Yuan Wang1, Hui Xu1, Chenguang Guo1, and Ming Zhang1
1Department of Medical Imaging, the first affiliated hospital of Xi'an Jiaotong University, Xi'an, China
Synopsis
Hemifacial spasm (HFS) is characterized by
unilateral and paroxysmal contraction of orofacial muscles. A group of HFS
patients and healthy controls underwent MRI examination and clinical assessment
for facial spasm and affective disorders. HFS patients showed thickened left
fusiform in cortex along with reduced subcortical volume in the right amygdala.
Increased amygdala-driven connections were revealed to the bilateral superior
frontal gyrus (SFG) and orbital gyrus (OG), and increased functional
connectivity (FC) was detected of fusiform seed to several subregions of frontal lobe.
These altered FC changes were associated with certain clinical indices, providing
new insight into pathophysiology of the disease.
Introduction
Hemifacial spasm (HFS) is defined as one of the
neuromuscular movement disorders characterized by
unilateral, involuntary, and paroxysmal orofacial contractions innervated by the
ipsilateral facial nerve. Only one study had assessed the
structural and functional alterations of the brain in HFS patients using voxel based morphometry (VBM) and regional homogeneity (ReHo) method until now. Compared to VBM approach, surface-based analysis
(SBA) can detect the abnormalities in cortical thickness and areas with subvoxel precision, and resting-state
functional connectivity (FC) is used to probe temporal correlations in spontaneous fluctuations across functionally
related and structurally distinct brain regions. Therefore, the objectives of this study are as follows: (1) to identify cortical
thickness changes in HFS patients and (2) to explore
the abnormal functional connectivity derived from these structural alterations compared to healthy controls.
Then we aim
to investigate the relationship of the structural and functional MRI indices
to the clinical variables in HFS group, which may be beneficial to better
understand the pathophysiology of this disease.
Methods
Thirty HFS patients and 30 age and gender matched healthy volunteers were
recruited in this study with three dimensional T1 and functional magnetic
resonance imaging (fMRI) acquired on a 3.0T GE scanner. SBA and FC analysis were applied to investigate the differences of structural
and resting-state fMRI properties in the whole brain between two groups. After
that, correlation analysis was employed between neuroimaging
data and severity of facial spasm and neuropsychological disorders in HFS patients, including degrees of facial spasm and scores of
Hamilton Depression Scale
(HAMD) and Hamilton Anxiety Scale (HAMA).Results
In comparison to healthy participants, HFS patients
showed significant increased cortical thickness in the
left fusiform, right supramarginal gyrus, and right parsobitalis region, along with decreased subcortical volume in the right amygdala. Increased amygdala-driven connections were detected to the bilateral superior frontal
gyrus (SFG), bilateral orbital gyrus (OG), and left posterior insula (L-PI),
together with increased functional connectivity of left fusiform seed to
several subregions of the frontal lobe, including the bilateral medial frontal
gyrus (MFG), right superior frontal gyrus (SFG) and right anterior cingulate
cortex (ACC). Moreover, a few of FC changes mentioned above were associated with the spasm degree and HAMA score in HFS.Discussion
Our results firstly demonstrated cortical
thickening in the left fusiform in HFS patients than
that of the controls. It is established that fusiform plays a
key role in face perception. The most consistent and prominent
face-selective fMRI activation was located on the lateral part of the fusiform
gyrus which was called as the “fusiform face area” or FFA. Given that the enrolled HFS
patients underwent chronic and severe facial spasm, most
of them were difficult to concentrate on other’s face during social contact. One possible mechanism for adaption to this situation is
the compensatory neural reorganization of FFA for the visual fixation
difficulty, which may be helpful for patients to identify people in a short period of time.
Moreover, the left fusiform may have altered
functional connectivity to medial prefrontal cortex (mPFC) in HFS patients. Based
on the current findings that linked the altered fusiform-mPFC functional connectivity to
the degree of orofacial spasm and anxiety, we suspect the connection abnormality
of the two regions in HFS was partly caused by mimetic muscular
contractions and spasm related affective disorders.
Last but not the least, the right amygdala cluster with decreased GMV in
patients demonstrated significantly increased connectivity to several subregions
of the frontal lobe, such as dorsal lateral prefrontal cortex (DLPFC), dorsal
medial prefrontal cortex (DMPFC), and OFC. Besides, the morphological and
functional alterations of amygdala may be linked to the spasm triggered visual
attentional deficit in patients with HFS, which was supported by bidirectional
communication between amygdala and fusiform gyrus during facial information
processing. Finally, the correlation analysis showed positive
associations of amygdala-frontal connectivity to the degree of facial spasm and
anxiety respectively, which may provide an alternative imaging marker for
predicting the characteristics of HFS condition.
Conclusion
In conclusion, the present study revealed thickened fusiform cortex and
dysfunctional fusiform-mPFC connection in HFS patients. Meanwhile, atrophic
right amygdala was detected in patients together with increased functional connectivity
of this seed to bilateral DLPFC. Moreover, the altered fusiform-mPFC and
amygdala-DLPFC networks were associated with severity of facial spasm and
anxiety state, which provide distinct aspect of clues for the evaluation of
HFS related disorders.Acknowledgements
We thank Dr. Faxiu Bao for their assistance with recruiting patients, as
well as Dr. Massieh Moayedi for his advice on functional connectivity analysis. The authors declared no potential conflicts of interest with respect to
the research, authorship, and/or publication of this article.
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