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Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology

Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity....

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Autores principales: Shen, Xinpeng, Ma, Sisi, Vemuri, Prashanthi, Simon, Gyorgy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031278/
https://www.ncbi.nlm.nih.gov/pubmed/32076020
http://dx.doi.org/10.1038/s41598-020-59669-x
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author Shen, Xinpeng
Ma, Sisi
Vemuri, Prashanthi
Simon, Gyorgy
author_facet Shen, Xinpeng
Ma, Sisi
Vemuri, Prashanthi
Simon, Gyorgy
author_sort Shen, Xinpeng
collection PubMed
description Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible.
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spelling pubmed-70312782020-02-27 Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology Shen, Xinpeng Ma, Sisi Vemuri, Prashanthi Simon, Gyorgy Sci Rep Article Causal Structure Discovery (CSD) is the problem of identifying causal relationships from large quantities of data through computational methods. With the limited ability of traditional association-based computational methods to discover causal relationships, CSD methodologies are gaining popularity. The goal of the study was to systematically examine whether (i) CSD methods can discover the known causal relationships from observational clinical data and (ii) to offer guidance to accurately discover known causal relationships. We used Alzheimer’s disease (AD), a complex progressive disease, as a model because the well-established evidence provides a “gold-standard” causal graph for evaluation. We evaluated two CSD methods, Fast Causal Inference (FCI) and Fast Greedy Equivalence Search (FGES) in their ability to discover this structure from data collected by the Alzheimer’s Disease Neuroimaging Initiative (ADNI). We used structural equation models (which is not designed for CSD) as control. We applied these methods under three scenarios defined by increasing amounts of background knowledge provided to the methods. The methods were evaluated by comparing the resulting causal relationships with the “gold standard” graph that was constructed from literature. Dedicated CSD methods managed to discover graphs that nearly coincided with the gold standard. For best results, CSD algorithms should be used with longitudinal data providing as much prior knowledge as possible. Nature Publishing Group UK 2020-02-19 /pmc/articles/PMC7031278/ /pubmed/32076020 http://dx.doi.org/10.1038/s41598-020-59669-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shen, Xinpeng
Ma, Sisi
Vemuri, Prashanthi
Simon, Gyorgy
Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title_full Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title_fullStr Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title_full_unstemmed Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title_short Challenges and Opportunities with Causal Discovery Algorithms: Application to Alzheimer’s Pathophysiology
title_sort challenges and opportunities with causal discovery algorithms: application to alzheimer’s pathophysiology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031278/
https://www.ncbi.nlm.nih.gov/pubmed/32076020
http://dx.doi.org/10.1038/s41598-020-59669-x
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