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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...

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Detalles Bibliográficos
Autores principales: Lin, Honghuang, Satizabal, Claudia, Xie, Zhijun, Yang, Qiong, Huan, Tianxiao, Joehanes, Roby, Wen, Chengping, Munson, Peter J., Beiser, Alexa, Levy, Daniel, Seshadri, Sudha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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
Descripción
Sumario: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.