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It’s not my fault I am aggressive, they picked on me: How early peer relations affect DNA methylation and neurocognitive development in children

Descripción del proyecto

El abecé de cómo las experiencias sociales afectan a la biología infantil

Los niños que viven sucesos sociales adversos en la guardería y la escuela primaria corren un mayor riesgo de desarrollar agresividad, una autorregulación deficiente y dificultades para controlar el estrés. Aunque las investigaciones han relacionado estas vivencias con consecuencias negativas, los mecanismos subyacentes a estos efectos no se conocen bien. Para abordar esta brecha del conocimiento, el equipo del proyecto socio-bio interplay, financiado por el Consejo Europeo de Investigación, pretende estudiar cómo afectan las vivencias sociales adversas a la neurobiología de los niños. Mediante un método multidisciplinar que combina estudios con gemelos, estudios observacionales y experimentos de laboratorio, los investigadores del proyecto se proponen descubrir las repercusiones del acoso y las vivencias sociales negativas en la metilación del ADN infantil y el desarrollo de las funciones neurocognitivas. El objetivo final es elaborar intervenciones para prevenir la agresividad y promover un desarrollo saludable de los niños vulnerables.

Objetivo

Think about the day you took your child to kindergarten for the first time. You were worried. Worried about the social experiences of your child. Would peers like your child, or would it get bullied, or rejected by classmates?
Many children have positive social school experiences, but 10-15% of children become rejected, victim of bullying, have few friends and have poor relations with teachers. Such experiences have been linked to aggression development, but we poorly understand how.
I hypothesize that adverse social experiences in kindergarten and elementary school affect the neurobiology of children. Specifically, I aim to study how adverse social experiences (1) affect DNA methylation of genes implicated with stress regulation, and (2) affect neurocognitive functions underlying self-regulation, thereby increasing aggression.
I will use a multidisciplinary approach to comprehensively study these hypotheses by using the strengths of twin-, observational and experimental studies. I will first study the impact of bully-victimization on children’s methylation of DNA and neurocognitive function development in monozygotic twins differing in bully-victimization, to test whether bully-victimization affects the neurobiology above and beyond possible genetic effects.
I will then focuses on cross-time influences of multiple social experiences on DNA methylation and neurocognitive functions. Adverse versus protective effects of peer- and teacher-relations on DNA methylation and neurocognitive functions will be studied to explore possible cascading, accentuation, and buffering effects. Further, sex differences will be addressed.
In the final set of (lab-experimental) studies I aim to unravel how DNA methylation of genes implicated with stress system responses, and altered neurocognitive functions lead to aggression by studying differences between chronically rejected and stable non-rejected children in stress-, and self-regulation following a social exclusion experience.

Régimen de financiación

ERC-COG - Consolidator Grant

Institución de acogida

STICHTING VU
Aportación neta de la UEn
€ 1 389 026,50
Dirección
DE BOELELAAN 1105
1081 HV Amsterdam
Países Bajos

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Región
West-Nederland Noord-Holland Groot-Amsterdam
Tipo de actividad
Higher or Secondary Education Establishments
Enlaces
Coste total
€ 1 389 026,50

Beneficiarios (2)