Serum Urate as a Predictor of Clinical and Radiographic Progression in Parkinson Disease
Top Cited Papers
- 1 June 2008
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 65 (6) , 716-23
- https://doi.org/10.1001/archneur.2008.65.6.nct70003
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. Prospective study. 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). Eight hundred four subjects with early PD enrolled in the PRECEPT study. 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. 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). 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.Keywords
This publication has 43 references indexed in Scilit:
- Genome-wide search for genes affecting serum uric acid levels: the Framingham Heart StudyMetabolism, 2005
- Mitochondria take center stage in aging and neurodegenerationAnnals of Neurology, 2005
- MOLECULAR PATHOPHYSIOLOGY OF PARKINSON'S DISEASEAnnual Review of Neuroscience, 2005
- Effect of ethanol on metabolism of purine bases (hypoxanthine, xanthine, and uric acid)Clinica Chimica Acta; International Journal of Clinical Chemistry, 2005
- Serum Uric Acid and Coronary Heart Disease in 9,458 Incident Cases and 155,084 Controls: Prospective Study and Meta-AnalysisPLoS Medicine, 2005
- Consumption of milk and calcium in midlife and the future risk of Parkinson diseaseNeurology, 2005
- Inosine Reduces Ischemic Brain Injury in RatsStroke, 2005
- Incidence and Risk Factors for Gout in White MenJAMA, 1991
- DATATOP: A Multicenter Controlled Clinical Trial in Early Parkinson's DiseaseArchives of Neurology, 1989
- Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis.Proceedings of the National Academy of Sciences, 1981