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Association Between Hyperuricemia, Gout, and the Risk of Parkinson’s Disease: An Updated Systematic Review and Meta-Analysis

F. Qtaishat, J. Yasin, R. Odat, M. Alsufi, A. Abunamoos (Irbid, Jordan)

Meeting: 2025 International Congress

Keywords: Parkinson’s

Category: Parkinson's Disease: Genetics

Objective: To explore and evaluate the association between gout, hyperuricemia, and Parkinson’s disease (PD) using a systematic review and meta-analysis, incorporating stratified analyses by age and gender.

Background: The metabolism of urate has been implicated in neuroprotection due to its antioxidant properties, while gout, a systemic inflammatory condition, has shown fluctuating associations with PD risk. This study provides available evidence to clarify the relationship between gout, hyperuricemia, and PD.

Method: A comprehensive literature search of PubMed, Embase, and Cochrane Library identified cohort and case-control studies assessing gout, hyperuricemia, and PD risk. Random-effects models were used to calculate pooled risk ratios (RR) with 95% confidence intervals (CI). Subgroup analyses were performed based on gender and age. Heterogeneity was assessed using I² statistics, and publication bias was evaluated using funnel plots and Egger’s test.

Results: Twelve studies met the inclusion criteria. Meta-analysis showed no significant association between gout and PD (RR: 0.99 [0.90, 1.08], I² = 87%), but hyperuricemia was associated with a reduced PD risk (RR: 0.69 [0.56, 0.85], I² = 73.4%). In gender-stratified analysis, gout showed no significant association with PD in males (RR: 0.94 [0.84, 1.05]) or females (RR: 1.07 [0.96, 1.19]), whereas hyperuricemia was more protective in males (RR: 0.48 [0.24, 0.97]) than in females (RR: 0.84 [0.44, 1.61]). Age-based analysis indicated that both hyperuricemia and gout were associated with lower PD risk in individuals <75 years, but no significant protective effect was observed in those ≥75 years.

Conclusion: No significant association between gout and PD was found using the meta analysis but the study supports a potential neuroprotective role of hyperuricemia, particularly in males and younger individuals. These findings suggest a biological basis for urate’s protective effect, warranting further research into urate-modulating strategies in PD prevention and management.

Gout (both sexes)

Gout (both sexes)

Gout (Stratified By Sex)

Gout (Stratified By Sex)

Gout (Stratified By Age)

Gout (Stratified By Age)

Urate (Q4 vs Q1)

Urate (Q4 vs Q1)

References: [1] M. Cortese, T. Riise, A. Engeland, A. Ascherio, and K. Bjørnevik, “Urate and the risk of Parkinson’s disease in men and women,” Parkinsonism Relat Disord, vol. 52, pp. 76–82, Jul. 2018, doi: 10.1016/J.PARKRELDIS.2018.03.026.
[2] M. De Vera, M. M. Rahman, J. Rankin, J. Kopec, X. Gao, and H. Choi, “Gout and the risk of Parkinson’s disease: a cohort study,” Arthritis Rheum, vol. 59, no. 11, pp. 1549–1554, Nov. 2008, doi: 10.1002/ART.24193.
[3] J. A. Singh and J. D. Cleveland, “Gout and the risk of Parkinson’s disease in older adults: A study of U.S. Medicare data,” BMC Neurol, vol. 19, no. 1, p. V, Jan. 2019, doi: 10.1186/S12883-018-1234-X/TABLES/3.
[4] J. H. Kim, I. A. Choi, A. Kim, and G. Kang, “Clinical Association between Gout and Parkinson’s Disease: A Nationwide Population-Based Cohort Study in Korea,” Medicina (Kaunas), vol. 57, no. 12, Dec. 2021, doi: 10.3390/MEDICINA57121292.
[5] S. W. Lai, C. H. Lin, C. L. Lin, and K. F. Liao, “Gout and Parkinson’s Disease in Older People: An Observation in Taiwan,” Int J Gerontol, vol. 8, no. 3, pp. 166–167, Sep. 2014, doi: 10.1016/J.IJGE.2013.01.006.
[6] J. Pakpoor, O. O. Seminog, S. V. Ramagopalan, and M. J. Goldacre, “Clinical associations between gout and multiple sclerosis, Parkinson’s disease and motor neuron disease: record-linkage studies,” BMC Neurol, vol. 15, no. 1, Feb. 2015, doi: 10.1186/S12883-015-0273-9.
[7] E. Schernhammer, J. Qiu, L. Wermuth, C. F. Lassen, S. Friis, and B. Ritz, “Gout and the risk of Parkinson’s disease in Denmark,” Eur J Epidemiol, vol. 28, no. 4, pp. 359–360, Apr. 2013, doi: 10.1007/S10654-013-9791-1/METRICS.
[8] M. A. Pou, F. Orfila, J. Pagonabarraga, S. Ferrer-Moret, H. Corominas, and C. Diaz-Torne, “Risk of Parkinson’s disease in a gout Mediterranean population: A case-control study,” Joint Bone Spine, vol. 89, no. 6, Nov. 2022, doi: 10.1016/J.JBSPIN.2022.105402.
[9] E. J. Lee et al., “Longitudinal follow-up study of the association with gout and Alzheimer’s disease and Parkinson’s disease in Korea,” Scientific Reports 2023 13:1, vol. 13, no. 1, pp. 1–11, Mar. 2023, doi: 10.1038/s41598-023-30379-4.
[10] L. Y. Hu et al., “Risk of Parkinson’s disease following gout: a population-based retrospective cohort study in Taiwan,” BMC Neurol, vol. 20, no. 1, Sep. 2020, doi: 10.1186/S12883-020-01916-9.
[11] A. Alonso, L. A. G. Rodríguez, G. Logroscino, and M. A. Hernán, “Gout and risk of Parkinson disease: a prospective study,” Neurology, vol. 69, no. 17, pp. 1696–1700, 2007, doi: 10.1212/01.WNL.0000279518.10072.DF.

To cite this abstract in AMA style:

F. Qtaishat, J. Yasin, R. Odat, M. Alsufi, A. Abunamoos. Association Between Hyperuricemia, Gout, and the Risk of Parkinson’s Disease: An Updated Systematic Review and Meta-Analysis [abstract]. Mov Disord. 2025; 40 (suppl 1). https://www.mdsabstracts.org/abstract/association-between-hyperuricemia-gout-and-the-risk-of-parkinsons-disease-an-updated-systematic-review-and-meta-analysis/. Accessed October 5, 2025.
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