Insomnia Clinical Trial
Official title:
The Sleepless Brain: Neuroimaging Support for a Differential Diagnosis of Insomnia
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.
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