Expired Study
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Bethesda, Maryland 20892


Purpose:

Background: The brain releases signals to mark rewards for certain behavior. Some medications for Parkinson disease (PD) can cause some patients to engage in compulsive behavior, possibly because the medications affect this reward system. By using transcranial magnetic stimulation (TMS), researchers can study brain activity when an individual receives a reward. Objectives: To learn how the brains of people with PD behave when rewarded. To learn whether two common Parkinson medications (levodopa and pramipexole) change this behavior. To compare reward signals in the brains of healthy volunteers with reward signals in the brains of people with PD. Eligibility: Women between 50 and 80 years of age and men between 45 and 80 years of age. Participants will be divided into healthy volunteers and volunteers who have mild to moderate PD. Design: Prescreening will consist of a neurological examination and a series of questions about gambling habits and drug and alcohol use. Participation in a TMS study involving a computer game simulation of a slot machine: - Before the simulation, participants will receive TMS to establish a baseline response rate. - During the simulation, participants will play a game in which they will receive real money. TMS will be administered to each patient under three different conditions: - TMS administered when patients have not taken any Parkinson medication. - TMS administered after patients have taken levodopa. - TMS administered after patients have taken pramipexole....


Study summary:

The role of mesencephalic dopamine neurons in reward processing has been established in primates using electrophysiological techniques and in humans using functional neuroimaging. Their role is thought to be dual: i) they show sustained activity with the expectation of a future reward and ii) a phasic response after reward. Animal data indicate that these neurons, located in the midbrain areas A8-10, behave as a single functional unit when activated. They have rich projections to both the prefrontal and motor cortices where they synapse on interneurons and cortical pyramidal cells, producing primarily inhibition. Though their function is not fully understood, these projections clearly play an important role in motivation and learning. We have recently developed a pair of paradigms to detect a reward related signal in the primary motor cortex, where transcranial magnetic stimulation can be used to measure brief events. So far, we have tested healthy volunteers; we now intend to study Parkinson disease (PD) patients in order to help clarify the role of dopamine in effect of reward. The Parkinson patients will be tested both on and off levodopa/carbidopa and dopamine agonist medications. Our hypothesis is that the dopamine reward related signal will alter level of evocable inhibition in primary motor cortex. Using a behavioral paradigm that deliver intermittent reward, we aim to demonstrate, in treated and untreated PD patients a difference in the amount of cortical inhibition, i) when reward is expected compared to when reward is not expected and ii) after rewarded compared to unrewarded trials. We also aim to demonstrate a difference between their response and that of healthy controls.


Criteria:

- INCLUSION CRITERIA: HEALTHY SUBJECTS: -Age 45-70 years PATIENTS: - Mild-moderate disease (Hoehn and Yahr stage 1-2). - Age 45-70 yrs EXCLUSION CRITERIA: - Pre-menopausal status in women: Preliminary data in healthy, cycling women suggests that the variation in paired-pulse inhibition caused by the menstrual cycle may obscure the change in the response induced by the behavioral task. - Significant neurological or psychiatric history other than PD - Exposure to DA agonists within a month of study - History of habitual gambling, defined as either visiting casinos more than once per month or playing cards for money more than once per week or gambling over the internet more than once per month - Habitual consumption of more than two drinks a day, marijuana more than once a week or any other illicit drug use within the last three months - Significant abnormality on neurological examination other than PD related signs - Metal in the cranial cavity or eye, pacemaker, implanted pumps or stimulators - Use of non-PD related medications affecting the DA system, such as phenothiazine antihistamines (promethazine), antiemetics or decongestants in the last month


Study is Available At:


Original ID:

080023


NCT ID:

NCT00558766


Secondary ID:

08-N-0023


Study Acronym:


Brief Title:

Motor Cortex Reward Signaling in Parkinson Disease


Official Title:

Motor Cortex Reward Signaling in Parkinson Disease


Overall Status:

Completed


Study Phase:

N/A


Genders:

N/A


Minimum Age:

45 Years


Maximum Age:

70 Years


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

National Institutes of Health Clinical Center (CC)


Oversight Authority:

United States: Federal Government


Reasons Why Stopped:


Study Type:

Observational


Study Design:


Number of Arms:

0


Number of Groups:

0


Total Enrollment:

35


Enrollment Type:

Actual


Study Dates

Start Date:November 8, 2007
Completion Date:June 13, 2011
Verification Date:June 13, 2011
Last Changed Date:June 30, 2017
First Received Date:November 14, 2007

Study Outcomes

There are no available Study Outcomes

Study Interventions

There are no available Study Interventions

Study Arms

There are no available Study Arms

Study Agencies

Agency Class:NIH
Agency Type:Lead Sponsor
Agency Name:National Institute of Neurological Disorders and Stroke (NINDS)

Sample and Retention Information

There are no available Sample and Retention Information

Study References

Reference Type:Reference
Citation:Strobel A, Spinath FM, Angleitner A, Riemann R, Lesch KP. Lack of association between polymorphisms of the dopamine D4 receptor gene and personality. Neuropsychobiology. 2003;47(1):52-6.
PMID:12606846
Reference Type:Reference
Citation:Cohen MX, Young J, Baek JM, Kessler C, Ranganath C. Individual differences in extraversion and dopamine genetics predict neural reward responses. Brain Res Cogn Brain Res. 2005 Dec;25(3):851-61. Epub 2005 Nov 11.
PMID:16289773
Reference Type:Reference
Citation:Avanzi M, Uber E, Bonfà F. Pathological gambling in two patients on dopamine replacement therapy for Parkinson's disease. Neurol Sci. 2004 Jun;25(2):98-101.
PMID:15221629

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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