<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31(22)</volume><submitter>D'Alessandra Y</submitter><pubmed_abstract>&lt;h4>Aims&lt;/h4>Circulating microRNAs (miRNAs) may represent a novel class of biomarkers; therefore, we examined whether acute myocardial infarction (MI) modulates miRNAs plasma levels in humans and mice.&lt;h4>Methods and results&lt;/h4>Healthy donors (n = 17) and patients (n = 33) with acute ST-segment elevation MI (STEMI) were evaluated. In one cohort (n = 25), the first plasma sample was obtained 517 ± 309 min after the onset of MI symptoms and after coronary reperfusion with percutaneous coronary intervention (PCI); miR-1, -133a, -133b, and -499-5p were ~15- to 140-fold control, whereas miR-122 and -375 were ~87-90% lower than control; 5 days later, miR-1, -133a, -133b, -499-5p, and -375 were back to baseline, whereas miR-122 remained lower than control through Day 30. In additional patients (</pubmed_abstract><journal>European heart journal</journal><pagination>2765-73</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2980809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Circulating microRNAs are new and sensitive biomarkers of myocardial infarction.</pubmed_title><pmcid>PMC2980809</pmcid><pubmed_authors>Achilli F</pubmed_authors><pubmed_authors>Di Carlo A</pubmed_authors><pubmed_authors>Maggiolini S</pubmed_authors><pubmed_authors>Carena MC</pubmed_authors><pubmed_authors>Biglioli P</pubmed_authors><pubmed_authors>Straino S</pubmed_authors><pubmed_authors>Devanna P</pubmed_authors><pubmed_authors>Spazzafumo L</pubmed_authors><pubmed_authors>Micheli B</pubmed_authors><pubmed_authors>Capogrossi MC</pubmed_authors><pubmed_authors>Marenzi G</pubmed_authors><pubmed_authors>D'Alessandra Y</pubmed_authors><pubmed_authors>Rubino M</pubmed_authors><pubmed_authors>Limana F</pubmed_authors><pubmed_authors>Martelli F</pubmed_authors><pubmed_authors>Pompilio G</pubmed_authors><pubmed_authors>De Simone M</pubmed_authors><pubmed_authors>Brambilla PG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circulating microRNAs are new and sensitive biomarkers of myocardial infarction.</name><description>&lt;h4>Aims&lt;/h4>Circulating microRNAs (miRNAs) may represent a novel class of biomarkers; therefore, we examined whether acute myocardial infarction (MI) modulates miRNAs plasma levels in humans and mice.&lt;h4>Methods and results&lt;/h4>Healthy donors (n = 17) and patients (n = 33) with acute ST-segment elevation MI (STEMI) were evaluated. In one cohort (n = 25), the first plasma sample was obtained 517 ± 309 min after the onset of MI symptoms and after coronary reperfusion with percutaneous coronary intervention (PCI); miR-1, -133a, -133b, and -499-5p were ~15- to 140-fold control, whereas miR-122 and -375 were ~87-90% lower than control; 5 days later, miR-1, -133a, -133b, -499-5p, and -375 were back to baseline, whereas miR-122 remained lower than control through Day 30. In additional patients (</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Nov</publication><modification>2026-07-15T10:07:21.654Z</modification><creation>2026-07-03T03:12:02.358Z</creation></dates><accession>S-EPMC2980809</accession><cross_references><pubmed>20534597</pubmed><doi>10.1093/eurheartj/ehq167</doi></cross_references></HashMap>