Imaging of Brain Receptors in Healthy Volunteers and in Patients With Schizophrenia
NCT ID: NCT00061789
Last Updated: 2008-03-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
100 participants
INTERVENTIONAL
2003-02-28
2004-08-31
Brief Summary
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The following individuals between 21 and 50 years of age (or between 21 and 80 years of age for Group 1 only) are eligible for this study: healthy non-smokers (Group 1); schizophrenia patients who smoke (Group 2); schizophrenia patients who do not smoke (Group 3); healthy smokers (Group 4); healthy non-smokers (Group 5). Patients with schizophrenia must be taking olanzapine (Zyprexa) or risperidone (Risperdal) for at least 6 months. All candidates will be screened at the first visit. Group 1 participants will have three more visits; Groups 2 through 5 will have two more visits.
Visit 1
All participants will be screened with physical and neurological examinations; blood and urine tests; and neuropsychological tests to assess their ability to learn and remember words and numbers, to pay attention, and to quickly perform motor tasks, such as putting pegs into a piece of wood. In addition, they will have an eye movement test and event-related potential testing. For the eye test, the subject sits in a chair and leans forward with the chin on a chin rest. A band is tied around the head and very small amounts of invisible (infrared) light are shined into the eyes. The light is reflected back and measured. Wire electrodes are placed around the area of the eye and cheek to monitor eye blinks and eye movements. Subjects are asked to follow a light with their eyes and to look away from a light. For event- related potential testing, electrodes are placed on the scalp, forehead and cheeks, and brain activity is recorded while the subject identifies particular pictures and sounds.
Visit 2 (and Visit 3 for Group 1)
Participants will have a SPECT scan. On the night before the scan, the day of the scan, and for 4 days after the scan, subject take an oral dose of potassium iodide to protect the thyroid gland from the radioactive tracer used in the SPECT procedure. (Individuals allergic to potassium iodide will take potassium perchlorate instead.) For the SPECT scan, small radioactive markers containing 99mTc are glued to the subject's head. Two catheters (thin, flexible tubes) are placed in veins in the arms to inject the radioactive tracer \[123I\]5-I-A-85380 and to draw blood samples. During the scan, the subject lies on a bed with his or her head held still with a headholder. The scans are taken over a 9-hour period after injection of the tracer injection. An electrocardiogram, respiration, and blood pressure measures are taken before injection of \[123I\]5-I-A-85380, then 5 minutes after the injection, and again 30 to 60 minutes after the injection. Breath samples are collected every 60 minutes. Blood and urine samples are collected 5 to 6 hours after starting the scan. Group 1 subjects will have a second SPECT scan within 4 weeks of the first.
Visit 3 (Visit 4 for Group 1)
Participants will have a magnetic resonance imaging (MRI) scan. For this procedure, the subject lies on a table that slides into a narrow metal cylinder with a strong magnetic field for the scan. The scanner uses a magnetic field and radio waves to produce images that show structural and chemical changes in tissues. The test lasts up to 1 hour.
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Detailed Description
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We plan to use a new single photon emission computed tomography (SPECT) tracer, \[(123)I\]5-I-A-85380, which appears suitable for imaging the high affinity Alpha 4 Beta 2 subtype of nAChRs. We plan to compare four groups, 1) schizophrenia smokers, 2) schizophrenia non-smokers, 3) healthy smokers, and 4) healthy non-smokers. All patients will be on stable doses of olanzapine or risperidone. In addition to comparing \[(123)I\]5-I-A-85380 binding among these groups, relationship will be studied between psychiatric symptoms or cognitive dysfunction and the SPECT measurement of the receptors. Further, to study the reliability of the SPECT measurement, a test retest study will be preformed in healthy subjects with a wide range. The proposed study will explore the roles of nAChRs in the psychiatric symptoms, particularly the cognitive deficits in schizophrenia, which is the central impairment of this disorder. New findings in this research will lead to enhanced treatment of the cognitive deficits.
Conditions
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Study Design
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TREATMENT
Interventions
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SPECT Imaging of Nicotinic Acetylcholine Receptors in Brain
Eligibility Criteria
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Inclusion Criteria
Healthy Diagnosis;
21-80 years;
No Cigarette Smoking;
Plasma Cotinine less than 3 ng/mL;
No olanzapine or risperidone
Smoker Patients-Group 2:
Diagnosis of Schizophrenia;
21-50 years;
Cigarette Smoking greater than 20 per day and greater than 5 years;
Plasma Cotinine greater than 100 ng/mL;
Olanzapine or risperidone greater than 6 mo. and same dose for 2 weeks
Non-Smoker Patients-Group 3:
Diagnosis of Schizophrenia;
21-50 years;
No Cigarette Smoking;
Plasma Cotinine less than 3 ng/mL;
Olanzapine or risperidone greater than 6 mo. and same dose for 2 weeks
Smoker Controls-Group 4:
Healthy Diagnosis;
21-50 years;
Cigarette Smoking greater than 20 per day and greater than 5 years;
Plasma Cotinine greater than 100 ng/mL;
No olanzapine or risperidone
Non-Smoker Controls-Group 5:
Healthy Diagnosis;
21-50 years;
No Cigarette Smoking;
Plasma Cotinine less than 3 ng/mL;
No olanzapine or risperidone
ALL
Yes
Sponsors
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National Institute of Mental Health (NIMH)
NIH
Locations
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National Institute of Mental Health (NIMH)
Bethesda, Maryland, United States
Countries
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Other Identifiers
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03-M-0003
Identifier Type: -
Identifier Source: secondary_id
030003
Identifier Type: -
Identifier Source: org_study_id
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