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Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder.
Overs, Bronwyn J; Roberts, Gloria; Ridgway, Kate; Toma, Claudio; Hadzi-Pavlovic, Dusan; Wilcox, Holly C; Hulvershorn, Leslie A; Nurnberger, John I; Schofield, Peter R; Mitchell, Philip B; Fullerton, Janice M.
Afiliação
  • Overs BJ; Neuroscience Research Australia, Randwick, New South Wales, Australia.
  • Roberts G; School of Psychiatry, University of New South Wales, Kensington, New South Wales, Australia.
  • Ridgway K; School of Psychiatry, University of New South Wales, Kensington, New South Wales, Australia.
  • Toma C; Neuroscience Research Australia, Randwick, New South Wales, Australia.
  • Hadzi-Pavlovic D; Centro de Biología Molecular "Severo Ochoa," Universidad Autónoma de Madrid/CSIC, Madrid, Spain.
  • Wilcox HC; School of Psychiatry, University of New South Wales, Kensington, New South Wales, Australia.
  • Hulvershorn LA; Child Psychiatry and Public Health, Johns Hopkins University, Baltimore, Maryland, USA.
  • Nurnberger JI; Department of Psychiatry, Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Schofield PR; Department of Psychiatry, Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Mitchell PB; Department of Medical and Molecular Genetics, Indiana University, Indianapolis, Indiana, USA.
  • Fullerton JM; Neuroscience Research Australia, Randwick, New South Wales, Australia.
Am J Med Genet B Neuropsychiatr Genet ; 186(8): 485-507, 2021 12.
Article em En | MEDLINE | ID: mdl-34726322
Bipolar disorder (BD) is associated with a 20-30-fold increased suicide risk compared to the general population. First-degree relatives of BD patients show inflated rates of psychopathology including suicidal behaviors. As reliable biomarkers of suicide attempts (SA) are lacking, we examined associations between suicide-related polygenic risk scores (PRSs)-a quantitative index of genomic risk-and variability in brain structures implicated in SA. Participants (n = 206; aged 12-30 years) were unrelated individuals of European ancestry and comprised three groups: 41 BD cases, 96 BD relatives ("high risk"), and 69 controls. Genotyping employed PsychArray, followed by imputation. Three PRSs were computed using genome-wide association data for SA in BD (SA-in-BD), SA in major depressive disorder (SA-in-MDD) (Mullins et al., 2019, The American Journal of Psychiatry, 176(8), 651-660), and risky behavior (Karlsson Linnér et al., 2019, Nature Genetics, 51(2), 245-257). Structural magnetic resonance imaging processing employed FreeSurfer v5.3.0. General linear models were constructed using 32 regions-of-interest identified from suicide neuroimaging literature, with false-discovery-rate correction. SA-in-MDD and SA-in-BD PRSs negatively predicted parahippocampal thickness, with the latter association modified by group membership. SA-in-BD and Risky Behavior PRSs inversely predicted rostral and caudal anterior cingulate structure, respectively, with the latter effect driven by the "high risk" group. SA-in-MDD and SA-in-BD PRSs positively predicted cuneus structure, irrespective of group. This study demonstrated associations between PRSs for suicide-related phenotypes and structural variability in brain regions implicated in SA. Future exploration of extended PRSs, in conjunction with a range of biological, phenotypic, environmental, and experiential data in high risk populations, may inform predictive models for suicidal behaviors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Humans Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Transtorno Depressivo Maior Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Humans Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Austrália