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Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males

Juvenile delinquency is related to several biological factors, yet very few vulnerability biomarkers have been identified. Previous data suggest that the enzyme monoamine oxidase B (MAO-B) influences several personality traits linked to the propensity to engage in delinquent behavior. Building on th...

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Autores principales: Podobnik, Josip, Nikolac Perkovic, Matea, Nedic Erjavec, Gordana, Dodig Curkovic, Katarina, Curkovic, Mario, Kovac, Vlatka, Svob Strac, Dubravka, Cusek, Melita, Bortolato, Marco, Pivac, Nela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697475/
https://www.ncbi.nlm.nih.gov/pubmed/33203099
http://dx.doi.org/10.3390/biom10111555
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author Podobnik, Josip
Nikolac Perkovic, Matea
Nedic Erjavec, Gordana
Dodig Curkovic, Katarina
Curkovic, Mario
Kovac, Vlatka
Svob Strac, Dubravka
Cusek, Melita
Bortolato, Marco
Pivac, Nela
author_facet Podobnik, Josip
Nikolac Perkovic, Matea
Nedic Erjavec, Gordana
Dodig Curkovic, Katarina
Curkovic, Mario
Kovac, Vlatka
Svob Strac, Dubravka
Cusek, Melita
Bortolato, Marco
Pivac, Nela
author_sort Podobnik, Josip
collection PubMed
description Juvenile delinquency is related to several biological factors, yet very few vulnerability biomarkers have been identified. Previous data suggest that the enzyme monoamine oxidase B (MAO-B) influences several personality traits linked to the propensity to engage in delinquent behavior. Building on this evidence, we assessed whether conduct disorder (CD), juvenile delinquency adjudications, or detention in a correctional facility were associated with either platelet MAO-B activity or the MAOB rs1799836 polymorphism. The study enrolled 289 medication-free male youths, including 182 individuals detained in a correctional facility (with or without a diagnosis of CD). Of the remaining 107 participants, 26 subjects had a diagnosis of CD, and 81 were mentally healthy controls. Platelet MAO-B activity was determined by spectrophotofluorometry, while MAOB rs1799836 was genotyped using qPCR. Platelet MAO-B activity, corrected for age and smoking, was significantly higher in juvenile detainees (p < 0.001), irrespective of CD diagnosis. MAOB rs1799836 was not associated with platelet MAO-B activity or with detention in a correctional facility, CD diagnosis, or delinquent behavior. These data suggest that detention in a juvenile correctional facility increases platelet MAO-B activity in male adolescents. Future studies are needed to determine the mechanisms and functional significance of MAO-B peripheral elevation in juvenile male detainees.
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spelling pubmed-76974752020-11-29 Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males Podobnik, Josip Nikolac Perkovic, Matea Nedic Erjavec, Gordana Dodig Curkovic, Katarina Curkovic, Mario Kovac, Vlatka Svob Strac, Dubravka Cusek, Melita Bortolato, Marco Pivac, Nela Biomolecules Article Juvenile delinquency is related to several biological factors, yet very few vulnerability biomarkers have been identified. Previous data suggest that the enzyme monoamine oxidase B (MAO-B) influences several personality traits linked to the propensity to engage in delinquent behavior. Building on this evidence, we assessed whether conduct disorder (CD), juvenile delinquency adjudications, or detention in a correctional facility were associated with either platelet MAO-B activity or the MAOB rs1799836 polymorphism. The study enrolled 289 medication-free male youths, including 182 individuals detained in a correctional facility (with or without a diagnosis of CD). Of the remaining 107 participants, 26 subjects had a diagnosis of CD, and 81 were mentally healthy controls. Platelet MAO-B activity was determined by spectrophotofluorometry, while MAOB rs1799836 was genotyped using qPCR. Platelet MAO-B activity, corrected for age and smoking, was significantly higher in juvenile detainees (p < 0.001), irrespective of CD diagnosis. MAOB rs1799836 was not associated with platelet MAO-B activity or with detention in a correctional facility, CD diagnosis, or delinquent behavior. These data suggest that detention in a juvenile correctional facility increases platelet MAO-B activity in male adolescents. Future studies are needed to determine the mechanisms and functional significance of MAO-B peripheral elevation in juvenile male detainees. MDPI 2020-11-15 /pmc/articles/PMC7697475/ /pubmed/33203099 http://dx.doi.org/10.3390/biom10111555 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Podobnik, Josip
Nikolac Perkovic, Matea
Nedic Erjavec, Gordana
Dodig Curkovic, Katarina
Curkovic, Mario
Kovac, Vlatka
Svob Strac, Dubravka
Cusek, Melita
Bortolato, Marco
Pivac, Nela
Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title_full Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title_fullStr Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title_full_unstemmed Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title_short Detention in Juvenile Correctional Facilities Is Associated with Higher Platelet Monoamine Oxidase B Activity in Males
title_sort detention in juvenile correctional facilities is associated with higher platelet monoamine oxidase b activity in males
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697475/
https://www.ncbi.nlm.nih.gov/pubmed/33203099
http://dx.doi.org/10.3390/biom10111555
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