DYT1 dystonia increases risk taking in humans

Author:

Arkadir David1,Radulescu Angela23,Raymond Deborah4,Lubarr Naomi4,Bressman Susan B4,Mazzoni Pietro5,Niv Yael23ORCID

Affiliation:

1. Department of Neurology, Hadassah Medical Center and the Hebrew University, Jerusalem, Israel

2. Department of Psychology, Princeton University, Princeton, United States

3. Princeton Neuroscience Institute, Princeton University, Princeton, United States

4. Department of Neurology, Beth Israel Medical Center, New York, United States

5. The Neurological Institute, Columbia University, New York, United States

Abstract

It has been difficult to link synaptic modification to overt behavioral changes. Rodent models of DYT1 dystonia, a motor disorder caused by a single gene mutation, demonstrate increased long-term potentiation and decreased long-term depression in corticostriatal synapses. Computationally, such asymmetric learning predicts risk taking in probabilistic tasks. Here we demonstrate abnormal risk taking in DYT1 dystonia patients, which is correlated with disease severity, thereby supporting striatal plasticity in shaping choice behavior in humans.

Funder

Parkinson's Disease Foundation

National Institutes of Health

National Institute for Psychobiology in Israel, Hebrew University of Jerusalem

Alfred P. Sloan Foundation

National Institute of Mental Health

Army Research Office

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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