Biomedical signals and machine learning in amyotrophic lateral sclerosis: a systematic review

Abstract Introduction The use of machine learning (ML) techniques in healthcare encompasses an emerging concept that envisages vast contributions to the tackling of rare diseases. In this scenario, amyotrophic lateral sclerosis (ALS) involves complexities that are yet not demystified. In ALS, the bi...

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Main Authors: Felipe Fernandes, Ingridy Barbalho, Daniele Barros, Ricardo Valentim, César Teixeira, Jorge Henriques, Paulo Gil, Mário Dourado Júnior
Format: Article
Language:English
Published: BMC 2021-06-01
Series:BioMedical Engineering OnLine
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Online Access:https://doi.org/10.1186/s12938-021-00896-2
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Summary:Abstract Introduction The use of machine learning (ML) techniques in healthcare encompasses an emerging concept that envisages vast contributions to the tackling of rare diseases. In this scenario, amyotrophic lateral sclerosis (ALS) involves complexities that are yet not demystified. In ALS, the biomedical signals present themselves as potential biomarkers that, when used in tandem with smart algorithms, can be useful to applications within the context of the disease. Methods This Systematic Literature Review (SLR) consists of searching for and investigating primary studies that use ML techniques and biomedical signals related to ALS. Following the definition and execution of the SLR protocol, 18 articles met the inclusion, exclusion, and quality assessment criteria, and answered the SLR research questions. Discussions Based on the results, we identified three classes of ML applications combined with biomedical signals in the context of ALS: diagnosis (72.22%), communication (22.22%), and survival prediction (5.56%). Conclusions Distinct algorithmic models and biomedical signals have been reported and present promising approaches, regardless of their classes. In summary, this SLR provides an overview of the primary studies analyzed as well as directions for the construction and evolution of technology-based research within the scope of ALS.
ISSN:1475-925X