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将多种多模态语音特征整合为一个可解释的指数评分,以捕捉肌萎缩侧索硬化症的疾病进展。

Combining Multiple Multimodal Speech Features into an Interpretable Index Score for Capturing Disease Progression in Amyotrophic Lateral Sclerosis.

作者信息

Neumann Michael, Kothare Hardik, Ramanarayanan Vikram

机构信息

Modality.AI, Inc., San Francisco, USA.

出版信息

Interspeech. 2023 Aug;2023:2353-2357. doi: 10.21437/interspeech.2023-2100.

DOI:10.21437/interspeech.2023-2100
PMID:39006832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11246072/
Abstract

Multiple speech biomarkers have been shown to carry useful information regarding Amyotrophic Lateral Sclerosis (ALS) pathology. We propose a two-step framework to compute optimal linear combinations (indexes) of these biomarkers that are more discriminative and noise-robust than the individual markers, which is important for clinical care and pharmaceutical trial applications. First, we use a hierarchical clustering based method to select representative speech metrics from a dataset comprising 143 people with ALS and 135 age- and sex-matched healthy controls. Second, we analyze three methods of index computation that optimize linear discriminability, Youden Index, and sparsity of logistic regression model weights, respectively, and evaluate their performance with 5-fold cross validation. We find that the proposed indexes are generally more discriminative of bulbar vs non-bulbar onset in ALS than their individual component metrics as well as an equally-weighted baseline.

摘要

多种言语生物标志物已被证明携带有关肌萎缩侧索硬化症(ALS)病理学的有用信息。我们提出了一个两步框架来计算这些生物标志物的最佳线性组合(指标),这些组合比单个标志物更具区分性且对噪声更具鲁棒性,这对于临床护理和药物试验应用很重要。首先,我们使用一种基于层次聚类的方法从一个包含143例ALS患者和135例年龄及性别匹配的健康对照的数据集里选择有代表性的言语指标。其次,我们分析了三种分别优化线性可区分性、约登指数和逻辑回归模型权重稀疏性的指标计算方法,并通过五折交叉验证评估它们的性能。我们发现,所提出的指标通常比其单个组成指标以及等权重基线更能区分ALS中的延髓性发病与非延髓性发病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc58/11246072/43b0f251e1ac/nihms-2000963-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc58/11246072/43b0f251e1ac/nihms-2000963-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc58/11246072/43b0f251e1ac/nihms-2000963-f0001.jpg