Efficacy of adjunctive Garcinia mangostana Linn (mangosteen) pericarp for bipolar depression: study protocol for a proof-of-concept trial.

Journal: Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999)

Volume: 41

Issue: 3

Year of Publication: 2019

Affiliated Institutions:  Deakin University, Innovation in Mental and Physical Health and Clinical Treatment (IMPACT) Strategic Research Centre, School of Medicine, Barwon Health, Geelong, Australia. Department of Psychiatry, The Melbourne Clinic, University of Melbourne, Richmond, Australia. Florey Institute for Neuroscience and Mental Health, University of Melbourne, Parkville, Australia. Orygen, National Centre of Excellence in Youth Mental Health, Parkville, Australia. Centre for Population Health Research, Deakin Health Economics, Deakin University, Geelong, Australia. Center of Excellence for Pharmaceutical Sciences, School of Pharmacy, North-West University, Potchefstroom, South Africa. Academic Department of Psychiatry, Northern Sydney Local Health District, St. Leonards, Australia.

Abstract summary 

Bipolar depression is characterized by neurobiological features including perturbed oxidative biology, reduction in antioxidant levels, and a concomitant rise in oxidative stress markers. Bipolar depression manifests systemic inflammation, mitochondrial dysfunction, and changes in brain growth factors. The depressive phase of the disorder is the most common and responds the least to conventional treatments. Garcinia mangostana Linn, commonly known as mangosteen, is a tropical fruit. The pericarp's properties may reduce oxidative stress and inflammation and improve neurogenesis, making mangosteen pericarp a promising add-on therapy for bipolar depression.Participants will receive 24 weeks of either 1,000 mg mangosteen pericarp or placebo per day, in addition to their usual treatment. The primary outcome is change in severity of mood symptoms, measured using the Montgomery-Åsberg Depression Rating Scale (MADRS), over the treatment phase. Secondary outcomes include global psychopathology, quality of life, functioning, substance use, cognition, safety, biological data, and cost-effectiveness. A follow-up interview will be conducted 4 weeks post-treatment.The findings of this study may have implications for improving treatment outcomes for those with bipolar disorder and may contribute to our understanding of the pathophysiology of bipolar depression.Australian and New Zealand Clinical Trial Registry, ACTRN12616000028404.

Authors & Co-authors:  Ashton Melanie M MM Berk Michael M Ng Chee H CH Hopwood Malcolm M Dodd Seetal S Turner Alyna A Brown Ellie E Jacka Felice N FN Cotton Susan M SM Khoo Jon-Paul JP Chatterton Mary Lou ML Kavanagh Bianca E BE Nadjidai Sarah E SE Lo Monaco Samantha L SL Harvey Brian H BH Sarris Jerome J Malhi Gin S GS Dowling Nathan L NL Dean Olivia M OM

Study Outcome 

Source Link: Visit source

Statistics
Citations :  Judd LL, Akiskal HS, Schettler PJ, Endicott J, Maser J, Solomon DA, et al. The long-term natural history of the weekly symptomatic status of bipolar I disorder. Arch Gen Psychiatry. 2002;59:530–7.
Authors :  19
Identifiers
Doi : 10.1590/1516-4446-2018-0114
SSN : 1809-452X
Study Population
Male,Female
Mesh Terms
Antioxidants
Other Terms
Study Design
Cross Sectional Study
Study Approach
Systemic Review
Country of Study
Publication Country
Brazil