Causal Inference Analysis for Poorly Soluble Low Toxicity Particles, Lung Function, and Malignancy
Author
Harber, P.Affiliation
Mel and Enid Zuckerman College of Public Health, University of ArizonaIssue Date
2022Keywords
carbon blackcausal inference analysis
causation analysis
chronic obstructive pulmonary disease (COPD)
directed acyclic graph
lung cancer
particulate toxicity
pulmonary inflammation
Metadata
Show full item recordPublisher
Frontiers Media S.A.Citation
Harber, P. (2022). Causal Inference Analysis for Poorly Soluble Low Toxicity Particles, Lung Function, and Malignancy. Frontiers in Public Health, 10.Journal
Frontiers in Public HealthRights
Copyright © 2022 Harber. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Poorly soluble low toxicity particles such as carbon black and titanium dioxide have raised concern about possible nonmalignant and malignant pulmonary effects. This paper illustrates application of causal inference analysis to assessing these effects. A framework for analysis is created using directed acyclic graphs to define pathways from exposure to potential lung cancer or chronic airflow obstruction outcomes. Directed acyclic graphs define influences of confounders, backdoor pathways, and analytic models. Potential mechanistic pathways such as intermediate pulmonary inflammation are illustrated. An overview of available data for each of the inter-node links is presented. Individual empirical epidemiologic studies have limited ability to confirm mechanisms of potential causal relationships due to the complexity of causal pathways and the extended time course over which disease may develop. Therefore, an explicit conceptual and graphical framework to facilitate synthesizing data from several studies to consider pulmonary inflammation as a common pathway for both chronic airflow obstruction and lung cancer is suggested. These methods are useful to clarify potential bona fide and artifactual observed relationships. They also delineate variables which should be included in analytic models for single study data and biologically relevant variables unlikely to be available from a single study. Copyright © 2022 Harber.Note
Open access journalISSN
2296-2565PubMed ID
35865253Version
Final published versionae974a485f413a2113503eed53cd6c53
10.3389/fpubh.2022.863402
Scopus Count
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Except where otherwise noted, this item's license is described as Copyright © 2022 Harber. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
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