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HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data

Mediation analysis plays a major role in identifying significant mediators in the pathway between environmental exposures and health outcomes. With advanced data collection technology for large-scale studies, there has been growing research interest in developing methodology for high-dimensional med...

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Autores principales: Perera, Chamila, Zhang, Haixiang, Zheng, Yinan, Hou, Lifang, Qu, Annie, Zheng, Cheng, Xie, Ke, Liu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310002/
https://www.ncbi.nlm.nih.gov/pubmed/35879655
http://dx.doi.org/10.1186/s12859-022-04748-1
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author Perera, Chamila
Zhang, Haixiang
Zheng, Yinan
Hou, Lifang
Qu, Annie
Zheng, Cheng
Xie, Ke
Liu, Lei
author_facet Perera, Chamila
Zhang, Haixiang
Zheng, Yinan
Hou, Lifang
Qu, Annie
Zheng, Cheng
Xie, Ke
Liu, Lei
author_sort Perera, Chamila
collection PubMed
description Mediation analysis plays a major role in identifying significant mediators in the pathway between environmental exposures and health outcomes. With advanced data collection technology for large-scale studies, there has been growing research interest in developing methodology for high-dimensional mediation analysis. In this paper we present HIMA2, an extension of the HIMA method (Zhang in Bioinformatics 32:3150–3154, 2016). First, the proposed HIMA2 reduces the dimension of mediators to a manageable level based on the sure independence screening (SIS) method (Fan in J R Stat Soc Ser B 70:849–911, 2008). Second, a de-biased Lasso procedure is implemented for estimating regression parameters. Third, we use a multiple-testing procedure to accurately control the false discovery rate (FDR) when testing high-dimensional mediation hypotheses. We demonstrate its practical performance using Monte Carlo simulation studies and apply our method to identify DNA methylation markers which mediate the pathway from smoking to reduced lung function in the Coronary Artery Risk Development in Young Adults (CARDIA) Study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04748-1.
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spelling pubmed-93100022022-07-25 HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data Perera, Chamila Zhang, Haixiang Zheng, Yinan Hou, Lifang Qu, Annie Zheng, Cheng Xie, Ke Liu, Lei BMC Bioinformatics Research Mediation analysis plays a major role in identifying significant mediators in the pathway between environmental exposures and health outcomes. With advanced data collection technology for large-scale studies, there has been growing research interest in developing methodology for high-dimensional mediation analysis. In this paper we present HIMA2, an extension of the HIMA method (Zhang in Bioinformatics 32:3150–3154, 2016). First, the proposed HIMA2 reduces the dimension of mediators to a manageable level based on the sure independence screening (SIS) method (Fan in J R Stat Soc Ser B 70:849–911, 2008). Second, a de-biased Lasso procedure is implemented for estimating regression parameters. Third, we use a multiple-testing procedure to accurately control the false discovery rate (FDR) when testing high-dimensional mediation hypotheses. We demonstrate its practical performance using Monte Carlo simulation studies and apply our method to identify DNA methylation markers which mediate the pathway from smoking to reduced lung function in the Coronary Artery Risk Development in Young Adults (CARDIA) Study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04748-1. BioMed Central 2022-07-25 /pmc/articles/PMC9310002/ /pubmed/35879655 http://dx.doi.org/10.1186/s12859-022-04748-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Perera, Chamila
Zhang, Haixiang
Zheng, Yinan
Hou, Lifang
Qu, Annie
Zheng, Cheng
Xie, Ke
Liu, Lei
HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title_full HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title_fullStr HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title_full_unstemmed HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title_short HIMA2: high-dimensional mediation analysis and its application in epigenome-wide DNA methylation data
title_sort hima2: high-dimensional mediation analysis and its application in epigenome-wide dna methylation data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310002/
https://www.ncbi.nlm.nih.gov/pubmed/35879655
http://dx.doi.org/10.1186/s12859-022-04748-1
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