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Nonlinear dimensionality reduction combining MR imaging with non-imaging information

机译:结合MR成像和非成像信息的非线性降维

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We propose a framework for the extraction of biomarkers from low-dimensional manifolds representing inter-subject brain variation. Manifold coordinates of each image capture information about structural shape and appearance and, when a phenotype exists, about the subject's clinical state. Our framework incorporates subject meta-information into the manifold learning step. Apart from gender and age, information such as genotype or a derived biomarker is often available in clinical studies and can inform the classification of a query subject. Such information, whether discrete or continuous, is used as an additional input to manifold learning, extending the Laplacian Eigenmap objective function and enriching a similarity measure derived from pairwise image similarities. The biomarkers identified with the proposed method are data-driven in contrast to a priori defined biomarkers derived from, e.g., manual or automated segmentations. They form a unified representation of both the imaging and non-imaging measurements, providing a natural use for data analysis and visualization. We test the method to classify subjects with Alzheimer's Disease (AD), mild cognitive impairment (MCI) and healthy controls enrolled in the ADNI study. Non-imaging metadata used are ApoE genotype, a risk factor associated with AD, and the CSF-concentration of Aβ 1-42, an established biomarker for AD. In addition, we use hippocampal volume as a derived imaging-biomarker to enrich the learned manifold. Our classification results compare favorably to what has been reported in a recent meta-analysis using established neuroimaging methods on the same database.
机译:我们提出了一个框架,用于从代表受试者间脑部变异的低维流形提取生物标志物。每个图像的流形坐标捕获有关结构形状和外观的信息,以及当存在表型时有关受试者的临床状态的信息。我们的框架将主题元信息纳入了多种学习步骤。除性别和年龄外,临床研究中经常可以获取诸如基因型或衍生生物标记之类的信息,这些信息可以为查询对象的分类提供信息。这种信息,无论是离散的还是连续的,都用作流形学习的附加输入,扩展了Laplacian特征图的目标函数并丰富了从成对图像相似性得出的相似性度量。与源自例如手动或自动分割的先验定义的生物标记相反,用所提出的方法鉴定的生物标记是数据驱动的。它们形成了成像和非成像测量的统一表示,自然地用于数据分析和可视化。我们测试了该方法以对参加ADNI研究的阿尔茨海默氏病(AD),轻度认知障碍(MCI)和健康对照的受试者进行分类。使用的非成像元数据是ApoE基因型,与AD相关的危险因素以及Aβ1-42的CSF浓度(已建立的AD生物标记)。此外,我们将海马体积用作衍生的成像生物标记物,以丰富学习的知识。我们的分类结果与最近在使用相同数据库上建立的神经影像学方法的荟萃分析中所报告的结果相比具有优势。

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