The Sleepless Brain: Neuroimaging Support for a Differential Diagnosis of Insomnia

NCT ID: NCT02821234

Last Updated: 2017-08-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-09-01
• Study Completion Date: 2017-04-03

Brief Summary

One-tenth of the population suffers from insomnia, increasing their risk on other health problems such as depression. Self-reported sleep quality only was historically leading for insomnia diagnosis, but more recently a state of 24-hour hyperarousal has been associated with insomnia, either physiological (increased heart rate, higher frequency EEG) or predominant cognitive-emotional hyperarousal (worry, rumination, repetitive thoughts). Strong evidence shows that those suffering from insomnia with physiological hyperarousal are at higher risk of short and long term severe health problems such as inflammation and hypertension than the group without physiological hyperarousal. The neurophysiological basis of these insomnia phenotypes has however barely been investigated, although its results can have major consequences for how this limiting condition will be treated.

To support the development of a differential diagnosis of insomnia, structural and functional brain connectivity in insomnia patients with different levels of hyperarousal will be investigated and related to sleep variables. Investigators will compare the insomnia group to a normal sleeping control group. Investigators expect that the emotion processing circuit (amygdala-ventromedial prefrontal cortex) is a) more affected in insomniacs compared to normal sleeping controls and b) the directionality of this effect to depend on the level and type of hyperarousal in insomniacs. Further, investigators expect c) amygdala activity to be positive correlated with physiological hyperarousal level and d) prefrontal activity to be positively correlated with cognitive-emotional hyperarousal level. Investigators expect a higher physiological hyperarousal level to be reflected in affected afferent pathways of the amygdala towards the ventromedial prefrontal cortex and investigators expect higher cognitive-emotional hyperarousal to be related to affected efferent pathways from the ventromedial prefrontal cortex to the amygdala. Investigators expect sleep quality to play a mediating role in both types of hyperarousal and their brain activation patterns in insomnia patients and normal sleeping controls.

These data can lead to the definition of new insomnia phenotypes and to new customized and effective insomnia treatment, focused not only on improving sleep but also on changing dysfunctional hyperarousal levels that currently put insomniacs at risk of numerous severe health problems.

Conditions

Insomnia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Insomnia group

Patients with insomnia: sleep complaints, of at least 3 nights a week, for at least 3 months, affected daytime functioning, objectified low sleep quality (SE \<85%) with 10 days actigraphy occurred in the last 2 months

Group Type: EXPERIMENTAL

MRI

Intervention Type: OTHER

Control group

Volunteer without sleep problems either self-reported or objectified through actigraphy (SE ≥85%)

Group Type: EXPERIMENTAL

MRI

Intervention Type: OTHER

Interventions

MRI

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Insomnia group: patients with insomnia: sleep complaints, of at least 3 nights a week, for at least 3 months, affected daytime functioning.
• control group: no self-reported sleep problems in the last 2 months.
• 20-50 years old.
• Male or female.
• having given written informed consent to participate in the research project.

Exclusion Criteria

• Night and shift-workers.
• Psychiatric disorder: clinical mood disorder, anxiety disorder, psychosis, bipolar disorder.
• For insomnia group: all sleep disorders other than persistent insomnia.
• For control group: all sleep disorders.
• Progressive neurological diseases that include restless legs syndrome.
• Cardiovascular disease other than treated hypertension.
• Unstable respiratory or endocrinological diseases.
• Drug addiction, alcohol addiction during the previous 6 months.
• Having undertaken trans-meridian travel (± 3H) in the previous 1 month.
• Pregnant or lactating women.
• Chronic pain.
• Hypnotic and psychotropic medication taking or stopped less than 5 half-life periods of molecules before screening V0.
• Patient participating to any other interventional study.
• For MRI: presence of a ferromagnetic foreign body (in particular certain intracranial clips, certain cardiac valves, intraocular foreign body, or subject having worked with metals), the presence of an implanted pacemaker, subject with cardiac or brain valves of ventricular derivation (risk of maladjustment), claustrophobia.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Institut des Maladies Neurodégénératives (UMR5293)

UNKNOWN

Sponsor Role: collaborator

University Hospital, Bordeaux

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU de Bordeaux

Bordeaux, , France

Countries

France

References

Sanz-Arigita E, Daviaux Y, Joliot M, Dilharreguy B, Micoulaud-Franchi JA, Bioulac S, Taillard J, Philip P, Altena E. Brain reactivity to humorous films is affected by insomnia. Sleep. 2021 Sep 13;44(9):zsab081. doi: 10.1093/sleep/zsab081.

Reference Type: DERIVED

PMID: 33772591 (View on PubMed)

Other Identifiers

CHUBX 2016/05

Identifier Type: -

Identifier Source: org_study_id