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Uric acid as a potential disease modifier in patients with multiple system atrophy

Identifieur interne : 001488 ( Main/Corpus ); précédent : 001487; suivant : 001489

Uric acid as a potential disease modifier in patients with multiple system atrophy

Auteurs : Ji E. Lee ; Sook K. Song ; Young H. Sohn ; Phil Hyu Lee

Source :

RBID : ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33

English descriptors

Abstract

Background:: Recent studies have suggested that mitochondrial dysfunction and oxidative stress play a key role in the pathogenesis of multiple system atrophy. Methods:: 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. Results:: 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). Conclusions:: These data suggest that serum uric acid may act as a potential disease modifier in multiple system atrophy. © 2011 Movement Disorder Society

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DOI: 10.1002/mds.23556

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ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33

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<p>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.</p>
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<b>Funding agencies</b>
: 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.
<b>Relevant conflicts of interest/financial disclosures</b>
: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article.</p>
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<titleInfo lang="en">
<title>Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
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<titleInfo type="abbreviated" lang="en">
<title>Brief Report</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en">
<title>Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
</titleInfo>
<name type="personal">
<namePart type="given">Ji E.</namePart>
<namePart type="family">Lee</namePart>
<namePart type="termsOfAddress">MD,</namePart>
<affiliation>Department of Neurology, Yonsei University College of Medicine, Seoul, Korea</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Sook K.</namePart>
<namePart type="family">Song</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, Jeju University College of Medicine, Jeju, Korea</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Young H.</namePart>
<namePart type="family">Sohn</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Department of Neurology, Yonsei University College of Medicine, Seoul, Korea</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Phil Hyu</namePart>
<namePart type="family">Lee</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Department of Neurology, Yonsei University College of Medicine, Seoul, Korea</affiliation>
<affiliation>Severance Biomedical Science Institute, Yonsei University, Seoul, South Korea</affiliation>
<description>Correspondence: Department of Neurology, Yonsei University Medical College, 250 Seongsanno, Seodaemun‐gu, Seoul 120‐752, South Korea</description>
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<roleTerm type="text">author</roleTerm>
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<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<place>
<placeTerm type="text">Hoboken</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2011-07</dateIssued>
<dateCaptured encoding="w3cdtf">2010-09-08</dateCaptured>
<dateValid encoding="w3cdtf">2010-11-04</dateValid>
<copyrightDate encoding="w3cdtf">2011</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<internetMediaType>text/html</internetMediaType>
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<abstract lang="en">Background:: Recent studies have suggested that mitochondrial dysfunction and oxidative stress play a key role in the pathogenesis of multiple system atrophy. Methods:: 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. Results:: 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). Conclusions:: These data suggest that serum uric acid may act as a potential disease modifier in multiple system atrophy. © 2011 Movement Disorder Society</abstract>
<note type="content">*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.</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>uric acid</topic>
<topic>multiple system atrophy</topic>
<topic>progression</topic>
</subject>
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<title>Movement Disorders</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="Journal">journal</genre>
<subject>
<genre>article category</genre>
<topic>Brief Report</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2011</date>
<detail type="volume">
<caption>vol.</caption>
<number>26</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>8</number>
</detail>
<extent unit="pages">
<start>1533</start>
<end>1536</end>
<total>4</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">9FDA783E1D171D8F0B82711CD9D73384D43B8E33</identifier>
<identifier type="DOI">10.1002/mds.23556</identifier>
<identifier type="ArticleID">MDS23556</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2010 Movement Disorder Society</accessCondition>
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