Abnormal dynamic functional connectivity of hippocampal subregions associated with working memory impairment in
Lai Shunkai1,2, Ting Su1,3, Shuming Zhong2
1Medical Imaging Center, First Affiliated Hospital of Jinan University, Guangzhou 510630, China.
Background:
Previous studies have demonstrated structural and functional changes of the hippocampus in patients with major depressive disorder (MDD). However, no studies have analyzed the dynamic functional connectivity (dFC) of hippocampal subregions in melancholic MDD. We aimed to reveal the patterns for dFC variability in hippocampus subregions - including the bilateral rostral and caudal areas and its associations with cognitive impairment in melancholic MDD.
Methods:
Forty-two treatment-naive MDD patients with melancholic features and 55 demographically matched healthy controls were included. The sliding-window analysis was used to evaluate whole-brain dFC for each hippocampal subregions seed. We assessed between-group differences in the dFC variability values of each hippocampal subregion in the whole brain and cognitive performance on the MATRICS Consensus Cognitive Battery (MCCB). Finally, association analysis was conducted to investigate their relationships.
Results:
Patients with melancholic MDD showed decreased dFC variability between the left rostral hippocampus and left anterior lobe of cerebellum compared with healthy controls (voxel p < 0.005, cluster p < 0.0125, GRF corrected), and poorer cognitive scores in working memory, verbal learning, visual learning, and social cognition (all p < 0.05). Association analysis showed that working memory was positively correlated with the dFC variability values of the left rostral hippocampus-left anterior lobe of the cerebellum (r = 0.338, p = 0.029) in melancholic MDD.
Conclusions:
These findings confirmed the distinct dynamic functional pathway of hippocampal subregions in patients with melancholic MDD, and suggested that the dysfunction of hippocampus-cerebellum connectivity may be underlying the neural substrate of working memory impairment in melancholic MDD.
Insights
Major depressive disorder (MDD) with melancholic features shows altered hippocampus connectivity. This dysfunction, particularly involving the hippocampus and cerebellum, is linked to working memory deficits in patients.
Area of Science:
- Neuroscience
- Psychiatry
- Cognitive Science
Background:
- Previous research indicates hippocampal structural and functional changes in major depressive disorder (MDD).
- Dynamic functional connectivity (dFC) of hippocampal subregions in melancholic MDD has not been previously analyzed.
- This study investigates dFC variability in hippocampal subregions and its association with cognitive impairment in melancholic MDD.
Purpose of the Study:
- To analyze dFC variability in hippocampal subregions (rostral and caudal) in melancholic MDD.
- To examine the association between altered dFC and cognitive impairments in this patient group.
- To identify potential neural substrates underlying cognitive deficits in melancholic MDD.
Main Methods:
- Utilized sliding-window analysis to assess whole-brain dFC for hippocampal subregion seeds.
- Included 42 treatment-naive melancholic MDD patients and 55 healthy controls.
- Assessed cognitive performance using the MATRICS Consensus Cognitive Battery (MCCB) and conducted association analyses.
Main Results:
- Melancholic MDD patients exhibited decreased dFC variability between the left rostral hippocampus and left anterior cerebellum compared to controls.
- Patients showed poorer cognitive performance in working memory, verbal learning, visual learning, and social cognition.
- Working memory performance positively correlated with left rostral hippocampus-left anterior cerebellum dFC variability in MDD patients.
Conclusions:
- Confirmed distinct dynamic functional pathways involving hippocampal subregions in melancholic MDD.
- Suggests hippocampus-cerebellum connectivity dysfunction underlies working memory impairment in melancholic MDD.
- Highlights the role of specific neural pathways in cognitive deficits associated with melancholic depression.
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