<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Winzeler B</submitter><funding>Swiss National Science Foundation</funding><funding>Swiss Academy of Medical Sciences</funding><funding>G.&amp;amp; J. Bangerter-Rhyner Foundation</funding><funding>, University Hospital and University of Basel</funding><pagination>e151800</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8516458</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>131(20)</volume><pubmed_abstract>BackgroundPrimary polydipsia, characterized by excessive fluid intake, carries the risk of water intoxication and hyponatremia, but treatment options are scarce. Glucagon-like peptide 1 (GLP-1) reduces appetite and food intake. In experimental models, GLP-1 has also been shown to play a role in thirst and drinking behavior. The aim of this trial was to investigate whether GLP-1 receptor agonists reduce fluid intake in patients with primary polydipsia.MethodsIn this randomized, double-blind, placebo-controlled, 3-week crossover trial, 34 patients with primary polydipsia received weekly dulaglutide (1.5 mg, Trulicity) in one treatment segment and placebo (0.9% sodium chloride) in the other. During the last treatment week, patients attended an 8-hour evaluation visit with free access to water</pubmed_abstract><journal>The Journal of clinical investigation</journal><pubmed_title>A randomized controlled trial of the GLP-1 receptor agonist dulaglutide in primary polydipsia.</pubmed_title><pmcid>PMC8516458</pmcid><funding_grant_id>162608</funding_grant_id><funding_grant_id>-</funding_grant_id><pubmed_authors>Sailer CO</pubmed_authors><pubmed_authors>Christ-Crain M</pubmed_authors><pubmed_authors>Coynel D</pubmed_authors><pubmed_authors>Refardt J</pubmed_authors><pubmed_authors>Vogt DR</pubmed_authors><pubmed_authors>Urwyler SA</pubmed_authors><pubmed_authors>Zanchi D</pubmed_authors><pubmed_authors>Winzeler B</pubmed_authors></additional><is_claimable>false</is_claimable><name>A randomized controlled trial of the GLP-1 receptor agonist dulaglutide in primary polydipsia.</name><description>BackgroundPrimary polydipsia, characterized by excessive fluid intake, carries the risk of water intoxication and hyponatremia, but treatment options are scarce. Glucagon-like peptide 1 (GLP-1) reduces appetite and food intake. In experimental models, GLP-1 has also been shown to play a role in thirst and drinking behavior. The aim of this trial was to investigate whether GLP-1 receptor agonists reduce fluid intake in patients with primary polydipsia.MethodsIn this randomized, double-blind, placebo-controlled, 3-week crossover trial, 34 patients with primary polydipsia received weekly dulaglutide (1.5 mg, Trulicity) in one treatment segment and placebo (0.9% sodium chloride) in the other. During the last treatment week, patients attended an 8-hour evaluation visit with free access to water</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-08T22:37:43.104Z</modification><creation>2022-02-11T16:20:03.204Z</creation></dates><accession>S-EPMC8516458</accession><cross_references><pubmed>34473645</pubmed><doi>10.1172/JCI151800</doi><doi>10.1172/jci151800</doi></cross_references></HashMap>