TY - JOUR
T1 - Identification of novel urinary biomarkers for assessing disease activity and prognosis of rheumatoid arthritis
AU - Park, Yune Jung
AU - Yoo, Seung Ah
AU - Hwang, Daehee
AU - Cho, Chul Soo
AU - Kim, Wan Uk
N1 - Publisher Copyright:
© 2016 KSBMB.
PY - 2016/2/5
Y1 - 2016/2/5
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84978639970&partnerID=8YFLogxK
U2 - 10.1038/emm.2015.120
DO - 10.1038/emm.2015.120
M3 - Article
C2 - 26915672
AN - SCOPUS:84978639970
SN - 1226-3613
VL - 48
JO - Experimental and Molecular Medicine
JF - Experimental and Molecular Medicine
IS - 2
M1 - e211
ER -