{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Leistner DM"],"funding":["American Heart Association","Deutsche Stiftung für Herzforschung","National Heart, Lung, and Blood Institute","Berlin Institute of Health","NHLBI NIH HHS","German Centre for Cardiovascular Research","Abbott Vascular"],"pagination":["3549-3560"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7780480"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["41(37)"],"pubmed_abstract":["Aims
Acute coronary syndromes with intact fibrous cap (IFC-ACS), i.e. caused by coronary plaque erosion, account for approximately one-third of ACS. However, the underlying pathophysiological mechanisms as compared with ACS caused by plaque rupture (RFC-ACS) remain largely undefined. The prospective translational OPTICO-ACS study programme investigates for the first time the microenvironment of ACS-causing culprit lesions (CL) with intact fibrous cap by molecular high-resolution intracoronary imaging and simultaneous local immunological phenotyping.Methods and results
The CL of 170 consecutive ACS patients were investigated by optical coherence tomography (OCT) and simultaneous immunophenotyping by flow cytometric analysis as well as by effector molecule concentration measu"],"journal":["European heart journal"],"pubmed_title":["Differential immunological signature at the culprit site distinguishes acute coronary syndrome with intact from acute coronary syndrome with ruptured fibrous cap: results from the prospective translational OPTICO-ACS study."],"pmcid":["PMC7780480"],"funding_grant_id":["1R01HL134892","81Z2100202","R01 HL134892","18CSA34080399"],"pubmed_authors":["Landmesser U","Kia S","Steiner JK","Mueller DN","Flores E","Stahli BE","Riedel M","Rai H","Rauch-Krohnert U","Abdelwahed YS","Krankel N","Leistner DM","Mochmann HC","Volk HD","Sieronski L","Klotsche J","Strassler E","Haghikia A","Meteva D","Lauten A","Frohlich G","Libby P","Dirks F","Joner M","Skurk C","Seppelt C"],"additional_accession":[]},"is_claimable":false,"name":"Differential immunological signature at the culprit site distinguishes acute coronary syndrome with intact from acute coronary syndrome with ruptured fibrous cap: results from the prospective translational OPTICO-ACS study.","description":"Aims
Acute coronary syndromes with intact fibrous cap (IFC-ACS), i.e. caused by coronary plaque erosion, account for approximately one-third of ACS. However, the underlying pathophysiological mechanisms as compared with ACS caused by plaque rupture (RFC-ACS) remain largely undefined. The prospective translational OPTICO-ACS study programme investigates for the first time the microenvironment of ACS-causing culprit lesions (CL) with intact fibrous cap by molecular high-resolution intracoronary imaging and simultaneous local immunological phenotyping.Methods and results
The CL of 170 consecutive ACS patients were investigated by optical coherence tomography (OCT) and simultaneous immunophenotyping by flow cytometric analysis as well as by effector molecule concentration measu","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Oct","modification":"2026-04-07T16:13:48.962Z","creation":"2025-04-06T00:00:57.896Z"},"accession":"S-EPMC7780480","cross_references":{"pubmed":["33080003"],"doi":["10.1093/eurheartj/ehaa703"]}}