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Serum urate as a predictor of clinical and radiographic progression in Parkinson disease.

Identifieur interne : 000140 ( PubMed/Corpus ); précédent : 000139; suivant : 000141

Serum urate as a predictor of clinical and radiographic progression in Parkinson disease.

Auteurs : Michael. Schwarzschild ; Steven. Schwid ; Kenneth Marek ; Arthur Watts ; Anthony. Lang ; David Oakes ; Ira Shoulson ; Alberto Ascherio ; Christopher Hyson ; Emily Gorbold ; Alice Rudolph ; Karl Kieburtz ; Stanley Fahn ; Lisa Gauger ; Christopher Goetz ; John Seibyl ; Misser Forrest ; John Ondrasik

Source :

RBID : pubmed:18413464

English descriptors

Abstract

To determine whether concentration of serum urate, a purine metabolite and potent antioxidant that has been linked to a reduced risk of Parkinson disease (PD), predicts prognosis in PD.

DOI: 10.1001/archneur.2008.65.6.nct70003
PubMed: 18413464

Links to Exploration step

pubmed:18413464

Le document en format XML

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<term>Biomarkers (blood)</term>
<term>Cohort Studies</term>
<term>Disease Progression</term>
<term>Double-Blind Method</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Longitudinal Studies</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (blood)</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (radiography)</term>
<term>Predictive Value of Tests</term>
<term>Prospective Studies</term>
<term>Uric Acid (blood)</term>
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<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Biomarkers</term>
<term>Uric Acid</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en">
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="radiography" xml:lang="en">
<term>Parkinson Disease</term>
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<term>Cohort Studies</term>
<term>Disease Progression</term>
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<front>
<div type="abstract" xml:lang="en">To determine whether concentration of serum urate, a purine metabolite and potent antioxidant that has been linked to a reduced risk of Parkinson disease (PD), predicts prognosis in PD.</div>
</front>
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<DateCreated>
<Year>2008</Year>
<Month>06</Month>
<Day>10</Day>
</DateCreated>
<DateCompleted>
<Year>2008</Year>
<Month>06</Month>
<Day>26</Day>
</DateCompleted>
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<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
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<ISSN IssnType="Electronic">1538-3687</ISSN>
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<Volume>65</Volume>
<Issue>6</Issue>
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<Year>2008</Year>
<Month>Jun</Month>
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<Title>Archives of neurology</Title>
<ISOAbbreviation>Arch. Neurol.</ISOAbbreviation>
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<ArticleTitle>Serum urate as a predictor of clinical and radiographic progression in Parkinson disease.</ArticleTitle>
<Pagination>
<MedlinePgn>716-23</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1001/archneur.2008.65.6.nct70003</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To determine whether concentration of serum urate, a purine metabolite and potent antioxidant that has been linked to a reduced risk of Parkinson disease (PD), predicts prognosis in PD.</AbstractText>
<AbstractText Label="DESIGN" NlmCategory="METHODS">Prospective study.</AbstractText>
<AbstractText Label="SETTING" NlmCategory="METHODS">The Parkinson Research Examination of CEP-1347 Trial (PRECEPT) study, which investigated the effects of a potential neuroprotectant on rates of PD progression, was conducted between April 2002 and August 2005 (average follow-up time 21.4 months).</AbstractText>
<AbstractText Label="PARTICIPANTS" NlmCategory="METHODS">Eight hundred four subjects with early PD enrolled in the PRECEPT study.</AbstractText>
<AbstractText Label="MAIN OUTCOME MEASURES" NlmCategory="METHODS">The primary study end point was progression to clinical disability sufficient to warrant dopaminergic therapy. Cox proportional hazards models were used to estimate the hazard ratio (HR) of reaching end point according to quintiles of baseline serum urate concentration, adjusting for sex, age, and other potential covariates. Change in striatal uptake of iodine I 123-labeled 2-beta-carbomethoxy-3-beta-(4-iodophenyl)tropane ([(123)I]beta-CIT), a marker for the presynaptic dopamine transporter, was assessed with linear regression for a subset of 399 subjects.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The adjusted HR of reaching end point declined with increasing baseline concentrations of urate; subjects in the top quintile reached the end point at only half the rate of subjects in the bottom quintile (HR, 0.51; 95% confidence interval [CI], 0.37-0.72; P for trend < .001). This association was markedly stronger in men (HR, 0.39; 95% CI, 0.26-0.60; P for trend < .001) than in women (HR, 0.77; 95% CI, 0.39-1.50; P for trend = .33). The percentage of loss in striatal [(123)I]beta-CIT uptake also improved with increasing serum urate concentrations (overall P for trend = .002; men, P = .001; women, P = .43).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">These findings identify serum urate as the first molecular factor directly linked to the progression of typical PD and suggest that targeting urate or its determinants could be an effective disease-modifying therapy in PD. Trial Registration clinicaltrials.gov Identifier: NCT00040404.</AbstractText>
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<LastName>Schwarzschild</LastName>
<ForeName>Michael A</ForeName>
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<LastName>Ondrasik</LastName>
<ForeName>John</ForeName>
<Initials>J</Initials>
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<Language>eng</Language>
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