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Whole blood gene expression and white matter Hyperintensities
BACKGROUND: White matter hyperintensities (WMH) are an important biomarker of cumulative vascular brain injury and have been associated with cognitive decline and an increased risk of dementia, stroke, depression, and gait impairments. The pathogenesis of white matter lesions however, remains uncert...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604498/ https://www.ncbi.nlm.nih.gov/pubmed/28923099 http://dx.doi.org/10.1186/s13024-017-0209-5 |
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author | Lin, Honghuang Satizabal, Claudia Xie, Zhijun Yang, Qiong Huan, Tianxiao Joehanes, Roby Wen, Chengping Munson, Peter J. Beiser, Alexa Levy, Daniel Seshadri, Sudha |
author_facet | Lin, Honghuang Satizabal, Claudia Xie, Zhijun Yang, Qiong Huan, Tianxiao Joehanes, Roby Wen, Chengping Munson, Peter J. Beiser, Alexa Levy, Daniel Seshadri, Sudha |
author_sort | Lin, Honghuang |
collection | PubMed |
description | BACKGROUND: White matter hyperintensities (WMH) are an important biomarker of cumulative vascular brain injury and have been associated with cognitive decline and an increased risk of dementia, stroke, depression, and gait impairments. The pathogenesis of white matter lesions however, remains uncertain. The characterization of gene expression profiles associated with WMH might help uncover molecular mechanisms underlying WMH. METHODS: We performed a transcriptome-wide association study of gene expression profiles with WMH in 3248 participants from the Framingham Heart Study using the Affymetrix Human Exon 1.0 ST Array. RESULTS: We identified 13 genes that were significantly associated with WMH (FDR < 0.05) after adjusting for age, sex and blood cell components. Many of these genes are involved in inflammation-related pathways. CONCLUSION: Thirteen genes were significantly associated with WMH. Our study confirms the hypothesis that inflammation might be an important factor contributing to white matter lesions. Future work is needed to explore if these gene products might serve as potential therapeutic targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13024-017-0209-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5604498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56044982017-09-20 Whole blood gene expression and white matter Hyperintensities Lin, Honghuang Satizabal, Claudia Xie, Zhijun Yang, Qiong Huan, Tianxiao Joehanes, Roby Wen, Chengping Munson, Peter J. Beiser, Alexa Levy, Daniel Seshadri, Sudha Mol Neurodegener Research Article BACKGROUND: White matter hyperintensities (WMH) are an important biomarker of cumulative vascular brain injury and have been associated with cognitive decline and an increased risk of dementia, stroke, depression, and gait impairments. The pathogenesis of white matter lesions however, remains uncertain. The characterization of gene expression profiles associated with WMH might help uncover molecular mechanisms underlying WMH. METHODS: We performed a transcriptome-wide association study of gene expression profiles with WMH in 3248 participants from the Framingham Heart Study using the Affymetrix Human Exon 1.0 ST Array. RESULTS: We identified 13 genes that were significantly associated with WMH (FDR < 0.05) after adjusting for age, sex and blood cell components. Many of these genes are involved in inflammation-related pathways. CONCLUSION: Thirteen genes were significantly associated with WMH. Our study confirms the hypothesis that inflammation might be an important factor contributing to white matter lesions. Future work is needed to explore if these gene products might serve as potential therapeutic targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13024-017-0209-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-18 /pmc/articles/PMC5604498/ /pubmed/28923099 http://dx.doi.org/10.1186/s13024-017-0209-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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. |
spellingShingle | Research Article Lin, Honghuang Satizabal, Claudia Xie, Zhijun Yang, Qiong Huan, Tianxiao Joehanes, Roby Wen, Chengping Munson, Peter J. Beiser, Alexa Levy, Daniel Seshadri, Sudha Whole blood gene expression and white matter Hyperintensities |
title | Whole blood gene expression and white matter Hyperintensities |
title_full | Whole blood gene expression and white matter Hyperintensities |
title_fullStr | Whole blood gene expression and white matter Hyperintensities |
title_full_unstemmed | Whole blood gene expression and white matter Hyperintensities |
title_short | Whole blood gene expression and white matter Hyperintensities |
title_sort | whole blood gene expression and white matter hyperintensities |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604498/ https://www.ncbi.nlm.nih.gov/pubmed/28923099 http://dx.doi.org/10.1186/s13024-017-0209-5 |
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