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Clustered photoplethysmogram pulse wave shapes and their associations with clinical data

Photopletysmography (PPG) is a non-invasive and well known technology that enables the recording of the digital volume pulse (DVP). Although PPG is largely employed in research, several aspects remain unknown. One of these is represented by the lack of information about how many waveform classes bes...

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Detalles Bibliográficos
Autores principales: Zanelli, Serena, Eveilleau, Kornelia, Charlton, Peter H., Ammi, Mehdi, Hallab, Magid, El Yacoubi, Mounim A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10637540/
https://www.ncbi.nlm.nih.gov/pubmed/37954447
http://dx.doi.org/10.3389/fphys.2023.1176753
Descripción
Sumario:Photopletysmography (PPG) is a non-invasive and well known technology that enables the recording of the digital volume pulse (DVP). Although PPG is largely employed in research, several aspects remain unknown. One of these is represented by the lack of information about how many waveform classes best express the variability in shape. In the literature, it is common to classify DVPs into four classes based on the dicrotic notch position. However, when working with real data, labelling waveforms with one of these four classes is no longer straightforward and may be challenging. The correct identification of the DVP shape could enhance the precision and the reliability of the extracted bio markers. In this work we proposed unsupervised machine learning and deep learning approaches to overcome the data labelling limitations. Concretely we performed a K-medoids based clustering that takes as input 1) DVP handcrafted features, 2) similarity matrix computed with the Derivative Dynamic Time Warping and 3) DVP features extracted from a CNN AutoEncoder. All the cited methods have been tested first by imposing four medoids representative of the Dawber classes, and after by automatically searching four clusters. We then searched the optimal number of clusters for each method using silhouette score, the prediction strength and inertia. To validate the proposed approaches we analyse the dissimilarities in the clinical data related to obtained clusters.