<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Enkhmaa B</submitter><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>Women’s Health Program Award</funding><funding>National Institutes of Health</funding><funding>UC Davis Clinical and Translational Center</funding><pagination>bvaa073</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7358566</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(7)</volume><pubmed_abstract>&lt;h4>Context&lt;/h4>Inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) reduces lipoprotein(a) [Lp(a)] levels, but the association of PCSK9 with Lp(a) level and its major determinant, apolipoprotein(a) [apo(a)] size, is not fully understood.&lt;h4>Objective&lt;/h4>To assess the relationship between PCSK9, Lp(a) level, apo(a) size, age, and ethnicity/race.&lt;h4>Design&lt;/h4>Cross-sectional.&lt;h4>Setting&lt;/h4>General population.&lt;h4>Participants&lt;/h4>Healthy African Americans and Caucasians (n = 267); age range: 6 to 74 years.&lt;h4>Interventions&lt;/h4>None.&lt;h4>Main outcome measures&lt;/h4>PCSK9 levels, apo(a) isoform and &lt;i>LPA&lt;/i> allele sizes, and isoform-specific Lp(a) levels.&lt;h4>Results&lt;/h4>Plasma PCSK9 levels were significantly higher in African Americans vs Caucasians, in females vs males, and i</pubmed_abstract><journal>Journal of the Endocrine Society</journal><pubmed_title>PCSK9 in African Americans and Caucasians in Relation to Lp(a) Level, Apo(a) Size and Heritability.</pubmed_title><pmcid>PMC7358566</pmcid><funding_grant_id>#TR001860</funding_grant_id><funding_grant_id>R01#HL62705</funding_grant_id><funding_grant_id>UL1 TR001860</funding_grant_id><funding_grant_id>R01 HL062705</funding_grant_id><funding_grant_id>K12 HD051958</funding_grant_id><funding_grant_id>#NIH 2K12HD051958</funding_grant_id><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Prakash N</pubmed_authors><pubmed_authors>Berglund L</pubmed_authors><pubmed_authors>Kim K</pubmed_authors><pubmed_authors>Anuurad E</pubmed_authors><pubmed_authors>Enkhmaa B</pubmed_authors><pubmed_authors>Truax K</pubmed_authors></additional><is_claimable>false</is_claimable><name>PCSK9 in African Americans and Caucasians in Relation to Lp(a) Level, Apo(a) Size and Heritability.</name><description>&lt;h4>Context&lt;/h4>Inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) reduces lipoprotein(a) [Lp(a)] levels, but the association of PCSK9 with Lp(a) level and its major determinant, apolipoprotein(a) [apo(a)] size, is not fully understood.&lt;h4>Objective&lt;/h4>To assess the relationship between PCSK9, Lp(a) level, apo(a) size, age, and ethnicity/race.&lt;h4>Design&lt;/h4>Cross-sectional.&lt;h4>Setting&lt;/h4>General population.&lt;h4>Participants&lt;/h4>Healthy African Americans and Caucasians (n = 267); age range: 6 to 74 years.&lt;h4>Interventions&lt;/h4>None.&lt;h4>Main outcome measures&lt;/h4>PCSK9 levels, apo(a) isoform and &lt;i>LPA&lt;/i> allele sizes, and isoform-specific Lp(a) levels.&lt;h4>Results&lt;/h4>Plasma PCSK9 levels were significantly higher in African Americans vs Caucasians, in females vs males, and i</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-04T23:46:35.988Z</modification><creation>2025-04-04T23:46:35.988Z</creation></dates><accession>S-EPMC7358566</accession><cross_references><pubmed>32685870</pubmed><doi>10.1210/jendso/bvaa073</doi></cross_references></HashMap>