<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hou Y</submitter><funding>NIA NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>1334-1349</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10916937</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(2)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The molecular mechanisms that contribute to sex differences, in particular female predominance, in Alzheimer's disease (AD) prevalence, symptomology, and pathology, are incompletely understood.&lt;h4>Methods&lt;/h4>To address this problem, we investigated cellular metabolism and immune responses ("immunometabolism endophenotype") across AD individuals as a function of sex with diverse clinical diagnosis of cognitive status at death (cogdx), Braak staging, and Consortium to Establish a Registry for AD (CERAD) scores using human cortex metabolomics and transcriptomics data from the Religious Orders Study / Memory and Aging Project (ROSMAP) cohort.&lt;h4>Results&lt;/h4>We identified sex-specific metabolites, immune and metabolic genes, and pathways associated with the AD diagnosis an</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>Microglial immunometabolism endophenotypes contribute to sex difference in Alzheimer's disease.</pubmed_title><pmcid>PMC10916937</pmcid><funding_grant_id>R01 AG082118</funding_grant_id><funding_grant_id>R01 AG015819</funding_grant_id><funding_grant_id>U01 AG061356</funding_grant_id><funding_grant_id>R01 AG074392</funding_grant_id><funding_grant_id>R01 AG036836</funding_grant_id><funding_grant_id>R01 AG066707</funding_grant_id><funding_grant_id>U01 NS093334</funding_grant_id><funding_grant_id>R01 AG053798</funding_grant_id><funding_grant_id>P20 AG068053</funding_grant_id><funding_grant_id>U01 AG073323</funding_grant_id><funding_grant_id>R01 AG069901</funding_grant_id><funding_grant_id>U01 AG046152</funding_grant_id><funding_grant_id>P01 CA245705</funding_grant_id><funding_grant_id>R35 AG071476</funding_grant_id><funding_grant_id>P30 AG072959</funding_grant_id><funding_grant_id>P20 GM109025</funding_grant_id><funding_grant_id>R01 AG030146</funding_grant_id><funding_grant_id>RF1 NS133812</funding_grant_id><funding_grant_id>R01 AG076448</funding_grant_id><funding_grant_id>P30 AG010161</funding_grant_id><funding_grant_id>R56 AG074001</funding_grant_id><funding_grant_id>R01 AG084250</funding_grant_id><funding_grant_id>R21 AG083003</funding_grant_id><funding_grant_id>U19 AG063744</funding_grant_id><funding_grant_id>U01 AG032984</funding_grant_id><funding_grant_id>K08 AG065463</funding_grant_id><funding_grant_id>RF1 AG082211</funding_grant_id><funding_grant_id>R01 AG017917</funding_grant_id><pubmed_authors>Cheng F</pubmed_authors><pubmed_authors>Caldwell JZK</pubmed_authors><pubmed_authors>Leverenz JB</pubmed_authors><pubmed_authors>Pieper AA</pubmed_authors><pubmed_authors>Lathia JD</pubmed_authors><pubmed_authors>Hou Y</pubmed_authors><pubmed_authors>Cummings J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microglial immunometabolism endophenotypes contribute to sex difference in Alzheimer's disease.</name><description>&lt;h4>Introduction&lt;/h4>The molecular mechanisms that contribute to sex differences, in particular female predominance, in Alzheimer's disease (AD) prevalence, symptomology, and pathology, are incompletely understood.&lt;h4>Methods&lt;/h4>To address this problem, we investigated cellular metabolism and immune responses ("immunometabolism endophenotype") across AD individuals as a function of sex with diverse clinical diagnosis of cognitive status at death (cogdx), Braak staging, and Consortium to Establish a Registry for AD (CERAD) scores using human cortex metabolomics and transcriptomics data from the Religious Orders Study / Memory and Aging Project (ROSMAP) cohort.&lt;h4>Results&lt;/h4>We identified sex-specific metabolites, immune and metabolic genes, and pathways associated with the AD diagnosis an</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-07-15T13:51:34.393Z</modification><creation>2026-07-05T03:11:27.74Z</creation></dates><accession>S-EPMC10916937</accession><cross_references><pubmed>37985399</pubmed><doi>10.1002/alz.13546</doi></cross_references></HashMap>