Literature DB >> 25355443

DNA extracted from saliva for methylation studies of psychiatric traits: evidence tissue specificity and relatedness to brain.

Alicia K Smith1, Varun Kilaru, Torsten Klengel, Kristina B Mercer, Bekh Bradley, Karen N Conneely, Kerry J Ressler, Elisabeth B Binder.   

Abstract

DNA methylation has become increasingly recognized in the etiology of psychiatric disorders. Because brain tissue is not accessible in living humans, epigenetic studies are most often conducted in blood. Saliva is often collected for genotyping studies but is rarely used to examine DNA methylation because the proportion of epithelial cells and leukocytes varies extensively between individuals. The goal of this study was to evaluate whether saliva DNA is informative for studies of psychiatric disorders. DNA methylation (HumanMethylation450 BeadChip) was assessed in saliva and blood samples from 64 adult African Americans. Analyses were conducted using linear regression adjusted for appropriate covariates, including estimated cellular proportions. DNA methylation from brain tissues (cerebellum, frontal cortex, entorhinal cortex, and superior temporal gyrus) was obtained from a publically available dataset. Saliva and blood methylation was clearly distinguishable though there was positive correlation overall. There was little correlation in CpG sites within relevant candidate genes. Correlated CpG sites were more likely to occur in areas of low CpG density (i.e., CpG shores and open seas). There was more variability in CpG sites from saliva than blood, which may reflect its heterogeneity. Finally, DNA methylation in saliva appeared more similar to patterns from each of the brain regions examined overall than methylation in blood. Thus, this study provides a framework for using DNA methylation from saliva and suggests that DNA methylation of saliva may offer distinct opportunities for epidemiological and longitudinal studies of psychiatric traits.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  EWAS; HumanMethylation450; biomarker; epigenetic; oragene

Mesh:

Substances:

Year:  2014        PMID: 25355443      PMCID: PMC4610814          DOI: 10.1002/ajmg.b.32278

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  43 in total

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4.  Alterations in DNA methylation of Fkbp5 as a determinant of blood-brain correlation of glucocorticoid exposure.

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5.  DNA hypomethylation of MB-COMT promoter in the DNA derived from saliva in schizophrenia and bipolar disorder.

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7.  DNA methylation analysis of BDNF gene promoters in peripheral blood cells of schizophrenia patients.

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10.  Validation of DNA methylation profiling in formalin-fixed paraffin-embedded samples using the Infinium HumanMethylation450 Microarray.

Authors:  Sebastián Moran; Miguel Vizoso; Anna Martinez-Cardús; Antonio Gomez; Xavier Matías-Guiu; Sebastián M Chiavenna; Andrés G Fernandez; Manel Esteller
Journal:  Epigenetics       Date:  2014-04-14       Impact factor: 4.528

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2.  Relation of Promoter Methylation of the Oxytocin Gene to Stressful Life Events and Depression Severity.

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3.  Early Experiences of Threat, but Not Deprivation, Are Associated With Accelerated Biological Aging in Children and Adolescents.

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4.  Caregiver maltreatment causes altered neuronal DNA methylation in female rodents.

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6.  Dopaminergic gene methylation is associated with cognitive performance in a childhood monozygotic twin study.

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7.  Don't brush off buccal data heterogeneity.

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Review 8.  Review: DNA methylation and alcohol use disorders: Progress and challenges.

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9.  Combining Human Epigenetics and Sleep Studies in Caenorhabditis elegans: A Cross-Species Approach for Finding Conserved Genes Regulating Sleep.

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Review 10.  Evidence from clinical and animal model studies of the long-term and transgenerational impact of stress on DNA methylation.

Authors:  Jennifer Blaze; Tania L Roth
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