DNA methylation and brain structure and function across the life course: A systematic review
•60 studies of association between DNAm and human brain MRI were identified.•Differential DNAm is associated with brain structure and function throughout life.•There is modest consistency between DNAm and image endophenotypes.•Approaches for reducing heterogeneity in DNAm-MRI analyses are proposed....
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Veröffentlicht in: | Neuroscience and biobehavioral reviews 2020-06, Vol.113, p.133-156 |
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Sprache: | eng |
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Zusammenfassung: | •60 studies of association between DNAm and human brain MRI were identified.•Differential DNAm is associated with brain structure and function throughout life.•There is modest consistency between DNAm and image endophenotypes.•Approaches for reducing heterogeneity in DNAm-MRI analyses are proposed.
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. |
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ISSN: | 0149-7634 1873-7528 |
DOI: | 10.1016/j.neubiorev.2020.03.007 |