Université de Lyon, CREATIS ; CNRS UMR5220 ; Inserm U1206 ; INSA-Lyon ; Université Lyon 1, Lyon, France.
Med Image Anal. 2017 May;38:117-132. doi: 10.1016/j.media.2017.02.006. Epub 2017 Feb 20.
This paper presents a methodology to access the 3D local myocyte arrangements in fresh human post-mortem heart samples. We investigated the cardiac micro-structure at a high and isotropic resolution of 3.5 µm in three dimensions using X-ray phase micro-tomography at the European Synchrotron Radiation Facility. We then processed the reconstructed volumes to extract the 3D local orientation of the myocytes using a multi-scale approach with no segmentation. We created a simplified 3D model of tissue sample made of simulated myocytes with known size and orientations, to evaluate our orientation extraction method. Afterwards, we applied it to 2D histological cuts and to eight 3D left ventricular (LV) cardiac tissue samples. Then, the variation of the helix angles, from the endocardium to the epicardium, was computed at several spatial resolutions ranging from 3.6 mm to 112 µm. We measure an increased range of 20° to 30° from the coarsest resolution level to the finest level in the experimental samples. This result is in line with the higher values measured from histology. The displayed tractography demonstrates a rather smooth evolution of the transmural helix angle in six LV samples and a sudden discontinuity of the helix angle in two septum samples. These measurements bring a new vision of the human heart architecture from macro- to micro-scale.
本文提出了一种方法,用于获取新鲜人体死后心脏样本中的 3D 局部心肌排列。我们使用欧洲同步辐射设施的 X 射线相衬微断层摄影术以 3.5 µm 的高各向同性分辨率研究了心脏微结构。然后,我们使用无分割的多尺度方法处理重构体积,以提取心肌的 3D 局部取向。我们创建了一个由具有已知大小和取向的模拟心肌组成的组织样本的简化 3D 模型,以评估我们的取向提取方法。然后,我们将其应用于 2D 组织学切片和 8 个 3D 左心室 (LV) 心脏组织样本。然后,在从 3.6mm 到 112µm 的几个空间分辨率下,计算了从心内膜到心外膜的螺旋角的变化。我们在实验样本中从最粗的分辨率级别到最细的分辨率级别测量到增加了 20°到 30°的范围。这一结果与组织学测量到的较高值相符。显示的轨迹描绘表明,在六个 LV 样本中,跨壁螺旋角的演变相当平滑,而在两个隔样本中,螺旋角突然中断。这些测量从宏观到微观尺度为人类心脏结构提供了新的视角。