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Data-driven modelling of neurodegenerative disease progression: thinking outside the black box.
Young, Alexandra L; Oxtoby, Neil P; Garbarino, Sara; Fox, Nick C; Barkhof, Frederik; Schott, Jonathan M; Alexander, Daniel C.
Afiliación
  • Young AL; UCL Centre for Medical Image Computing, Department of Computer Science, University College London, London, UK. alexandra.young@ucl.ac.uk.
  • Oxtoby NP; Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK. alexandra.young@ucl.ac.uk.
  • Garbarino S; UCL Centre for Medical Image Computing, Department of Computer Science, University College London, London, UK. n.oxtoby@ucl.ac.uk.
  • Fox NC; Life Science Computational Laboratory, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Barkhof F; Dementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.
  • Schott JM; UCL Centre for Medical Image Computing, Department of Computer Science, University College London, London, UK.
  • Alexander DC; Department of Radiology & Nuclear Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Nat Rev Neurosci ; 25(2): 111-130, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38191721
ABSTRACT
Data-driven disease progression models are an emerging set of computational tools that reconstruct disease timelines for long-term chronic diseases, providing unique insights into disease processes and their underlying mechanisms. Such methods combine a priori human knowledge and assumptions with large-scale data processing and parameter estimation to infer long-term disease trajectories from short-term data. In contrast to 'black box' machine learning tools, data-driven disease progression models typically require fewer data and are inherently interpretable, thereby aiding disease understanding in addition to enabling classification, prediction and stratification. In this Review, we place the current landscape of data-driven disease progression models in a general framework and discuss their enhanced utility for constructing a disease timeline compared with wider machine learning tools that construct static disease profiles. We review the insights they have enabled across multiple neurodegenerative diseases, notably Alzheimer disease, for applications such as determining temporal trajectories of disease biomarkers, testing hypotheses about disease mechanisms and uncovering disease subtypes. We outline key areas for technological development and translation to a broader range of neuroscience and non-neuroscience applications. Finally, we discuss potential pathways and barriers to integrating disease progression models into clinical practice and trial settings.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Neurodegenerativas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Rev Neurosci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Neurodegenerativas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Rev Neurosci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido
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