3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Development of a cardiovascular magnetic resonance‐compatible large animal isolated heart model for direct comparison of beating and arrested hearts

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cardiac motion results in image artefacts and quantification errors in many cardiovascular magnetic resonance (CMR) techniques, including microstructural assessment using diffusion tensor cardiovascular magnetic resonance (DT‐CMR). Here, we develop a CMR‐compatible isolated perfused porcine heart model that allows comparison of data obtained in beating and arrested states. Ten porcine hearts (8/10 for protocol optimisation) were harvested using a donor heart retrieval protocol and transported to the remote CMR facility. Langendorff perfusion in a 3D‐printed chamber and perfusion circuit re‐established contraction. Hearts were imaged using cine, parametric mapping and STEAM DT‐CMR at cardiac phases with the minimum and maximum wall thickness. High potassium and lithium perfusates were then used to arrest the heart in a slack and contracted state, respectively. Imaging was repeated in both arrested states. After imaging, tissue was removed for subsequent histology in a location matched to the DT‐CMR data using fiducial markers. Regular sustained contraction was successfully established in six out of 10 hearts, including the final five hearts. Imaging was performed in four hearts and one underwent the full protocol, including colocalised histology. The image quality was good and there was good agreement between DT‐CMR data in equivalent beating and arrested states. Despite the use of autologous blood and dextran within the perfusate, T2 mapping results, DT‐CMR measures and an increase in mass were consistent with development of myocardial oedema, resulting in failure to achieve a true diastolic‐like state. A contiguous stack of 313 5‐μm histological sections at and a 100‐μm thick section showing cell morphology on 3D fluorescent confocal microscopy colocalised to DT‐CMR data were obtained. A CMR‐compatible isolated perfused beating heart setup for large animal hearts allows direct comparisons of beating and arrested heart data with subsequent colocalised histology, without the need for onsite preclinical facilities.

          Abstract

          A cardiovascular magnetic resonance (CMR)‐compatible isolated perfused beating porcine heart model was developed that allows direct comparison of data acquired in multiple states of contraction between the beating and arrested heart. We describe the development of this model, its successes and failures, including the presence of oedema in the hearts. In this study, microstructural measures were obtained from the porcine hearts using diffusion tensor CMR in the most and least contracted states with subsequent colocalised histology.

          Related collections

          Most cited references50

          • Record: found
          • Abstract: found
          • Article: not found

          Imaging three-dimensional myocardial mechanics using navigator-gated volumetric spiral cine DENSE MRI.

          A navigator-gated 3D spiral cine displacement encoding with stimulated echoes (DENSE) pulse sequence for imaging 3D myocardial mechanics was developed. In addition, previously described 2D postprocessing algorithms including phase unwrapping, tissue tracking, and strain tensor calculation for the left ventricle (LV) were extended to 3D. These 3D methods were evaluated in five healthy volunteers, using 2D cine DENSE and historical 3D myocardial tagging as reference standards. With an average scan time of 20.5 ± 5.7 min, 3D data sets with a matrix size of 128 × 128 × 22, voxel size of 2.8 × 2.8 × 5.0 mm(3), and temporal resolution of 32 msec were obtained with displacement encoding in three orthogonal directions. Mean values for end-systolic mid-ventricular mid-wall radial, circumferential, and longitudinal strain were 0.33 ± 0.10, -0.17 ± 0.02, and -0.16 ± 0.02, respectively. Transmural strain gradients were detected in the radial and circumferential directions, reflecting high spatial resolution. Good agreement by linear correlation and Bland-Altman analysis was achieved when comparing normal strains measured by 2D and 3D cine DENSE. Also, the 3D strains, twist, and torsion results obtained by 3D cine DENSE were in good agreement with historical values measured by 3D myocardial tagging.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            In vivo cardiovascular magnetic resonance diffusion tensor imaging shows evidence of abnormal myocardial laminar orientations and mobility in hypertrophic cardiomyopathy

            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° vs 56.4° controls, p = 0.026) and markedly raised E2A in diastole (46.8° vs 24.0° 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°, p = 0.0028, LGE absent 54.8°, p = 0.0022 vs normal thickness 38.1°). 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. Electronic supplementary material The online version of this article (doi:10.1186/s12968-014-0087-8) contains supplementary material, which is available to authorized users.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Assessment of Myocardial Microstructural Dynamics by In Vivo Diffusion Tensor Cardiac Magnetic Resonance

              BACKGROUND Cardiomyocytes are organized in microstructures termed sheetlets that reorientate during left ventricular thickening. Diffusion tensor cardiac magnetic resonance (DT-CMR) may enable noninvasive interrogation of in vivo cardiac microstructural dynamics. Dilated cardiomyopathy (DCM) is a condition of abnormal myocardium with unknown sheetlet function. OBJECTIVES This study sought to validate in vivo DT-CMR measures of cardiac microstructure against histology, characterize microstructural dynamics during left ventricular wall thickening, and apply the technique in hypertrophic cardiomyopathy (HCM) and DCM. METHODS In vivo DT-CMR was acquired throughout the cardiac cycle in healthy swine, followed by in situ and ex vivo DT-CMR, then validated against histology. In vivo DT-CMR was performed in 19 control subjects, 19 DCM, and 13 HCM patients. RESULTS In swine, a DT-CMR index of sheetlet reorientation (E2A) changed substantially (E2A mobility ~46°). E2A changes correlated with wall thickness changes (in vivo r 2 = 0.75; in situ r 2 = 0.89), were consistently observed under all experimental conditions, and accorded closely with histological analyses in both relaxed and contracted states. The potential contribution of cyclical strain effects to in vivo E2A was ~17%. In healthy human control subjects, E2A increased from diastole (18°) to systole (65°; p < 0.001; E2A mobility = 45°). HCM patients showed significantly greater E2A in diastole than control subjects did (48 ; p < 0.001) with impaired E2A mobility (23°; p < 0.001). In DCM, E2A was similar to control subjects in diastole, but systolic values were markedly lower (40° ; p < 0.001) with impaired E2A mobility (20°; p < 0.001). CONCLUSIONS Myocardial microstructure dynamics can be characterized by in vivo DT-CMR. Sheetlet function was abnormal in DCM with altered systolic conformation and reduced mobility, contrasting with HCM, which showed reduced mobility with altered diastolic conformation. These novel insights significantly improve understanding of contractile dysfunction at a level of noninvasive interrogation not previously available in humans. (J Am Coll Cardiol 2017;69:661–76) Published by Elsevier on behalf of the American College of Cardiology Foundation.
                Bookmark

                Author and article information

                Contributors
                r.desilva@imperial.ac.uk
                Journal
                NMR Biomed
                NMR Biomed
                10.1002/(ISSN)1099-1492
                NBM
                Nmr in Biomedicine
                John Wiley and Sons Inc. (Hoboken )
                0952-3480
                1099-1492
                12 February 2022
                July 2022
                : 35
                : 7 ( doiID: 10.1002/nbm.v35.7 )
                : e4692
                Affiliations
                [ 1 ] Cardiovascular Magnetic Resonance Unit Royal Brompton Hospital London UK
                [ 2 ] National Heart and Lung Institute Imperial College London UK
                [ 3 ] Department of Perfusion Royal Brompton Hospital London UK
                [ 4 ] Translational Biomedical Research Centre University of Bristol Bristol UK
                [ 5 ] Bristol Heart Institute University Hospital Bristol NHS Foundation Trust Bristol UK
                [ 6 ] Imperial Centre for Cardiac Engineering Imperial College London UK
                [ 7 ] Cardiac Morphology Unit Royal Brompton Hospital London UK
                [ 8 ] Magdi Yacoub Institute, National Heart and Lung Institute Imperial College London UK
                [ 9 ] Department of Aeronautics Imperial College London UK
                Author notes
                [*] [* ] Correspondence

                Ranil de Silva, Cardiovascular Magnetic Resonance Unit, Royal Brompton Hospital, Sydney Street, London, UK.

                Email: r.desilva@ 123456imperial.ac.uk .

                Author information
                https://orcid.org/0000-0001-7656-3123
                https://orcid.org/0000-0002-0977-4796
                https://orcid.org/0000-0002-8193-9559
                https://orcid.org/0000-0003-4204-1014
                https://orcid.org/0000-0002-0436-3496
                https://orcid.org/0000-0002-2273-7439
                https://orcid.org/0000-0001-5523-1314
                https://orcid.org/0000-0001-8045-5619
                Article
                NBM4692
                10.1002/nbm.4692
                9286060
                35040195
                19e693e2-671a-41e3-9b57-f41e4684e348
                © 2022 The Authors. NMR in Biomedicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 December 2021
                : 21 July 2021
                : 07 January 2022
                Page count
                Figures: 11, Tables: 0, Pages: 15, Words: 10201
                Funding
                Funded by: British Heart Foundation (BHF) , doi 10.13039/501100000274;
                Award ID: RG/19/1/34160
                Award ID: RE/13/4/30184
                Award ID: PG/14/68/30798
                Award ID: IG/14/2/30991
                Award ID: PG/16/104/32652
                Award ID: PG/16/17/32069
                Funded by: Institute of Physics and Engineering in Medicine Research
                Funded by: Medical Research Council , doi 10.13039/501100000265;
                Award ID: MR/L012723/1
                Funded by: Bristol National Institute for Health Research Biomedical Research Centre , doi 10.13039/100015250;
                Funded by: Rosetrees Trust , doi 10.13039/501100000833;
                Award ID: JS15/M645
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                July 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:15.07.2022

                Radiology & Imaging
                cardiovascular magnetic resonance,diffusion tensor imaging,langendorff perfusion,microstructure,myocardial tissue characterization,oedema,preclinical

                Comments

                Comment on this article