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Using path signatures to predict a diagnosis of Alzheimer’s disease

机译:使用路径签名预测阿尔茨海默病的诊断

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The path signature is a means of feature generation that can encode nonlinear interactions in data in addition to the usual linear terms. It provides interpretable features and its output is a fixed length vector irrespective of the number of input points or their sample times. In this paper we use the path signature to provide features for identifying people whose diagnosis subsequently converts to Alzheimer’s disease. In two separate classification tasks we distinguish converters from 1) healthy individuals, and 2) individuals with mild cognitive impairment. The data used are time-ordered measurements of the whole brain, ventricles and hippocampus from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We find two nonlinear interactions which are predictive in both cases. The first interaction is change of hippocampal volume with time, and the second is a change of hippocampal volume relative to the volume of the whole brain. While hippocampal and brain volume changes are well known in Alzheimer’s disease, we demonstrate the power of the path signature in their identification and analysis without manual feature selection. Sequential data is becoming increasingly available as monitoring technology is applied, and the path signature method is shown to be a useful tool in the processing of this data.
机译:路径签名是除了通常的线性术语之外,可以在数据中编码非线性交互的特征生成手段。它提供可解释的特征,其输出是固定长度矢量,而不管输入点的数量或其采样时间。在本文中,我们使用路径签名来提供识别其诊断随后转化为阿尔茨海默病的人的功能。在两个单独的分类任务中,我们将转换器与1)的转换器区分开,2)个体具有轻度认知障碍的个人。所用的数据是来自阿尔茨海默病神经影像序(ADNI)的全脑,心室和海马的时间有序测量。我们发现两种情况下的两个非线性相互作用。第一种相互作用是随着时间的推移而改变海马体积的变化,第二个是相对于全脑体积的海马体积的变化。虽然海马和脑体积变化在阿尔茨海默病中众所周知,但我们在没有手动特征选择的情况下展示了路径签名的力量。顺序数据变得越来越多,因为应用了监视技术,并且路径签名方法被示出为处理此数据的有用工具。

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