<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Moscoso A</submitter><funding>NCATS NIH HHS</funding><funding>NIBIB NIH HHS</funding><funding>European Research Council</funding><funding>NIA NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>RRD VA</funding><funding>NIMH NIH HHS</funding><funding>NIDCD NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>Wellcome Trust</funding><funding>NIH HHS</funding><pagination>229-242</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12848857</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>334(3)</volume><pubmed_abstract>&lt;h4>Importance&lt;/h4>Tau positron emission tomography (PET) allows in vivo detection of neurofibrillary tangles, a core neuropathologic feature of Alzheimer disease (AD).&lt;h4>Objective&lt;/h4>To provide estimates of the frequency of tau PET positivity and its associated risk of clinical outcomes.&lt;h4>Design, setting, and participants&lt;/h4>Longitudinal study using data pooled from 21 cohorts, comprising a convenience sample of 6514 participants from 13 countries, collected between January 2013 and June 2024. Cognitively unimpaired individuals and patients with a clinical diagnosis of mild cognitive impairment (MCI), AD dementia, or other neurodegenerative disorders were included.&lt;h4>Exposures&lt;/h4>Tau PET with flortaucipir F 18, amyloid-β (Aβ) PET, and clinical examinations. Tau PET scans were visua</pubmed_abstract><journal>JAMA</journal><pubmed_title>Frequency and Clinical Outcomes Associated With Tau Positron Emission Tomography Positivity.</pubmed_title><pmcid>PMC12848857</pmcid><funding_grant_id>R01 AG058724</funding_grant_id><funding_grant_id>P30 AG028283</funding_grant_id><funding_grant_id>R56 AG045571</funding_grant_id><funding_grant_id>P30 AG053760</funding_grant_id><funding_grant_id>U01 AG057195</funding_grant_id><funding_grant_id>R01 AG079142</funding_grant_id><funding_grant_id>P50 AG047266</funding_grant_id><funding_grant_id>P20 AG068053</funding_grant_id><funding_grant_id>R35 AG072362</funding_grant_id><funding_grant_id>P30 AG066444</funding_grant_id><funding_grant_id>P30 AG019610</funding_grant_id><funding_grant_id>R01 AG062276</funding_grant_id><funding_grant_id>P30 AG072958</funding_grant_id><funding_grant_id>P30 AG072959</funding_grant_id><funding_grant_id>P50 AG047270</funding_grant_id><funding_grant_id>P30 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D</pubmed_authors><pubmed_authors>Bischof GN</pubmed_authors><pubmed_authors>Marshall G</pubmed_authors><pubmed_authors>Morris JC</pubmed_authors><pubmed_authors>Donohue M</pubmed_authors><pubmed_authors>Jimenez G</pubmed_authors><pubmed_authors>Wingo TS</pubmed_authors><pubmed_authors>Smith S</pubmed_authors><pubmed_authors>Smith R</pubmed_authors><pubmed_authors>Thomopoulos SI</pubmed_authors><pubmed_authors>Boutin S</pubmed_authors><pubmed_authors>PREVENT-AD Research Group, the Harvard Aging Brain Study, the LEADS Consortium, and the Alzheimer’s Disease Neuroimaging Initiative</pubmed_authors><pubmed_authors>Tariot P</pubmed_authors><pubmed_authors>Moscoso A</pubmed_authors><pubmed_authors>Mahar L</pubmed_authors><pubmed_authors>Shaw LM</pubmed_authors><pubmed_authors>Gonneaud J</pubmed_authors><pubmed_authors>Polsinelli A</pubmed_authors><pubmed_authors>Kantarci K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Frequency and Clinical Outcomes Associated With Tau Positron Emission Tomography Positivity.</name><description>&lt;h4>Importance&lt;/h4>Tau positron emission tomography (PET) allows in vivo detection of neurofibrillary tangles, a core neuropathologic feature of Alzheimer disease (AD).&lt;h4>Objective&lt;/h4>To provide estimates of the frequency of tau PET positivity and its associated risk of clinical outcomes.&lt;h4>Design, setting, and participants&lt;/h4>Longitudinal study using data pooled from 21 cohorts, comprising a convenience sample of 6514 participants from 13 countries, collected between January 2013 and June 2024. Cognitively unimpaired individuals and patients with a clinical diagnosis of mild cognitive impairment (MCI), AD dementia, or other neurodegenerative disorders were included.&lt;h4>Exposures&lt;/h4>Tau PET with flortaucipir F 18, amyloid-β (Aβ) PET, and clinical examinations. Tau PET scans were visua</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-06-11T05:38:24.383Z</modification><creation>2026-06-11T03:08:06.012Z</creation></dates><accession>S-EPMC12848857</accession><cross_references><pubmed>40522652</pubmed><doi>10.1001/jama.2025.7817</doi></cross_references></HashMap>