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Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension

INTRODUCTION: Plasmin and its precursor, plasminogen, are detectable in urine from patients with glomerular disease. Urinary plasmin(ogen) levels correlate with blood pressure (BP) and may contribute to renal Na(+) retention by activating the epithelial Na(+) channel (ENaC). In a longitudinal nested...

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Autores principales: Ray, Evan C., Miller, Rachel G., Demko, John E., Costacou, Tina, Kinlough, Carol L., Demko, Casey L., Unruh, Mark L., Orchard, Trevor J., Kleyman, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224670/
https://www.ncbi.nlm.nih.gov/pubmed/30450470
http://dx.doi.org/10.1016/j.ekir.2018.06.007
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author Ray, Evan C.
Miller, Rachel G.
Demko, John E.
Costacou, Tina
Kinlough, Carol L.
Demko, Casey L.
Unruh, Mark L.
Orchard, Trevor J.
Kleyman, Thomas R.
author_facet Ray, Evan C.
Miller, Rachel G.
Demko, John E.
Costacou, Tina
Kinlough, Carol L.
Demko, Casey L.
Unruh, Mark L.
Orchard, Trevor J.
Kleyman, Thomas R.
author_sort Ray, Evan C.
collection PubMed
description INTRODUCTION: Plasmin and its precursor, plasminogen, are detectable in urine from patients with glomerular disease. Urinary plasmin(ogen) levels correlate with blood pressure (BP) and may contribute to renal Na(+) retention by activating the epithelial Na(+) channel (ENaC). In a longitudinal nested-cohort study, we asked whether urinary plasmin(ogen) levels predict subsequent increase in BP, incident hypertension, or mortality in subjects with type I diabetes, who often develop proteinuria. METHODS: The Pittsburgh Epidemiology of Diabetes Complications (EDC) study followed up type I diabetic subjects for 25 years. Urine specimens from 70 subjects with a spectrum of baseline urinary albumin levels were examined. Outcomes included increased BP after 2 years (≥1 SD over baseline systolic or diastolic BP, examined via logistic regression), 25-year incident hypertension (≥140/90 mm Hg or initiating BP-lowering medications), and all-cause or cardiovascular mortality, examined using Cox regression. RESULTS: Subjects experiencing a 2-year increase in BP had higher baseline urinary plasmin(ogen)/creatinine levels (uPl/Cr) than other subjects (P = 0.04); the difference in baseline urinary albumin/creatinine levels (uAlb/Cr) was similar (P = 0.07). Baseline uPl/Cr was associated with increased 25-year hypertension incidence (hazard ratio = 2.05, P = 0.001), all-cause mortality (HR = 2.05, P = 0.01) and cardiovascular mortality (HR = 3.30, P = 0.005), although not independent of uAlb/Cr. CONCLUSION: This is the first long-term prospective study addressing clinical outcomes associated with increased urinary plasmin(ogen). Findings are consistent with a role for plasmin(ogen) in promoting increased BP, but also demonstrate the difficulty in distinguishing effects due to plasmin(ogen) from those of albuminuria.
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spelling pubmed-62246702018-11-16 Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension Ray, Evan C. Miller, Rachel G. Demko, John E. Costacou, Tina Kinlough, Carol L. Demko, Casey L. Unruh, Mark L. Orchard, Trevor J. Kleyman, Thomas R. Kidney Int Rep Clinical Research INTRODUCTION: Plasmin and its precursor, plasminogen, are detectable in urine from patients with glomerular disease. Urinary plasmin(ogen) levels correlate with blood pressure (BP) and may contribute to renal Na(+) retention by activating the epithelial Na(+) channel (ENaC). In a longitudinal nested-cohort study, we asked whether urinary plasmin(ogen) levels predict subsequent increase in BP, incident hypertension, or mortality in subjects with type I diabetes, who often develop proteinuria. METHODS: The Pittsburgh Epidemiology of Diabetes Complications (EDC) study followed up type I diabetic subjects for 25 years. Urine specimens from 70 subjects with a spectrum of baseline urinary albumin levels were examined. Outcomes included increased BP after 2 years (≥1 SD over baseline systolic or diastolic BP, examined via logistic regression), 25-year incident hypertension (≥140/90 mm Hg or initiating BP-lowering medications), and all-cause or cardiovascular mortality, examined using Cox regression. RESULTS: Subjects experiencing a 2-year increase in BP had higher baseline urinary plasmin(ogen)/creatinine levels (uPl/Cr) than other subjects (P = 0.04); the difference in baseline urinary albumin/creatinine levels (uAlb/Cr) was similar (P = 0.07). Baseline uPl/Cr was associated with increased 25-year hypertension incidence (hazard ratio = 2.05, P = 0.001), all-cause mortality (HR = 2.05, P = 0.01) and cardiovascular mortality (HR = 3.30, P = 0.005), although not independent of uAlb/Cr. CONCLUSION: This is the first long-term prospective study addressing clinical outcomes associated with increased urinary plasmin(ogen). Findings are consistent with a role for plasmin(ogen) in promoting increased BP, but also demonstrate the difficulty in distinguishing effects due to plasmin(ogen) from those of albuminuria. Elsevier 2018-06-30 /pmc/articles/PMC6224670/ /pubmed/30450470 http://dx.doi.org/10.1016/j.ekir.2018.06.007 Text en © 2018 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Ray, Evan C.
Miller, Rachel G.
Demko, John E.
Costacou, Tina
Kinlough, Carol L.
Demko, Casey L.
Unruh, Mark L.
Orchard, Trevor J.
Kleyman, Thomas R.
Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title_full Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title_fullStr Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title_full_unstemmed Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title_short Urinary Plasmin(ogen) as a Prognostic Factor for Hypertension
title_sort urinary plasmin(ogen) as a prognostic factor for hypertension
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224670/
https://www.ncbi.nlm.nih.gov/pubmed/30450470
http://dx.doi.org/10.1016/j.ekir.2018.06.007
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