DYT1 dystonia increases risk taking in humans

Elife. 2016 Jun 1:5:e14155. doi: 10.7554/eLife.14155.

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.

Keywords: dystonia; human; neuroscience; reinforcement learning; risk aversion.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, N.I.H., Extramural

MeSH terms

  • Dystonia / genetics*
  • Dystonia / psychology*
  • Humans
  • Molecular Chaperones / genetics*
  • Risk-Taking*

Substances

  • Molecular Chaperones
  • TOR1A protein, human