Mesocorticolimbic hemodynamic response in Parkinson's disease patients with compulsive behaviors. Issue 11 (19th June 2017)

• Record Type: Journal Article
• Authors: Claassen, Daniel O.; Stark, Adam J.; Spears, Charis A.; Petersen, Kalen J.; van Wouwe, Nelleke C.; Kessler, Robert M.; Zald, David H.; Donahue, Manus J.
• Is Part Of: Movement disorders. Volume 32:Issue 11(2017)
• Page Start: 1574
• Page End: 1583
• Publication Date: 2017-06-19
• Subjects: cerebral blood flow -- dopamine -- impulsive compulsive behaviors -- impulse control disorder -- Parkinson's disease; Movement disorders -- Periodicals; 610
• DOI: 10.1002/mds.27047
• Languages: English
• ISSNs: 0885-3185

Abstract

ABSTRACT: Background: PD patients treated with dopamine therapy can develop maladaptive impulsive and compulsive behaviors, manifesting as repetitive participation in reward‐driven activities. This behavioral phenotype implicates aberrant mesocorticolimbic network function, a concept supported by past literature. However, no study has investigated the acute hemodynamic response to dopamine agonists in this subpopulation. Objectives: We tested the hypothesis that dopamine agonists differentially alter mesocortical and mesolimbic network activity in patients with impulsive‐compulsive behaviors. Methods: Dopamine agonist effects on neuronal metabolism were quantified using arterial‐spin‐labeling MRI measures of cerebral blood flow in the on ‐dopamine agonist and off ‐dopamine states. The within‐subject design included 34 PD patients, 17 with active impulsive compulsive behavior symptoms, matched for age, sex, disease duration, and PD severity. Results: Patients with impulsive‐compulsive behaviors have a significant increase in ventral striatal cerebral blood flow in response to dopamine agonists. Across all patients, ventral striatal cerebral blood flow on ‐dopamine agonist is significantly correlated with impulsive‐compulsive behavior severity (Questionnaire for Impulsive Compulsive Disorders in Parkinson's Disease‐ Rating Scale). Voxel‐wise analysis of dopamine agonist–induced cerebral blood flow revealed group differences in mesocortical (ventromedial prefrontal cortex; insular cortex), mesolimbic (ventral striatum), and midbrain (SN; periaqueductal gray) regions. Conclusions: These results indicate that dopamine agonist therapy can augment mesocorticolimbic and striato‐nigro‐striatal network activity in patients susceptible to impulsive‐compulsive behaviors. Our findings reinforce a wider literature linking studies of maladaptive behaviors to mesocorticolimbic networks and extend our understanding of biological mechanisms of impulsive compulsive behaviors in PD. © 2017 International Parkinson and Movement Disorder Society