Caruyer Emmanuel, Verma Ragini
Section of Biomedical Image Analysis, Department of Radiology, University of Pennsylvania, 3600 Market Street, Suite 380, Philadelphia, PA 19104, United States.
Section of Biomedical Image Analysis, Department of Radiology, University of Pennsylvania, 3600 Market Street, Suite 380, Philadelphia, PA 19104, United States.
Med Image Anal. 2015 Feb;20(1):87-96. doi: 10.1016/j.media.2014.10.009. Epub 2014 Nov 8.
We design and evaluate a novel method to compute rotationally invariant features using High Angular Resolution Diffusion Imaging (HARDI) data. These measures quantify the complexity of the angular diffusion profile modeled using a higher order model, thereby giving more information than classical diffusion tensor-derived parameters. The method is based on the spherical harmonic (SH) representation of the angular diffusion information, and is generalizable to a range of HARDI reconstruction models. These scalars are obtained as homogeneous polynomials of the SH representation of a HARDI reconstruction model. We show that finding such polynomials is equivalent to solving a large linear system of equations, and present a numerical method based on sparse matrices to efficiently solve this system. Among the solutions, we only keep a subset of algebraically independent polynomials, using an algorithm based on a numerical implementation of the Jacobian criterion. We compute a set of 12 or 25 rotationally invariant measures representative of the underlying white matter for the rank-4 or rank-6 spherical harmonics (SHs) representation of the apparent diffusion coefficient (ADC) profile, respectively. Synthetic data was used to investigate and quantify the difference in contrast. Real data acquired with multiple repetitions showed that within subject variation in the invariants was less than the difference across subjects - facilitating their use to study population differences. These results demonstrate that our measures are able to characterize white matter, especially complex white matter found in regions of fiber crossings and hence can be used to derive new biomarkers for HARDI and can be used for HARDI-based population analysis.
我们设计并评估了一种利用高角分辨率扩散成像(HARDI)数据计算旋转不变特征的新方法。这些测量方法量化了使用高阶模型建模的角扩散剖面的复杂性,从而比传统的扩散张量衍生参数提供更多信息。该方法基于角扩散信息的球谐(SH)表示,并且可以推广到一系列HARDI重建模型。这些标量是作为HARDI重建模型的SH表示的齐次多项式获得的。我们表明,找到这样的多项式等同于求解一个大型线性方程组,并提出了一种基于稀疏矩阵的数值方法来有效地求解该系统。在这些解中,我们仅保留代数独立多项式的一个子集,使用基于雅可比准则数值实现的算法。我们分别针对表观扩散系数(ADC)剖面的四阶或六阶球谐(SH)表示计算了一组12个或25个代表潜在白质的旋转不变测量值。使用合成数据来研究和量化对比度差异。多次重复采集的真实数据表明,受试者内部不变量的变化小于受试者之间的差异——这便于使用它们来研究群体差异。这些结果表明,我们的测量方法能够表征白质,特别是在纤维交叉区域发现的复杂白质,因此可用于为HARDI推导新的生物标志物,并可用于基于HARDI的群体分析。