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Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study

Non-invasive and simple methods enabling easy identification of individuals at high risk of cognitive decline are needed as preventive measures against dementia. This pilot study aimed to explore protein biomarkers that can predict cognitive decline using urine, which can be collected non-invasively...

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Autores principales: Watanabe, Yumi, Hirao, Yoshitoshi, Kasuga, Kensaku, Kitamura, Kaori, Nakamura, Kazutoshi, Yamamoto, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061132/
https://www.ncbi.nlm.nih.gov/pubmed/37006491
http://dx.doi.org/10.3389/fneur.2023.1134976
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author Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Kitamura, Kaori
Nakamura, Kazutoshi
Yamamoto, Tadashi
author_facet Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Kitamura, Kaori
Nakamura, Kazutoshi
Yamamoto, Tadashi
author_sort Watanabe, Yumi
collection PubMed
description Non-invasive and simple methods enabling easy identification of individuals at high risk of cognitive decline are needed as preventive measures against dementia. This pilot study aimed to explore protein biomarkers that can predict cognitive decline using urine, which can be collected non-invasively. Study subjects were selected from participants in a cohort study of middle-aged and older community-dwelling adults who underwent cognitive testing using the Mini-Mental State Examination and provided spot urine samples at two time points with an interval of approximately 5 years. Seven participants whose cognitive function declined 4 or more points from baseline (Group D) and 7 sex- and age-matched participants whose cognitive function remained within the normal range during the same period (Group M) were selected. Urinary proteomics using mass spectrometry was performed and discriminant models were created using orthogonal partial least squares-discriminant analysis (OPLS-DA). OPLS-DA yielded two models that significantly discriminated between the two groups at baseline and follow-up. Both models had ORM1, ORM2, and SERPINA3 in common. A further OPLS-DA model using baseline ORM1, ORM2, and SERPINA3 data showed similar predictive performance for data at follow-up as it did for baseline data (sensitivity: 0.85, specificity: 0.85), with the receiver operating characteristic curve analysis yielding an area under the curve of 0.878. This prospective study demonstrated the potential for using urine to identify biomarkers of cognitive decline.
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spelling pubmed-100611322023-03-31 Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study Watanabe, Yumi Hirao, Yoshitoshi Kasuga, Kensaku Kitamura, Kaori Nakamura, Kazutoshi Yamamoto, Tadashi Front Neurol Neurology Non-invasive and simple methods enabling easy identification of individuals at high risk of cognitive decline are needed as preventive measures against dementia. This pilot study aimed to explore protein biomarkers that can predict cognitive decline using urine, which can be collected non-invasively. Study subjects were selected from participants in a cohort study of middle-aged and older community-dwelling adults who underwent cognitive testing using the Mini-Mental State Examination and provided spot urine samples at two time points with an interval of approximately 5 years. Seven participants whose cognitive function declined 4 or more points from baseline (Group D) and 7 sex- and age-matched participants whose cognitive function remained within the normal range during the same period (Group M) were selected. Urinary proteomics using mass spectrometry was performed and discriminant models were created using orthogonal partial least squares-discriminant analysis (OPLS-DA). OPLS-DA yielded two models that significantly discriminated between the two groups at baseline and follow-up. Both models had ORM1, ORM2, and SERPINA3 in common. A further OPLS-DA model using baseline ORM1, ORM2, and SERPINA3 data showed similar predictive performance for data at follow-up as it did for baseline data (sensitivity: 0.85, specificity: 0.85), with the receiver operating characteristic curve analysis yielding an area under the curve of 0.878. This prospective study demonstrated the potential for using urine to identify biomarkers of cognitive decline. Frontiers Media S.A. 2023-03-16 /pmc/articles/PMC10061132/ /pubmed/37006491 http://dx.doi.org/10.3389/fneur.2023.1134976 Text en Copyright © 2023 Watanabe, Hirao, Kasuga, Kitamura, Nakamura and Yamamoto. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Watanabe, Yumi
Hirao, Yoshitoshi
Kasuga, Kensaku
Kitamura, Kaori
Nakamura, Kazutoshi
Yamamoto, Tadashi
Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title_full Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title_fullStr Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title_full_unstemmed Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title_short Urinary proteome profiles associated with cognitive decline in community elderly residents—A pilot study
title_sort urinary proteome profiles associated with cognitive decline in community elderly residents—a pilot study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061132/
https://www.ncbi.nlm.nih.gov/pubmed/37006491
http://dx.doi.org/10.3389/fneur.2023.1134976
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