Altered volumetric and functional connectivity of the habenula in chronic insomnia disorder
Jingjing Sun1, Kai Zhang2, Panpan Li1
1Zhenjiang Mental Health Center, Zhenjiang Fifth Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Insights
Chronic insomnia disorder involves altered habenula connectivity, particularly the left habenula
Area of Science:
- Neuroimaging
- Neuroscience
- Brain Connectivity
Background:
- The habenula (Hb) is recognized for its roles in sleep and emotion processing.
- Its specific involvement in chronic insomnia disorder (CID) is not well understood.
- Investigating the habenula's structure and connectivity in CID is crucial.
Purpose of the Study:
- To examine structural characteristics of the habenula in CID patients.
- To assess functional connectivity (FC) of the habenula with brain networks in CID.
- To identify neuroimaging markers for CID pathophysiology.
Main Methods:
- Structural MRI (sMRI) and resting-state fMRI (rs-fMRI) were used.
- 42 CID patients and 31 healthy controls (HC) participated.
- Clinical questionnaires and neuroimaging data were collected and analyzed.
Main Results:
- No significant differences in habenula volume or laterality were found between groups.
- CID patients showed altered left habenula FC with frontal, angular, and caudate regions.
- Decreased left habenula connectivity with somatomotor (SM) and dorsal attention networks (DAN) was observed.
Conclusions:
- Chronic insomnia disorder is associated with asymmetric habenula functional connectivity.
- Impaired connectivity between the left habenula and SM/DAN networks is a key finding.
- These FC abnormalities, without structural changes, offer insights into CID and suggest the left habenula as a therapeutic target.
Background:
Previous findings have demonstrated that habenula (Hb) is a key hub for sleep regulation and emotion processing. However, its role in chronic insomnia disorder (CID) remains understudied. This study aimed to investigate the structural characteristics of the Hb and its functional connectivity (FC) with large-scale brain networks in CID patients.
Methods:
A total of 42 CID patients and 31 age-, gender-, and education-matched healthy controls (HC) completed clinical questionnaires, structural magnetic resonance imaging (sMRI) and resting-state fMRI (rs-fMRI).
Results:
No significant group differences were observed in the relative volumes or the laterality index between CID patients and HC. However, voxel-wise FC analysis showed increased FC between the left Hb and the right inferior frontal gyrus, right middle frontal gyrus, and left angular gyrus in CID patients, alongside decreased FC between the left Hb and left inferior frontal gyrus, left precentral gyrus, and right caudate nucleus. The right Hb exhibited decreased FC with the right middle cingulate cortex, supramarginal gyrus and postcentral gyrus. Region-of-interest (ROI)-wise analysis further demonstrated that the left Hb had significantly decreased connectivity with the posterior/anterior somatomotor networks (SM-d, SM-v) and posterior dorsal attention network (DAN-p) in CID patients.
Conclusion:
Our findings indicate that CID is characterized by asymmetric FC abnormalities of the bilateral Hb, particularly impaired connectivity between the left Hb and SM and DAN networks, without structural changes. These aberrations provide novel neuroimaging insights into the pathophysiology of CID and highlight the left Hb as a potential target for targeted interventions.
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