<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(4)</volume><submitter>Tardif JC</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Dalcetrapib effects on cardiovascular outcomes are determined by adenylate cyclase 9 gene polymorphisms. Our aim was to determine whether these clinical end point results are also associated with changes in reverse cholesterol transport and inflammation.&lt;h4>Methods and results&lt;/h4>Participants of the dal-OUTCOMES and dal-PLAQUE-2 trials were randomly assigned to receive dalcetrapib or placebo in addition to standard care. High-sensitivity C-reactive protein was measured at baseline and at end of study in 5243 patients from dal-OUTCOMES also genotyped for the rs1967309 polymorphism in adenylate cyclase 9. Cholesterol efflux capacity of high-density lipoproteins from J774 macrophages after cAMP stimulation was determined at baseline and 12 months in 171 genotyped patients </pubmed_abstract><journal>Circulation. Cardiovascular genetics</journal><pagination>340-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4982759</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes.</pubmed_title><pmcid>PMC4982759</pmcid><pubmed_authors>Feroz Zada Y</pubmed_authors><pubmed_authors>Brodeur M</pubmed_authors><pubmed_authors>Rheaume E</pubmed_authors><pubmed_authors>Boule M</pubmed_authors><pubmed_authors>Fouodjio R</pubmed_authors><pubmed_authors>L'Allier PL</pubmed_authors><pubmed_authors>Alem S</pubmed_authors><pubmed_authors>Dube MP</pubmed_authors><pubmed_authors>Rhainds D</pubmed_authors><pubmed_authors>Gregoire JC</pubmed_authors><pubmed_authors>Mongrain I</pubmed_authors><pubmed_authors>Schwartz GG</pubmed_authors><pubmed_authors>Provost S</pubmed_authors><pubmed_authors>Guertin MC</pubmed_authors><pubmed_authors>Ibrahim R</pubmed_authors><pubmed_authors>Tardif JC</pubmed_authors><pubmed_authors>Olsson AG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes.</name><description>&lt;h4>Background&lt;/h4>Dalcetrapib effects on cardiovascular outcomes are determined by adenylate cyclase 9 gene polymorphisms. Our aim was to determine whether these clinical end point results are also associated with changes in reverse cholesterol transport and inflammation.&lt;h4>Methods and results&lt;/h4>Participants of the dal-OUTCOMES and dal-PLAQUE-2 trials were randomly assigned to receive dalcetrapib or placebo in addition to standard care. High-sensitivity C-reactive protein was measured at baseline and at end of study in 5243 patients from dal-OUTCOMES also genotyped for the rs1967309 polymorphism in adenylate cyclase 9. Cholesterol efflux capacity of high-density lipoproteins from J774 macrophages after cAMP stimulation was determined at baseline and 12 months in 171 genotyped patients </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Aug</publication><modification>2026-06-16T04:56:25.918Z</modification><creation>2019-03-27T02:20:31Z</creation></dates><accession>S-EPMC4982759</accession><cross_references><pubmed>27418594</pubmed><doi>10.1161/CIRCGENETICS.116.001405</doi></cross_references></HashMap>