Department of Computer Science and Engineering, NYU Tandon School of Engineering, NY, USA.
Department of Computer Science and Engineering, NYU Tandon School of Engineering, NY, USA.
Med Image Anal. 2019 Aug;56:96-109. doi: 10.1016/j.media.2019.05.009. Epub 2019 May 31.
Autofluorescence is the emission of light by naturally occurring tissue components on the absorption of incident light. Autofluorescence within the eye is associated with several disorders, such as Age-related Macular Degeneration (AMD) which is a leading cause of central vision loss. Its pathogenesis is incompletely understood, but endogenous fluorophores in retinal tissue might play a role. Hyperspectral fluorescence microscopy of ex-vivo retinal tissue can be used to determine the fluorescence emission spectra of these fluorophores. Comparisons of spectra in healthy and diseased tissues can provide important insights into the pathogenesis of AMD. However, the spectrum from each pixel of the hyperspectral image is a superposition of spectra from multiple overlapping tissue components. As spectra cannot be negative, there is a need for a non-negative blind source separation model to isolate individual spectra. We propose a tensor formulation by leveraging multiple excitation wavelengths to excite the tissue sample. Arranging images from different excitation wavelengths as a tensor, a non-negative tensor decomposition can be performed to recover a provably unique low-rank model with factors representing emission and excitation spectra of these materials and corresponding abundance maps of autofluorescent substances in the tissue sample. We iteratively impute missing values common in fluorescence measurements using Expectation-Maximization and use L regularization to reduce ill-posedness. Further, we present a framework for performing group hypothesis testing on hyperspectral images, finding significant differences in spectra between AMD and control groups in the peripheral macula. In the absence of ground truth, i.e. molecular identification of fluorophores, we provide a rigorous validation of chosen methods on both synthetic and real images where fluorescence spectra are known. These methodologies can be applied to the study of other pathologies presenting autofluorescence that can be captured by hyperspectral imaging.
自发荧光是指在吸收入射光时,自然存在的组织成分发出的光。眼睛内的自发荧光与几种疾病有关,例如年龄相关性黄斑变性(AMD),这是导致中心视力丧失的主要原因。其发病机制尚未完全了解,但视网膜组织中的内源性荧光团可能起作用。离体视网膜组织的高光谱荧光显微镜可用于确定这些荧光团的荧光发射光谱。比较健康和患病组织的光谱可以为 AMD 的发病机制提供重要的见解。然而,高光谱图像中每个像素的光谱是来自多个重叠组织成分的光谱的叠加。由于光谱不能为负,因此需要使用非负盲源分离模型来分离单个光谱。我们通过利用多个激发波长来激发组织样本提出了张量公式。将来自不同激发波长的图像排列为张量,可以执行非负张量分解,以恢复具有唯一低秩模型的证明,该模型的因子代表这些材料的发射和激发光谱以及组织样本中自发荧光物质的相应丰度图。我们使用期望最大化迭代地估算荧光测量中常见的缺失值,并使用 L 正则化来减少不适定性。此外,我们提出了一种在高光谱图像上进行组假设检验的框架,在周边黄斑中发现 AMD 和对照组之间的光谱存在显着差异。在没有荧光团的分子识别的情况下,我们在荧光光谱已知的合成和真实图像上对选定方法进行了严格的验证。这些方法可以应用于呈现自发荧光的其他病理学的研究,可以通过高光谱成像来捕获。