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Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review

Alzheimer’s disease is a neurodegenerative disorder and the most common form of dementia. Early diagnosis may assist interventions to delay onset and reduce the progression rate of the disease. We systematically reviewed the use of machine learning algorithms for predicting Alzheimer’s disease using...

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Autores principales: Rowe, Thomas W, Katzourou, Ioanna K, Stevenson-Hoare, Joshua O, Bracher-Smith, Matthew R, Ivanov, Dobril K, Escott-Price, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598986/
https://www.ncbi.nlm.nih.gov/pubmed/34805994
http://dx.doi.org/10.1093/braincomms/fcab246
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author Rowe, Thomas W
Katzourou, Ioanna K
Stevenson-Hoare, Joshua O
Bracher-Smith, Matthew R
Ivanov, Dobril K
Escott-Price, Valentina
author_facet Rowe, Thomas W
Katzourou, Ioanna K
Stevenson-Hoare, Joshua O
Bracher-Smith, Matthew R
Ivanov, Dobril K
Escott-Price, Valentina
author_sort Rowe, Thomas W
collection PubMed
description Alzheimer’s disease is a neurodegenerative disorder and the most common form of dementia. Early diagnosis may assist interventions to delay onset and reduce the progression rate of the disease. We systematically reviewed the use of machine learning algorithms for predicting Alzheimer’s disease using single nucleotide polymorphisms and instances where these were combined with other types of data. We evaluated the ability of machine learning models to distinguish between controls and cases, while also assessing their implementation and potential biases. Articles published between December 2009 and June 2020 were collected using Scopus, PubMed and Google Scholar. These were systematically screened for inclusion leading to a final set of 12 publications. Eighty-five per cent of the included studies used the Alzheimer's Disease Neuroimaging Initiative dataset. In studies which reported area under the curve, discrimination varied (0.49–0.97). However, more than half of the included manuscripts used other forms of measurement, such as accuracy, sensitivity and specificity. Model calibration statistics were also found to be reported inconsistently across all studies. The most frequent limitation in the assessed studies was sample size, with the total number of participants often numbering less than a thousand, whilst the number of predictors usually ran into the many thousands. In addition, key steps in model implementation and validation were often not performed or unreported, making it difficult to assess the capability of machine learning models.
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spelling pubmed-85989862021-11-18 Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review Rowe, Thomas W Katzourou, Ioanna K Stevenson-Hoare, Joshua O Bracher-Smith, Matthew R Ivanov, Dobril K Escott-Price, Valentina Brain Commun Review Article Alzheimer’s disease is a neurodegenerative disorder and the most common form of dementia. Early diagnosis may assist interventions to delay onset and reduce the progression rate of the disease. We systematically reviewed the use of machine learning algorithms for predicting Alzheimer’s disease using single nucleotide polymorphisms and instances where these were combined with other types of data. We evaluated the ability of machine learning models to distinguish between controls and cases, while also assessing their implementation and potential biases. Articles published between December 2009 and June 2020 were collected using Scopus, PubMed and Google Scholar. These were systematically screened for inclusion leading to a final set of 12 publications. Eighty-five per cent of the included studies used the Alzheimer's Disease Neuroimaging Initiative dataset. In studies which reported area under the curve, discrimination varied (0.49–0.97). However, more than half of the included manuscripts used other forms of measurement, such as accuracy, sensitivity and specificity. Model calibration statistics were also found to be reported inconsistently across all studies. The most frequent limitation in the assessed studies was sample size, with the total number of participants often numbering less than a thousand, whilst the number of predictors usually ran into the many thousands. In addition, key steps in model implementation and validation were often not performed or unreported, making it difficult to assess the capability of machine learning models. Oxford University Press 2021-10-21 /pmc/articles/PMC8598986/ /pubmed/34805994 http://dx.doi.org/10.1093/braincomms/fcab246 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Rowe, Thomas W
Katzourou, Ioanna K
Stevenson-Hoare, Joshua O
Bracher-Smith, Matthew R
Ivanov, Dobril K
Escott-Price, Valentina
Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title_full Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title_fullStr Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title_full_unstemmed Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title_short Machine learning for the life-time risk prediction of Alzheimer’s disease: a systematic review
title_sort machine learning for the life-time risk prediction of alzheimer’s disease: a systematic review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598986/
https://www.ncbi.nlm.nih.gov/pubmed/34805994
http://dx.doi.org/10.1093/braincomms/fcab246
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