Abstract

Tourette syndrome is a neurodevelopmental disorder associated with hyperactivity in dopaminergic networks. Dopaminergic hyperactivity in the basal ganglia has previously been linked to increased sensitivity to positive reinforcement and increases in choice impulsivity. In this study, we examine whether this extends to changes in temporal discounting, where impulsivity is operationalized as an increased preference for smaller-but-sooner over larger-but-later rewards. We assessed intertemporal choice in two studies including nineteen adolescents (age: mean[sd] = 14.21[±2.37], 13 male subjects) and twenty-five adult patients (age: mean[sd] = 29.88 [±9.03]; 19 male subjects) with Tourette syndrome and healthy age- and education matched controls. Computational modeling using exponential and hyperbolic discounting models via hierarchical Bayesian parameter estimation revealed reduced temporal discounting in adolescent patients, and no evidence for differences in adult patients. Results are discussed with respect to neural models of temporal discounting, dopaminergic alterations in Tourette syndrome and the developmental trajectory of temporal discounting. Specifically, adolescents might show attenuated discounting due to improved inhibitory functions that also affect choice impulsivity and/or the developmental trajectory of executive control functions. Future studies would benefit from a longitudinal approach to further elucidate the developmental trajectory of these effects.

Highlights

  • We did not find any difference in intertemporal choice in adults

  • Tourette syndrome (TS) is a complex neuropsychiatric disorder associated with developmental disturbances in dopaminergic transmission which possibly result in failure to control motor output [1, 2, 14, 15, 71]

  • Some studies point towards reductions in temporal discounting due to pharmacological elevation of DA levels, whereas others point to an increase [18]

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Summary

Introduction

Fewer studies have explored alterations in value-based decision-making in TS This question is of particular interest because motor and choice impulsivity might at least in part be supported by common neural systems. Regarding choice and motor impulsivity, the dorsal striatum might be a key region of interest where top down inhibitory processes (originating in the PFC) modulate the execution or the re-evaluation of choice outcomes [47] These anatomical regions and attributed functions might be affected in TS pathophysiology [48]. We compared adolescents (Study 1, Hamburg) and adults (Study 2, Cologne) with TS to controls, using two modified temporal discounting tasks to broaden the understanding of value based decisions in TS on one operational measure of choice impulsivity [32, 33]

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