<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chang CY</submitter><funding>NIA NIH HHS</funding><funding>F. Hoffmann-La Roche</funding><pagination>26668</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11535522</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Early detection of Alzheimer's disease (AD) is crucial to maximize clinical outcomes. Most disease progression analyses include people with diagnoses of cognitive impairment, limiting understanding of AD risk among those with normal cognition. The objective was to establish AD progression models through a deep learning approach to analyze heterogeneous, multi-modal datasets, including clustering analyses of population subsets. A multi-head deep-learning architecture was built to process and learn from biomedical and imaging data from the National Alzheimer's Coordinating Center. Shapley additive explanation algorithms for feature importance ranking and pairwise correlation analysis were used to identify predictors of disease progression. Four primary disease progression clusters (slow, mod</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Prediction and clustering of Alzheimer's disease by race and sex: a multi-head deep-learning approach to analyze irregular and heterogeneous data.</pubmed_title><pmcid>PMC11535522</pmcid><funding_grant_id>P30 AG062677</funding_grant_id><funding_grant_id>P30 AG066514</funding_grant_id><funding_grant_id>P30 AG066515</funding_grant_id><funding_grant_id>P30 AG066518</funding_grant_id><funding_grant_id>P30 AG062715</funding_grant_id><funding_grant_id>P30 AG066519</funding_grant_id><funding_grant_id>P20 AG068053</funding_grant_id><funding_grant_id>P30 AG072931</funding_grant_id><funding_grant_id>P30 AG066462</funding_grant_id><funding_grant_id>P30 AG072975</funding_grant_id><funding_grant_id>P30 AG072976</funding_grant_id><funding_grant_id>P20 AG068077</funding_grant_id><funding_grant_id>P30 AG072977</funding_grant_id><funding_grant_id>P30 AG066444</funding_grant_id><funding_grant_id>P30 AG072972</funding_grant_id><funding_grant_id>P30 AG072973</funding_grant_id><funding_grant_id>P30 AG066468</funding_grant_id><funding_grant_id>P30 AG072978</funding_grant_id><funding_grant_id>R01 AG079280</funding_grant_id><funding_grant_id>P30 AG072979</funding_grant_id><funding_grant_id>P30 AG072958</funding_grant_id><funding_grant_id>P30 AG072959</funding_grant_id><funding_grant_id>P30 AG062421</funding_grant_id><funding_grant_id>P30 AG062422</funding_grant_id><funding_grant_id>P30 AG066546</funding_grant_id><funding_grant_id>P30 AG066506</funding_grant_id><funding_grant_id>P30 AG066507</funding_grant_id><funding_grant_id>P30 AG066508</funding_grant_id><funding_grant_id>P30 AG062429</funding_grant_id><funding_grant_id>P30 AG066509</funding_grant_id><funding_grant_id>P30 AG066530</funding_grant_id><funding_grant_id>P20 AG068082</funding_grant_id><funding_grant_id>P30 AG066511</funding_grant_id><funding_grant_id>P30 AG066512</funding_grant_id><funding_grant_id>U24 AG072122</funding_grant_id><funding_grant_id>P20 AG068024</funding_grant_id><funding_grant_id>P30 AG072946</funding_grant_id><funding_grant_id>P30 AG072947</funding_grant_id><pubmed_authors>Win N</pubmed_authors><pubmed_authors>Chang CY</pubmed_authors><pubmed_authors>Slowiejko D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction and clustering of Alzheimer's disease by race and sex: a multi-head deep-learning approach to analyze irregular and heterogeneous data.</name><description>Early detection of Alzheimer's disease (AD) is crucial to maximize clinical outcomes. Most disease progression analyses include people with diagnoses of cognitive impairment, limiting understanding of AD risk among those with normal cognition. The objective was to establish AD progression models through a deep learning approach to analyze heterogeneous, multi-modal datasets, including clustering analyses of population subsets. A multi-head deep-learning architecture was built to process and learn from biomedical and imaging data from the National Alzheimer's Coordinating Center. Shapley additive explanation algorithms for feature importance ranking and pairwise correlation analysis were used to identify predictors of disease progression. Four primary disease progression clusters (slow, mod</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-07-16T13:17:37.347Z</modification><creation>2025-04-20T03:54:13.323Z</creation></dates><accession>S-EPMC11535522</accession><cross_references><pubmed>39496718</pubmed><doi>10.1038/s41598-024-77829-1</doi></cross_references></HashMap>