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Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection

PURPOSE: Human infection with Dobrava-Belgrade virus (DOBV) in Northern Germany causes a mild form of hantavirus disease predominantly characterized by acute kidney injury due to interstitial nephritis. We evaluated the largest number of DOBV-infected patients so far regarding clinical course, prote...

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Autores principales: Meier, Markus, Kramer, Jan, Jabs, Wolfram J., Nolte, Claudia, Hofmann, Jörg, Krüger, Detlev H., Lehnert, Hendrik, Nitschke, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968261/
https://www.ncbi.nlm.nih.gov/pubmed/29849535
http://dx.doi.org/10.1159/000486322
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author Meier, Markus
Kramer, Jan
Jabs, Wolfram J.
Nolte, Claudia
Hofmann, Jörg
Krüger, Detlev H.
Lehnert, Hendrik
Nitschke, Martin
author_facet Meier, Markus
Kramer, Jan
Jabs, Wolfram J.
Nolte, Claudia
Hofmann, Jörg
Krüger, Detlev H.
Lehnert, Hendrik
Nitschke, Martin
author_sort Meier, Markus
collection PubMed
description PURPOSE: Human infection with Dobrava-Belgrade virus (DOBV) in Northern Germany causes a mild form of hantavirus disease predominantly characterized by acute kidney injury due to interstitial nephritis. We evaluated the largest number of DOBV-infected patients so far regarding clinical course, proteinuria, and prognostic markers. PATIENTS AND METHODS: Patients with DOBV-associated hantavirus disease admitted to the Renal Division of the University of Lübeck (Germany) between 1997 and 2012 were included in this study. Symptoms, clinical course, laboratory parameters, and urinary protein analysis were investigated at admission (baseline, t(0)), 3–5 days (t(3–5)), 10–17 days (t(10–17)), and after 1 year of follow-up (t(365)). RESULTS: Of the 34 patients (male/female ratio: 23/11; age: 41 ± 14 years) included in the study, 4 underwent hemodialysis (HD). Glomerular filtration rate was 17 ± 14 mL/min at t(0) and increased to 27 ± 26 mL/min (t(3–5)), 57 ± 20 mL/min (t(10–17)), and 84 ± 16 mL/min (t(365)). Albuminuria and tubular proteinuria (α(1)- and β(2)-microglobulin) decreased during follow-up; the urinary α(1)-microglobulin concentration in patients who required HD was significantly higher than that in patients not requiring HD (t(0): 186 ± 51 vs. 45 ± 26 mg/g creatinine; t(3–5): 87 ± 14 vs. 32 ± 16 mg/g creatinine; t(10–17): 63 ± 18 vs. 28 ± 12 mg/g creatinine; p < 0.001). CONCLUSIONS: DOBV infection of inpatients in Northern Germany is associated with severe kidney injury that recovers within a few weeks and normalizes within 1 year. Tubular proteinuria is associated with the severity of kidney injury and the necessity of renal replacement therapy in these DOBV-infected patients.
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spelling pubmed-59682612018-05-30 Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection Meier, Markus Kramer, Jan Jabs, Wolfram J. Nolte, Claudia Hofmann, Jörg Krüger, Detlev H. Lehnert, Hendrik Nitschke, Martin Nephron Extra Original Paper PURPOSE: Human infection with Dobrava-Belgrade virus (DOBV) in Northern Germany causes a mild form of hantavirus disease predominantly characterized by acute kidney injury due to interstitial nephritis. We evaluated the largest number of DOBV-infected patients so far regarding clinical course, proteinuria, and prognostic markers. PATIENTS AND METHODS: Patients with DOBV-associated hantavirus disease admitted to the Renal Division of the University of Lübeck (Germany) between 1997 and 2012 were included in this study. Symptoms, clinical course, laboratory parameters, and urinary protein analysis were investigated at admission (baseline, t(0)), 3–5 days (t(3–5)), 10–17 days (t(10–17)), and after 1 year of follow-up (t(365)). RESULTS: Of the 34 patients (male/female ratio: 23/11; age: 41 ± 14 years) included in the study, 4 underwent hemodialysis (HD). Glomerular filtration rate was 17 ± 14 mL/min at t(0) and increased to 27 ± 26 mL/min (t(3–5)), 57 ± 20 mL/min (t(10–17)), and 84 ± 16 mL/min (t(365)). Albuminuria and tubular proteinuria (α(1)- and β(2)-microglobulin) decreased during follow-up; the urinary α(1)-microglobulin concentration in patients who required HD was significantly higher than that in patients not requiring HD (t(0): 186 ± 51 vs. 45 ± 26 mg/g creatinine; t(3–5): 87 ± 14 vs. 32 ± 16 mg/g creatinine; t(10–17): 63 ± 18 vs. 28 ± 12 mg/g creatinine; p < 0.001). CONCLUSIONS: DOBV infection of inpatients in Northern Germany is associated with severe kidney injury that recovers within a few weeks and normalizes within 1 year. Tubular proteinuria is associated with the severity of kidney injury and the necessity of renal replacement therapy in these DOBV-infected patients. S. Karger AG 2018-02-09 /pmc/articles/PMC5968261/ /pubmed/29849535 http://dx.doi.org/10.1159/000486322 Text en Copyright © 2018 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Original Paper
Meier, Markus
Kramer, Jan
Jabs, Wolfram J.
Nolte, Claudia
Hofmann, Jörg
Krüger, Detlev H.
Lehnert, Hendrik
Nitschke, Martin
Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title_full Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title_fullStr Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title_full_unstemmed Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title_short Proteinuria and the Clinical Course of Dobrava-Belgrade Hantavirus Infection
title_sort proteinuria and the clinical course of dobrava-belgrade hantavirus infection
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5968261/
https://www.ncbi.nlm.nih.gov/pubmed/29849535
http://dx.doi.org/10.1159/000486322
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