Cargando…

Lagged WQS regression for mixtures with many components

The developmental timing of exposures to toxic chemicals or combinations of chemicals may be as important as the dosage itself. This concept is called “critical windows of exposure.” The time boundaries of such windows can be detected if exposure data are collected repeatedly in short time intervals...

Descripción completa

Detalles Bibliográficos
Autores principales: Gennings, Chris, Curtin, Paul, Bello, Ghalib, Wright, Robert, Arora, Manish, Austin, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489300/
https://www.ncbi.nlm.nih.gov/pubmed/32371274
http://dx.doi.org/10.1016/j.envres.2020.109529
_version_ 1783581853135929344
author Gennings, Chris
Curtin, Paul
Bello, Ghalib
Wright, Robert
Arora, Manish
Austin, Christine
author_facet Gennings, Chris
Curtin, Paul
Bello, Ghalib
Wright, Robert
Arora, Manish
Austin, Christine
author_sort Gennings, Chris
collection PubMed
description The developmental timing of exposures to toxic chemicals or combinations of chemicals may be as important as the dosage itself. This concept is called “critical windows of exposure.” The time boundaries of such windows can be detected if exposure data are collected repeatedly in short time intervals. The development of tooth-matrix biomarkers which provide prenatal and postnatal exposure measures in repeated intervals can provide such data. Using teeth, we use reverse distributed lagged models (DLMs) to incorporate weekly prenatal and postnatal measures of exposures to estimate time-varying associations with developmental effects. The analysis of such data using lagged weighted quantile sum (WQS) regression as an extension to reverse DLMs for complex mixtures was first proposed by Bello et al. This prior algorithm was not operationally generalizable to large numbers of components (say, more than five or six). We propose a revised algorithm that may be useful for larger mixtures by combining time-specific WQS(t) indices in a reverse DLM. We demonstrate the new algorithm using tooth data in association with a neurodevelopmental score and in simulated data from 3 cases wherein different components of a mixture have time varying associations and in the case where none have associations. The new algorithm correctly detects the simulated associations when the number of samples within the time-specific analyses is moderate to large.
format Online
Article
Text
id pubmed-7489300
institution National Center for Biotechnology Information
language English
publishDate 2020
record_format MEDLINE/PubMed
spelling pubmed-74893002020-09-14 Lagged WQS regression for mixtures with many components Gennings, Chris Curtin, Paul Bello, Ghalib Wright, Robert Arora, Manish Austin, Christine Environ Res Article The developmental timing of exposures to toxic chemicals or combinations of chemicals may be as important as the dosage itself. This concept is called “critical windows of exposure.” The time boundaries of such windows can be detected if exposure data are collected repeatedly in short time intervals. The development of tooth-matrix biomarkers which provide prenatal and postnatal exposure measures in repeated intervals can provide such data. Using teeth, we use reverse distributed lagged models (DLMs) to incorporate weekly prenatal and postnatal measures of exposures to estimate time-varying associations with developmental effects. The analysis of such data using lagged weighted quantile sum (WQS) regression as an extension to reverse DLMs for complex mixtures was first proposed by Bello et al. This prior algorithm was not operationally generalizable to large numbers of components (say, more than five or six). We propose a revised algorithm that may be useful for larger mixtures by combining time-specific WQS(t) indices in a reverse DLM. We demonstrate the new algorithm using tooth data in association with a neurodevelopmental score and in simulated data from 3 cases wherein different components of a mixture have time varying associations and in the case where none have associations. The new algorithm correctly detects the simulated associations when the number of samples within the time-specific analyses is moderate to large. 2020-04-21 2020-07 /pmc/articles/PMC7489300/ /pubmed/32371274 http://dx.doi.org/10.1016/j.envres.2020.109529 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Gennings, Chris
Curtin, Paul
Bello, Ghalib
Wright, Robert
Arora, Manish
Austin, Christine
Lagged WQS regression for mixtures with many components
title Lagged WQS regression for mixtures with many components
title_full Lagged WQS regression for mixtures with many components
title_fullStr Lagged WQS regression for mixtures with many components
title_full_unstemmed Lagged WQS regression for mixtures with many components
title_short Lagged WQS regression for mixtures with many components
title_sort lagged wqs regression for mixtures with many components
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489300/
https://www.ncbi.nlm.nih.gov/pubmed/32371274
http://dx.doi.org/10.1016/j.envres.2020.109529
work_keys_str_mv AT genningschris laggedwqsregressionformixtureswithmanycomponents
AT curtinpaul laggedwqsregressionformixtureswithmanycomponents
AT belloghalib laggedwqsregressionformixtureswithmanycomponents
AT wrightrobert laggedwqsregressionformixtureswithmanycomponents
AT aroramanish laggedwqsregressionformixtureswithmanycomponents
AT austinchristine laggedwqsregressionformixtureswithmanycomponents