Assessing midbrain neuromelanin and its relationship to reward learning in anorexia nervosa: Stage 1 of a registered report

Author:

Murray Stuart B.1ORCID,Diaz‐Fong Joel P.234,Mak Vienna W. T.2,Feusner Jamie D.23456

Affiliation:

1. Department of Psychiatry & Behavioral Sciences University of Southern California Los Angeles California USA

2. Centre for Addiction and Mental Health Toronto Ontario Canada

3. Institute of Medical Science, Temerty Faculty of Medicine University of Toronto Toronto Ontario Canada

4. Semel Institute for Neuroscience & Human Behavior, Department of Psychiatry & Biobehavioral Science University of California, Los Angeles Los Angeles California USA

5. Department of Psychiatry, Temerty Faculty of Medicine University of Toronto Toronto Ontario Canada

6. Department of Women's and Children's Health Karolinska Institutet Stockholm Sweden

Abstract

AbstractIntroductionAnorexia nervosa (AN) is a debilitating and potentially chronic eating disorder, characterized by low hedonic drive toward food, which has been linked with perturbations in both reward processing and dopaminergic activity. Neuromelanin‐sensitive magnetic resonance imaging (MRI) is an emerging method to index midbrain neuromelanin—a by‐product of dopaminergic synthesis. The assessment of midbrain neuromelanin, and its association with AN psychopathology and reward‐related processes, may provide critical insights into reward circuit function in AN.MethodsThis study will incorporate neuromelanin‐sensitive MRI into an existing study of appetitive conditioning in those with AN. Specifically, those with acute and underweight AN (N = 30), those with weight‐restored AN (N = 30), and age‐matched healthy controls (N = 30) will undergo clinical assessment of current and previous psychopathology, in addition to structural neuromelanin‐sensitive MRI, diffusion MRI, and functional MRI (fMRI) during appetitive conditioning.ConclusionThis study will be among the first to interrogate midbrain neuromelanin in AN—a disorder characterized by altered dopaminergic activity. Results will help establish whether abnormalities in the midbrain synthesis of dopamine are evident in those with AN and are associated with symptomatic behavior and reduced ability to experience pleasure and reward.

Funder

Klarman Family Foundation

Publisher

Wiley

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