<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zeng L</submitter><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>National Institute on Aging</funding><pagination>e6108</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11265565</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(6)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>To examine clinically important adverse events (AEs) associated with methylphenidate (MPH) treatment of apathy in Alzheimer's Disease (AD) versus placebo, including weight loss, vital signs, falls, and insomnia.&lt;h4>Methods&lt;/h4>The Apathy in Dementia Methylphenidate Trial 2 (ADMET2) trial was a multicenter randomized, placebo-controlled trial of MPH to treat apathy in individuals with apathy and AD. Participants in ADMET2 had vital signs and weight measured at monthly visits through 6 months. AEs, including insomnia, falls, and cardiovascular events, were reported at every visit by participants and families using a symptom checklist.&lt;h4>Results&lt;/h4>The study included 98 participants in the MPH group and 101 in the placebo group. Participants in the MPH group experienced g</pubmed_abstract><journal>International journal of geriatric psychiatry</journal><pubmed_title>Adverse effects of methylphenidate for apathy in patients with Alzheimer's disease (ADMET2 trial).</pubmed_title><pmcid>PMC11265565</pmcid><funding_grant_id>U01 AG061357</funding_grant_id><funding_grant_id>P30 AG066511</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>R01 AG055132</funding_grant_id><funding_grant_id>U54 AG065187</funding_grant_id><funding_grant_id>P30 AG066507</funding_grant_id><funding_grant_id>P30 AG072947</funding_grant_id><funding_grant_id>R01 AG046543</funding_grant_id><pubmed_authors>Lerner AJ</pubmed_authors><pubmed_authors>Brawman-Mintzer O</pubmed_authors><pubmed_authors>Herrmann N</pubmed_authors><pubmed_authors>Craft S</pubmed_authors><pubmed_authors>Zeng L</pubmed_authors><pubmed_authors>Gross AL</pubmed_authors><pubmed_authors>Perin J</pubmed_authors><pubmed_authors>Shade D</pubmed_authors><pubmed_authors>Levey A</pubmed_authors><pubmed_authors>Padala PR</pubmed_authors><pubmed_authors>Mintzer JE</pubmed_authors><pubmed_authors>van Dyck CH</pubmed_authors><pubmed_authors>Rosenberg PB</pubmed_authors><pubmed_authors>Lanctot KL</pubmed_authors><pubmed_authors>Porsteinsson AP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Adverse effects of methylphenidate for apathy in patients with Alzheimer's disease (ADMET2 trial).</name><description>&lt;h4>Objectives&lt;/h4>To examine clinically important adverse events (AEs) associated with methylphenidate (MPH) treatment of apathy in Alzheimer's Disease (AD) versus placebo, including weight loss, vital signs, falls, and insomnia.&lt;h4>Methods&lt;/h4>The Apathy in Dementia Methylphenidate Trial 2 (ADMET2) trial was a multicenter randomized, placebo-controlled trial of MPH to treat apathy in individuals with apathy and AD. Participants in ADMET2 had vital signs and weight measured at monthly visits through 6 months. AEs, including insomnia, falls, and cardiovascular events, were reported at every visit by participants and families using a symptom checklist.&lt;h4>Results&lt;/h4>The study included 98 participants in the MPH group and 101 in the placebo group. Participants in the MPH group experienced g</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-01T16:07:24.018Z</modification><creation>2026-04-08T13:59:19.951Z</creation></dates><accession>S-EPMC11265565</accession><cross_references><pubmed>38858522</pubmed><doi>10.1002/gps.6108</doi></cross_references></HashMap>