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Plasma glutathione suggests oxidative stress is equally present in early- and late-onset bipolar disorder.
Singh, Nisha; McMahon, Hannah; Bilderbeck, Amy; Reed, Zoe E; Tunbridge, Elizabeth; Brett, Daniel; Geddes, John R; Churchill, Grant C; Goodwin, Guy M.
Afiliación
  • Singh N; Department of Psychiatry and Oxford Health NHS Trust, Warneford Hospital, University of Oxford, Oxford, UK.
  • McMahon H; Department of Pharmacology, University of Oxford, Oxford, UK.
  • Bilderbeck A; Centre for Neuroimaging Sciences, IoPPN, King's College, London, UK.
  • Reed ZE; Department of Psychiatry and Oxford Health NHS Trust, Warneford Hospital, University of Oxford, Oxford, UK.
  • Tunbridge E; Department of Psychiatry and Oxford Health NHS Trust, Warneford Hospital, University of Oxford, Oxford, UK.
  • Brett D; P1Vital, Wallingford, UK.
  • Geddes JR; Department of Psychiatry and Oxford Health NHS Trust, Warneford Hospital, University of Oxford, Oxford, UK.
  • Churchill GC; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Goodwin GM; Department of Psychiatry and Oxford Health NHS Trust, Warneford Hospital, University of Oxford, Oxford, UK.
Bipolar Disord ; 21(1): 61-67, 2019 02.
Article en En | MEDLINE | ID: mdl-29600584
OBJECTIVES: We previously demonstrated oxidative stress in bipolar patients and a relationship between the age of illness onset and total glutathione, a principal antioxidant. In this study, we sought to replicate these findings in a new cohort of patients. METHODS: We recruited bipolar patients from Warneford Hospital, Oxford, UK, of similar age and grouped them according to age of onset of illness. The early-onset group comprised patients with onset at <23 years, and the late group comprised patients with onset at >30 years. A third group, comprising age-matched healthy volunteers, was also included. Reduced and oxidized glutathione, cysteine, and cystine were determined in plasma, using high-performance liquid chromatography. Mitochondrial DNA copy number, measured in whole blood, was also compared between patients and healthy controls. RESULTS: Significant increases in oxidative stress were observed in the patient groups, compared with the control group; however, no differences in glutathione-related oxidative stress measures were detected between the early- and late-onset bipolar patient groups. No differences were observed in the amount of mitochondrial DNA, and there was no correlation with mood state. CONCLUSION: Using a more accurate method to quantify oxidative stress than in our previous study, we show that oxidative stress is a consistent feature of bipolar disorder. Although we did not reproduce our finding correlating age of onset of illness to oxidative stress, we have shown, once again, that oxidative stress is a consistent feature of bipolar disorder.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Bipolar / Estrés Oxidativo / Glutatión Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Bipolar Disord Asunto de la revista: PSIQUIATRIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno Bipolar / Estrés Oxidativo / Glutatión Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Bipolar Disord Asunto de la revista: PSIQUIATRIA Año: 2019 Tipo del documento: Article