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Protective Factors for Psychotic Symptoms Among Poly-victimized Children

BACKGROUND: Experiencing victimization in early life has been repeatedly shown to be associated with the emergence of psychotic symptoms in childhood. However, most victimized children do not develop psychotic symptoms and why this occurs is not fully understood. This study investigated which indivi...

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Autores principales: Crush, Eloise, Arseneault, Louise, Jaffee, Sara R, Danese, Andrea, Fisher, Helen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890453/
https://www.ncbi.nlm.nih.gov/pubmed/28981896
http://dx.doi.org/10.1093/schbul/sbx111
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author Crush, Eloise
Arseneault, Louise
Jaffee, Sara R
Danese, Andrea
Fisher, Helen L
author_facet Crush, Eloise
Arseneault, Louise
Jaffee, Sara R
Danese, Andrea
Fisher, Helen L
author_sort Crush, Eloise
collection PubMed
description BACKGROUND: Experiencing victimization in early life has been repeatedly shown to be associated with the emergence of psychotic symptoms in childhood. However, most victimized children do not develop psychotic symptoms and why this occurs is not fully understood. This study investigated which individual, family-level, and wider community characteristics were associated with an absence of psychotic symptoms among children at risk for psychosis by virtue of their exposure to multiple victimization experiences (poly-victimization). METHODS: Participants were from the Environmental Risk Longitudinal Twin Study, a nationally representative cohort of 2232 UK-born twins. Exposure to maltreatment, bullying and domestic violence prior to age 12 was determined from interviews with mothers, children, and observations by research workers at ages 5, 7, 10, and 12. Children were interviewed about psychotic symptoms at age 12. Protective factors were measured at ages 5, 7, 10, and 12. RESULTS: Childhood poly-victimization was associated with age-12 psychotic symptoms (OR = 4.61, 95% CI 2.82–7.52), but the majority of poly-victimized children did not report symptoms (80.7%). Having a relatively high IQ, more positive atmosphere at home, and higher levels of neighborhood social cohesion were found to be protective against childhood psychotic symptoms among poly-victimized children and also in the whole sample. However, “protected” poly-victimized children displayed elevated levels of other mental health problems compared to nonvictimized children. CONCLUSIONS: Children’s characteristics, family context, and the wider community were all found to protect children from developing early psychotic symptoms, even when they were victimized multiple times. These findings indicate targets for multilevel preventive interventions.
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spelling pubmed-58904532018-04-13 Protective Factors for Psychotic Symptoms Among Poly-victimized Children Crush, Eloise Arseneault, Louise Jaffee, Sara R Danese, Andrea Fisher, Helen L Schizophr Bull Regular Articles BACKGROUND: Experiencing victimization in early life has been repeatedly shown to be associated with the emergence of psychotic symptoms in childhood. However, most victimized children do not develop psychotic symptoms and why this occurs is not fully understood. This study investigated which individual, family-level, and wider community characteristics were associated with an absence of psychotic symptoms among children at risk for psychosis by virtue of their exposure to multiple victimization experiences (poly-victimization). METHODS: Participants were from the Environmental Risk Longitudinal Twin Study, a nationally representative cohort of 2232 UK-born twins. Exposure to maltreatment, bullying and domestic violence prior to age 12 was determined from interviews with mothers, children, and observations by research workers at ages 5, 7, 10, and 12. Children were interviewed about psychotic symptoms at age 12. Protective factors were measured at ages 5, 7, 10, and 12. RESULTS: Childhood poly-victimization was associated with age-12 psychotic symptoms (OR = 4.61, 95% CI 2.82–7.52), but the majority of poly-victimized children did not report symptoms (80.7%). Having a relatively high IQ, more positive atmosphere at home, and higher levels of neighborhood social cohesion were found to be protective against childhood psychotic symptoms among poly-victimized children and also in the whole sample. However, “protected” poly-victimized children displayed elevated levels of other mental health problems compared to nonvictimized children. CONCLUSIONS: Children’s characteristics, family context, and the wider community were all found to protect children from developing early psychotic symptoms, even when they were victimized multiple times. These findings indicate targets for multilevel preventive interventions. Oxford University Press 2018-04 2017-08-31 /pmc/articles/PMC5890453/ /pubmed/28981896 http://dx.doi.org/10.1093/schbul/sbx111 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Crush, Eloise
Arseneault, Louise
Jaffee, Sara R
Danese, Andrea
Fisher, Helen L
Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title_full Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title_fullStr Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title_full_unstemmed Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title_short Protective Factors for Psychotic Symptoms Among Poly-victimized Children
title_sort protective factors for psychotic symptoms among poly-victimized children
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890453/
https://www.ncbi.nlm.nih.gov/pubmed/28981896
http://dx.doi.org/10.1093/schbul/sbx111
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