Reduced antioxidant defense in early onset first-episode psychosis: a case-control study

Background:Our objective is to determine the activity of the antioxidant defense system at admission in patients with early onset first psychotic episodes compared with a control group. Methods: Total antioxidant status (TAS) and lipid peroxidation (LOOH) were determined in plasma. Enzyme activities...

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Detalhes bibliográficos
Autores: Micó, Juan Antonio, Rojas Corrales, Maria Olga, Gibert Rahola, Juan, Parellada, Mara, Moreno, Dolores, Fraguas, David, Graell, Montserrat, Gil, Javier, Irazusta, Jon, Castro Fornieles, Josefina, Soutullo, Cesar, Arango, Celso, Otero, Soraya, Navarro, Ana, Baeza, Inmaculada, 1970-, Martínez Cengotitabengoa, Mónica, González-Pinto, Ana
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2011
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositório:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/35753
Acesso em linha:https://hdl.handle.net/2445/35753
Access Level:Acceso aberto
Palavra-chave:Psicosi
Glutatió
Estrès oxidatiu
Psychoses
Glutathione
Oxidative stress
Descrição
Resumo:Background:Our objective is to determine the activity of the antioxidant defense system at admission in patients with early onset first psychotic episodes compared with a control group. Methods: Total antioxidant status (TAS) and lipid peroxidation (LOOH) were determined in plasma. Enzyme activities and total glutathione levels were determined in erythrocytes in 102 children and adolescents with a first psychotic episode and 98 healthy controls. Results: A decrease in antioxidant defense was found in patients, measured as decreased TAS and glutathione levels. Lipid damage (LOOH) and glutathione peroxidase activity was higher in patients than controls. Our study shows a decrease in the antioxidant defense system in early onset first episode psychotic patients. Conclusions: Glutathione deficit seems to be implicated in psychosis, and may be an important indirect biomarker of oxidative stress in early-onset schizophrenia. Oxidative damage is present in these patients, and may contribute to its pathophysiology.