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Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease
BACKGROUND: Genome-wide association studies (GWAS) have identified many individual genes associated with brain imaging quantitative traits (QTs) in Alzheimer’s disease (AD). However single marker level association discovery may not be able to address the underlying biological interactions with disea...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771059/ https://www.ncbi.nlm.nih.gov/pubmed/33372590 http://dx.doi.org/10.1186/s12864-020-07282-7 |
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author | Meng, Xianglian Li, Jin Zhang, Qiushi Chen, Feng Bian, Chenyuan Yao, Xiaohui Yan, Jingwen Xu, Zhe Risacher, Shannon L. Saykin, Andrew J. Liang, Hong Shen, Li |
author_facet | Meng, Xianglian Li, Jin Zhang, Qiushi Chen, Feng Bian, Chenyuan Yao, Xiaohui Yan, Jingwen Xu, Zhe Risacher, Shannon L. Saykin, Andrew J. Liang, Hong Shen, Li |
author_sort | Meng, Xianglian |
collection | PubMed |
description | BACKGROUND: Genome-wide association studies (GWAS) have identified many individual genes associated with brain imaging quantitative traits (QTs) in Alzheimer’s disease (AD). However single marker level association discovery may not be able to address the underlying biological interactions with disease mechanism. RESULTS: In this paper, we used the MGAS (Multivariate Gene-based Association test by extended Simes procedure) tool to perform multivariate GWAS on eight AD-relevant subcortical imaging measures. We conducted multiple iPINBPA (integrative Protein-Interaction-Network-Based Pathway Analysis) network analyses on MGAS findings using protein-protein interaction (PPI) data, and identified five Consensus Modules (CMs) from the PPI network. Functional annotation and network analysis were performed on the identified CMs. The MGAS yielded significant hits within APOE, TOMM40 and APOC1 genes, which were known AD risk factors, as well as a few new genes such as LAMA1, XYLB, HSD17B7P2, and NPEPL1. The identified five CMs were enriched by biological processes related to disorders such as Alzheimer’s disease, Legionellosis, Pertussis, and Serotonergic synapse. CONCLUSIONS: The statistical power of coupling MGAS with iPINBPA was higher than traditional GWAS method, and yielded new findings that were missed by GWAS. This study provides novel insights into the molecular mechanism of Alzheimer’s Disease and will be of value to novel gene discovery and functional genomic studies. |
format | Online Article Text |
id | pubmed-7771059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77710592020-12-30 Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease Meng, Xianglian Li, Jin Zhang, Qiushi Chen, Feng Bian, Chenyuan Yao, Xiaohui Yan, Jingwen Xu, Zhe Risacher, Shannon L. Saykin, Andrew J. Liang, Hong Shen, Li BMC Genomics Research BACKGROUND: Genome-wide association studies (GWAS) have identified many individual genes associated with brain imaging quantitative traits (QTs) in Alzheimer’s disease (AD). However single marker level association discovery may not be able to address the underlying biological interactions with disease mechanism. RESULTS: In this paper, we used the MGAS (Multivariate Gene-based Association test by extended Simes procedure) tool to perform multivariate GWAS on eight AD-relevant subcortical imaging measures. We conducted multiple iPINBPA (integrative Protein-Interaction-Network-Based Pathway Analysis) network analyses on MGAS findings using protein-protein interaction (PPI) data, and identified five Consensus Modules (CMs) from the PPI network. Functional annotation and network analysis were performed on the identified CMs. The MGAS yielded significant hits within APOE, TOMM40 and APOC1 genes, which were known AD risk factors, as well as a few new genes such as LAMA1, XYLB, HSD17B7P2, and NPEPL1. The identified five CMs were enriched by biological processes related to disorders such as Alzheimer’s disease, Legionellosis, Pertussis, and Serotonergic synapse. CONCLUSIONS: The statistical power of coupling MGAS with iPINBPA was higher than traditional GWAS method, and yielded new findings that were missed by GWAS. This study provides novel insights into the molecular mechanism of Alzheimer’s Disease and will be of value to novel gene discovery and functional genomic studies. BioMed Central 2020-12-29 /pmc/articles/PMC7771059/ /pubmed/33372590 http://dx.doi.org/10.1186/s12864-020-07282-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Meng, Xianglian Li, Jin Zhang, Qiushi Chen, Feng Bian, Chenyuan Yao, Xiaohui Yan, Jingwen Xu, Zhe Risacher, Shannon L. Saykin, Andrew J. Liang, Hong Shen, Li Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title | Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title_full | Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title_fullStr | Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title_full_unstemmed | Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title_short | Multivariate genome wide association and network analysis of subcortical imaging phenotypes in Alzheimer’s disease |
title_sort | multivariate genome wide association and network analysis of subcortical imaging phenotypes in alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771059/ https://www.ncbi.nlm.nih.gov/pubmed/33372590 http://dx.doi.org/10.1186/s12864-020-07282-7 |
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