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Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis

To optimize treatment for rheumatoid arthritis (RA), it is ideal to monitor the disease activity on a daily basis because RA activity fluctuates over time. Urine can be collected routinely at home by patients. Recently, we identified four urinary biomarker candidates—gelsolin (GSN), orosomucoid (ORM...

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Autores principales: Park, Yune-Jung, Yoo, Seung-Ah, Hwang, Daehee, Cho, Chul-Soo, Kim, Wan-Uk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892870/
https://www.ncbi.nlm.nih.gov/pubmed/26915672
http://dx.doi.org/10.1038/emm.2015.120
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author Park, Yune-Jung
Yoo, Seung-Ah
Hwang, Daehee
Cho, Chul-Soo
Kim, Wan-Uk
author_facet Park, Yune-Jung
Yoo, Seung-Ah
Hwang, Daehee
Cho, Chul-Soo
Kim, Wan-Uk
author_sort Park, Yune-Jung
collection PubMed
description To optimize treatment for rheumatoid arthritis (RA), it is ideal to monitor the disease activity on a daily basis because RA activity fluctuates over time. Urine can be collected routinely at home by patients. Recently, we identified four urinary biomarker candidates—gelsolin (GSN), orosomucoid (ORM)1, ORM2 and soluble CD14 (sCD14)—in RA patients through transcriptomic and proteomic studies. Here, we investigated the clinical significance of the aforementioned urinary biomarker candidates in a prospective manner. For the first time, we found that urinary ORM1, ORM2 and sCD14 levels, but not GSN, were elevated in RA patients and had a positive correlation with the status of the disease activity. In particular, urine tests for ORM 1, ORM 2 and sCD14 efficiently represented the presence of high RA activity without the need for measuring blood markers. In a parallel study, a more rapid radiographic progression over 3 years was observed in patients with higher ORM2 levels. Combined measurements of urinary ORM2 and serum C-reactive protein synergistically increased the predictability of the radiographic progression of RA (odds ratio: 46.5). Collectively, our data provide evidence that blood-free, urinary biomarkers are promising surrogates for assessing disease activity and prognosis of RA. We anticipate that our urinary biomarkers will provide novel candidates for patient-driven measurements of RA activity at home and can shift the paradigm from blood to urine testing in the assessment of RA activity and prognosis in hospitals.
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spelling pubmed-48928702016-07-27 Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis Park, Yune-Jung Yoo, Seung-Ah Hwang, Daehee Cho, Chul-Soo Kim, Wan-Uk Exp Mol Med Original Article To optimize treatment for rheumatoid arthritis (RA), it is ideal to monitor the disease activity on a daily basis because RA activity fluctuates over time. Urine can be collected routinely at home by patients. Recently, we identified four urinary biomarker candidates—gelsolin (GSN), orosomucoid (ORM)1, ORM2 and soluble CD14 (sCD14)—in RA patients through transcriptomic and proteomic studies. Here, we investigated the clinical significance of the aforementioned urinary biomarker candidates in a prospective manner. For the first time, we found that urinary ORM1, ORM2 and sCD14 levels, but not GSN, were elevated in RA patients and had a positive correlation with the status of the disease activity. In particular, urine tests for ORM 1, ORM 2 and sCD14 efficiently represented the presence of high RA activity without the need for measuring blood markers. In a parallel study, a more rapid radiographic progression over 3 years was observed in patients with higher ORM2 levels. Combined measurements of urinary ORM2 and serum C-reactive protein synergistically increased the predictability of the radiographic progression of RA (odds ratio: 46.5). Collectively, our data provide evidence that blood-free, urinary biomarkers are promising surrogates for assessing disease activity and prognosis of RA. We anticipate that our urinary biomarkers will provide novel candidates for patient-driven measurements of RA activity at home and can shift the paradigm from blood to urine testing in the assessment of RA activity and prognosis in hospitals. Nature Publishing Group 2016-02 2016-02-26 /pmc/articles/PMC4892870/ /pubmed/26915672 http://dx.doi.org/10.1038/emm.2015.120 Text en Copyright © 2016 KSBMB. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Park, Yune-Jung
Yoo, Seung-Ah
Hwang, Daehee
Cho, Chul-Soo
Kim, Wan-Uk
Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title_full Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title_fullStr Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title_full_unstemmed Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title_short Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
title_sort identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892870/
https://www.ncbi.nlm.nih.gov/pubmed/26915672
http://dx.doi.org/10.1038/emm.2015.120
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