Your browser doesn't support javascript.
loading
Glutathione levels and activities of glutathione metabolism enzymes in patients with schizophrenia: A systematic review and meta-analysis.
Tsugawa, Sakiko; Noda, Yoshihiro; Tarumi, Ryosuke; Mimura, Yu; Yoshida, Kazunari; Iwata, Yusuke; Elsalhy, Muhammad; Kuromiya, Minori; Kurose, Shin; Masuda, Fumi; Morita, Shinji; Ogyu, Kamiyu; Plitman, Eric; Wada, Masataka; Miyazaki, Takahiro; Graff-Guerrero, Ariel; Mimura, Masaru; Nakajima, Shinichiro.
Afiliación
  • Tsugawa S; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Noda Y; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Tarumi R; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Mimura Y; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Yoshida K; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Iwata Y; Pharmacogenetic Research Clinic, Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Elsalhy M; Multimodal Imaging Group, University of Toronto, Toronto, ON, Canada.
  • Kuromiya M; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Kurose S; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Masuda F; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Morita S; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Ogyu K; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Plitman E; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Wada M; Multimodal Imaging Group, University of Toronto, Toronto, ON, Canada.
  • Miyazaki T; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Graff-Guerrero A; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
  • Mimura M; Multimodal Imaging Group, University of Toronto, Toronto, ON, Canada.
  • Nakajima S; Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
J Psychopharmacol ; 33(10): 1199-1214, 2019 10.
Article en En | MEDLINE | ID: mdl-31039654
BACKGROUND: Glutathione is among the important antioxidants to prevent oxidative stress. However, the relationships between abnormality in the glutathione system and pathophysiology of schizophrenia remain uncertain due to inconsistent findings on glutathione levels and/or glutathione-related enzyme activities in patients with schizophrenia. METHODS: A systematic literature search was conducted using Embase, Medline, PsycINFO, and PubMed. Original studies, in which three metabolite levels (glutathione, glutathione disulfide, and total glutathione (glutathione+glutathione disulfide)) and five enzyme activities (glutathione peroxidase, glutathione reductase, glutamate-cysteine ligase, glutathione synthetase, and glutathione S-transferase) were measured with any techniques in both patients with schizophrenia and healthy controls, were included. Standardized mean differences were calculated to determine the group differences in the glutathione levels with a random-effects model. RESULTS: We identified 41, 9, 15, 38, and seven studies which examined glutathione, glutathione disulfide, total glutathione, glutathione peroxidase, and glutathione reductase, respectively. Patients with schizophrenia had lower levels of both glutathione and total glutathione and decreased activity of glutathione peroxidase compared to controls. Glutathione levels were lower in unmedicated patients with schizophrenia than those in controls while glutathione levels did not differ between patients with first-episode psychosis and controls. CONCLUSIONS: Our findings suggested that there may be glutathione deficits and abnormalities in the glutathione redox cycle in patients with schizophrenia. However, given the small number of studies examined the entire glutathione system, further studies are needed to elucidate a better understanding of disrupted glutathione function in schizophrenia, which may pave the way for the development of novel therapeutic strategies in this disorder.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esquizofrenia / Estrés Oxidativo / Glutamato-Cisteína Ligasa / Glutatión / Glutatión Peroxidasa / Glutatión Reductasa / Glutatión Sintasa / Glutatión Transferasa Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Psychopharmacol Asunto de la revista: PSICOFARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esquizofrenia / Estrés Oxidativo / Glutamato-Cisteína Ligasa / Glutatión / Glutatión Peroxidasa / Glutatión Reductasa / Glutatión Sintasa / Glutatión Transferasa Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Psychopharmacol Asunto de la revista: PSICOFARMACOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón