<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schworer EK</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>National Institute of Child Health and Human Development</funding><funding>National Institute on Aging</funding><pagination>1214-1224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12207984</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Adults with Down syndrome are at risk for Alzheimer's disease. Natural history cohort studies have characterised the progression of Alzheimer's disease biomarkers in people with Down syndrome, with a focus on amyloid β-PET and tau-PET. In this study, we aimed to leverage these well characterised imaging biomarkers in a large cohort of individuals with Down syndrome, to examine the timeline to symptomatic Alzheimer's disease based on estimated years since the detection on PET of amyloid β-positivity, referred to here as amyloid age, and in relation to tau burden as assessed by PET.&lt;h4>Methods&lt;/h4>In this prospective, longitudinal, observational cohort study, data were collected at four university research sites in the UK and USA as part of the Alzheimer's Biomarker Consor</pubmed_abstract><journal>The Lancet. Neurology</journal><pubmed_title>Timeline to symptomatic Alzheimer's disease in people with Down syndrome as assessed by amyloid-PET and tau-PET: a longitudinal cohort study.</pubmed_title><pmcid>PMC12207984</pmcid><funding_grant_id>P50 AG008702</funding_grant_id><funding_grant_id>R01 AG080766</funding_grant_id><funding_grant_id>UL1 TR002373</funding_grant_id><funding_grant_id>T32 HD007489</funding_grant_id><funding_grant_id>UL1 TR001873</funding_grant_id><funding_grant_id>UL1 TR002345</funding_grant_id><funding_grant_id>P30 AG062421</funding_grant_id><funding_grant_id>U54 HD087011</funding_grant_id><funding_grant_id>P50 AG005681</funding_grant_id><funding_grant_id>UL1 TR001414</funding_grant_id><funding_grant_id>U19 AG068054</funding_grant_id><funding_grant_id>P50 HD105353</funding_grant_id><funding_grant_id>P50 AG005133</funding_grant_id><funding_grant_id>UL1 TR001857</funding_grant_id><funding_grant_id>P30 AG062715</funding_grant_id><funding_grant_id>P30 AG066519</funding_grant_id><funding_grant_id>U24 AG021886</funding_grant_id><funding_grant_id>P30 AG066462</funding_grant_id><funding_grant_id>R01 AG070028</funding_grant_id><funding_grant_id>U01 AG051412</funding_grant_id><funding_grant_id>U01 AG051406</funding_grant_id><funding_grant_id>K99 AG084738</funding_grant_id><funding_grant_id>U54 HD090256</funding_grant_id><funding_grant_id>P50 AG016570</funding_grant_id><pubmed_authors>Zammit MD</pubmed_authors><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Zaman S</pubmed_authors><pubmed_authors>Clark L</pubmed_authors><pubmed_authors>O'Bryant S</pubmed_authors><pubmed_authors>Schupf N</pubmed_authors><pubmed_authors>Cheema A</pubmed_authors><pubmed_authors>Minhas D</pubmed_authors><pubmed_authors>Nadkarni N</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Zaman SH</pubmed_authors><pubmed_authors>Clare I</pubmed_authors><pubmed_authors>Varadarajan B</pubmed_authors><pubmed_authors>Constantino J</pubmed_authors><pubmed_authors>Henson R</pubmed_authors><pubmed_authors>Handen BL</pubmed_authors><pubmed_authors>Honig L</pubmed_authors><pubmed_authors>Reiman E</pubmed_authors><pubmed_authors>Kofler J</pubmed_authors><pubmed_authors>Alzheimer's Biomarker Consortium–Down Syndrome (ABC–DS)</pubmed_authors><pubmed_authors>Keator D</pubmed_authors><pubmed_authors>Pang D</pubmed_authors><pubmed_authors>Mapstone M</pubmed_authors><pubmed_authors>Mathis C</pubmed_authors><pubmed_authors>Christian BT</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Feingold E</pubmed_authors><pubmed_authors>Rosas D</pubmed_authors><pubmed_authors>Foroud T</pubmed_authors><pubmed_authors>Betthauser T</pubmed_authors><pubmed_authors>Fagan A</pubmed_authors><pubmed_authors>Tudorascu DL</pubmed_authors><pubmed_authors>Klunk W</pubmed_authors><pubmed_authors>Parisi M</pubmed_authors><pubmed_authors>Schworer EK</pubmed_authors><pubmed_authors>Hartley S</pubmed_authors><pubmed_authors>Bulova P</pubmed_authors><pubmed_authors>Head E</pubmed_authors><pubmed_authors>Doran E</pubmed_authors><pubmed_authors>Pulsifer M</pubmed_authors><pubmed_authors>Aizenstein H</pubmed_authors><pubmed_authors>Petersen M</pubmed_authors><pubmed_authors>Laymon CM</pubmed_authors><pubmed_authors>Rizvi B</pubmed_authors><pubmed_authors>Ryan L</pubmed_authors><pubmed_authors>Jordan C</pubmed_authors><pubmed_authors>Lai F</pubmed_authors><pubmed_authors>Tudorascu D</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Birn R</pubmed_authors><pubmed_authors>Ances BM</pubmed_authors><pubmed_authors>Ances B</pubmed_authors><pubmed_authors>Johnson S</pubmed_authors><pubmed_authors>Andrews H</pubmed_authors><pubmed_authors>Lott I</pubmed_authors><pubmed_authors>Tycko B</pubmed_authors><pubmed_authors>Krinsky-McHale S</pubmed_authors><pubmed_authors>Rafii M</pubmed_authors><pubmed_authors>White D</pubmed_authors><pubmed_authors>Yassa M</pubmed_authors><pubmed_authors>Cohen AD</pubmed_authors><pubmed_authors>Christian B</pubmed_authors><pubmed_authors>Price J</pubmed_authors><pubmed_authors>Hom C</pubmed_authors><pubmed_authors>Harp J</pubmed_authors><pubmed_authors>Brickman A</pubmed_authors><pubmed_authors>Handen B</pubmed_authors><pubmed_authors>Tumuluru R</pubmed_authors><pubmed_authors>Kreisl W</pubmed_authors><pubmed_authors>Bell K</pubmed_authors><pubmed_authors>Ikonomovic M</pubmed_authors><pubmed_authors>Laymon C</pubmed_authors><pubmed_authors>Schmitt F</pubmed_authors><pubmed_authors>Cohen A</pubmed_authors><pubmed_authors>Hartley SL</pubmed_authors><pubmed_authors>Kamboh MI</pubmed_authors><pubmed_authors>Lao P</pubmed_authors><pubmed_authors>Lupson V</pubmed_authors><pubmed_authors>Silverman W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Timeline to symptomatic Alzheimer's disease in people with Down syndrome as assessed by amyloid-PET and tau-PET: a longitudinal cohort study.</name><description>&lt;h4>Background&lt;/h4>Adults with Down syndrome are at risk for Alzheimer's disease. Natural history cohort studies have characterised the progression of Alzheimer's disease biomarkers in people with Down syndrome, with a focus on amyloid β-PET and tau-PET. In this study, we aimed to leverage these well characterised imaging biomarkers in a large cohort of individuals with Down syndrome, to examine the timeline to symptomatic Alzheimer's disease based on estimated years since the detection on PET of amyloid β-positivity, referred to here as amyloid age, and in relation to tau burden as assessed by PET.&lt;h4>Methods&lt;/h4>In this prospective, longitudinal, observational cohort study, data were collected at four university research sites in the UK and USA as part of the Alzheimer's Biomarker Consor</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-09T05:40:10.783Z</modification><creation>2026-06-09T03:08:01.91Z</creation></dates><accession>S-EPMC12207984</accession><cross_references><pubmed>39577922</pubmed><doi>10.1016/S1474-4422(24)00426-5</doi><doi>10.1016/s1474-4422(24)00426-5</doi></cross_references></HashMap>