PMID- 25388867 OWN - NLM STAT- MEDLINE DCOM- 20150330 LR - 20240117 IS - 1532-429X (Electronic) IS - 1097-6647 (Print) IS - 1097-6647 (Linking) VI - 16 IP - 1 DP - 2014 Nov 12 TI - In vivo cardiovascular magnetic resonance diffusion tensor imaging shows evidence of abnormal myocardial laminar orientations and mobility in hypertrophic cardiomyopathy. PG - 87 LID - 10.1186/s12968-014-0087-8 [doi] LID - 87 AB - BACKGROUND: Cardiac diffusion tensor imaging (cDTI) measures the magnitudes and directions of intramyocardial water diffusion. Assuming the cross-myocyte components to be constrained by the laminar microstructures of myocardium, we hypothesized that cDTI at two cardiac phases might identify any abnormalities of laminar orientation and mobility in hypertrophic cardiomyopathy (HCM). METHODS: We performed cDTI in vivo at 3 Tesla at end-systole and late diastole in 11 healthy controls and 11 patients with HCM, as well as late gadolinium enhancement (LGE) for detection of regional fibrosis. RESULTS: Voxel-wise analysis of diffusion tensors relative to left ventricular coordinates showed expected transmural changes of myocardial helix-angle, with no significant differences between phases or between HCM and control groups. In controls, the angle of the second eigenvector of diffusion (E2A) relative to the local wall tangent plane was larger in systole than diastole, in accord with previously reported changes of laminar orientation. HCM hearts showed higher than normal global E2A in systole (63.9 degrees vs 56.4 degrees controls, p=0.026) and markedly raised E2A in diastole (46.8 degrees vs 24.0 degrees controls, p<0.001). In hypertrophic regions, E2A retained a high, systole-like angulation even in diastole, independent of LGE, while regions of normal wall thickness did not (LGE present 57.8 degrees , p=0.0028, LGE absent 54.8 degrees , p=0.0022 vs normal thickness 38.1 degrees ). CONCLUSIONS: In healthy controls, the angles of cross-myocyte components of diffusion were consistent with previously reported transmural orientations of laminar microstructures and their changes with contraction. In HCM, especially in hypertrophic regions, they were consistent with hypercontraction in systole and failure of relaxation in diastole. Further investigation of this finding is required as previously postulated effects of strain might be a confounding factor. FAU - Ferreira, Pedro F AU - Ferreira PF FAU - Kilner, Philip J AU - Kilner PJ FAU - McGill, Laura-Ann AU - McGill LA FAU - Nielles-Vallespin, Sonia AU - Nielles-Vallespin S FAU - Scott, Andrew D AU - Scott AD FAU - Ho, Siew Y AU - Ho SY FAU - McCarthy, Karen P AU - McCarthy KP FAU - Haba, Margarita M AU - Haba MM FAU - Ismail, Tevfik F AU - Ismail TF FAU - Gatehouse, Peter D AU - Gatehouse PD FAU - de Silva, Ranil AU - de Silva R FAU - Lyon, Alexander R AU - Lyon AR FAU - Prasad, Sanjay K AU - Prasad SK FAU - Firmin, David N AU - Firmin DN AD - National Institute of Health Research Cardiovascular Biomedical Research Unit, Royal Brompton Hospital and Imperial College, London, UK. d.firmin@ic.ac.uk. FAU - Pennell, Dudley J AU - Pennell DJ LA - eng GR - FS/11/67/28954/BHF_/British Heart Foundation/United Kingdom PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141112 PL - England TA - J Cardiovasc Magn Reson JT - Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance JID - 9815616 SB - IM CIN - J Cardiovasc Magn Reson. 2014;16:89. PMID: 25388937 MH - Aged MH - Cardiomyopathy, Hypertrophic/*diagnosis/pathology/physiopathology MH - Case-Control Studies MH - *Diffusion Magnetic Resonance Imaging MH - *Diffusion Tensor Imaging MH - Female MH - Fibrosis MH - Humans MH - Image Interpretation, Computer-Assisted MH - *Magnetic Resonance Imaging, Cine MH - Male MH - Middle Aged MH - *Myocardial Contraction MH - Myocardium/*pathology MH - Predictive Value of Tests MH - *Ventricular Function, Left PMC - PMC4229618 EDAT- 2014/11/13 06:00 MHDA- 2015/03/31 06:00 PMCR- 2014/11/12 CRDT- 2014/11/13 06:00 PHST- 2014/03/03 00:00 [received] PHST- 2014/09/24 00:00 [accepted] PHST- 2014/11/13 06:00 [entrez] PHST- 2014/11/13 06:00 [pubmed] PHST- 2015/03/31 06:00 [medline] PHST- 2014/11/12 00:00 [pmc-release] AID - S1097-6647(23)00154-0 [pii] AID - 87 [pii] AID - 10.1186/s12968-014-0087-8 [doi] PST - epublish SO - J Cardiovasc Magn Reson. 2014 Nov 12;16(1):87. doi: 10.1186/s12968-014-0087-8.