7T MRS in depression associated with MetS

  • Research type

    Research Study

  • Full title

    Translating potential neuroimaging biomarkers into clinics: fingerprinting mood disorders related to metabolic syndrome (MetS)

  • IRAS ID

    313113

  • Contact name

    Antoine Cherix

  • Contact email

    antoine.cherix@ndcn.ox.ac.uk

  • Sponsor organisation

    University of Oxford / Research Governance, Ethics and Assurance

  • Duration of Study in the UK

    1 years, 11 months, 30 days

  • Research summary

    Mood disorders, and in particular depression, are a major burden on society and improving therapeutic strategies requires to better characterize their underlying pathophysiology and to identify reliable biological markers. Insulin resistance has been recently put forward as a potential link between metabolic deregulations, typically observed in metabolic syndrome (MetS), and depression. MetS has a high co-occurrence with depression and could thus represent an etiological factor for a large subset of patients with mood disorders. The goal of this project is to study how insulin signalling regulates brain metabolic homeostasis and impacts depressive behaviour. By combining neuroimaging and behavioural measurements in humans, this project aims at identifying translatable neuroimaging markers based on preclinical findings in mice. In particular, this project focuses on how magnetic resonance spectroscopy (MRS) can be exploited to provide useful imaging markers indicative of neuroenergetic impairments in brain structures of depressed patients.

  • REC name

    Wales REC 4

  • REC reference

    22/WA/0243

  • Date of REC Opinion

    15 Sep 2022

  • REC opinion

    Favourable Opinion