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Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis

BACKGROUND: As osteoarthritis (OA) is a highly heterogeneous disease in terms of progression, establishment of prognostic biomarkers would be highly beneficial for treatment. The present study was performed to identify novel biomarkers capable of predicting the progression of knee OA. METHODS: A tot...

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Autores principales: Takinami, Yoshihiko, Yoshimatsu, Shinya, Uchiumi, Takaoki, Toyosaki-Maeda, Tomoko, Morita, Atsushi, Ishihara, Takeshi, Yamane, Shoji, Fukuda, Isao, Okamoto, Hiroyuki, Numata, Yoshito, Fukui, Naoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735238/
https://www.ncbi.nlm.nih.gov/pubmed/23935359
http://dx.doi.org/10.4137/BMI.S11966
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author Takinami, Yoshihiko
Yoshimatsu, Shinya
Uchiumi, Takaoki
Toyosaki-Maeda, Tomoko
Morita, Atsushi
Ishihara, Takeshi
Yamane, Shoji
Fukuda, Isao
Okamoto, Hiroyuki
Numata, Yoshito
Fukui, Naoshi
author_facet Takinami, Yoshihiko
Yoshimatsu, Shinya
Uchiumi, Takaoki
Toyosaki-Maeda, Tomoko
Morita, Atsushi
Ishihara, Takeshi
Yamane, Shoji
Fukuda, Isao
Okamoto, Hiroyuki
Numata, Yoshito
Fukui, Naoshi
author_sort Takinami, Yoshihiko
collection PubMed
description BACKGROUND: As osteoarthritis (OA) is a highly heterogeneous disease in terms of progression, establishment of prognostic biomarkers would be highly beneficial for treatment. The present study was performed to identify novel biomarkers capable of predicting the progression of knee OA. METHODS: A total of 69 plasma samples (OA patients undergoing radiographic progression, n = 25; nonprogression, n = 33; healthy donors, n = 11) were analyzed by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS), and ion peaks of interest were identified by liquid chromatography and matrix-assisted laser desorption/ionization (MALDI)-TOF MS. The identities of these proteins were further validated by immunoprecipitation combined with SELDI-TOF MS analysis. RESULTS: SELDI-TOF MS analysis indicated that the intensities of 3 ion peaks differed significantly between progressors and nonprogressors. Subsequent analyses indicated that these peaks corresponded to apolipoprotein C-I, C-III, and an N-terminal truncated form of transthyretin, respectively. The identities of these proteins were confirmed by the loss of ion peaks in SELDI-TOF MS spectra by immunoprecipitation using specific antibodies for the respective proteins. CONCLUSIONS: Three potential biomarkers were identified whose serum levels differed significantly between OA progressors and nonprogressors. These biomarkers are expected to be prognostic biomarkers for knee OA and to facilitate the development of novel disease-modifying treatments for OA.
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spelling pubmed-37352382013-08-09 Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis Takinami, Yoshihiko Yoshimatsu, Shinya Uchiumi, Takaoki Toyosaki-Maeda, Tomoko Morita, Atsushi Ishihara, Takeshi Yamane, Shoji Fukuda, Isao Okamoto, Hiroyuki Numata, Yoshito Fukui, Naoshi Biomark Insights Original Research BACKGROUND: As osteoarthritis (OA) is a highly heterogeneous disease in terms of progression, establishment of prognostic biomarkers would be highly beneficial for treatment. The present study was performed to identify novel biomarkers capable of predicting the progression of knee OA. METHODS: A total of 69 plasma samples (OA patients undergoing radiographic progression, n = 25; nonprogression, n = 33; healthy donors, n = 11) were analyzed by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS), and ion peaks of interest were identified by liquid chromatography and matrix-assisted laser desorption/ionization (MALDI)-TOF MS. The identities of these proteins were further validated by immunoprecipitation combined with SELDI-TOF MS analysis. RESULTS: SELDI-TOF MS analysis indicated that the intensities of 3 ion peaks differed significantly between progressors and nonprogressors. Subsequent analyses indicated that these peaks corresponded to apolipoprotein C-I, C-III, and an N-terminal truncated form of transthyretin, respectively. The identities of these proteins were confirmed by the loss of ion peaks in SELDI-TOF MS spectra by immunoprecipitation using specific antibodies for the respective proteins. CONCLUSIONS: Three potential biomarkers were identified whose serum levels differed significantly between OA progressors and nonprogressors. These biomarkers are expected to be prognostic biomarkers for knee OA and to facilitate the development of novel disease-modifying treatments for OA. Libertas Academica 2013-07-29 /pmc/articles/PMC3735238/ /pubmed/23935359 http://dx.doi.org/10.4137/BMI.S11966 Text en © 2013 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Original Research
Takinami, Yoshihiko
Yoshimatsu, Shinya
Uchiumi, Takaoki
Toyosaki-Maeda, Tomoko
Morita, Atsushi
Ishihara, Takeshi
Yamane, Shoji
Fukuda, Isao
Okamoto, Hiroyuki
Numata, Yoshito
Fukui, Naoshi
Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title_full Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title_fullStr Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title_full_unstemmed Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title_short Identification of Potential Prognostic Markers for Knee Osteoarthritis by Serum Proteomic Analysis
title_sort identification of potential prognostic markers for knee osteoarthritis by serum proteomic analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735238/
https://www.ncbi.nlm.nih.gov/pubmed/23935359
http://dx.doi.org/10.4137/BMI.S11966
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