Beg Mirza Faisal, Helm Patrick A, McVeigh Elliot, Miller Michael I, Winslow Raimond L
Center for Imaging Science, The Whitaker Biomedical Engineering Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Magn Reson Med. 2004 Nov;52(5):1167-74. doi: 10.1002/mrm.20255.
Ventricular geometry and fiber orientation may undergo global or local remodeling in cardiac disease. However, there are as yet no mathematical and computational methods for quantifying variation of geometry and fiber orientation or the nature of their remodeling in disease. Toward this goal, a landmark and image intensity-based large deformation diffeomorphic metric mapping (LDDMM) method to transform heart geometry into common coordinates for quantification of shape and form was developed. Two automated landmark placement methods for modeling tissue deformations expected in different cardiac pathologies are presented. The transformations, computed using the combined use of landmarks and image intensities, yields high-registration accuracy of heart anatomies even in the presence of significant variation of cardiac shape and form. Once heart anatomies have been registered, properties of tissue geometry and cardiac fiber orientation in corresponding regions of different hearts may be quantified.
在心脏疾病中,心室几何形状和纤维方向可能会发生整体或局部重塑。然而,目前尚无数学和计算方法来量化几何形状和纤维方向的变化或疾病中其重塑的性质。为了实现这一目标,开发了一种基于地标和图像强度的大变形微分同胚度量映射(LDDMM)方法,用于将心脏几何形状转换为通用坐标,以量化形状和形态。提出了两种自动地标放置方法,用于模拟不同心脏病理情况下预期的组织变形。使用地标和图像强度的组合计算的变换,即使在心脏形状和形态存在显著变化的情况下,也能产生心脏解剖结构的高配准精度。一旦心脏解剖结构配准完成,就可以量化不同心脏相应区域的组织几何形状和心脏纤维方向的属性。