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Updated: Sep 6, 2026
Design and Implementation of an fMRI Study Examining Thought Suppression in Young Women with, and At-risk, for Depression
Published on: May 19, 2015
Left Cerebellar-Right Frontal Uncoupling in Female First-Episode Major Depressive Disorder: Synaptic Evidence From
Juehan Wang1, Yajun Lin2, Tianfang Zhang1
1Department of Physical Medicine and Rehabilitation, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Background:
Synaptic loss is a neuropathological feature of depression.
Objective:
Cerebello-cerebral synaptic function was evaluated in female first-episode major depressive disorder (MDD) patients using [18F]UCB-H positron emission tomography (PET).
Materials And Methods:
PET was performed on female first-episode MDD patients (FMD group, n = 7), healthy controls (HC group, n = 9), and chronic restraint stress (CRS) mice (n = 9). Standardized uptake value ratios (SUVR), voxel-wise tracer uptake analysis, functional connectivity (FC), and network analysis were performed at the cerebello-cerebral level. Associations with Hamilton depression scale (HAMD) and Hamilton anxiety scale (HAMA) scores were assessed by Pearson correlation and logistic regression analysis.
Results:
In the FMD group, SUVR in the left cerebellum 7b was significantly reduced and negatively correlated with HAMD (r = -0.57) and HAMA (r = -0.55) scores. The cluster centered on the left cerebellar lobule VIII showed reduced tracer uptake and was negatively correlated with HAMD scores. FC was significantly reduced in the right frontal lobe but enhanced in the midbrain and occipital regions. The network was characterized by bilateral frontal lobe concentration in the FMD group, while the cerebellar network was more uniform. Cerebello-cerebral uncoupling between the left cerebellum and the right frontal lobe was observed, manifested as reduced SUVR correlation and weakened FC. CRS mice also showed reduced brain [18F]UCB-H uptake.
Conclusions:
Left cerebellar-right frontal uncoupling may serve as a potential neural correlate of first-episode MDD in females.