Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder

Author:

Hesam-Shariati Sonia,Overs Bronwyn J.ORCID,Roberts Gloria,Toma ClaudioORCID,Watkeys Oliver J.ORCID,Green Melissa J.ORCID,Pierce Kerrie D.ORCID,Edenberg Howard J.ORCID,Wilcox Holly C.,Stapp Emma K.ORCID,McInnis Melvin G.ORCID,Hulvershorn Leslie A.,Nurnberger John I.ORCID,Schofield Peter R.ORCID,Mitchell Philip B.,Fullerton Janice M.ORCID

Abstract

AbstractEnvironmental factors contribute to risk of bipolar disorder (BD), but how environmental factors impact the development of psychopathology within the context of elevated genetic risk is unknown. We herein sought to identify epigenetic signatures operating in the context of polygenic risk for BD in young people at high familial risk (HR) of BD. Peripheral blood-derived DNA was assayed using Illumina PsychArray, and Methylation-450K or -EPIC BeadChips. Polygenic risk scores (PRS) were calculated using summary statistics from recent genome-wide association studies for BD, major depressive disorder (MDD) and cross-disorder (meta-analysis of eight psychiatric disorders). Unrelated HR participants of European ancestry (n = 103) were stratified based on their BD-PRS score within the HR-population distribution, and the top two quintiles (High-BD-PRS;n = 41) compared against the bottom two quintiles (Low-BD-PRS;n = 41). The High-BD-PRS stratum also had higher mean cross-disorder-PRS and MDD-PRS (ANCOVAp = 0.035 andp = 0.024, respectively). We evaluated DNA methylation differences between High-BD-PRS and Low-BD-PRS strata using linear models. One differentially methylated probe (DMP) (cg00933603;p = 3.54 × 10−7) inVARS2, a mitochondrial aminoacyl-tRNA synthetase, remained significantly hypomethylated after multiple-testing correction. Overall, BD-PRS appeared to broadly impact epigenetic processes, with 1,183 genes mapped to nominal DMPs (p < 0.05); these displayed convergence with genes previously associated with BD, schizophrenia, chronotype, and risk taking. We tested poly-methylomic epigenetic profiles derived from nominal DMPs in two independent samples (n = 54 andn = 82, respectively), and conducted an exploratory evaluation of the effects of family environment, indexing cohesion and flexibility. This study highlights an important interplay between heritable risk and epigenetic factors, which warrant further exploration.

Funder

Department of Health | National Health and Medical Research Council

U.S. Department of Health & Human Services | NIH | National Institute of Mental Health

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

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