The Role of Serotonin in Seizures
Imaging Serotoninergic Neurotransmission in Epilepsy
2 other identifiers
observational
46
1 country
1
Brief Summary
This study will investigate the role that a brain chemical called serotonin plays in seizures. Serotonin, present naturally in the brain, helps transmit signals between nerve cells. Glucose is a sugar that is the main fuel of the brain. Studying these two chemicals may help explain why people with epilepsy get seizures and are more likely to be depressed. Healthy volunteers and patients 18 to 60 years of age who have epilepsy with or without depression and whose seizures are not controlled by medication may be eligible for this study. Candidates are screened with a review of their medical history, a physical examination and an electroencephalogram (EEG, brain wave recording). Participants undergo the following procedures:
- Positron emission tomography (PET) scans: The first of three PET scans measures brain blood flow and the activity at some of the brain serotonin receptors (the parts of brain cells to which serotonin attaches). A second scan measures the amount of serotonin transported between brain cells. A third scan measures glucose use. The PET scanner is shaped like a doughnut. The subject lies on a bed that slides in and out of the scanner with his or her head inside the opening. A special mask is fitted to the subject s head to help keep it still during the procedure so the images will be clear. For the first scan, catheters (plastic tubes) are placed in an arm vein to inject a radioactive substance and in an artery in the wrist to collect blood samples. The other two scans require only the catheter in the arm.
- Magnetic resonance imaging: This test uses a strong magnetic field and radio waves to obtain images of the brain. The scanner is a metal cylinder surrounded by a strong magnetic field. The subject lies on a table that can slide in and out of the cylinder. Most scans last between 45 and 90 minutes. Subjects wear earplugs to muffle loud knocking noises that occur during scanning.
- Psychological evaluation: Subjects are interviewed and fill out questionnaires to help study sadness and depression in epilepsy.
- Blood draw: Blood tests look for differences in genes between people with epilepsy who are depressed and those who are not.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2007
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 20, 2007
CompletedFirst Submitted
Initial submission to the registry
February 22, 2007
CompletedFirst Posted
Study publicly available on registry
February 23, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
June 5, 2015
CompletedJuly 5, 2018
June 5, 2015
February 22, 2007
July 3, 2018
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Patients must have seizures documented by appropriate clinical and laboratory studies . This criterion will be established by studies performed by the referring physicians, preliminary screening in the NINDS Clinical Epilepsy Section outpatient clinic, or if necessary, inpatient video-EEG monitoring.
- Male and Female subjects aged between 18 and 60 years
- Healthy control subjects will also be recruited.
- Subjects must be able to give written informed consent prior to participation in this study.
You may not qualify if:
- Patients younger than 18 or older than 60 years old. There is evidence for reduced 5HT1A receptor binding in patients over 60.
- Patients with a known treatable seizure etiology such as neoplastic or infectious disease.
- Patients with MRI findings consistent with brain tumors, trauma or AVMs.
- Patients with progressive neurologic disorders.
- Patients with a history of significant medical disorders, or requiring treatment with drugs
- that can not be stopped, and would interfere with the study, except for antidepressants.
- Patients with cancer.
- Patients not capable of giving an informed consent.
- Patients who had seizure activity 24 hours prior to the study.
- Women who are pregnant or nursing
- Subjects who are current smokers, and cannot stop for at least two weeks before the PET scan, as smoking may affect serotonergic neurotransmission.
- Healthy subjects must be free from a personal history of seizure disorders
- Patients with coagulation abnormalities.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, 20892, United States
Related Publications (3)
Bromfield EB, Altshuler L, Leiderman DB, Balish M, Ketter TA, Devinsky O, Post RM, Theodore WH. Cerebral metabolism and depression in patients with complex partial seizures. Arch Neurol. 1992 Jun;49(6):617-23. doi: 10.1001/archneur.1992.00530300049010.
PMID: 1596197BACKGROUNDKanner AM. Depression in epilepsy: prevalence, clinical semiology, pathogenic mechanisms, and treatment. Biol Psychiatry. 2003 Aug 1;54(3):388-98. doi: 10.1016/s0006-3223(03)00469-4.
PMID: 12893113BACKGROUNDLambert MV, Robertson MM. Depression in epilepsy: etiology, phenomenology, and treatment. Epilepsia. 1999;40 Suppl 10:S21-47. doi: 10.1111/j.1528-1157.1999.tb00884.x.
PMID: 10609603BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
William H Theodore, M.D.
National Institute of Neurological Disorders and Stroke (NINDS)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
February 22, 2007
First Posted
February 23, 2007
Study Start
February 20, 2007
Study Completion
June 5, 2015
Last Updated
July 5, 2018
Record last verified: 2015-06-05