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Prepulse Inhibition in Cocaine Addiction and Dual Pathologies
Cocaine addiction is frequently associated with different psychiatric disorders, especially schizophrenia and antisocial personality disorder. A small number of studies have used prepulse inhibition (PPI) as a discriminating factor between these disorders. This work evaluated PPI and the phenotype o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924364/ https://www.ncbi.nlm.nih.gov/pubmed/33672693 http://dx.doi.org/10.3390/brainsci11020269 |
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author | Gil-Miravet, Isis Fuertes-Saiz, Alejandro Benito, Ana Almodóvar, Isabel Ochoa, Enrique Haro, Gonzalo |
author_facet | Gil-Miravet, Isis Fuertes-Saiz, Alejandro Benito, Ana Almodóvar, Isabel Ochoa, Enrique Haro, Gonzalo |
author_sort | Gil-Miravet, Isis |
collection | PubMed |
description | Cocaine addiction is frequently associated with different psychiatric disorders, especially schizophrenia and antisocial personality disorder. A small number of studies have used prepulse inhibition (PPI) as a discriminating factor between these disorders. This work evaluated PPI and the phenotype of patients with cocaine-related disorder (CRD) who presented a dual diagnosis of schizophrenia or antisocial personality disorder. A total of 74 men aged 18–60 years were recruited for this research. The sample was divided into four groups: CRD (n = 14), CRD and schizophrenia (n = 21), CRD and antisocial personality disorder (n = 16), and a control group (n = 23). We evaluated the PPI and other possible vulnerability factors in these patients by using different assessment scales. PPI was higher in the CRD group at 30 ms (F(3, 64) = 2.972, p = 0.038). Three discriminant functions were obtained which allowed us to use the overall Hare Psychopathy Checklist Revised score, reward sensitivity, and PPI at 30 ms to predict inclusion of these patients in the different groups with a success rate of 79.7% (42.9% for CRD, 76.2% for CRD and schizophrenia, 100% for CRD and antisocial personality disorder, and 91.3% in the control group). Despite the differences we observed in PPI, this factor is of little use for discriminating between the different diagnostic groups and it acts more as a non-specific endophenotype in certain mental disorders, such as in patients with a dual diagnosis. |
format | Online Article Text |
id | pubmed-7924364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79243642021-03-03 Prepulse Inhibition in Cocaine Addiction and Dual Pathologies Gil-Miravet, Isis Fuertes-Saiz, Alejandro Benito, Ana Almodóvar, Isabel Ochoa, Enrique Haro, Gonzalo Brain Sci Article Cocaine addiction is frequently associated with different psychiatric disorders, especially schizophrenia and antisocial personality disorder. A small number of studies have used prepulse inhibition (PPI) as a discriminating factor between these disorders. This work evaluated PPI and the phenotype of patients with cocaine-related disorder (CRD) who presented a dual diagnosis of schizophrenia or antisocial personality disorder. A total of 74 men aged 18–60 years were recruited for this research. The sample was divided into four groups: CRD (n = 14), CRD and schizophrenia (n = 21), CRD and antisocial personality disorder (n = 16), and a control group (n = 23). We evaluated the PPI and other possible vulnerability factors in these patients by using different assessment scales. PPI was higher in the CRD group at 30 ms (F(3, 64) = 2.972, p = 0.038). Three discriminant functions were obtained which allowed us to use the overall Hare Psychopathy Checklist Revised score, reward sensitivity, and PPI at 30 ms to predict inclusion of these patients in the different groups with a success rate of 79.7% (42.9% for CRD, 76.2% for CRD and schizophrenia, 100% for CRD and antisocial personality disorder, and 91.3% in the control group). Despite the differences we observed in PPI, this factor is of little use for discriminating between the different diagnostic groups and it acts more as a non-specific endophenotype in certain mental disorders, such as in patients with a dual diagnosis. MDPI 2021-02-20 /pmc/articles/PMC7924364/ /pubmed/33672693 http://dx.doi.org/10.3390/brainsci11020269 Text en © 2021 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 Gil-Miravet, Isis Fuertes-Saiz, Alejandro Benito, Ana Almodóvar, Isabel Ochoa, Enrique Haro, Gonzalo Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title | Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title_full | Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title_fullStr | Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title_full_unstemmed | Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title_short | Prepulse Inhibition in Cocaine Addiction and Dual Pathologies |
title_sort | prepulse inhibition in cocaine addiction and dual pathologies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924364/ https://www.ncbi.nlm.nih.gov/pubmed/33672693 http://dx.doi.org/10.3390/brainsci11020269 |
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