<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Edwards NC</submitter><funding>US National Institutes of Health</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><pagination>fcae331</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11472828</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(5)</volume><pubmed_abstract>By age 40 years, over 90% of adults with Down syndrome have Alzheimer's disease pathology and most progress to dementia. Despite having few systemic vascular risk factors, individuals with Down syndrome have elevated cerebrovascular disease markers that track with the clinical progression of Alzheimer's disease, suggesting a role of cerebrovascular disease that is hypothesized to be mediated by inflammatory factors. This study examined the pathways through which small vessel cerebrovascular disease contributes to Alzheimer's disease-related pathophysiology and neurodegeneration in adults with Down syndrome. One hundred eighty-five participants from the Alzheimer's Biomarkers Consortium-Down Syndrome [mean (SD) age = 45.2 (9.3) years] with available MRI and plasma biomarker data were includ</pubmed_abstract><journal>Brain communications</journal><pubmed_title>Cerebrovascular disease is associated with Alzheimer's plasma biomarker concentrations in adults with Down syndrome.</pubmed_title><pmcid>PMC11472828</pmcid><funding_grant_id>P50 AG008702</funding_grant_id><funding_grant_id>UL1 TR002373</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>RF1 AG079519</funding_grant_id><funding_grant_id>UL1 TR001414</funding_grant_id><funding_grant_id>P50 AG005681</funding_grant_id><funding_grant_id>P50 HD105353</funding_grant_id><funding_grant_id>U19 AG068054</funding_grant_id><funding_grant_id>P50 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N</pubmed_authors><pubmed_authors>Doran EW</pubmed_authors><pubmed_authors>Clare I</pubmed_authors><pubmed_authors>Varadarajan B</pubmed_authors><pubmed_authors>Edwards NC</pubmed_authors><pubmed_authors>Alzheimer’s Biomarkers Consortium–Down Syndrome (ABC-DS) Investigators</pubmed_authors><pubmed_authors>Gutierrez J</pubmed_authors><pubmed_authors>Henson R</pubmed_authors><pubmed_authors>Handen BL</pubmed_authors><pubmed_authors>Honig L</pubmed_authors><pubmed_authors>Birn RM</pubmed_authors><pubmed_authors>Reiman E</pubmed_authors><pubmed_authors>Keator D</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors><pubmed_authors>Silverman WP</pubmed_authors><pubmed_authors>Pang D</pubmed_authors><pubmed_authors>Mapstone M</pubmed_authors><pubmed_authors>Alshikho MJ</pubmed_authors><pubmed_authors>Janelidze S</pubmed_authors><pubmed_authors>Price JC</pubmed_authors><pubmed_authors>Christian BT</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Feingold E</pubmed_authors><pubmed_authors>Hansson O</pubmed_authors><pubmed_authors>Fagan A</pubmed_authors><pubmed_authors>Tudorascu DL</pubmed_authors><pubmed_authors>Parisi M</pubmed_authors><pubmed_authors>Ericsson OM</pubmed_authors><pubmed_authors>Ikonomovic MD</pubmed_authors><pubmed_authors>Kreisl WC</pubmed_authors><pubmed_authors>Bulova P</pubmed_authors><pubmed_authors>White DA</pubmed_authors><pubmed_authors>Head E</pubmed_authors><pubmed_authors>Pulsifer M</pubmed_authors><pubmed_authors>Petersen M</pubmed_authors><pubmed_authors>Rizvi B</pubmed_authors><pubmed_authors>Simoes S</pubmed_authors><pubmed_authors>Mathis CA</pubmed_authors><pubmed_authors>Ryan L</pubmed_authors><pubmed_authors>Jordan C</pubmed_authors><pubmed_authors>Lai F</pubmed_authors><pubmed_authors>Wilcock DM</pubmed_authors><pubmed_authors>Ances BM</pubmed_authors><pubmed_authors>Tycko B</pubmed_authors><pubmed_authors>Lott IT</pubmed_authors><pubmed_authors>Johnson SC</pubmed_authors><pubmed_authors>Aizenstein HJ</pubmed_authors><pubmed_authors>Lao PJ</pubmed_authors><pubmed_authors>Constantino JN</pubmed_authors><pubmed_authors>Cohen AD</pubmed_authors><pubmed_authors>Foroud TM</pubmed_authors><pubmed_authors>Hom C</pubmed_authors><pubmed_authors>Krinsky-McHale SJ</pubmed_authors><pubmed_authors>Minhas DS</pubmed_authors><pubmed_authors>Harp J</pubmed_authors><pubmed_authors>Aguilar LF</pubmed_authors><pubmed_authors>Rafii MS</pubmed_authors><pubmed_authors>Tumuluru R</pubmed_authors><pubmed_authors>Bell K</pubmed_authors><pubmed_authors>Laymon C</pubmed_authors><pubmed_authors>Schmitt F</pubmed_authors><pubmed_authors>Kofler JK</pubmed_authors><pubmed_authors>Hartley SL</pubmed_authors><pubmed_authors>Kamboh MI</pubmed_authors><pubmed_authors>Lao P</pubmed_authors><pubmed_authors>Yassa MA</pubmed_authors><pubmed_authors>Lupson V</pubmed_authors><pubmed_authors>Andrews HF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cerebrovascular disease is associated with Alzheimer's plasma biomarker concentrations in adults with Down syndrome.</name><description>By age 40 years, over 90% of adults with Down syndrome have Alzheimer's disease pathology and most progress to dementia. Despite having few systemic vascular risk factors, individuals with Down syndrome have elevated cerebrovascular disease markers that track with the clinical progression of Alzheimer's disease, suggesting a role of cerebrovascular disease that is hypothesized to be mediated by inflammatory factors. This study examined the pathways through which small vessel cerebrovascular disease contributes to Alzheimer's disease-related pathophysiology and neurodegeneration in adults with Down syndrome. One hundred eighty-five participants from the Alzheimer's Biomarkers Consortium-Down Syndrome [mean (SD) age = 45.2 (9.3) years] with available MRI and plasma biomarker data were includ</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-07-09T10:29:48.931Z</modification><creation>2025-04-04T02:22:31.371Z</creation></dates><accession>S-EPMC11472828</accession><cross_references><pubmed>39403075</pubmed><doi>10.1093/braincomms/fcae331</doi></cross_references></HashMap>