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Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits
Background. A growing body of evidence suggests an association between altered hypothalamic-pituitary-adrenal axis reactivity and the development of persistent antisocial behavior in children. However the effects of altered cortisol levels remain poorly understood in the complex context of conduct d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693123/ https://www.ncbi.nlm.nih.gov/pubmed/23841064 http://dx.doi.org/10.1155/2013/349530 |
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author | von Polier, Georg G. Herpertz-Dahlmann, Beate Konrad, Kerstin Wiesler, Kristine Rieke, Jana Heinzel-Gutenbrunner, Monika Bachmann, Christian J. Vloet, Timo D. |
author_facet | von Polier, Georg G. Herpertz-Dahlmann, Beate Konrad, Kerstin Wiesler, Kristine Rieke, Jana Heinzel-Gutenbrunner, Monika Bachmann, Christian J. Vloet, Timo D. |
author_sort | von Polier, Georg G. |
collection | PubMed |
description | Background. A growing body of evidence suggests an association between altered hypothalamic-pituitary-adrenal axis reactivity and the development of persistent antisocial behavior in children. However the effects of altered cortisol levels remain poorly understood in the complex context of conduct disorder, callous-unemotional (CU) personality traits, and frequent comorbidities, such as attention deficit hyperactivity disorder (ADHD). The aim of the current study was to investigate associations among CU traits, antisocial behavior, and comorbid ADHD symptomatology with cortisol levels in male children and adolescents. Methods. The study included 37 boys with early-onset conduct disorder (EO-CD, mean age 11.9 years) and 38 healthy boys (mean age 12.5 years). Participants were subjected to multiple daytime salivary cortisol measurements and a psychometric characterization. Results. Subjects in the EO-CD group with elevated CU traits showed a diminished cortisol awakening response compared to healthy participants. In the EO-CD group, high CU traits and impulsivity were associated with decreased diurnal cortisol levels, while associations with antisocial behavior were not detected. The cortisol awakening response was significantly inversely associated with hyperactivity (P = 0.02) and marginally significant with CU traits (P = 0.07). Conclusions. These results indicate a specific association between CU traits and a diminished stress response, which is not explained by antisocial behavior in general. |
format | Online Article Text |
id | pubmed-3693123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36931232013-07-09 Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits von Polier, Georg G. Herpertz-Dahlmann, Beate Konrad, Kerstin Wiesler, Kristine Rieke, Jana Heinzel-Gutenbrunner, Monika Bachmann, Christian J. Vloet, Timo D. Biomed Res Int Clinical Study Background. A growing body of evidence suggests an association between altered hypothalamic-pituitary-adrenal axis reactivity and the development of persistent antisocial behavior in children. However the effects of altered cortisol levels remain poorly understood in the complex context of conduct disorder, callous-unemotional (CU) personality traits, and frequent comorbidities, such as attention deficit hyperactivity disorder (ADHD). The aim of the current study was to investigate associations among CU traits, antisocial behavior, and comorbid ADHD symptomatology with cortisol levels in male children and adolescents. Methods. The study included 37 boys with early-onset conduct disorder (EO-CD, mean age 11.9 years) and 38 healthy boys (mean age 12.5 years). Participants were subjected to multiple daytime salivary cortisol measurements and a psychometric characterization. Results. Subjects in the EO-CD group with elevated CU traits showed a diminished cortisol awakening response compared to healthy participants. In the EO-CD group, high CU traits and impulsivity were associated with decreased diurnal cortisol levels, while associations with antisocial behavior were not detected. The cortisol awakening response was significantly inversely associated with hyperactivity (P = 0.02) and marginally significant with CU traits (P = 0.07). Conclusions. These results indicate a specific association between CU traits and a diminished stress response, which is not explained by antisocial behavior in general. Hindawi Publishing Corporation 2013 2013-06-11 /pmc/articles/PMC3693123/ /pubmed/23841064 http://dx.doi.org/10.1155/2013/349530 Text en Copyright © 2013 Georg G. von Polier et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study von Polier, Georg G. Herpertz-Dahlmann, Beate Konrad, Kerstin Wiesler, Kristine Rieke, Jana Heinzel-Gutenbrunner, Monika Bachmann, Christian J. Vloet, Timo D. Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title | Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title_full | Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title_fullStr | Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title_full_unstemmed | Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title_short | Reduced Cortisol in Boys with Early-Onset Conduct Disorder and Callous-Unemotional Traits |
title_sort | reduced cortisol in boys with early-onset conduct disorder and callous-unemotional traits |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693123/ https://www.ncbi.nlm.nih.gov/pubmed/23841064 http://dx.doi.org/10.1155/2013/349530 |
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