<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schindler SE</submitter><funding>NIA NIH HHS</funding><pagination>e571</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8054965</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To evaluate for racial differences in triggering receptor expressed on myeloid cells 2 (TREM2), a key immune mediator in Alzheimer disease, the levels of CSF soluble TREM2 (sTREM2), and the frequency of associated genetic variants were compared in groups of individuals who self-reported their race as African American (AA) or non-Hispanic White (NHW).&lt;h4>Methods&lt;/h4>Community-dwelling older research participants underwent measurement of CSF sTREM2 concentrations and genetic analyses.&lt;h4>Results&lt;/h4>The primary cohort included 91 AAs and 868 NHWs. CSF sTREM2 levels were lower in the AA compared with the NHW group (1,336 ± 470 vs 1,856 ± 624 pg/mL, &lt;i>p&lt;/i> &lt; 0.0001). AAs were more likely to carry &lt;i>TREM2&lt;/i> coding variants (15% vs 3%, &lt;i>p&lt;/i> &lt; 0.0001), which were associ</pubmed_abstract><journal>Neurology. Genetics</journal><pubmed_title>African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic Variants.</pubmed_title><pmcid>PMC8054965</pmcid><funding_grant_id>R01 AG070941</funding_grant_id><funding_grant_id>P30 AG066444</funding_grant_id><funding_grant_id>RF1 AG071706</funding_grant_id><funding_grant_id>R03 AG050921</funding_grant_id><funding_grant_id>U01 AG024904</funding_grant_id><funding_grant_id>P50 AG005681</funding_grant_id><funding_grant_id>P01 AG026276</funding_grant_id><funding_grant_id>K23 AG053426</funding_grant_id><funding_grant_id>T32 AG000213</funding_grant_id><funding_grant_id>P01 AG003991</funding_grant_id><pubmed_authors>Llibre-Guerra JJ</pubmed_authors><pubmed_authors>Farias FHG</pubmed_authors><pubmed_authors>Fagan AM</pubmed_authors><pubmed_authors>Holtzman DM</pubmed_authors><pubmed_authors>Ances BM</pubmed_authors><pubmed_authors>Piccio L</pubmed_authors><pubmed_authors>Morris JC</pubmed_authors><pubmed_authors>Deming Y</pubmed_authors><pubmed_authors>Schindler SE</pubmed_authors><pubmed_authors>Cruchaga C</pubmed_authors><pubmed_authors>Mikesell RJ</pubmed_authors><pubmed_authors>Henson RL</pubmed_authors><pubmed_authors>Wilkins CH</pubmed_authors><pubmed_authors>Xiong C</pubmed_authors><pubmed_authors>Joseph A</pubmed_authors><pubmed_authors>Moulder KL</pubmed_authors><pubmed_authors>Benzinger TLS</pubmed_authors><pubmed_authors>McCue L</pubmed_authors></additional><is_claimable>false</is_claimable><name>African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic Variants.</name><description>&lt;h4>Objective&lt;/h4>To evaluate for racial differences in triggering receptor expressed on myeloid cells 2 (TREM2), a key immune mediator in Alzheimer disease, the levels of CSF soluble TREM2 (sTREM2), and the frequency of associated genetic variants were compared in groups of individuals who self-reported their race as African American (AA) or non-Hispanic White (NHW).&lt;h4>Methods&lt;/h4>Community-dwelling older research participants underwent measurement of CSF sTREM2 concentrations and genetic analyses.&lt;h4>Results&lt;/h4>The primary cohort included 91 AAs and 868 NHWs. CSF sTREM2 levels were lower in the AA compared with the NHW group (1,336 ± 470 vs 1,856 ± 624 pg/mL, &lt;i>p&lt;/i> &lt; 0.0001). AAs were more likely to carry &lt;i>TREM2&lt;/i> coding variants (15% vs 3%, &lt;i>p&lt;/i> &lt; 0.0001), which were associ</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-22T00:37:37.556Z</modification><creation>2022-02-10T09:25:22.836Z</creation></dates><accession>S-EPMC8054965</accession><cross_references><pubmed>33884297</pubmed><doi>10.1212/NXG.0000000000000571</doi></cross_references></HashMap>