<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang T</submitter><funding>345 Talent Project of Shengjing Hospital of China Medical University</funding><funding>Peking University Clinical Medicine + X youth program</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Major Project of the Anhui Provincial Department of Education</funding><funding>Young Elite Scientists Sponsorship Program by China Association for Science and Technology</funding><funding>Beijing Hospitals Authority Youth Programme</funding><funding>Youth Key Talents Program of Wannan Medical College</funding><funding>Beijing Chao-Yang Hospital Golden Seeds Foundation</funding><pagination>106</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11088014</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Previous studies on the associations between serum urate levels and neurodegenerative outcomes have yielded inconclusive results, and the causality remains unclear. This study aimed to investigate whether urate levels are associated with the risks of Alzheimer's disease and related dementias (ADRD), Parkinson's disease (PD), and neurodegenerative deaths.&lt;h4>Methods&lt;/h4>This prospective study included 382,182 participants (45.7% men) from the UK Biobank cohort. Cox proportional hazards models were used to assess the associations between urate levels and risk of neurodegenerative outcomes. In the Mendelian randomization (MR) analysis, urate-related single-nucleotide polymorphisms were identified through a genome-wide association study. Both linear and non-linear MR approac</pubmed_abstract><journal>Alzheimer's research &amp; therapy</journal><pubmed_title>Serum urate levels and neurodegenerative outcomes: a prospective cohort study and mendelian randomization analysis of the UK Biobank.</pubmed_title><pmcid>PMC11088014</pmcid><funding_grant_id>QML20230301</funding_grant_id><funding_grant_id>82003456</funding_grant_id><funding_grant_id>PKU2023LCXQ009</funding_grant_id><funding_grant_id>WK202211</funding_grant_id><funding_grant_id>M0294</funding_grant_id><funding_grant_id>2022AH051233</funding_grant_id><funding_grant_id>CYJZ202102</funding_grant_id><funding_grant_id>2020QNRC001</funding_grant_id><funding_grant_id>82103811</funding_grant_id><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Xia Y</pubmed_authors><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Shen Z</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>An Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serum urate levels and neurodegenerative outcomes: a prospective cohort study and mendelian randomization analysis of the UK Biobank.</name><description>&lt;h4>Background&lt;/h4>Previous studies on the associations between serum urate levels and neurodegenerative outcomes have yielded inconclusive results, and the causality remains unclear. This study aimed to investigate whether urate levels are associated with the risks of Alzheimer's disease and related dementias (ADRD), Parkinson's disease (PD), and neurodegenerative deaths.&lt;h4>Methods&lt;/h4>This prospective study included 382,182 participants (45.7% men) from the UK Biobank cohort. Cox proportional hazards models were used to assess the associations between urate levels and risk of neurodegenerative outcomes. In the Mendelian randomization (MR) analysis, urate-related single-nucleotide polymorphisms were identified through a genome-wide association study. Both linear and non-linear MR approac</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-01T05:35:07.616Z</modification><creation>2026-04-08T09:35:57.539Z</creation></dates><accession>S-EPMC11088014</accession><cross_references><pubmed>38730474</pubmed><doi>10.1186/s13195-024-01476-x</doi></cross_references></HashMap>