Cargando…
Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder
Early life stress may have a lasting impact on the developmental programming of the dopamine (DA) system implicated in psychosis. Early adversity could promote resilience by calibrating the prefrontal stress-regulatory dopaminergic neurotransmission to improve the individual’s fit with the predicted...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805207/ https://www.ncbi.nlm.nih.gov/pubmed/27007554 http://dx.doi.org/10.1371/journal.pone.0150746 |
_version_ | 1782423110450937856 |
---|---|
author | Kasanova, Zuzana Hernaus, Dennis Vaessen, Thomas van Amelsvoort, Thérèse Winz, Oliver Heinzel, Alexander Pruessner, Jens Mottaghy, Felix M. Collip, Dina Myin-Germeys, Inez |
author_facet | Kasanova, Zuzana Hernaus, Dennis Vaessen, Thomas van Amelsvoort, Thérèse Winz, Oliver Heinzel, Alexander Pruessner, Jens Mottaghy, Felix M. Collip, Dina Myin-Germeys, Inez |
author_sort | Kasanova, Zuzana |
collection | PubMed |
description | Early life stress may have a lasting impact on the developmental programming of the dopamine (DA) system implicated in psychosis. Early adversity could promote resilience by calibrating the prefrontal stress-regulatory dopaminergic neurotransmission to improve the individual’s fit with the predicted stressful environment. Aberrant reactivity to such match between proximal and distal environments may, however, enhance psychosis disease risk. We explored the combined effects of childhood adversity and adult stress by exposing 12 unmedicated individuals with a diagnosis of non-affective psychotic disorder (NAPD) and 12 healthy controls (HC) to psychosocial stress during an [(18)F]fallypride positron emission tomography. Childhood trauma divided into early (ages 0–11 years) and late (12–18 years) was assessed retrospectively using a questionnaire. A significant group x childhood trauma interaction on the spatial extent of stress-related [(18)F]fallypride displacement was observed in the mPFC for early (b = -8.45, t(1,23) = -3.35, p = .004) and late childhood trauma (b = -7.86, t(1,23) = -2.48, p = .023). In healthy individuals, the spatial extent of mPFC DA activity under acute psychosocial stress was positively associated with the severity of early (b = 7.23, t(11) = 3.06, p = .016) as well as late childhood trauma (b = -7.86, t(1,23) = -2.48, p = .023). Additionally, a trend-level main effect of early childhood trauma on subjective stress response emerged within this group (b = -.7, t(11) = -2, p = .07), where higher early trauma correlated with lower subjective stress response to the task. In the NAPD group, childhood trauma was not associated with the spatial extent of the tracer displacement in mPFC (b = -1.22, t(11) = -0.67), nor was there a main effect of trauma on the subjective perception of stress within this group (b = .004, t(11) = .01, p = .99). These findings reveal a potential mechanism of neuroadaptation of prefrontal DA transmission to early life stress and suggest its role in resilience and vulnerability to psychosis. |
format | Online Article Text |
id | pubmed-4805207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48052072016-03-25 Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder Kasanova, Zuzana Hernaus, Dennis Vaessen, Thomas van Amelsvoort, Thérèse Winz, Oliver Heinzel, Alexander Pruessner, Jens Mottaghy, Felix M. Collip, Dina Myin-Germeys, Inez PLoS One Research Article Early life stress may have a lasting impact on the developmental programming of the dopamine (DA) system implicated in psychosis. Early adversity could promote resilience by calibrating the prefrontal stress-regulatory dopaminergic neurotransmission to improve the individual’s fit with the predicted stressful environment. Aberrant reactivity to such match between proximal and distal environments may, however, enhance psychosis disease risk. We explored the combined effects of childhood adversity and adult stress by exposing 12 unmedicated individuals with a diagnosis of non-affective psychotic disorder (NAPD) and 12 healthy controls (HC) to psychosocial stress during an [(18)F]fallypride positron emission tomography. Childhood trauma divided into early (ages 0–11 years) and late (12–18 years) was assessed retrospectively using a questionnaire. A significant group x childhood trauma interaction on the spatial extent of stress-related [(18)F]fallypride displacement was observed in the mPFC for early (b = -8.45, t(1,23) = -3.35, p = .004) and late childhood trauma (b = -7.86, t(1,23) = -2.48, p = .023). In healthy individuals, the spatial extent of mPFC DA activity under acute psychosocial stress was positively associated with the severity of early (b = 7.23, t(11) = 3.06, p = .016) as well as late childhood trauma (b = -7.86, t(1,23) = -2.48, p = .023). Additionally, a trend-level main effect of early childhood trauma on subjective stress response emerged within this group (b = -.7, t(11) = -2, p = .07), where higher early trauma correlated with lower subjective stress response to the task. In the NAPD group, childhood trauma was not associated with the spatial extent of the tracer displacement in mPFC (b = -1.22, t(11) = -0.67), nor was there a main effect of trauma on the subjective perception of stress within this group (b = .004, t(11) = .01, p = .99). These findings reveal a potential mechanism of neuroadaptation of prefrontal DA transmission to early life stress and suggest its role in resilience and vulnerability to psychosis. Public Library of Science 2016-03-23 /pmc/articles/PMC4805207/ /pubmed/27007554 http://dx.doi.org/10.1371/journal.pone.0150746 Text en © 2016 Kasanova et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kasanova, Zuzana Hernaus, Dennis Vaessen, Thomas van Amelsvoort, Thérèse Winz, Oliver Heinzel, Alexander Pruessner, Jens Mottaghy, Felix M. Collip, Dina Myin-Germeys, Inez Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title | Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title_full | Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title_fullStr | Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title_full_unstemmed | Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title_short | Early-Life Stress Affects Stress-Related Prefrontal Dopamine Activity in Healthy Adults, but Not in Individuals with Psychotic Disorder |
title_sort | early-life stress affects stress-related prefrontal dopamine activity in healthy adults, but not in individuals with psychotic disorder |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805207/ https://www.ncbi.nlm.nih.gov/pubmed/27007554 http://dx.doi.org/10.1371/journal.pone.0150746 |
work_keys_str_mv | AT kasanovazuzana earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT hernausdennis earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT vaessenthomas earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT vanamelsvoorttherese earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT winzoliver earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT heinzelalexander earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT pruessnerjens earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT mottaghyfelixm earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT collipdina earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder AT myingermeysinez earlylifestressaffectsstressrelatedprefrontaldopamineactivityinhealthyadultsbutnotinindividualswithpsychoticdisorder |