TY - JOUR
T1 - Prospective study of plasma urate and risk of Parkinson disease in men and women
AU - Gao, Xiang
AU - O'Reilly, Eílis J.
AU - Schwarzschild, Michael A.
AU - Ascherio, Alberto
N1 - Funding Information:
Supported by grants (P01 CA055075, UM1 CA186107, UM1 CA167552, R01 NS061858, and R21 NS087235-01A1) from the NIH. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. X. Gao received funding from the NIH/NINDS. E. O''Reilly received funding from the NHS/NINDS. M. Schwarzschild has received research support from the NIH/NINDS, the US Department of Defense, the Michael J. Fox Foundation, the Parkinson Disease Foundation, the RJG Parkinson''s Disease Foundation, the American Parkinson Disease Association, and the American Federation for Aging Research. A. Ascherio serves on a scientific advisory board for the Michael J. Fox Foundation; serves on the editorial boards of Neurology®, Annals of Neurology, and the American Journal of Epidemiology; and receives research support from the NIH, the US Department of Defense, and the Michael J. Fox Foundation. Go to Neurology.org for full disclosures.
Funding Information:
Supported by grants (P01 CA055075, UM1 CA186107, UM1 CA167552, R01 NS061858, and R21 NS087235-01A1) from the NIH. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. X. Gao received funding from the NIH/NINDS. E. O''Reilly received funding from the NHS/NINDS. M. Schwarzschild has received research support from the NIH/NINDS, the US Department of Defense, the Michael J. Fox Foundation, the Parkinson Disease Foundation, the RJG Parkinson''s Disease Foundation, the American Parkinson Disease Association, and the American Federation for Aging Research. A. Ascherio serves on a scientific advisory board for the Michael J. Fox Foundation; serves on the editorial boards of Neurology?, Annals of Neurology, and the American Journal of Epidemiology; and receives research support from the NIH, the US Department of Defense, and the Michael J. Fox Foundation. Go to Neurology.org for full disclosures.
Publisher Copyright:
© 2016 American Academy of Neurology.
PY - 2016/2/9
Y1 - 2016/2/9
N2 - Objective: To examine whether higher plasma urate concentrations are associated with a lower risk of developing Parkinson disease (PD) and whether there is a sex difference in the potential urate-PD relationship. Methods: We conducted a nested case-control study based on 90,214 participants of 3 ongoing US cohorts. We identified 388 new PD cases (202 men and 186 women) since blood collection, which were then matched to 1,267 controls. PD cases were confirmed by medical record review. Conditional logistic regression estimated relative risks (RRs) and 95% confidence intervals (95% CIs), after adjustment for age, smoking, caffeine intake, plasma concentrations of cholesterol and ferritin, and other covariates. We also conducted a meta-analysis to combine our study with 3 previously published prospective studies on urate and PD risk. Results: In the present nested case-control study, the multivariate-adjusted RRs of PD comparing extreme quartiles of urate were 0.63 (95% CI 0.35, 1.10; p trend 0.049) in men and 1.04 (95% CI 0.61, 1.78; p trend 0.44) in women (p heterogeneity 0.001). In the meta-analysis, the pooled RRs comparing 2 extreme quartiles of urate were 0.63 (95% CI 0.42, 0.95) in men and 0.89 (95% CI 0.57, 1.40) in women. Conclusion: We observed that men, but not women, with higher urate concentrations had a lower future risk of developing PD, suggesting that urate could be protective against PD risk or could slow disease progression during the preclinical stage of disease.
AB - Objective: To examine whether higher plasma urate concentrations are associated with a lower risk of developing Parkinson disease (PD) and whether there is a sex difference in the potential urate-PD relationship. Methods: We conducted a nested case-control study based on 90,214 participants of 3 ongoing US cohorts. We identified 388 new PD cases (202 men and 186 women) since blood collection, which were then matched to 1,267 controls. PD cases were confirmed by medical record review. Conditional logistic regression estimated relative risks (RRs) and 95% confidence intervals (95% CIs), after adjustment for age, smoking, caffeine intake, plasma concentrations of cholesterol and ferritin, and other covariates. We also conducted a meta-analysis to combine our study with 3 previously published prospective studies on urate and PD risk. Results: In the present nested case-control study, the multivariate-adjusted RRs of PD comparing extreme quartiles of urate were 0.63 (95% CI 0.35, 1.10; p trend 0.049) in men and 1.04 (95% CI 0.61, 1.78; p trend 0.44) in women (p heterogeneity 0.001). In the meta-analysis, the pooled RRs comparing 2 extreme quartiles of urate were 0.63 (95% CI 0.42, 0.95) in men and 0.89 (95% CI 0.57, 1.40) in women. Conclusion: We observed that men, but not women, with higher urate concentrations had a lower future risk of developing PD, suggesting that urate could be protective against PD risk or could slow disease progression during the preclinical stage of disease.
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U2 - 10.1212/WNL.0000000000002351
DO - 10.1212/WNL.0000000000002351
M3 - Article
C2 - 26764029
AN - SCOPUS:84957824775
SN - 0028-3878
VL - 86
SP - 520
EP - 526
JO - Neurology
JF - Neurology
IS - 6
ER -