Artificial intelligence and statistical methods for stratification and prediction of progression in amyotrophic lateral sclerosis: A systematic review

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disorder characterised by the progressive loss of motor neurons in the brain and spinal cord. The fact that ALS’s disease course is highly heterogeneous, and its determinants not fully known, combined with ALS’s relatively low prevalen...

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Veröffentlicht in:Artificial intelligence in medicine 2023-08, Vol.142, p.102588-102588, Article 102588
Hauptverfasser: Tavazzi, Erica, Longato, Enrico, Vettoretti, Martina, Aidos, Helena, Trescato, Isotta, Roversi, Chiara, Martins, Andreia S., Castanho, Eduardo N., Branco, Ruben, Soares, Diogo F., Guazzo, Alessandro, Birolo, Giovanni, Pala, Daniele, Bosoni, Pietro, Chiò, Adriano, Manera, Umberto, de Carvalho, Mamede, Miranda, Bruno, Gromicho, Marta, Alves, Inês, Bellazzi, Riccardo, Dagliati, Arianna, Fariselli, Piero, Madeira, Sara C., Di Camillo, Barbara
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Sprache:eng
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Zusammenfassung:Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disorder characterised by the progressive loss of motor neurons in the brain and spinal cord. The fact that ALS’s disease course is highly heterogeneous, and its determinants not fully known, combined with ALS’s relatively low prevalence, renders the successful application of artificial intelligence (AI) techniques particularly arduous. This systematic review aims at identifying areas of agreement and unanswered questions regarding two notable applications of AI in ALS, namely the automatic, data-driven stratification of patients according to their phenotype, and the prediction of ALS progression. Differently from previous works, this review is focused on the methodological landscape of AI in ALS. We conducted a systematic search of the Scopus and PubMed databases, looking for studies on data-driven stratification methods based on unsupervised techniques resulting in (A) automatic group discovery or (B) a transformation of the feature space allowing patient subgroups to be identified; and for studies on internally or externally validated methods for the prediction of ALS progression. We described the selected studies according to the following characteristics, when applicable: variables used, methodology, splitting criteria and number of groups, prediction outcomes, validation schemes, and metrics. Of the starting 1604 unique reports (2837 combined hits between Scopus and PubMed), 239 were selected for thorough screening, leading to the inclusion of 15 studies on patient stratification, 28 on prediction of ALS progression, and 6 on both stratification and prediction. In terms of variables used, most stratification and prediction studies included demographics and features derived from the ALSFRS or ALSFRS-R scores, which were also the main prediction targets. The most represented stratification methods were K-means, and hierarchical and expectation-maximisation clustering; while random forests, logistic regression, the Cox proportional hazard model, and various flavours of deep learning were the most widely used prediction methods. Predictive model validation was, albeit unexpectedly, quite rarely performed in absolute terms (leading to the exclusion of 78 eligible studies), with the overwhelming majority of included studies resorting to internal validation only. This systematic review highlighted a general agreement in terms of input variable selection for both stratification and prediction o
ISSN:0933-3657
1873-2860
DOI:10.1016/j.artmed.2023.102588