Movement Disorders (revue)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

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

Identifieur interne : 001290 ( Main/Curation ); précédent : 001289; suivant : 001291

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

Auteurs : Ji E. Lee [Corée du Sud] ; Sook K. Song [Corée du Sud] ; Young H. Sohn [Corée du Sud] ; Phil Hyu Lee [Corée du Sud]

Source :

RBID : ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33

Descripteurs français

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

Url:
DOI: 10.1002/mds.23556

Links toward previous steps (curation, corpus...)


Links to Exploration step

ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
</author>
<author>
<name sortKey="Lee, Phil Hyu" sort="Lee, Phil Hyu" uniqKey="Lee P" first="Phil Hyu" last="Lee">Phil Hyu Lee</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33</idno>
<date when="2011" year="2011">2011</date>
<idno type="doi">10.1002/mds.23556</idno>
<idno type="url">https://api.istex.fr/document/9FDA783E1D171D8F0B82711CD9D73384D43B8E33/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000984</idno>
<idno type="wicri:Area/Istex/Curation">000984</idno>
<idno type="wicri:Area/Istex/Checkpoint">000022</idno>
<idno type="wicri:doubleKey">0885-3185:2011:Lee J:uric:acid:as</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:21542015</idno>
<idno type="wicri:Area/PubMed/Corpus">001226</idno>
<idno type="wicri:Area/PubMed/Curation">001226</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001007</idno>
<idno type="wicri:Area/Ncbi/Merge">003201</idno>
<idno type="wicri:Area/Ncbi/Curation">003201</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">003201</idno>
<idno type="wicri:Area/Main/Merge">001343</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:11-0353402</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000506</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002812</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000333</idno>
<idno type="wicri:doubleKey">0885-3185:2011:Lee J:uric:acid:as</idno>
<idno type="wicri:Area/Main/Merge">001923</idno>
<idno type="wicri:Area/Main/Curation">001290</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Jeju University College of Medicine, Jeju</wicri:regionArea>
<wicri:noRegion>Jeju</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lee, Phil Hyu" sort="Lee, Phil Hyu" uniqKey="Lee P" first="Phil Hyu" last="Lee">Phil Hyu Lee</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Severance Biomedical Science Institute, Yonsei University, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2011-07">2011-07</date>
<biblScope unit="vol">26</biblScope>
<biblScope unit="issue">8</biblScope>
<biblScope unit="page" from="1533">1533</biblScope>
<biblScope unit="page" to="1536">1536</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">9FDA783E1D171D8F0B82711CD9D73384D43B8E33</idno>
<idno type="DOI">10.1002/mds.23556</idno>
<idno type="ArticleID">MDS23556</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Enzyme Assays</term>
<term>Female</term>
<term>Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (blood)</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Prospective Studies</term>
<term>Regression Analysis</term>
<term>Seasons</term>
<term>Uric Acid (blood)</term>
<term>Uric acid</term>
<term>multiple system atrophy</term>
<term>progression</term>
<term>uric acid</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Uric Acid</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en">
<term>Multiple System Atrophy</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Enzyme Assays</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Prospective Studies</term>
<term>Regression Analysis</term>
<term>Seasons</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Acide urique</term>
<term>Atrophie multisystématisée</term>
<term>Homme</term>
<term>Pathologie du système nerveux</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Homme</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml: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</div>
</front>
</TEI>
<double idat="0885-3185:2011:Lee J:uric:acid:as">
<INIST>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en" level="a">Uric Acid as a Potential Disease Modifier in Patients with Multiple System Atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Department of Neurology, Jeju University College of Medicine</s1>
<s2>Jeju</s2>
<s3>KOR</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<wicri:noRegion>Jeju</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Phil Hyu Lee" sort="Phil Hyu Lee" uniqKey="Phil Hyu Lee" last="Phil Hyu Lee">PHIL HYU LEE</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<inist:fA14 i1="03">
<s1>Severance Biomedical Science Institute, Yonsei University</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">INIST</idno>
<idno type="inist">11-0353402</idno>
<date when="2011">2011</date>
<idno type="stanalyst">PASCAL 11-0353402 INIST</idno>
<idno type="RBID">Pascal:11-0353402</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000506</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002812</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000333</idno>
<idno type="wicri:doubleKey">0885-3185:2011:Lee J:uric:acid:as</idno>
<idno type="wicri:Area/Main/Merge">001923</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a">Uric Acid as a Potential Disease Modifier in Patients with Multiple System Atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Department of Neurology, Jeju University College of Medicine</s1>
<s2>Jeju</s2>
<s3>KOR</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<wicri:noRegion>Jeju</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Phil Hyu Lee" sort="Phil Hyu Lee" uniqKey="Phil Hyu Lee" last="Phil Hyu Lee">PHIL HYU LEE</name>
<affiliation wicri:level="3">
<inist:fA14 i1="01">
<s1>Department of Neurology, Yonsei University College of Medicine</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<inist:fA14 i1="03">
<s1>Severance Biomedical Science Institute, Yonsei University</s1>
<s2>Seoul</s2>
<s3>KOR</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>Corée du Sud</country>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2011">2011</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Human</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Uric acid</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Atrophie multisystématisée</term>
<term>Pathologie du système nerveux</term>
<term>Acide urique</term>
<term>Homme</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml: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.</div>
</front>
</TEI>
</INIST>
<ISTEX>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
</author>
<author>
<name sortKey="Lee, Phil Hyu" sort="Lee, Phil Hyu" uniqKey="Lee P" first="Phil Hyu" last="Lee">Phil Hyu Lee</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33</idno>
<date when="2011" year="2011">2011</date>
<idno type="doi">10.1002/mds.23556</idno>
<idno type="url">https://api.istex.fr/document/9FDA783E1D171D8F0B82711CD9D73384D43B8E33/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000984</idno>
<idno type="wicri:Area/Istex/Curation">000984</idno>
<idno type="wicri:Area/Istex/Checkpoint">000022</idno>
<idno type="wicri:doubleKey">0885-3185:2011:Lee J:uric:acid:as</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:21542015</idno>
<idno type="wicri:Area/PubMed/Corpus">001226</idno>
<idno type="wicri:Area/PubMed/Curation">001226</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001007</idno>
<idno type="wicri:Area/Ncbi/Merge">003201</idno>
<idno type="wicri:Area/Ncbi/Curation">003201</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">003201</idno>
<idno type="wicri:Area/Main/Merge">001343</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Uric acid as a potential disease modifier in patients with multiple system atrophy</title>
<author>
<name sortKey="Lee, Ji E" sort="Lee, Ji E" uniqKey="Lee J" first="Ji E." last="Lee">Ji E. Lee</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Song, Sook K" sort="Song, Sook K" uniqKey="Song S" first="Sook K." last="Song">Sook K. Song</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Jeju University College of Medicine, Jeju</wicri:regionArea>
<wicri:noRegion>Jeju</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Sohn, Young H" sort="Sohn, Young H" uniqKey="Sohn Y" first="Young H." last="Sohn">Young H. Sohn</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lee, Phil Hyu" sort="Lee, Phil Hyu" uniqKey="Lee P" first="Phil Hyu" last="Lee">Phil Hyu Lee</name>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yonsei University College of Medicine, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
<affiliation wicri:level="3">
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Severance Biomedical Science Institute, Yonsei University, Seoul</wicri:regionArea>
<placeName>
<settlement type="city">Séoul</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2011-07">2011-07</date>
<biblScope unit="vol">26</biblScope>
<biblScope unit="issue">8</biblScope>
<biblScope unit="page" from="1533">1533</biblScope>
<biblScope unit="page" to="1536">1536</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">9FDA783E1D171D8F0B82711CD9D73384D43B8E33</idno>
<idno type="DOI">10.1002/mds.23556</idno>
<idno type="ArticleID">MDS23556</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Enzyme Assays</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (blood)</term>
<term>Prospective Studies</term>
<term>Regression Analysis</term>
<term>Seasons</term>
<term>Uric Acid (blood)</term>
<term>multiple system atrophy</term>
<term>progression</term>
<term>uric acid</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Uric Acid</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en">
<term>Multiple System Atrophy</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Enzyme Assays</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Prospective Studies</term>
<term>Regression Analysis</term>
<term>Seasons</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml: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</div>
</front>
</TEI>
</ISTEX>
</double>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001290 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 001290 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Curation
   |type=    RBID
   |clé=     ISTEX:9FDA783E1D171D8F0B82711CD9D73384D43B8E33
   |texte=   Uric acid as a potential disease modifier in patients with multiple system atrophy
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024