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Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder.
Hesam-Shariati, Sonia; Overs, Bronwyn J; Roberts, Gloria; Toma, Claudio; Watkeys, Oliver J; Green, Melissa J; Pierce, Kerrie D; Edenberg, Howard J; Wilcox, Holly C; Stapp, Emma K; McInnis, Melvin G; Hulvershorn, Leslie A; Nurnberger, John I; Schofield, Peter R; Mitchell, Philip B; Fullerton, Janice M.
Afiliação
  • Hesam-Shariati S; Neuroscience Research Australia, Sydney, NSW, Australia.
  • Overs BJ; School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Roberts G; Neuroscience Research Australia, Sydney, NSW, Australia.
  • Toma C; School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Watkeys OJ; Neuroscience Research Australia, Sydney, NSW, Australia.
  • Green MJ; School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Pierce KD; Centro de Biología Molecular "Severo Ochoa", Universidad Autónoma de Madrid/CSIC, Madrid, Spain.
  • Edenberg HJ; Neuroscience Research Australia, Sydney, NSW, Australia.
  • Wilcox HC; School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Stapp EK; Neuroscience Research Australia, Sydney, NSW, Australia.
  • McInnis MG; School of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
  • Hulvershorn LA; Neuroscience Research Australia, Sydney, NSW, Australia.
  • Nurnberger JI; Department of Medical and Molecular Genetics, Indiana University, Indianapolis, IN, USA.
  • Schofield PR; Department of Biochemistry and Molecular Biology, Indiana University, Indianapolis, IN, USA.
  • Mitchell PB; Child Psychiatry & Public Health, Johns Hopkins University, Baltimore, MD, USA.
  • Fullerton JM; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Transl Psychiatry ; 12(1): 310, 2022 08 03.
Article em En | MEDLINE | ID: mdl-35922419
ABSTRACT
Environmental 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 (ANCOVA p = 0.035 and p = 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) in VARS2, 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 and n = 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adolescent / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article