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Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis
Early diagnosis and treatment of rheumatoid arthritis are associated with improved outcomes but current diagnostic tools such as rheumatoid factor or anti-citrullinated protein antibodies have shown limited sensitivity. In this pilot study we set out to establish a panel of urinary biomarkers associ...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140712/ https://www.ncbi.nlm.nih.gov/pubmed/25144639 http://dx.doi.org/10.1371/journal.pone.0104625 |
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author | Stalmach, Angelique Johnsson, Hanna McInnes, Iain B. Husi, Holger Klein, Julie Dakna, Mohammed Mullen, William Mischak, Harald Porter, Duncan |
author_facet | Stalmach, Angelique Johnsson, Hanna McInnes, Iain B. Husi, Holger Klein, Julie Dakna, Mohammed Mullen, William Mischak, Harald Porter, Duncan |
author_sort | Stalmach, Angelique |
collection | PubMed |
description | Early diagnosis and treatment of rheumatoid arthritis are associated with improved outcomes but current diagnostic tools such as rheumatoid factor or anti-citrullinated protein antibodies have shown limited sensitivity. In this pilot study we set out to establish a panel of urinary biomarkers associated with rheumatoid arthritis using capillary electrophoresis coupled to mass spectrometry. We compared the urinary proteome of 33 participants of the Scottish Early Rheumatoid Arthritis inception cohort study with 30 healthy controls and identified 292 potential rheumatoid arthritis-specific peptides. Amongst them, 39 were used to create a classifier model using support vector machine algorithms. Specific peptidic fragments were differentially excreted between groups; fragments of protein S100-A9 and gelsolin were less abundant in rheumatoid arthritis while fragments of uromodulin, complement C3 and fibrinogen were all increasingly excreted. The model generated was subsequently tested in an independent test-set of 31 samples. The classifier demonstrated a sensitivity of 88% and a specificity of 93% in diagnosing the condition, with an area under the receiver operating characteristic curve of 0.93 (p<0.0001). These preliminary results suggest that urinary biomarkers could be useful in the early diagnosis of rheumatoid arthritis. Further studies are currently being undertaken in larger cohorts of patients with rheumatoid arthritis and other athridities to assess the potential of the urinary peptide based classifier in the early detection of rheumatoid arthritis. |
format | Online Article Text |
id | pubmed-4140712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41407122014-08-25 Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis Stalmach, Angelique Johnsson, Hanna McInnes, Iain B. Husi, Holger Klein, Julie Dakna, Mohammed Mullen, William Mischak, Harald Porter, Duncan PLoS One Research Article Early diagnosis and treatment of rheumatoid arthritis are associated with improved outcomes but current diagnostic tools such as rheumatoid factor or anti-citrullinated protein antibodies have shown limited sensitivity. In this pilot study we set out to establish a panel of urinary biomarkers associated with rheumatoid arthritis using capillary electrophoresis coupled to mass spectrometry. We compared the urinary proteome of 33 participants of the Scottish Early Rheumatoid Arthritis inception cohort study with 30 healthy controls and identified 292 potential rheumatoid arthritis-specific peptides. Amongst them, 39 were used to create a classifier model using support vector machine algorithms. Specific peptidic fragments were differentially excreted between groups; fragments of protein S100-A9 and gelsolin were less abundant in rheumatoid arthritis while fragments of uromodulin, complement C3 and fibrinogen were all increasingly excreted. The model generated was subsequently tested in an independent test-set of 31 samples. The classifier demonstrated a sensitivity of 88% and a specificity of 93% in diagnosing the condition, with an area under the receiver operating characteristic curve of 0.93 (p<0.0001). These preliminary results suggest that urinary biomarkers could be useful in the early diagnosis of rheumatoid arthritis. Further studies are currently being undertaken in larger cohorts of patients with rheumatoid arthritis and other athridities to assess the potential of the urinary peptide based classifier in the early detection of rheumatoid arthritis. Public Library of Science 2014-08-21 /pmc/articles/PMC4140712/ /pubmed/25144639 http://dx.doi.org/10.1371/journal.pone.0104625 Text en © 2014 Stalmach et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Stalmach, Angelique Johnsson, Hanna McInnes, Iain B. Husi, Holger Klein, Julie Dakna, Mohammed Mullen, William Mischak, Harald Porter, Duncan Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title | Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title_full | Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title_fullStr | Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title_full_unstemmed | Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title_short | Identification of Urinary Peptide Biomarkers Associated with Rheumatoid Arthritis |
title_sort | identification of urinary peptide biomarkers associated with rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140712/ https://www.ncbi.nlm.nih.gov/pubmed/25144639 http://dx.doi.org/10.1371/journal.pone.0104625 |
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