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Association of subcortical gray-matter volumes with life-course-persistent antisocial behavior in a population-representative longitudinal birth cohort.
Carlisi, Christina O; Moffitt, Terrie E; Knodt, Annchen R; Harrington, HonaLee; Langevin, Stephanie; Ireland, David; Melzer, Tracy R; Poulton, Richie; Ramrakha, Sandhya; Caspi, Avshalom; Hariri, Ahmad R; Viding, Essi.
Afiliação
  • Carlisi CO; Division of Psychology and Language Sciences, University College London, London, UK.
  • Moffitt TE; Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
  • Knodt AR; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
  • Harrington H; PROMENTA, Department of Psychology, University of Oslo, Oslo, Norway.
  • Langevin S; Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
  • Ireland D; Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
  • Melzer TR; Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
  • Poulton R; School of Criminology, University of Montreal, Quebec, Canada.
  • Ramrakha S; Dunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.
  • Caspi A; New Zealand Brain Research Institute, Christchurch, New Zealand.
  • Hariri AR; Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Viding E; Brain Research New Zealand - Rangahau Roro Aotearo Centre of Research Excellence, Dunedin, New Zealand.
Dev Psychopathol ; : 1-11, 2021 Oct 18.
Article em En | MEDLINE | ID: mdl-34657646
ABSTRACT
Neuropsychological evidence supports the developmental taxonomy theory of antisocial behavior, suggesting that abnormal brain development distinguishes life-course-persistent from adolescence-limited antisocial behavior. Recent neuroimaging work confirmed that prospectively-measured life-course-persistent antisocial behavior is associated with differences in cortical brain structure. Whether this extends to subcortical brain structures remains uninvestigated. This study compared subcortical gray-matter volumes between 672 members of the Dunedin Study previously defined as exhibiting life-course-persistent, adolescence-limited or low-level antisocial behavior based on repeated assessments at ages 7-26 years. Gray-matter volumes of 10 subcortical structures were compared across groups. The life-course-persistent group had lower volumes of amygdala, brain stem, cerebellum, hippocampus, pallidum, thalamus, and ventral diencephalon compared to the low-antisocial group. Differences between life-course-persistent and adolescence-limited individuals were comparable in effect size to differences between life-course-persistent and low-antisocial individuals, but were not statistically significant due to less statistical power. Gray-matter volumes in adolescence-limited individuals were near the norm in this population-representative cohort and similar to volumes in low-antisocial individuals. Although this study could not establish causal links between brain volume and antisocial behavior, it constitutes new biological evidence that all people with antisocial behavior are not the same, supporting a need for greater developmental and diagnostic precision in clinical, forensic, and policy-based interventions.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article