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Neurodevelopmental vulnerability to psychosis: developmentally-based methods enable detection of early life inhibitory control deficits that predict psychotic-like experiences at the transition to adolescence.
Zarubin, Vanessa C; Damme, Katherine S F; Vargas, Teresa; Osborne, K Juston; Norton, Elizabeth S; Briggs-Gowan, Margaret; Allen, Norrina B; Wakschlag, Laurie; Mittal, Vijay A.
Afiliação
  • Zarubin VC; Department of Psychology, Northwestern University, Evanston, IL, USA.
  • Damme KSF; Department of Psychology, Northwestern University, Evanston, IL, USA.
  • Vargas T; Institute for Innovations in Developmental Sciences (DevSci), Northwestern University, Evanston and Chicago, IL, USA.
  • Osborne KJ; Department of Psychology, Northwestern University, Evanston, IL, USA.
  • Norton ES; Department of Psychology, Northwestern University, Evanston, IL, USA.
  • Briggs-Gowan M; Institute for Innovations in Developmental Sciences (DevSci), Northwestern University, Evanston and Chicago, IL, USA.
  • Allen NB; Department of Medical Social Sciences, Northwestern University, Chicago, IL, USA.
  • Wakschlag L; Department of Communication Sciences & Disorders, School of Communication, Northwestern University, Evanston, IL, USA.
  • Mittal VA; Department of Psychiatry, University of Connecticut Health Center, Farmington, CT, USA.
Psychol Med ; 53(16): 7746-7755, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37395596
BACKGROUND: Inhibitory control develops in early childhood, and atypical development may be a measurable marker of risk for the later development of psychosis. Additionally, inhibitory control may be a target for intervention. METHODS: Behavioral performance on a developmentally appropriate Go/No-Go task including a frustration manipulation completed by children ages 3-5 years (early childhood; n = 107) was examined in relation to psychotic-like experiences (PLEs; 'tween'; ages 9-12), internalizing symptoms, and externalizing symptoms self-reported at long-term follow-up (pre-adolescence; ages 8-11). ERP N200 amplitude for a subset of these children (n = 34) with electrophysiological data during the task was examined as an index of inhibitory control. RESULTS: Children with lower accuracy on No-Go trials compared to Go trials in early childhood (F(1,101) = 3.976, p = 0.049), evidenced higher PLEs at the transition to adolescence 4-9 years later, reflecting a specific deficit in inhibitory control. No association was observed with internalizing or externalizing symptoms. Decreased accuracy during the frustration manipulation predicted higher internalizing, F(2,202) = 5.618, p = 0.004, and externalizing symptoms, F(2,202) = 4.663, p = 0.010. Smaller N200 amplitudes were observed on No-Go trials for those with higher PLEs, F(1,101) = 6.075, p = 0.020; no relationship was observed for internalizing or externalizing symptoms. CONCLUSIONS: Long-term follow-up demonstrates for the first time a specific deficit in inhibitory control behaviorally and electrophysiology, for individuals who later report more PLEs. Decreases in task performance under frustration induction indicated risk for internalizing and externalizing symptoms. These findings suggest that pathophysiological mechanisms for psychosis are relevant and discriminable in early childhood, and further, suggest an identifiable and potentially modifiable target for early intervention.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos