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Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients

BACKGROUND/AIMS: The identification of predictive biomarkers for Alzheimer's disease (AD) from urine would aid in screening for the disease, but information about biological and pathophysiological changes in the urine of AD patients is limited. This study aimed to explore the comprehensive prof...

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Autores principales: Watanabe, Yumi, Hirao, Yoshitoshi, Kasuga, Kensaku, Tokutake, Takayoshi, Semizu, Yuka, Kitamura, Kaori, Ikeuchi, Takeshi, Nakamura, Kazutoshi, Yamamoto, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477484/
https://www.ncbi.nlm.nih.gov/pubmed/31043964
http://dx.doi.org/10.1159/000496100
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author Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Tokutake, Takayoshi
Semizu, Yuka
Kitamura, Kaori
Ikeuchi, Takeshi
Nakamura, Kazutoshi
Yamamoto, Tadashi
author_facet Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Tokutake, Takayoshi
Semizu, Yuka
Kitamura, Kaori
Ikeuchi, Takeshi
Nakamura, Kazutoshi
Yamamoto, Tadashi
author_sort Watanabe, Yumi
collection PubMed
description BACKGROUND/AIMS: The identification of predictive biomarkers for Alzheimer's disease (AD) from urine would aid in screening for the disease, but information about biological and pathophysiological changes in the urine of AD patients is limited. This study aimed to explore the comprehensive profile and molecular network relations of urinary proteins in AD patients. METHODS: Urine samples collected from 18 AD patients and 18 age- and sex-matched cognitively normal controls were analyzed by mass spectrometry and semiquantified with the normalized spectral index method. Bioinformatics analyses were performed on proteins which significantly increased by more than 2-fold or decreased by less than 0.5-fold compared to the control (p < 0.05) using DAVID bioinformatics resources and KeyMolnet software. RESULTS: The levels of 109 proteins significantly differed between AD patients and controls. Among these, annotation clusters related to lysosomes, complement activation, and gluconeogenesis were significantly enriched. The molecular relation networks derived from these proteins were mainly associated with pathways of lipoprotein metabolism, heat shock protein 90 signaling, matrix metalloproteinase signaling, and redox regulation by thioredoxin. CONCLUSION: Our findings suggest that changes in the urinary proteome of AD patients reflect systemic changes related to AD pathophysiology.
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spelling pubmed-64774842019-05-01 Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients Watanabe, Yumi Hirao, Yoshitoshi Kasuga, Kensaku Tokutake, Takayoshi Semizu, Yuka Kitamura, Kaori Ikeuchi, Takeshi Nakamura, Kazutoshi Yamamoto, Tadashi Dement Geriatr Cogn Dis Extra Original Research Article BACKGROUND/AIMS: The identification of predictive biomarkers for Alzheimer's disease (AD) from urine would aid in screening for the disease, but information about biological and pathophysiological changes in the urine of AD patients is limited. This study aimed to explore the comprehensive profile and molecular network relations of urinary proteins in AD patients. METHODS: Urine samples collected from 18 AD patients and 18 age- and sex-matched cognitively normal controls were analyzed by mass spectrometry and semiquantified with the normalized spectral index method. Bioinformatics analyses were performed on proteins which significantly increased by more than 2-fold or decreased by less than 0.5-fold compared to the control (p < 0.05) using DAVID bioinformatics resources and KeyMolnet software. RESULTS: The levels of 109 proteins significantly differed between AD patients and controls. Among these, annotation clusters related to lysosomes, complement activation, and gluconeogenesis were significantly enriched. The molecular relation networks derived from these proteins were mainly associated with pathways of lipoprotein metabolism, heat shock protein 90 signaling, matrix metalloproteinase signaling, and redox regulation by thioredoxin. CONCLUSION: Our findings suggest that changes in the urinary proteome of AD patients reflect systemic changes related to AD pathophysiology. S. Karger AG 2019-02-08 /pmc/articles/PMC6477484/ /pubmed/31043964 http://dx.doi.org/10.1159/000496100 Text en Copyright © 2019 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 Research Article
Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Tokutake, Takayoshi
Semizu, Yuka
Kitamura, Kaori
Ikeuchi, Takeshi
Nakamura, Kazutoshi
Yamamoto, Tadashi
Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title_full Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title_fullStr Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title_full_unstemmed Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title_short Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients
title_sort molecular network analysis of the urinary proteome of alzheimer's disease patients
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477484/
https://www.ncbi.nlm.nih.gov/pubmed/31043964
http://dx.doi.org/10.1159/000496100
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