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Urinary proteomic pattern in female stress urinary incontinence: a pilot study

INTRODUCTION AND HYPOTHESIS: Previous studies aiming to identify specific pre-defined urine protein biomarkers for stress urinary incontinence (SUI) have not identified clinically important differences. The hypothesis of our study was that the global distribution of urinary proteins, the proteome, d...

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Autores principales: Koch, Marianne, Mitulovic, Goran, Hanzal, Engelbert, Umek, Wolfgang, Seyfert, Sonja, Mohr, Thomas, Koelbl, Heinz, Laterza, Rosa Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065895/
https://www.ncbi.nlm.nih.gov/pubmed/27193112
http://dx.doi.org/10.1007/s00192-016-3033-5
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author Koch, Marianne
Mitulovic, Goran
Hanzal, Engelbert
Umek, Wolfgang
Seyfert, Sonja
Mohr, Thomas
Koelbl, Heinz
Laterza, Rosa Maria
author_facet Koch, Marianne
Mitulovic, Goran
Hanzal, Engelbert
Umek, Wolfgang
Seyfert, Sonja
Mohr, Thomas
Koelbl, Heinz
Laterza, Rosa Maria
author_sort Koch, Marianne
collection PubMed
description INTRODUCTION AND HYPOTHESIS: Previous studies aiming to identify specific pre-defined urine protein biomarkers for stress urinary incontinence (SUI) have not identified clinically important differences. The hypothesis of our study was that the global distribution of urinary proteins, the proteome, differs between women with and those without SUI. METHODS: In this age-matched case–control study, we compared the urinary proteome of 20 women with SUI and 20 controls. Proteins were identified by applying high-performance liquid chromatography separation and tandem mass spectrometry detection. Data analysis was performed using Mascot 2.4.1 embedded in ProteinScape 3.1. RESULTS: We identified 828 different proteins. The concentration of six of those showed a significant difference between urine samples of SUI patients and those of controls (q value < 0.25). Four proteins showed a higher abundance in SUI samples compared with controls: plasma serine protease inhibitor (logFC 1.11), leucine-rich alpha-2-glycoprotein (logFC 3.91), lysosomal alpha-glucosidase (logFC 1.24), and peptidyl-prolyl cis- trans isomerase A (logFC 1.96). We identified two proteins in lower abundance in SUI samples compared with controls: uromodulin (logFC −4.87) and TALPID3 (logFC −1.99). CONCLUSIONS: Overexpression of plasma serine protease inhibitor, leucine-rich alpha-2-glycoprotein, lysosomal alpha-glucosidase, and peptidyl-prolyl cis- trans isomerase A, and lower expression of uromodulin and TALPID3, in urine may be associated with female SUI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00192-016-3033-5) contains supplementary material, which is available to authorized users
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spelling pubmed-50658952016-10-28 Urinary proteomic pattern in female stress urinary incontinence: a pilot study Koch, Marianne Mitulovic, Goran Hanzal, Engelbert Umek, Wolfgang Seyfert, Sonja Mohr, Thomas Koelbl, Heinz Laterza, Rosa Maria Int Urogynecol J Original Article INTRODUCTION AND HYPOTHESIS: Previous studies aiming to identify specific pre-defined urine protein biomarkers for stress urinary incontinence (SUI) have not identified clinically important differences. The hypothesis of our study was that the global distribution of urinary proteins, the proteome, differs between women with and those without SUI. METHODS: In this age-matched case–control study, we compared the urinary proteome of 20 women with SUI and 20 controls. Proteins were identified by applying high-performance liquid chromatography separation and tandem mass spectrometry detection. Data analysis was performed using Mascot 2.4.1 embedded in ProteinScape 3.1. RESULTS: We identified 828 different proteins. The concentration of six of those showed a significant difference between urine samples of SUI patients and those of controls (q value < 0.25). Four proteins showed a higher abundance in SUI samples compared with controls: plasma serine protease inhibitor (logFC 1.11), leucine-rich alpha-2-glycoprotein (logFC 3.91), lysosomal alpha-glucosidase (logFC 1.24), and peptidyl-prolyl cis- trans isomerase A (logFC 1.96). We identified two proteins in lower abundance in SUI samples compared with controls: uromodulin (logFC −4.87) and TALPID3 (logFC −1.99). CONCLUSIONS: Overexpression of plasma serine protease inhibitor, leucine-rich alpha-2-glycoprotein, lysosomal alpha-glucosidase, and peptidyl-prolyl cis- trans isomerase A, and lower expression of uromodulin and TALPID3, in urine may be associated with female SUI. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00192-016-3033-5) contains supplementary material, which is available to authorized users Springer London 2016-05-18 2016 /pmc/articles/PMC5065895/ /pubmed/27193112 http://dx.doi.org/10.1007/s00192-016-3033-5 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Koch, Marianne
Mitulovic, Goran
Hanzal, Engelbert
Umek, Wolfgang
Seyfert, Sonja
Mohr, Thomas
Koelbl, Heinz
Laterza, Rosa Maria
Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title_full Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title_fullStr Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title_full_unstemmed Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title_short Urinary proteomic pattern in female stress urinary incontinence: a pilot study
title_sort urinary proteomic pattern in female stress urinary incontinence: a pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065895/
https://www.ncbi.nlm.nih.gov/pubmed/27193112
http://dx.doi.org/10.1007/s00192-016-3033-5
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