Investigation of Serotonin Receptor Binding in the Migraine Brain Using Positron Emission Tomography

Sponsor
Danish Headache Center (Other)
Overall Status
Completed
CT.gov ID
NCT02309606
Collaborator
(none)
56
1
35
1.6

Study Details

Study Description

Brief Summary

Migraine affects 16% of the world population and is one of the most disabling of all disorders. It is a complex brain disorder characterized primarily by recurrent headache attacks. The signaling molecule serotonin (5-hydroxytryptamine, 5-HT) has for decades been thought to play a central role in migraine pathophysiology. The most effective class of abortive migraine drugs, the triptans, act on 5-HT receptors. However, the migraine-specific actions of serotonin and the mechanisms of triptans are still unknown. In this project the investigators will use high-resolution positron emission tomography and specific radioligands to investigate the significance of serotonin in migraine. Two newly developed radioligands that are specific for the 5-HT1B and 5-HT4 receptor, respectively, will be applied. To investigate the level and distribution of serotonin in the migraine brain the investigators will compare the binding of these ligands in episodic migraine patients with healthy controls. In addition, the investigators will include chronic migraine patients to evaluate the relation between the level of serotonin in the brain and the frequency of migraine attacks. To investigate the changes in the serotonin level during a migraine attack and the effects of triptans on the central nervous system the investigators will repeat the scans using the 5-HT1B specific ligand during induced migraine attacks and following treatment with sumatriptan. The results from this study will shed light on the role of serotonin in the migraine brain and elucidate the migraine-specific action of triptans. This will improve our understanding of the migraine pathophysiology and, potentially, facilitate the development of more efficient treatment of migraine.

Condition or Disease Intervention/Treatment Phase
  • Other: PET scan with 5-HT receptor ligands

Study Design

Study Type:
Observational
Actual Enrollment :
56 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Investigation of Serotonin Receptor Binding in the Migraine Brain Using Positron Emission Tomography
Actual Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Aug 1, 2017
Actual Study Completion Date :
Dec 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Migraine without aura

Migraine patients suffering from migraine 0-4 days per month.

Other: PET scan with 5-HT receptor ligands
Interictal episodic migraine patients and healthy controls will be scanned with a 5-HT1B and a 5-HT4 receptor radioligand. Episodic migraine patients will further be scanned during a cilostazol induced migraine attack and after treatment with sumatriptan. Chronic migraine patients will be scanned with only the 5-HT4 receptor radioligand.

Healthy controls

Healthy controls with no history of migraine or other primary headaches.

Other: PET scan with 5-HT receptor ligands
Interictal episodic migraine patients and healthy controls will be scanned with a 5-HT1B and a 5-HT4 receptor radioligand. Episodic migraine patients will further be scanned during a cilostazol induced migraine attack and after treatment with sumatriptan. Chronic migraine patients will be scanned with only the 5-HT4 receptor radioligand.

Chronic migraine

Migraine patients with chronic migraine

Other: PET scan with 5-HT receptor ligands
Interictal episodic migraine patients and healthy controls will be scanned with a 5-HT1B and a 5-HT4 receptor radioligand. Episodic migraine patients will further be scanned during a cilostazol induced migraine attack and after treatment with sumatriptan. Chronic migraine patients will be scanned with only the 5-HT4 receptor radioligand.

Outcome Measures

Primary Outcome Measures

  1. Differences in binding of the 5-HT1B radioligand [Up to 1 year]

    Differences in bindingpotentials for the 5-HT1B ligand between migraine patients and healthy controls will be assessed using the Simplified Reference Tissue Model.

  2. Differences in binding of the 5-HT4 radioligand [Up to 1 year]

    Differences in bindingpotentials for the 5-HT4 ligand between migraine patients and healthy controls will be assessed using the Simplified Reference Tissue Model.

  3. Differences in binding of the 5-HT4 radioligand [Up to 1 year]

    Differences in bindingpotentials for the 5-HT4 ligand between chronic migraine patients and healthy controls and between chronic and episodic migraine patients will be assessed using the Simplified Reference Tissue Model.

  4. Correlation with migraine frequency and 5-HT4 receptor binding [Up to 1 year]

    Correlations between migraine days and 5-HT4 receptor binding will be investigated using pooled data from episodic and chronic migraine patients on migraine frequency and their 5-HT4 receptor binding potentials assessed using the simplified reference tissue model

  5. Differences in binding of the 5-HT1B radioligand [Up to 1 year]

    Differences in binding between ictal and interictal binding and between ictal and post-treatment binding in episodic migraine patients will be assessed using the simplified reference tissue model

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria, both groups:

• Written informed consent

Inclusion Criteria, episodic migraine patients:
  • Migraine without aura according to the International Headache Society (IHS) 0-4 days per month

  • The migraine is treatable with sumatriptan

Inclusion Criteria, chronic migraine patients: Fulfill IHS criteria for chronic migraine

Inclusion Criteria, healthy controls:
  • Do not suffer from migraine according to IHS

  • Do not have any first degree relatives with migraine

Exclusion Criteria:
  • Tension type headache more than 5 days per month during the last year.

  • Tension type headache on the experimental day.

  • Any other primary headache disorder

  • Migraine 48 hour before and after the experimental day (only episodic migraine patients)

  • Use of antimigraine medication or pain-killer on the experimental day before PET

  • Pregnant or breastfeeding women.

  • Contraindications against MRI.

  • History or clinical sign of cardio- or cerebrovascular disease.

  • Untreated severe mental disorder or drug abuse.

  • Other diseases or disorders interpreted, by the examining doctor, to interfere with participation in the study.

  • Not accepting information about potential accidental findings during the experiment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Danish Headache Center, Glostrup Hospital Glostrup, Copenhagen Denmark 2600

Sponsors and Collaborators

  • Danish Headache Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marie Deen Christensen, Medical Doctor, Danish Headache Center
ClinicalTrials.gov Identifier:
NCT02309606
Other Study ID Numbers:
  • H-6-2014-057
First Posted:
Dec 5, 2014
Last Update Posted:
Jan 31, 2018
Last Verified:
Jan 1, 2018
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 31, 2018