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Antioxidant defense system and family environment in adolescents with family history of psychosis
BACKGROUND: Our objective was to determine antioxidant defence activity in healthy controls (HC) and healthy unaffected second-degree relatives of patients with early onset psychosis (HC-FHP), and to assess its relationship with familiar environment measured using the Family Environment Scale (FES)....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539933/ https://www.ncbi.nlm.nih.gov/pubmed/23158023 http://dx.doi.org/10.1186/1471-244X-12-200 |
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author | Gonzalez-Pinto, Ana Martinez-Cengotitabengoa, Monica Arango, Celso Baeza, Immaculada Otero-Cuesta, Soraya Graell-Berna, Montserrat Soutullo, César Leza, Juan Carlos Micó, Juan Antonio |
author_facet | Gonzalez-Pinto, Ana Martinez-Cengotitabengoa, Monica Arango, Celso Baeza, Immaculada Otero-Cuesta, Soraya Graell-Berna, Montserrat Soutullo, César Leza, Juan Carlos Micó, Juan Antonio |
author_sort | Gonzalez-Pinto, Ana |
collection | PubMed |
description | BACKGROUND: Our objective was to determine antioxidant defence activity in healthy controls (HC) and healthy unaffected second-degree relatives of patients with early onset psychosis (HC-FHP), and to assess its relationship with familiar environment measured using the Family Environment Scale (FES). METHODS: We included 82 HC and 14 HC-FHP aged between 9 and 17 years. Total antioxidant status, lipid peroxidation, antioxidant enzyme activities and glutathione levels were determined in blood samples. RESULTS: There was a significant decrease in the total antioxidant level in the HC-FHP group compared with the HC group (OR = 2.94; p = 0.009), but no between-group differences in the Global Assessment of Functioning (GAF) scale scores. For the FES, the HC-FHP group had significantly higher scores in the cohesion (p = 0.007) and intellectual-cultural dimensions (p=0.025). After adjusting for these two FES dimensions, total antioxidant status remained significantly different between groups (OR = 10.86, p = 0.009). CONCLUSIONS: Although causal relationships cannot be assumed, we can state that family environment is not playing a role in inducing oxidative stress in these healthy subjects. It could be hypothesized that families with affected relatives protect themselves from psychosis with positive environmental factors such as cohesion and intellectual-cultural activities. |
format | Online Article Text |
id | pubmed-3539933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35399332013-01-10 Antioxidant defense system and family environment in adolescents with family history of psychosis Gonzalez-Pinto, Ana Martinez-Cengotitabengoa, Monica Arango, Celso Baeza, Immaculada Otero-Cuesta, Soraya Graell-Berna, Montserrat Soutullo, César Leza, Juan Carlos Micó, Juan Antonio BMC Psychiatry Research Article BACKGROUND: Our objective was to determine antioxidant defence activity in healthy controls (HC) and healthy unaffected second-degree relatives of patients with early onset psychosis (HC-FHP), and to assess its relationship with familiar environment measured using the Family Environment Scale (FES). METHODS: We included 82 HC and 14 HC-FHP aged between 9 and 17 years. Total antioxidant status, lipid peroxidation, antioxidant enzyme activities and glutathione levels were determined in blood samples. RESULTS: There was a significant decrease in the total antioxidant level in the HC-FHP group compared with the HC group (OR = 2.94; p = 0.009), but no between-group differences in the Global Assessment of Functioning (GAF) scale scores. For the FES, the HC-FHP group had significantly higher scores in the cohesion (p = 0.007) and intellectual-cultural dimensions (p=0.025). After adjusting for these two FES dimensions, total antioxidant status remained significantly different between groups (OR = 10.86, p = 0.009). CONCLUSIONS: Although causal relationships cannot be assumed, we can state that family environment is not playing a role in inducing oxidative stress in these healthy subjects. It could be hypothesized that families with affected relatives protect themselves from psychosis with positive environmental factors such as cohesion and intellectual-cultural activities. BioMed Central 2012-11-16 /pmc/articles/PMC3539933/ /pubmed/23158023 http://dx.doi.org/10.1186/1471-244X-12-200 Text en Copyright ©2012 Gonzalez-Pinto et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gonzalez-Pinto, Ana Martinez-Cengotitabengoa, Monica Arango, Celso Baeza, Immaculada Otero-Cuesta, Soraya Graell-Berna, Montserrat Soutullo, César Leza, Juan Carlos Micó, Juan Antonio Antioxidant defense system and family environment in adolescents with family history of psychosis |
title | Antioxidant defense system and family environment in adolescents with family history of psychosis |
title_full | Antioxidant defense system and family environment in adolescents with family history of psychosis |
title_fullStr | Antioxidant defense system and family environment in adolescents with family history of psychosis |
title_full_unstemmed | Antioxidant defense system and family environment in adolescents with family history of psychosis |
title_short | Antioxidant defense system and family environment in adolescents with family history of psychosis |
title_sort | antioxidant defense system and family environment in adolescents with family history of psychosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539933/ https://www.ncbi.nlm.nih.gov/pubmed/23158023 http://dx.doi.org/10.1186/1471-244X-12-200 |
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