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Adversity in childhood linked to elevated striatal dopamine function in adulthood
Childhood adversity increases the risk of psychosis in adulthood. Theoretical and animal models suggest that this effect may be mediated by increased striatal dopamine neurotransmission. The primary objective of this study was to examine the relationship between adversity in childhood and striatal d...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publisher B. V
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147458/ https://www.ncbi.nlm.nih.gov/pubmed/27344984 http://dx.doi.org/10.1016/j.schres.2016.06.005 |
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author | Egerton, Alice Valmaggia, Lucia R. Howes, Oliver D. Day, Fern Chaddock, Christopher A. Allen, Paul Winton-Brown, Toby T. Bloomfield, Michael A.P. Bhattacharyya, Sagnik Chilcott, Jack Lappin, Julia M. Murray, Robin M. McGuire, Philip |
author_facet | Egerton, Alice Valmaggia, Lucia R. Howes, Oliver D. Day, Fern Chaddock, Christopher A. Allen, Paul Winton-Brown, Toby T. Bloomfield, Michael A.P. Bhattacharyya, Sagnik Chilcott, Jack Lappin, Julia M. Murray, Robin M. McGuire, Philip |
author_sort | Egerton, Alice |
collection | PubMed |
description | Childhood adversity increases the risk of psychosis in adulthood. Theoretical and animal models suggest that this effect may be mediated by increased striatal dopamine neurotransmission. The primary objective of this study was to examine the relationship between adversity in childhood and striatal dopamine function in early adulthood. Secondary objectives were to compare exposure to childhood adversity and striatal dopamine function in young people at ultra high risk (UHR) of psychosis and healthy volunteers. Sixty-seven young adults, comprising 47 individuals at UHR for psychosis and 20 healthy volunteers were recruited from the same geographic area and were matched for age, gender and substance use. Presynaptic dopamine function in the associative striatum was assessed using 18F-DOPA positron emission tomography. Childhood adversity was assessed using the Childhood Experience of Care and Abuse questionnaire. Within the sample as a whole, both severe physical or sexual abuse (T63 = 2.92; P = 0.005), and unstable family arrangements (T57 = 2.80; P = 0.007) in childhood were associated with elevated dopamine function in the associative striatum in adulthood. Comparison of the UHR and volunteer subgroups revealed similar incidence of childhood adverse experiences, and there was no significant group difference in dopamine function. This study provides evidence that childhood adversity is linked to elevated striatal dopamine function in adulthood. |
format | Online Article Text |
id | pubmed-5147458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier Science Publisher B. V |
record_format | MEDLINE/PubMed |
spelling | pubmed-51474582016-12-15 Adversity in childhood linked to elevated striatal dopamine function in adulthood Egerton, Alice Valmaggia, Lucia R. Howes, Oliver D. Day, Fern Chaddock, Christopher A. Allen, Paul Winton-Brown, Toby T. Bloomfield, Michael A.P. Bhattacharyya, Sagnik Chilcott, Jack Lappin, Julia M. Murray, Robin M. McGuire, Philip Schizophr Res Article Childhood adversity increases the risk of psychosis in adulthood. Theoretical and animal models suggest that this effect may be mediated by increased striatal dopamine neurotransmission. The primary objective of this study was to examine the relationship between adversity in childhood and striatal dopamine function in early adulthood. Secondary objectives were to compare exposure to childhood adversity and striatal dopamine function in young people at ultra high risk (UHR) of psychosis and healthy volunteers. Sixty-seven young adults, comprising 47 individuals at UHR for psychosis and 20 healthy volunteers were recruited from the same geographic area and were matched for age, gender and substance use. Presynaptic dopamine function in the associative striatum was assessed using 18F-DOPA positron emission tomography. Childhood adversity was assessed using the Childhood Experience of Care and Abuse questionnaire. Within the sample as a whole, both severe physical or sexual abuse (T63 = 2.92; P = 0.005), and unstable family arrangements (T57 = 2.80; P = 0.007) in childhood were associated with elevated dopamine function in the associative striatum in adulthood. Comparison of the UHR and volunteer subgroups revealed similar incidence of childhood adverse experiences, and there was no significant group difference in dopamine function. This study provides evidence that childhood adversity is linked to elevated striatal dopamine function in adulthood. Elsevier Science Publisher B. V 2016-10 /pmc/articles/PMC5147458/ /pubmed/27344984 http://dx.doi.org/10.1016/j.schres.2016.06.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Egerton, Alice Valmaggia, Lucia R. Howes, Oliver D. Day, Fern Chaddock, Christopher A. Allen, Paul Winton-Brown, Toby T. Bloomfield, Michael A.P. Bhattacharyya, Sagnik Chilcott, Jack Lappin, Julia M. Murray, Robin M. McGuire, Philip Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title | Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title_full | Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title_fullStr | Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title_full_unstemmed | Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title_short | Adversity in childhood linked to elevated striatal dopamine function in adulthood |
title_sort | adversity in childhood linked to elevated striatal dopamine function in adulthood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147458/ https://www.ncbi.nlm.nih.gov/pubmed/27344984 http://dx.doi.org/10.1016/j.schres.2016.06.005 |
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