Increased synaptic dopamine in the putamen in restless legs syndrome

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Abstract

Study Objectives: Prior studies using positron emission tomography (PET) or single-photon emission computed tomography techniques have reported inconsistent findings regarding differences between patients with restless legs syndrome (RLS) and control patients in the striatal dopamine-2 receptor (D2R) binding potentials (BP). D2R-BP does reflect receptor-ligand interactions such as receptor affinity (Kd) and density (βmax) or neurotransmitter synaptic concentrations. Thus, differences in D2R-BP reflect changes in these primary factors. PET techniques are currently available to estimate D2R βmax and Kd. Design: Separate morning and evening PET scans were performed. The D2R-BP were measured in basal ganglia using [11C]raclopride. Setting: Academic medical center. Patients or Participants: Thirty-one patients with primary RLS and 36 age- and sex-matched control patients completed the study. Measures and Results: Patients with RLS had lower D2R-BP in putamen and caudate but not the ventral striatum. A subgroups analysis of those RLS patients who had not previously taken dopaminergic medications continued to show a significantly lower D2R-BP in the posterior putamen. D2R-BP did not differ between night and day for either group. D2R βmax and Kd did not differ significantly between patients with RLS and control patients but did show a strong and significant increase at night in the ventral striatum. Primary and secondary clinical measures of disease status failed to show any relation to D2R in any brain region. Conclusions: Given the lack of any difference in either βmax or Kd and the prior studies supporting an increase in presynaptic dopaminergic activity, the current changes found in D2R-BP likely reflect an increase in synaptic dopamine.

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Earley, C. J., Kuwabara, H., Wong, D. F., Gamaldo, C., Salas, R. E., Brašíc, J. R., … Allen, R. P. (2013). Increased synaptic dopamine in the putamen in restless legs syndrome. Sleep, 36(1), 51–57. https://doi.org/10.5665/sleep.2300

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