| Literature DB >> 30043238 |
Sophie I Mavrogeni1, Petros P Sfikakis2, Theodoros Dimitroulas3, Loukia Koutsogeorgopoulou4, George Markousis-Mavrogenis5, George Poulos5, Genovefa Kolovou5, George Theodorakis5, George D Kitas6.
Abstract
Sudden cardiac death (SCD) is due to ventricular tachycardia/fibrillation (VT/VF) and may occur with or without any structural or functional heart disease. The presence of myocardial edema, ischemia and/or fibrosis plays a crucial role in the pathogenesis of VT/VF, irrespective of the pathophysiologic background of the disease. Specifically, in autoimmune rheumatic diseases (ARDs), various entities such as myocardial/vascular inflammation, ischemia and fibrosis may lead to VT/VF. Furthermore, autonomic dysfunction, commonly found in ARDs, may also contribute to SCD in these patients. The only non-invasive, radiation-free imaging modality that can perform functional assessment and tissue characterization is cardiovascular magnetic resonance (CMR). Due to its capability to detect and quantify edema, ischemia and fibrosis in parallel with ventricular function assessment, CMR has the great potential to identify ARD patients at high risk for VT/VF, thus influencing both cardiac and anti-rheumatic treatment and modifying perhaps the criteria for implantation of cardioverter defibrillators.Entities:
Keywords: Autoimmune diseases; Cardiovascular magnetic resonance; Edema; Fibrosis; Myocardial infarction; Myocarditis; Vasculitis; Ventricular fibrillation; Ventricular tachycardia
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Year: 2018 PMID: 30043238 DOI: 10.1007/s00296-018-4110-5
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631