Funding agencies: This research was supported by a grant from the Stem Cell Research Center of the 21st Century Frontier Research Program (SC-4111) funded by the Ministry of Science and Technology, Republic of Korea. Relevant conflicts of interest/financial disclosures: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article.
Uric acid as a potential disease modifier in patients with multiple system atrophy†
Version of Record online: 3 MAY 2011
Copyright © 2010 Movement Disorder Society
Volume 26, Issue 8, pages 1533–1536, July 2011
How to Cite
Lee, J. E., Song, S. K., Sohn, Y. H. and Lee, P. H. (2011), Uric acid as a potential disease modifier in patients with multiple system atrophy. Mov. Disord., 26: 1533–1536. doi: 10.1002/mds.23556
- Issue online: 21 JUL 2011
- Version of Record online: 3 MAY 2011
- Manuscript Accepted: 4 NOV 2010
- Manuscript Revised: 3 NOV 2010
- Manuscript Received: 8 SEP 2010
- uric acid;
- multiple system atrophy;
Recent studies have suggested that mitochondrial dysfunction and oxidative stress play a key role in the pathogenesis of multiple system atrophy.
We evaluated the influence of serum uric acid levels on disease progression in 52 patients with multiple system atrophy using changes in the annualized Unified Multiple System Atrophy Rating Scale scores.
The mean annualized Unified Multiple System Atrophy Rating Scale changes were significantly lower in patients with the highest uric acid quartile compared with those with the lowest quartile (8.4 ± 5.1 vs 20.2 ± 16.0, P = .038). Serum uric acid levels had a significant negative correlation with the annualized Unified Multiple System Atrophy Rating Scale changes (r = −0.40, P = .004). Multiple linear regression analysis showed that only serum uric acid concentration was significantly correlated with the annualized Unified Multiple System Atrophy Rating Scale changes (β = −2.687, P = .011).
These data suggest that serum uric acid may act as a potential disease modifier in multiple system atrophy. © 2011 Movement Disorder Society