PMID- 27005015 OWN - NLM STAT- MEDLINE DCOM- 20170310 LR - 20220318 IS - 1365-229X (Electronic) IS - 0009-9260 (Linking) VI - 71 IP - 8 DP - 2016 Aug TI - Assessment of myocardial fibrosis with T1 mapping MRI. PG - 768-78 LID - S0009-9260(16)00089-1 [pii] LID - 10.1016/j.crad.2016.02.013 [doi] AB - Myocardial fibrosis can arise from a range of pathological processes and its presence correlates with adverse clinical outcomes. Cardiac magnetic resonance (CMR) can provide a non-invasive assessment of cardiac structure, function, and tissue characteristics, which includes late gadolinium enhancement (LGE) techniques to identify focal irreversible replacement fibrosis with a high degree of accuracy and reproducibility. Importantly the presence of LGE is consistently associated with adverse outcomes in a range of common cardiac conditions; however, LGE techniques are qualitative and unable to detect diffuse myocardial fibrosis, which is an earlier form of fibrosis preceding replacement fibrosis that may be reversible. Novel T1 mapping techniques allow quantitative CMR assessment of diffuse myocardial fibrosis with the two most common measures being native T1 and extracellular volume (ECV) fraction. Native T1 differentiates normal from infarcted myocardium, is abnormal in hypertrophic cardiomyopathy, and may be particularly useful in the diagnosis of Anderson-Fabry disease and amyloidosis. ECV is a surrogate measure of the extracellular space and is equivalent to the myocardial volume of distribution of the gadolinium-based contrast medium. It is reproducible and correlates well with fibrosis on histology. ECV is abnormal in patients with cardiac failure and aortic stenosis, and is associated with functional impairment in these groups. T1 mapping techniques promise to allow earlier detection of disease, monitor disease progression, and inform prognosis; however, limitations remain. In particular, reference ranges are lacking for T1 mapping values as these are influenced by specific CMR techniques and magnetic field strength. In addition, there is significant overlap between T1 mapping values in healthy controls and most disease states, particularly using native T1, limiting the clinical application of these techniques at present. CI - Copyright (c) 2016 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved. FAU - Everett, R J AU - Everett RJ AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK. Electronic address: Russell.everett@ed.ac.uk. FAU - Stirrat, C G AU - Stirrat CG AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK. FAU - Semple, S I R AU - Semple SI AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK; Clinical Research Imaging Centre, University of Edinburgh, UK. FAU - Newby, D E AU - Newby DE AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK; Clinical Research Imaging Centre, University of Edinburgh, UK. FAU - Dweck, M R AU - Dweck MR AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK. FAU - Mirsadraee, S AU - Mirsadraee S AD - British Heart Foundation/University Centre for Cardiovascular Science, University of Edinburgh, UK; Clinical Research Imaging Centre, University of Edinburgh, UK. LA - eng GR - FS/14/78/31020/BHF_/British Heart Foundation/United Kingdom GR - G0701127/MRC_/Medical Research Council/United Kingdom PT - Journal Article PT - Review DEP - 20160319 PL - England TA - Clin Radiol JT - Clinical radiology JID - 1306016 SB - IM CIN - Clin Radiol. 2016 Dec;71(12 ):1309-1310. PMID: 27733276 MH - Cardiomyopathies/*diagnostic imaging/*pathology MH - Fibrosis MH - Heart/*diagnostic imaging MH - Image Enhancement/*methods MH - Magnetic Resonance Imaging/*methods MH - Myocardium/*pathology EDAT- 2016/03/24 06:00 MHDA- 2017/03/11 06:00 CRDT- 2016/03/24 06:00 PHST- 2015/11/10 00:00 [received] PHST- 2016/01/15 00:00 [revised] PHST- 2016/02/09 00:00 [accepted] PHST- 2016/03/24 06:00 [entrez] PHST- 2016/03/24 06:00 [pubmed] PHST- 2017/03/11 06:00 [medline] AID - S0009-9260(16)00089-1 [pii] AID - 10.1016/j.crad.2016.02.013 [doi] PST - ppublish SO - Clin Radiol. 2016 Aug;71(8):768-78. doi: 10.1016/j.crad.2016.02.013. Epub 2016 Mar 19.