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Associations between childhood family emotional health, fronto-limbic grey matter volume, and saliva 5mC in young adulthood.
Pfeiffer, J R; Bustamante, Angela C; Kim, Grace S; Armstrong, Don; Knodt, Annchen R; Koenen, Karestan C; Hariri, Ahmad R; Uddin, Monica.
Afiliação
  • Pfeiffer JR; Department of Psychology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
  • Bustamante AC; Carl R. Woese Institute for Genomic Biology, Urbana, IL, USA.
  • Kim GS; Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Armstrong D; Medical Scholars Program, University of Illinois College of Medicine, Urbana, IL, USA.
  • Knodt AR; Carl R. Woese Institute for Genomic Biology, Urbana, IL, USA.
  • Koenen KC; Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
  • Hariri AR; Laboratory of NeuroGenetics, Duke University, Durham, NC, USA.
  • Uddin M; Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.
Clin Epigenetics ; 13(1): 68, 2021 03 31.
Article em En | MEDLINE | ID: mdl-33789736
ABSTRACT

BACKGROUND:

Poor family emotional health (FEH) during childhood is prevalent and impactful, and likely confers similar neurodevelopmental risks as other adverse social environments. Pointed FEH study efforts are underdeveloped, and the mechanisms by which poor FEH are biologically embedded are unclear. The current exploratory study examined whether variability in 5-methyl-cytosine (5mC) and fronto-limbic grey matter volume may represent pathways through which FEH may become biologically embedded.

RESULTS:

In 98 university students aged 18-22 years, retrospective self-reported childhood FEH was associated with right hemisphere hippocampus (b = 10.4, p = 0.005), left hemisphere amygdala (b = 5.3, p = 0.009), and right hemisphere amygdala (b = 5.8, p = 0.016) volumes. After pre-processing and filtering to 5mC probes correlated between saliva and brain, analyses showed that childhood FEH was associated with 49 5mC principal components (module eigengenes; MEs) (prange = 3 × 10-6 to 0.047). Saliva-derived 5mC MEs partially mediated the association between FEH and right hippocampal volume (Burlywood ME indirect effect b = - 111, p = 0.014), and fully mediated the FEH and right amygdala volume relationship (Pink4 ME indirect effect b = - 48, p = 0.026). Modules were enriched with probes falling in genes with immune, central nervous system (CNS), cellular development/differentiation, and metabolic functions.

CONCLUSIONS:

Findings extend work highlighting neurodevelopmental variability associated with adverse social environment exposure during childhood by specifically implicating poor FEH, while informing a mechanism of biological embedding. FEH-associated epigenetic signatures could function as proxies of altered fronto-limbic grey matter volume associated with poor childhood FEH and inform further investigation into primarily affected tissues such as endocrine, immune, and CNS cell types.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saliva / Estresse Psicológico / Estudantes / Crisenos / Relações Familiares / Substância Cinzenta Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Clin Epigenetics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saliva / Estresse Psicológico / Estudantes / Crisenos / Relações Familiares / Substância Cinzenta Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Clin Epigenetics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos