European Heart Journal




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How inflammation heats the heart 

Filippo Crea

doi : 10.1093/eurheartj/ehab089

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 875–878

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Russian Society of Cardiology Activities in 2020 

Ekaterina Uvarova

doi : 10.1093/eurheartj/ehaa1055

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 879–880

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Professor Willibald Maier 

Thomas F Lüscher, Frank Ruschitzka

doi : 10.1093/eurheartj/ehaa1010

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Page 881

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Prof. S. Lale Tokg?zoglu 

doi : 10.1093/eurheartj/ehaa1037

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Page 881

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Re-purposed antiviral drugs without a purpose in COVID-19: a valuable lesson for clinicians 

Giovanna Liuzzo, MD, PhD, FESC, Carlo Patrono, MD, FESC

doi : 10.1093/eurheartj/ehab043

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 882–883

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The year in cardiovascular medicine 2020: acute coronary syndromes and intensive cardiac care 

Borja Ibanez, David Roque, Susanna Price

doi : 10.1093/eurheartj/ehaa1090

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 884–895

Highlights of 2020 publications on acute cardiac care–acute coronary syndromes. The statements in this figure are based on individual published articles and do not represent any kind of recommendation. ACS, acute coronary syndrome; CABG, coronary artery bypass grafting; COVID-19, coronavirus disease 19; DAPT, dual antiplatelet therapy; FFR, fractional flow reserve; I/R, ischaemia–reperfusion; IRA, infarct-related artery; MI, myocardial infarction; MINOCA, myocardial infarction with non-obstructive coronary arteries; MVD, multivessel disease; MVO, microvascular obstruction; NSTE-ACS, non-ST segment elevation acute coronary syndrome; PCI, percutaneous coronary intervention; SARS-CoV2, severe acute respiratory syndrome coronavirus 2; SCAD, spontaneous coronary artery dissection; STEMI, ST-segment elevation myocardial infarction; 4UDMI, fourth universal definition of myocardial infarction. Numbers correspond to the references in the text.

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The neutrophil–lymphocyte ratio and incident atherosclerotic events: analyses from five contemporary randomized trials 

Nicholas H Adamstein, Jean G MacFadyen, Lynda M Rose, Robert J Glynn, Amit K Dey 

doi : 10.1093/eurheartj/ehaa1034

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 896–903

The neutrophil–lymphocyte ratio (NLR) is a readily available inflammatory biomarker that may associate with atherosclerosis and predict cardiovascular (CV) events. The aims of this study are to determine whether the NLR predicts incident major adverse cardiovascular events (MACE) and is modified by anti-inflammatory therapy.

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Immune cell-based cardiovascular risk assessment: spotlight on the neutrophil–lymphocyte ratio 

Hendrik B Sager, Wolfgang Koenig

doi : 10.1093/eurheartj/ehaa1104

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 904–906

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Effect of long-term beta-blocker treatment following myocardial infarction among stable, optimally treated patients without heart failure in the reperfusion era: a Danish, nationwide cohort study 

Anders Holt, Paul Blanche, Bochra Zareini, Deepthi Rajan, Mohammed El-Sheikh

doi : 10.1093/eurheartj/ehaa1058

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 907–914

We aimed to investigate the long-term cardio-protective effect associated with beta-blocker (BB) treatment in stable, optimally treated myocardial infarction (MI) patients without heart failure (HF).

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Learning whether to subtract beta-blockers: it’s about time 

Sean van Diepen, Paul W Armstrong

doi : 10.1093/eurheartj/ehaa1033

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 915–918

Proposed framework for foundational and provisional secondary prevention therapy over time in low-risk post-MI patients. Foundational therapies should be considered in all patients without contraindications, while provisional therapies should be considered in selected patients with comorbidities or post-infarction complications. The horizontal time axis proposes duration of therapies and timeframes for pharmacotherapeutic re-assessment, and should be responsive to the temporal evolution of post-MI risk and events. ADP, adenosine diphosphate receptor inhibitors; ASA, acetylsalicylic acid; CKD, chronic kidney disease; DM, diabetes mellitus; HTN, hypertension; RAAS, renin–angiotensin–aldosterone system; RCT, randomized controlled trials; TG, triglyceride. *Pending guideline recommendations.

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Genome-wide analysis identifies novel susceptibility loci for myocardial infarction 

Jaana A Hartiala, Yi Han, Qiong Jia, James R Hilser, Pin Huang

doi : 10.1093/eurheartj/ehaa1040

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 919–933

While most patients with myocardial infarction (MI) have underlying coronary atherosclerosis, not all patients with coronary artery disease (CAD) develop MI. We sought to address the hypothesis that some of the genetic factors which establish atherosclerosis may be distinct from those that predispose to vulnerable plaques and thrombus formation.

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Unfolding and disentangling coronary vascular disease through genome-wide association studies 

Jeanette Erdmann, Sander W van der Laan

doi : 10.1093/eurheartj/ehaa1089

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 934–937

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Alarmin-activated B cells accelerate murine atherosclerosis after myocardial infarction via plasma cell-immunoglobulin-dependent mechanisms 

Tin Kyaw, Paula Loveland, Peter Kanellakis, Anh Cao, Axel Kallies 

doi : 10.1093/eurheartj/ehaa995

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 938–947

Myocardial infarction (MI) accelerates atherosclerosis and greatly increases the risk of recurrent cardiovascular events for many years, in particular, strokes and MIs. Because B cell-derived autoantibodies produced in response to MI also persist for years, we investigated the role of B cells in adaptive immune responses to MI.

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Does a myocardial infarction boost your (B cell) memory? 

Claudia Monaco, Jennifer Cole

doi : 10.1093/eurheartj/ehaa1059

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 948–950

Establishment of an autoreactive B cell memory after myocardial infarction: a working hypothesis. The demise of cardiac cells leads to the release of cryptoantigens that induce a humoral immune response that leads to accumulation of immunoglobulins in plaques and eventually amplifies atherogenesis at remote sites.

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Women who experience a myocardial infarction at a young age 

Michael Kolbe, Pedro Lopez-Ayala, Christian Mueller

doi : 10.1093/eurheartj/ehab012

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Page 951

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Women experiencing myocardial infarction at a young age have worse outcomes compared with men: only for non-cardiovascular deaths and when treated inadequately? 

Sudipta Chattopadhyay, Joseph John

doi : 10.1093/eurheartj/ehab009

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Pages 952–953

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Progression of artery aneurysm after transcatheter closure of coronary artery fistula 

Xinhui Wang, Chaowu Yan

doi : 10.1093/eurheartj/ehaa1029

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Page 918

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A flare up of idiopathic hypereosinophilic syndrome due to COVID-19 

Vahideh Laleh far, Seyed Reza Najafizadeh, Masoud Eslami, Reza Mollazadeh

doi : 10.1093/eurheartj/ehaa714

European Heart Journal, Volume 42, Issue 9, 1 March 2021, Page 954

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