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Male Inmate Profiles and Their Biological Correlates

OBJECTIVE: Borderline and antisocial personality disorders (PDs) share common clinical features (impulsivity, aggressiveness, substance use disorders [SUDs], and suicidal behaviours) that are greatly overrepresented in prison populations. These disorders have been associated biologically with testos...

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Autores principales: Horn, Mathilde, Potvin, Stephane, Allaire, Jean-François, Côté, Gilles, Gobbi, Gabriella, Benkirane, Karim, Vachon, Jeanne, Dumais, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Canadian Psychiatric Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143301/
https://www.ncbi.nlm.nih.gov/pubmed/25161069
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author Horn, Mathilde
Potvin, Stephane
Allaire, Jean-François
Côté, Gilles
Gobbi, Gabriella
Benkirane, Karim
Vachon, Jeanne
Dumais, Alexandre
author_facet Horn, Mathilde
Potvin, Stephane
Allaire, Jean-François
Côté, Gilles
Gobbi, Gabriella
Benkirane, Karim
Vachon, Jeanne
Dumais, Alexandre
author_sort Horn, Mathilde
collection PubMed
description OBJECTIVE: Borderline and antisocial personality disorders (PDs) share common clinical features (impulsivity, aggressiveness, substance use disorders [SUDs], and suicidal behaviours) that are greatly overrepresented in prison populations. These disorders have been associated biologically with testosterone and cortisol levels. However, the associations are ambiguous and the subject of controversy, perhaps because these heterogeneous disorders have been addressed as unitary constructs. A consideration of profiles of people, rather than of exclusive diagnoses, might yield clearer relationships. METHODS: In our study, multiple correspondence analysis and cluster analysis were employed to identify subgroups among 545 newly convicted inmates. The groups were then compared in terms of clinical features and biological markers, including levels of cortisol, testosterone, estradiol, progesterone, and sulfoconjugated dehydroepiandrosterone (DHEA-S). RESULTS: Four clusters with differing psychiatric, criminal, and biological profiles emerged. Clinically, one group had intermediate scores for each of the tested clinical features. Another group comprised people with little comorbidity. Two others displayed severe impulsivity, PD, and SUD. Biologically, cortisol levels were lowest in the last 2 groups and highest in the group with less comorbidity. In keeping with previous findings reported in the literature, testosterone was higher in a younger population with severe psychiatric symptoms. However, some apparently comparable behavioural outcomes were found to be related to distinct biological profiles. No differences were observed for estradiol, progesterone, or DHEA-S levels. CONCLUSIONS: The results not only confirm the importance of biological markers in the study of personality features but also demonstrate the need to consider the role of comorbidities and steroid coregulation.
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spelling pubmed-41433012015-02-01 Male Inmate Profiles and Their Biological Correlates Horn, Mathilde Potvin, Stephane Allaire, Jean-François Côté, Gilles Gobbi, Gabriella Benkirane, Karim Vachon, Jeanne Dumais, Alexandre Can J Psychiatry Original Research OBJECTIVE: Borderline and antisocial personality disorders (PDs) share common clinical features (impulsivity, aggressiveness, substance use disorders [SUDs], and suicidal behaviours) that are greatly overrepresented in prison populations. These disorders have been associated biologically with testosterone and cortisol levels. However, the associations are ambiguous and the subject of controversy, perhaps because these heterogeneous disorders have been addressed as unitary constructs. A consideration of profiles of people, rather than of exclusive diagnoses, might yield clearer relationships. METHODS: In our study, multiple correspondence analysis and cluster analysis were employed to identify subgroups among 545 newly convicted inmates. The groups were then compared in terms of clinical features and biological markers, including levels of cortisol, testosterone, estradiol, progesterone, and sulfoconjugated dehydroepiandrosterone (DHEA-S). RESULTS: Four clusters with differing psychiatric, criminal, and biological profiles emerged. Clinically, one group had intermediate scores for each of the tested clinical features. Another group comprised people with little comorbidity. Two others displayed severe impulsivity, PD, and SUD. Biologically, cortisol levels were lowest in the last 2 groups and highest in the group with less comorbidity. In keeping with previous findings reported in the literature, testosterone was higher in a younger population with severe psychiatric symptoms. However, some apparently comparable behavioural outcomes were found to be related to distinct biological profiles. No differences were observed for estradiol, progesterone, or DHEA-S levels. CONCLUSIONS: The results not only confirm the importance of biological markers in the study of personality features but also demonstrate the need to consider the role of comorbidities and steroid coregulation. The Canadian Psychiatric Association 2014-08 /pmc/articles/PMC4143301/ /pubmed/25161069 Text en © 2014 Canadian Psychiatric Association http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Original Research
Horn, Mathilde
Potvin, Stephane
Allaire, Jean-François
Côté, Gilles
Gobbi, Gabriella
Benkirane, Karim
Vachon, Jeanne
Dumais, Alexandre
Male Inmate Profiles and Their Biological Correlates
title Male Inmate Profiles and Their Biological Correlates
title_full Male Inmate Profiles and Their Biological Correlates
title_fullStr Male Inmate Profiles and Their Biological Correlates
title_full_unstemmed Male Inmate Profiles and Their Biological Correlates
title_short Male Inmate Profiles and Their Biological Correlates
title_sort male inmate profiles and their biological correlates
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143301/
https://www.ncbi.nlm.nih.gov/pubmed/25161069
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