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Moving towards personalized medicine in rheumatoid arthritis

To develop personalized medicine strategies for improvement of patient management in rheumatoid arthritis, the clinical and molecular properties of the individual patients need to be well characterized. A crucial step in this approach is to discover subgroups of patients that are characterized by a...

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Detalles Bibliográficos
Autores principales: de Jong, Tamarah D, Vosslamber, Saskia, Verweij, Cornelis L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060201/
https://www.ncbi.nlm.nih.gov/pubmed/25166016
http://dx.doi.org/10.1186/ar4565
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author de Jong, Tamarah D
Vosslamber, Saskia
Verweij, Cornelis L
author_facet de Jong, Tamarah D
Vosslamber, Saskia
Verweij, Cornelis L
author_sort de Jong, Tamarah D
collection PubMed
description To develop personalized medicine strategies for improvement of patient management in rheumatoid arthritis, the clinical and molecular properties of the individual patients need to be well characterized. A crucial step in this approach is to discover subgroups of patients that are characterized by a good or poor treatment outcome. Dennis and colleagues have identified distinct pretreatment gene expression profiles in affected synovial tissue specimens and a tissue type-related systemic protein pattern which are associated with a positive or negative clinical outcome to monotherapy with adalumimab (anti-TNFα) and tocilizumab (anti-IL-6 receptor). These observations assign biological pathways associated with response outcome and provide evidence for the existence of systemic, easy-to-measure predictive biomarkers for clinical benefit of these biologics.
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spelling pubmed-40602012014-06-17 Moving towards personalized medicine in rheumatoid arthritis de Jong, Tamarah D Vosslamber, Saskia Verweij, Cornelis L Arthritis Res Ther Editorial To develop personalized medicine strategies for improvement of patient management in rheumatoid arthritis, the clinical and molecular properties of the individual patients need to be well characterized. A crucial step in this approach is to discover subgroups of patients that are characterized by a good or poor treatment outcome. Dennis and colleagues have identified distinct pretreatment gene expression profiles in affected synovial tissue specimens and a tissue type-related systemic protein pattern which are associated with a positive or negative clinical outcome to monotherapy with adalumimab (anti-TNFα) and tocilizumab (anti-IL-6 receptor). These observations assign biological pathways associated with response outcome and provide evidence for the existence of systemic, easy-to-measure predictive biomarkers for clinical benefit of these biologics. BioMed Central 2014 2014-05-19 /pmc/articles/PMC4060201/ /pubmed/25166016 http://dx.doi.org/10.1186/ar4565 Text en Copyright © 2014 de Jong et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Editorial
de Jong, Tamarah D
Vosslamber, Saskia
Verweij, Cornelis L
Moving towards personalized medicine in rheumatoid arthritis
title Moving towards personalized medicine in rheumatoid arthritis
title_full Moving towards personalized medicine in rheumatoid arthritis
title_fullStr Moving towards personalized medicine in rheumatoid arthritis
title_full_unstemmed Moving towards personalized medicine in rheumatoid arthritis
title_short Moving towards personalized medicine in rheumatoid arthritis
title_sort moving towards personalized medicine in rheumatoid arthritis
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060201/
https://www.ncbi.nlm.nih.gov/pubmed/25166016
http://dx.doi.org/10.1186/ar4565
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