<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Parkinson Study Group SURE-PD3 Investigators</submitter><funding>NINDS NIH HHS</funding><pagination>926-939</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8441591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>326(10)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>Urate elevation, despite associations with crystallopathic, cardiovascular, and metabolic disorders, has been pursued as a potential disease-modifying strategy for Parkinson disease (PD) based on convergent biological, epidemiological, and clinical data.&lt;h4>Objective&lt;/h4>To determine whether sustained urate-elevating treatment with the urate precursor inosine slows early PD progression.&lt;h4>Design, participants, and setting&lt;/h4>Randomized, double-blind, placebo-controlled, phase 3 trial of oral inosine treatment in early PD. A total of 587 individuals consented, and 298 with PD not yet requiring dopaminergic medication, striatal dopamine transporter deficiency, and serum urate below the population median concentration (&lt;5.8 mg/dL) were randomized between August 2016 and D</pubmed_abstract><journal>JAMA</journal><pubmed_title>Effect of Urate-Elevating Inosine on Early Parkinson Disease Progression: The SURE-PD3 Randomized Clinical Trial.</pubmed_title><pmcid>PMC8441591</pmcid><funding_grant_id>U01 NS090259</funding_grant_id><funding_grant_id>U01 NS089666</funding_grant_id><pubmed_authors>Brodsky M</pubmed_authors><pubmed_authors>Waters C</pubmed_authors><pubmed_authors>Daley A</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Goetz C</pubmed_authors><pubmed_authors>LeWitt PA</pubmed_authors><pubmed_authors>Houghton DJ</pubmed_authors><pubmed_authors>James R</pubmed_authors><pubmed_authors>LaFaver K</pubmed_authors><pubmed_authors>Hunter C</pubmed_authors><pubmed_authors>Suski V</pubmed_authors><pubmed_authors>Langhammer A</pubmed_authors><pubmed_authors>Ahmed A</pubmed_authors><pubmed_authors>Pahwa R</pubmed_authors><pubmed_authors>Bwala G</pubmed_authors><pubmed_authors>Jain S</pubmed_authors><pubmed_authors>Rezak M</pubmed_authors><pubmed_authors>Espay AJ</pubmed_authors><pubmed_authors>de Marcaida JA</pubmed_authors><pubmed_authors>Mestre T</pubmed_authors><pubmed_authors>Russell D</pubmed_authors><pubmed_authors>Shah BB</pubmed_authors><pubmed_authors>Peterson C</pubmed_authors><pubmed_authors>Leehey M</pubmed_authors><pubmed_authors>Oakes D</pubmed_authors><pubmed_authors>Poon C</pubmed_authors><pubmed_authors>Serrano C</pubmed_authors><pubmed_authors>Casaceli C</pubmed_authors><pubmed_authors>Kostrzebski M</pubmed_authors><pubmed_authors>Ascherio A</pubmed_authors><pubmed_authors>Bodis-Wollner I</pubmed_authors><pubmed_authors>Curhan GC</pubmed_authors><pubmed_authors>Houston E</pubmed_authors><pubmed_authors>Macklin EA</pubmed_authors><pubmed_authors>Goudreau J</pubmed_authors><pubmed_authors>Bolger P</pubmed_authors><pubmed_authors>Rudolph A</pubmed_authors><pubmed_authors>Bhatti D</pubmed_authors><pubmed_authors>Pothier L</pubmed_authors><pubmed_authors>Thomas K</pubmed_authors><pubmed_authors>Schneider RB</pubmed_authors><pubmed_authors>Soileau M</pubmed_authors><pubmed_authors>Mihaila D</pubmed_authors><pubmed_authors>Laroche A</pubmed_authors><pubmed_authors>Shill HA</pubmed_authors><pubmed_authors>Rabin M</pubmed_authors><pubmed_authors>Bixby M</pubmed_authors><pubmed_authors>Shoulson I</pubmed_authors><pubmed_authors>Ratel AS</pubmed_authors><pubmed_authors>Togasaki DM</pubmed_authors><pubmed_authors>Videnovic A</pubmed_authors><pubmed_authors>Waikar SS</pubmed_authors><pubmed_authors>McMahon GM</pubmed_authors><pubmed_authors>Keith K</pubmed_authors><pubmed_authors>Bluett B</pubmed_authors><pubmed_authors>Zauber SE</pubmed_authors><pubmed_authors>Kumar R</pubmed_authors><pubmed_authors>Criswell SR</pubmed_authors><pubmed_authors>Litvan I</pubmed_authors><pubmed_authors>Gauger L</pubmed_authors><pubmed_authors>Ciccarello J</pubmed_authors><pubmed_authors>Mari Z</pubmed_authors><pubmed_authors>Lang A</pubmed_authors><pubmed_authors>Mozaffarian D</pubmed_authors><pubmed_authors>Christine C</pubmed_authors><pubmed_authors>Kaminski P</pubmed_authors><pubmed_authors>Dewey RB</pubmed_authors><pubmed_authors>Deik AF</pubmed_authors><pubmed_authors>Blindauer K</pubmed_authors><pubmed_authors>Gerald A</pubmed_authors><pubmed_authors>Hauser RA</pubmed_authors><pubmed_authors>Gunzler SA</pubmed_authors><pubmed_authors>Fitzgerald R</pubmed_authors><pubmed_authors>Crotty GF</pubmed_authors><pubmed_authors>Evatt M</pubmed_authors><pubmed_authors>Fang JY</pubmed_authors><pubmed_authors>Boyd JT</pubmed_authors><pubmed_authors>Simon DK</pubmed_authors><pubmed_authors>Mehta SH</pubmed_authors><pubmed_authors>Stover N</pubmed_authors><pubmed_authors>Schwarzschild MA</pubmed_authors><pubmed_authors>Marek K</pubmed_authors><pubmed_authors>Kurlan R</pubmed_authors><pubmed_authors>Park A</pubmed_authors><pubmed_authors>Friedman JH</pubmed_authors><pubmed_authors>Reich S</pubmed_authors><pubmed_authors>Ainslie M</pubmed_authors><pubmed_authors>Aldred J</pubmed_authors><pubmed_authors>Scott B</pubmed_authors><pubmed_authors>Hung A</pubmed_authors><pubmed_authors>Durphy J</pubmed_authors><pubmed_authors>Lungu C</pubmed_authors><pubmed_authors>Beck CA</pubmed_authors><pubmed_authors>Schiess MC</pubmed_authors><pubmed_authors>Chou K</pubmed_authors><pubmed_authors>Simuni T</pubmed_authors><pubmed_authors>Mosovsky S</pubmed_authors><pubmed_authors>LeDoux MS</pubmed_authors><pubmed_authors>Jimenez-Shahed J</pubmed_authors><pubmed_authors>Rosenthal L</pubmed_authors><pubmed_authors>Cloud L</pubmed_authors><pubmed_authors>Callahan KF</pubmed_authors><pubmed_authors>Shprecher D</pubmed_authors><pubmed_authors>Henchcliffe C</pubmed_authors><pubmed_authors>Klements D</pubmed_authors><pubmed_authors>Saint-Hilaire M</pubmed_authors><pubmed_authors>Parkinson Study Group SURE-PD3 Investigators</pubmed_authors><pubmed_authors>Kamp C</pubmed_authors><pubmed_authors>Hinson V</pubmed_authors><pubmed_authors>McGraw M</pubmed_authors><pubmed_authors>Morgan JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of Urate-Elevating Inosine on Early Parkinson Disease Progression: The SURE-PD3 Randomized Clinical Trial.</name><description>&lt;h4>Importance&lt;/h4>Urate elevation, despite associations with crystallopathic, cardiovascular, and metabolic disorders, has been pursued as a potential disease-modifying strategy for Parkinson disease (PD) based on convergent biological, epidemiological, and clinical data.&lt;h4>Objective&lt;/h4>To determine whether sustained urate-elevating treatment with the urate precursor inosine slows early PD progression.&lt;h4>Design, participants, and setting&lt;/h4>Randomized, double-blind, placebo-controlled, phase 3 trial of oral inosine treatment in early PD. A total of 587 individuals consented, and 298 with PD not yet requiring dopaminergic medication, striatal dopamine transporter deficiency, and serum urate below the population median concentration (&lt;5.8 mg/dL) were randomized between August 2016 and D</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-31T05:00:43.333Z</modification><creation>2026-04-08T08:11:38.853Z</creation></dates><accession>S-EPMC8441591</accession><cross_references><pubmed>34519802</pubmed><doi>10.1001/jama.2021.10207</doi></cross_references></HashMap>