology, Vascular Disease, Nephrology and Clinical Chemistry, University Hospital of Tuebingen, Tuebingen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2016,3,1]]},"reference":[{"key":"B1-20230813","doi-asserted-by":"crossref","first-page":"1153","DOI":"10.1007\/s00467-013-2435-6","article-title":"Over- or underfill: Not all nephrotic states are created equal.","volume":"28","author":"Bockenhauer","year":"2013","journal-title":"Pediatr Nephrol"},{"key":"B2-20230813","doi-asserted-by":"crossref","first-page":"531","DOI":"10.1007\/s00424-014-1661-5","article-title":"Urinary serine proteases and activation of ENaC in kidney--implications for physiological renal salt handling and hypertensive disorders with albuminuria.","volume":"467","author":"Svenningsen","year":"2015","journal-title":"Pflugers Arch"},{"key":"B3-20230813","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/j.coph.2013.11.010","article-title":"Epithelial sodium channel (ENaC) and the control of blood 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