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DNA methylation and brain structure and function across the life course: A systematic review
MRI has enhanced our capacity to understand variations in brain structure and function conferred by the genome. We identified 60 studies that report associations between DNA methylation (DNAm) and human brain structure/function. Forty-three studies measured candidate loci DNAm; seventeen measured ep...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237884/ https://www.ncbi.nlm.nih.gov/pubmed/32151655 http://dx.doi.org/10.1016/j.neubiorev.2020.03.007 |
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author | Wheater, Emily N.W. Stoye, David Q. Cox, Simon R. Wardlaw, Joanna M. Drake, Amanda J. Bastin, Mark E. Boardman, James P. |
author_facet | Wheater, Emily N.W. Stoye, David Q. Cox, Simon R. Wardlaw, Joanna M. Drake, Amanda J. Bastin, Mark E. Boardman, James P. |
author_sort | Wheater, Emily N.W. |
collection | PubMed |
description | MRI has enhanced our capacity to understand variations in brain structure and function conferred by the genome. We identified 60 studies that report associations between DNA methylation (DNAm) and human brain structure/function. Forty-three studies measured candidate loci DNAm; seventeen measured epigenome-wide DNAm. MRI features included region-of-interest and whole-brain structural, diffusion and functional imaging features. The studies report DNAm-MRI associations for: neurodevelopment and neurodevelopmental disorders; major depression and suicidality; alcohol use disorder; schizophrenia and psychosis; ageing, stroke, ataxia and neurodegeneration; post-traumatic stress disorder; and socio-emotional processing. Consistency between MRI features and differential DNAm is modest. Sources of bias: variable inclusion of comparator groups; different surrogate tissues used; variation in DNAm measurement methods; lack of control for genotype and cell-type composition; and variations in image processing. Knowledge of MRI features associated with differential DNAm may improve understanding of the role of DNAm in brain health and disease, but caution is required because conventions for linking DNAm and MRI data are not established, and clinical and methodological heterogeneity in existing literature is substantial. |
format | Online Article Text |
id | pubmed-7237884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Pergamon Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72378842020-06-01 DNA methylation and brain structure and function across the life course: A systematic review Wheater, Emily N.W. Stoye, David Q. Cox, Simon R. Wardlaw, Joanna M. Drake, Amanda J. Bastin, Mark E. Boardman, James P. Neurosci Biobehav Rev Article MRI has enhanced our capacity to understand variations in brain structure and function conferred by the genome. We identified 60 studies that report associations between DNA methylation (DNAm) and human brain structure/function. Forty-three studies measured candidate loci DNAm; seventeen measured epigenome-wide DNAm. MRI features included region-of-interest and whole-brain structural, diffusion and functional imaging features. The studies report DNAm-MRI associations for: neurodevelopment and neurodevelopmental disorders; major depression and suicidality; alcohol use disorder; schizophrenia and psychosis; ageing, stroke, ataxia and neurodegeneration; post-traumatic stress disorder; and socio-emotional processing. Consistency between MRI features and differential DNAm is modest. Sources of bias: variable inclusion of comparator groups; different surrogate tissues used; variation in DNAm measurement methods; lack of control for genotype and cell-type composition; and variations in image processing. Knowledge of MRI features associated with differential DNAm may improve understanding of the role of DNAm in brain health and disease, but caution is required because conventions for linking DNAm and MRI data are not established, and clinical and methodological heterogeneity in existing literature is substantial. Pergamon Press 2020-06 /pmc/articles/PMC7237884/ /pubmed/32151655 http://dx.doi.org/10.1016/j.neubiorev.2020.03.007 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wheater, Emily N.W. Stoye, David Q. Cox, Simon R. Wardlaw, Joanna M. Drake, Amanda J. Bastin, Mark E. Boardman, James P. DNA methylation and brain structure and function across the life course: A systematic review |
title | DNA methylation and brain structure and function across the life course: A systematic review |
title_full | DNA methylation and brain structure and function across the life course: A systematic review |
title_fullStr | DNA methylation and brain structure and function across the life course: A systematic review |
title_full_unstemmed | DNA methylation and brain structure and function across the life course: A systematic review |
title_short | DNA methylation and brain structure and function across the life course: A systematic review |
title_sort | dna methylation and brain structure and function across the life course: a systematic review |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237884/ https://www.ncbi.nlm.nih.gov/pubmed/32151655 http://dx.doi.org/10.1016/j.neubiorev.2020.03.007 |
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