Neural Plasticity
Volume 2019 (2019), Article ID 7235808, 9 pages
https://doi.org/10.1155/2019/7235808

Research Article

Motor Control Deficits in Facial Synkinesis Patients: Neuroimaging Evidences of Cerebral Cortex Involvement

Jia-jia Wu,¹ Ye-chen Lu,² Mou-xiong Zheng,1,3 Xu-yun Hua,1,3 Jian-guang Xu,1,2 Wei Ding,⁴ and Chun-lei Shan1,2

¹Center of Rehabilitation Medicine, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China
²School of Rehabilitation Science, Shanghai University of Traditional Chinese Medicine, Shanghai, China
³Department of Trauma and Orthopedics, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China
⁴Department of Plastic and Reconstructive Surgery, Shanghai Ninth People Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China

Correspondence should be addressed to Jian-guang Xu; jianguangxu@fudan.edu.cn and Wei Ding; drdingwei@outlook.com

Received 29 December 2018; Revised 5 February 2019; Accepted 3 March 2019; Published 27 March 2019

Academic Editor: Carlo Cavaliere

Copyright © 2019 Jia-jia Wu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Objective. Facial synkinesis is a severe sequelae of facial nerve malfunction. Once the synkinesis is established, it is extremely difficult for patients to recover. Given that the restoration of motor or sensory function after peripheral nerve injury was closely related with cortical plasticity, we investigated cortical plasticity in facial synkinesis patients by the frequency-specific data which remains largely uncharacterized. Materials and Methods. Resting-state fMRI was conducted in 20 facial synkinesis patients and 19 healthy controls, and the amplitude of low-frequency fluctuation (ALFF) in five different frequency bands (slow-6: 0-0.01 Hz; slow-5: 0.01-0.027 Hz; slow-4: 0.027-0.073 Hz; slow-3: 0.073-0.167 Hz; and slow-2: 0.167-0.25 Hz) was calculated, respectively. And the relationship between ALFF and clinical outcomes was also analyzed. Results. Comparing with the healthy controls, facial synkinesis patients showed significantly different ALFF values, mainly in the sensorimotor areas. Furthermore, increased ALFF of the ipsilateral insula in the slow-6 band was significantly related with better facial nerve function. Conclusion. Increased ALFF values in the ipsilateral insula might reflect an abnormal state of hypercompensation in motor control of facial synkinesis patients. It provided valuable spatial information about the functionally aberrant regions, which implied the possible involvement of motor control system in facial synkinesis.

1. Introduction

Facial synkinesis, one of the most troublesome sequelae of facial nerve paralysis, is characterized by synchronous and involuntary contractions of the muscles during volitional facial movements [1, 2]. Currently, despite the improved surgical techniques coupled with the use of botulinum toxin A injection, the results of these remained far from satisfactory [3, 4]. In the past years, researchers demonstrated several possible mechanisms of facial synkinesis, including aberrant regeneration and mismatch of axons [1, 5], ephaptic transmission between neighboring axons [5], and overacting of the facial nucleus in the pons [6]. However, none of them has perfectly interpreted all the issues about facial synkinesis. In other words, the underlying pathological mechanism of facial synkinesis is still not clearly elucidated. In the recent years, emerging evidences showed that functional outcome of peripheral neuropathy was closely associated with both peripheral recovery and cortical adaptation [7]. After years of digging peripheral reasons of facial synkinesis, we speculate that brain plasticity is also responsible for the deficits of facial motor control. Therefore, the investigation of cortical plasticity derived from facial synkinesis is now an interesting and vital question.

In our previous studies, we investigated the cortical functional alterations in patients with unilateral facial synkinesis using the task-designed fMRI [8, 9]. Results demonstrated that the distance of the representation sites during ipsilateral blinking and smiling tasks was decreased on the affected half face compared to the unaffected face in patients. And facial movements on either side performed by patients caused more intensive activation in the supplementary motor area on the contralateral side of the affected face than those on the unaffected side. Although we have successfully described alternation of activation in the primary sensorimotor area, higher order processing system, which also contributes to the complex motor control, is still out of our vision. The regulatory effect on facial motor control from other brain regions could not be ignored. There is a possibility that the facial synkinesis is not only a single problem of motor execution but also a complex problem concerning motor regulation or motor control. A resting-state fMRI study indicated that patients with facial palsy showed decreased connectivity mainly in areas responsible for sensorimotor integration and supervision, and the decreased connectivity between SII and the insula significantly correlated to the severity of the facial palsy [10]. Considering the persistency of facial nerve malfunction, some resting-state fMRI measurements such as amplitude of low-frequency fluctuation (ALFF) might provide more valuable information of the brain status.

ALFF is an effective measurement for detecting low-frequency oscillation (LFO) activities at resting state, which has been widely applied in functional neuroimaging [11]. Recent researches have indicated that neuronal oscillations are distributed linearly on the natural logarithmic scale and different spatial distributions of ALFF in distinct frequency bands may result from the neuronal input selection and plasticity [12–15]. However, the combination of every different band of ALFF results in insignificance of statistical analysis. In this study, the low-frequency fluctuation range is subdivided into five frequency bands: slow-6 (0-0.01 Hz), slow-5 (0.01-0.027 Hz), slow-4 (0.027-0.073 Hz), slow-3 (0.073-0.198 Hz), and slow-2 (0.198-0.25 Hz) [15]. And the power of different frequency bands varied among different anatomical and functional properties of the brain. With this method, we aimed to investigate the spontaneous changes of neural activity in facial synkinesis patients by the frequency-specific data, which would lead to a better understanding of facial synkinesis-related neuroplasticity. Furthermore, the relationship between ALFF and clinical outcomes was also analyzed. We also attempted to address the most correlated region and its frequency band, which might offer useful localization advices for researches of cortical interventions.

2. Methods and Materials

2.1. Participants

A total of 20 facial synkinesis patients and 19 healthy controls were enrolled in this study. Diagnosis of facial synkinesis was made by two experienced plastic surgeons from the Department of Plastic Surgery at The Ninth People’s Hospital, School of Medicine, Shanghai Jiaotong University, before the fMRI scans. We recruited patients with unilateral facial synkinesis, absence of nerve transposition, and with no other medical or psychological disorders. Participants were excluded if the facial palsy was recurrent or with concurrent peripheral neuropathy and with contraindications to investigation by MRI. The study was approved by the local ethics committee, and all patients provided written informed consent according to the Helsinki Declaration.

2.2. Clinical Assessments

The Sunnybrook facial grading system was applied for the clinical assessment of peripheral facial nerve palsy [16]. This grading system measures three components including facial resting symmetry, symmetry of voluntary movement, and synkinesis. The score ranges from 0 to 100, with higher score indicating better facial nerve function. In this study, the assessment of facial nerve function was directly evaluated by two experienced physicians after the fMRI scan.

2.3. fMRI Acquisition

The duration from facial palsy to fMRI scanning is provided in Table 1. The fMRI data were collected using a 3.0T MRI scanner (MR750, GE Healthcare, USA). Participants were instructed to lie still and rest quietly and their heads were immobilized with foam pads. The resting-state fMRI data were obtained with a single-shot gradient-recalled EPI sequence with the following parameters: interleaved scanning order, slice , matrix , , , , , (voxel size ), and number of .

Table 1: Demographic information of enrolled subjects.

Items
Facial synkinesis group ()
Healthy control group ()
value

Age

0.950a

Gender
2 (female)/18 (male)
2 (female)/17 (male)
0.957b

Duration

—
—

Affected side
9 (right)/11 (left)
—
—

Sunnybrook scores

—
—

aTwo independent sample -tests. bChi-square test.

2.4. Data Preprocessing

fMRI data were preprocessed in accordance with pipelines recommended by Yu-Feng et al. [17] using the Statistical Parametric Mapping 8 toolbox (http://www.fil.ion.ucl.ac.uk/spm/) on MATLAB 2014a platform. The brain images of right-sided facial synkinesis patients were flipped along the -axis prior to analysis to ensure the consistency of sides among patients. The first 10 images of each functional session were removed for the signal equilibrium. The acquired functional images were preprocessed as follows: (1) slice scan time correction, (2) head movement correction (the head movements were all less than 2.5 mm or 2.5 degrees in any direction), (3) spatial normalization of the functional images via standard EPI template, (4) regressing nuisance variables including the white matter and cerebral spinal fluid blood oxygen level-dependent (BOLD) signal and effects of head motion using six head motion profiles, (5) spatial smoothing using a Gaussian kernel of 4 mm full width at half maximum, and (6) removal of linear trends.

No temporal filtering during preprocessing assures that the entire frequency band below the Nyquist frequency (0.25 Hz) can be examined in subsequent analyses of ALFF.

2.5. ALFF Measures in Different Frequency Bands

Subsequent to data preprocessing, the time series for each voxel was transformed to the frequency domain using the fast Fourier transform. The power spectrum was obtained in different frequency bands at each voxel. The low-frequency range was subdivided into five bands as previously defined: slow-6 (0-0.01 Hz), slow-5 (0.01-0.027 Hz), slow-4 (0.027-0.073 Hz), slow-3 (0.073-0.198 Hz), and slow-2 (0.198-0.25 Hz) [15].

As the power of a given frequency was proportional to the square of the amplitude of this frequency component, the square root of the power spectrum was calculated at each frequency. Then, the averaged square root (i.e., ALFF value) of the power spectrum in different frequency bands was calculated [18]. Finally, each individual’s ALFF value was transformed to score to allow further comparison between groups.

2.6. Statistical Analysis

To investigate the effects of disease on different frequency bands, we performed an ANOVA (flexible factorial design, ) using the SPM8 software within a standard (Montreal Neurological Institute space) grey matter mask. The group was considered to be a between-subject factor with two levels (facial synkinesis patients vs. healthy controls). The frequency band was regarded as a correlated repeated measure factor with five levels. The interactions of group and frequency were considered as effects in the model. After the interaction effect analysis, significant clusters were generated within a binary mask. Further, post hoc two-sample -tests were performed for group comparison of each frequency band within the previously generated mask. All significance tests were conducted at a false discovery rate (FDR) threshold of .

2.7. Correlation Analysis

The correlation between ALFF values of the ROIs in each frequency band and Sunnybrook scores was also analyzed. The ROIs for correlation analysis were extracted from the largest significant cluster revealed by post hoc -tests between the two groups in each frequency band. Spearman’s correlative analyses were used to examine relationships between abnormal ALFF values and Sunnybrook scores in facial synkinesis patients using SPSS 22 software (SPSS Inc., Chicago, IL).

3. Results

3.1. Clinical Characteristics

There were no significant differences in age or gender between the facial synkinesis patients and the healthy controls. Among the facial synkinesis patients, 9 were with right-sided palsy and 11 were left-sided. The duration of facial palsy from onset to fMRI scanning was months. All patients showed a unilateral loss of facial function, with mean Sunnybrook score of points (Table 1).

3.2. ALFF Results

3.2.1. Interaction Effects of Group × Frequency Band

Significant interaction effects of were distributed over the left insula, right middle temporal cortex, left inferior temporal cortex, right cerebellum, bilateral superior temporal cortex, bilateral orbit frontal cortex, right postcentral cortex, right thalamus, and left anterior cingulate cortex (ACC) (Figure 1 and Table 2).

Figure 1: Interaction effects of by a two-way ANOVA. The red-yellow regions represent significant interaction between disease and frequency.

Table 2: Interaction effects of by a two-way ANOVA.

Brain regions
Cluster size
Cluster centroid (MNI)
value

Frontal_Med_Orbital_L
39
0
36
-12
24.4579

Insula_L
36
-42
3
-9
25.9851

Postcentral_R
36
51
-27
51
20.6439

Temporal_Sup_R
35
54
-39
15
15.8532

Cingulate_Ant_L
32
-3
36
24
12.3385

Insula_L
31
-30
21
6
9.2927

Temporal_Inf_L
24
-42
-39
-15
16.4087

Cerebellum_Crush1_R
18
39
-87
-33
21.6993

Temporal_Mid_R
18
60
-3
-18
15.6285

Postcentral_R
17
66
-12
21
13.1904

Orbital_frontal_med_R
16
15
48
-18
11.895

Thalamus_R
14
21
-21
6
12.5973

Orbital_frontal_post_L
13
-21
24
-18
11.873

Temporal_Pole_Mid_R
13
45
12
-30
10.9921

Temporal_Mid_R
12
69
-48
6
15.2749

Temporal_Sup_L
12
-57
-45
21
15.1745

Temporal_Pole_Sup_R
11
30
9
-24
20.7315

Temporal_Inf_L
11
-33
12
-39
18.3323

3.2.2. Post hoc Two-Sample -Tests between Groups

To investigate differences between the two groups in each frequency band, further post hoc two-sample -tests were performed (Figure 2 and Table 3).

Figure 2: Difference in the amplitude of low-frequency fluctuation (ALFF) between facial synkinesis patients and healthy controls. Each row in the figure displays difference of ALFF between facial synkinesis patients and healthy controls in each of the five frequency bands. The warm tone represents signal of patients greater than healthy controls, while the cold tone represents signal of patients less than healthy controls.

Table 3: Differences in ALFF between facial synkinesis patients and healthy controls in 5 frequency bands.

Brain regions
Cluster size
Cluster centroid(MNI)
value

Slow-2 band

    Facial synkinesis < healthy controls

        Insula_R
32
48
-6
3
-3.4274

        Temporal_Pole_Sup_R
30
30
18
-27
-2.6361

        Cingulate_Ant_R
30
9
42
0
-3.3372

        Postcentral_R
27
51
-27
48
-3.3814

        Cerebelum_Crus1_R
25
39
-87
-33
-4.0931

        Temporal_Mid_R
22
60
-3
-18
-2.4222

        Frontal_Sup_Medial_R
21
6
36
42
-2.899

        Temporal_Pole_Mid_R
19
48
9
-30
-2.8583

        Frontal_Sup_L
16
-21
36
36
-2.6557

        Cingulate_Ant_L
12
-6
30
18
-3.1261

Slow-3 band

    Facial synkinesis > healthy controls

        Thalamus_L
82
-18
-27
-3
2.8462

        Hippocampus_L
48
-21
-24
-9
4.9978

        Cerebelum_10_L
30
-21
-33
-45
4.8498

        Thalamus_R
11
12
-24
3
2.8505

    Facial synkinesis < healthy controls

        Frontal_Med_Orbital_R
42
12
48
-9
-2.7222

        Cingulate_Ant_L
22
-3
36
27
-3.8034

        Cerebelum_Crus1_R
22
39
-87
-33
-3.2934

        Temporal_Mid_R
10
60
-3
-21
-3.3251

        Postcentral_R
10
66
-15
15
-3.1111

        Cerebelum_Crus2_R
10
39
-75
-51
-2.7581

Slow-4 band

    Facial synkinesis > healthy controls

        Insula_L
36
-27
12
-21
2.5823

        Hippocampus_L
16
-21
-24
-9
3.222

        Cerebelum_9_R
15
12
-48
-54
4.2794

        Temporal_Pole_Sup_R
15
30
9
-24
4.137

        Frontal_Sup_Medial_L
12
-9
66
9
3.6189

        Hippocampus_L
10
-18
-12
-12
3.9069

        Frontal_Sup_2_R
10
24
36
42
2.7278

    Facial synkinesis < healthy controls

        Frontal_Med_Orbital_R
10
12
42
-6
-2.3628

Slow-5 band

    Facial synkinesis > healthy controls

        Insula_L
43
-33
15
9
3.353

        Frontal_Sup_2_R
12
27
9
66
2.9628

        Cingulate_Ant_L
12
-3
33
-9
2.8405

        Temporal_Inf_L
11
-42
6
-42
3.2313

        Hippocampus_L
11
-21
-24
-9
2.6231

        Frontal_Sup_2_R
10
24
39
42
2.3045

    Facial synkinesis < healthy controls

        Hippocampus_R
15
33
-12
-15
-2.9439

Slow-6 band

    Facial synkinesis > healthy controls

        Insula_L
61
-39
6
0
3.8307

        Postcentral_R
37
57
-21
45
3.3997

        Temporal_Pole_Mid_L
28
-21
9
-36
2.6843

        Cingulate_Ant_L
27
-3
39
18
3.3037

        Temporal_Inf_L
22
-42
6
-42
3.6417

        Frontal_Inf_Triangle_L
10
-48
39
3
3.9693

    Facial synkinesis < healthy controls

        Cerebelum_9_L
24
-9
-54
-51
-2.8445

        Hippocampus_R
15
30
-21
-15
-3.0374

In the slow-2 band, facial synkinesis patients exhibited significantly decreased ALFF values comparing with the healthy controls in the bilateral ACC, right insula, right cerebellum, right superior temporal cortex, left superior frontal cortex, right middle temporal cortex, right postcentral cortex, and right medial superior frontal gyrus.

In the slow-3 band, facial synkinesis patients showed significantly increased ALFF in the left hippocampus, left cerebellum, and bilateral thalamus and significantly decreased ALFF in the left ACC, right middle temporal cortex, right cerebellum, right postcentral cortex, and right orbit frontal cortex.

In the slow-4 band, facial synkinesis patients showed significantly increased ALFF in the right cerebellum, left insula, right superior temporal cortex, left hippocampus, left medial superior frontal cortex, and right superior frontal cortex and significantly decreased ALFF in the right orbit frontal cortex.

In the slow-5 band, facial synkinesis patients showed significantly increased ALFF in the left insula and left inferior temporal cortex, right superior frontal cortex, left ACC, and left hippocampus and significantly decreased ALFF in the right hippocampus.

In the slow-6 band, facial synkinesis patients showed significantly increased ALFF in the left insula, left inferior frontal cortex, left inferior temporal cortex, left middle temporal cortex, right postcentral cortex, left ACC, and right middle temporal cortex and significantly decreased ALFF in the right hippocampus, and left cerebellum.

3.3. Clinical Correlation

Significant correlation was found between the Sunnybrook scores and ALFF values in facial synkinesis patients for the cluster of the left insula in the slow-6 band (, ). However, ALFF values of the other significantly different clusters between groups in the slow-2 to slow-5 bands (the right insula in the slow-2 band, the left thalamus in the slow-3 band, the left insula in the slow-4 band, and the left insula in the slow-5 band) failed to show significant correlation with the Sunnybrook scores (Figure 3).

(a)

(b)

(c)

Figure 3: Spearman correlation analysis between Sunnybrook scores and ALFF values in five ROIs. The ROIs were extracted from the largest significant cluster revealed by post hoc -tests between the two groups in each frequency band. The bar graph showed the significant clusters of different ALFF between facial synkinesis patients and healthy controls by a post hoc two-sample -test in each frequency band. ROI 2-1: right insula; ROI 2-2: right superior temporal pole; ROI 2-3: right anterior cingulate cortex(ACC); ROI3-1: left thalamus; ROI3-2: left hippocampus; ROI3-3: right medial orbit frontal cortex; ROI4-1: left insula; ROI4-2: left hippocampus; ROI4-3: right cerebellum; ROI4-4: right superior temporal pole; ROI5-1: left insula; ROI5-2: right hippocampus; ROI5-3: right superior frontal gyrus; ROI5-4: left ACC; ROI6-1: left insula; ROI6-2: right postcentral gyrus; ROI6-3: left middle temporal pole.

4. Discussion

4.1. Main Findings

In the present study, we investigated frequency-specific ALFF alteration between facial synkinesis patients and healthy controls in the distribution of intrinsic brain hemodynamic oscillations across five frequency bands (slow-2 to slow-6). We also investigated the capability of the frequency-specific alterations in providing predictive information with the frequency-specific alterations. The main findings were concluded as follows: (1) a significant interaction effect of the band was observed mainly in the sensorimotor regions; (2) post hoc two-sample -tests showed significant differences in ALFF between the two groups in each frequency band; and (3) in the slow-6 band, ALFF values of facial synkinesis patients’ insula were most significantly related with facial synkinesis patients’ Sunnybrook scores.

4.2. Alterations of ALFF in Each Frequency Band

ALFF was reported to describe the local spontaneous neuronal activity [19]. Previous studies of electroencephalography have demonstrated that LFO represented spontaneous neural activity which generated its rhythmic activity patterns through information exchange with neighboring brain areas [15]. Most fMRI studies measured ALFF at a typical frequency range between 0.01 and 0.08 Hz which was thought to be physiologically meaningful [20, 21]. However, the fMRI scan objectively enabled possible detection of fluctuations over 0.1 Hz [21]. According to the Buzsáki framework, the full frequency range (0-0.25 Hz) was subdivided into five frequency bands (slow-2, slow-3, slow-4, slow-5, and slow-6 bands) [15]. Although the exact mechanism of different bands is still controversial, several researchers have tried to give some explanations of frequency-specific ALFF. The neurophysiological mechanisms that underlie oscillations within specific classes may be linked to specific neurophysiological processes, including input selection, plasticity, binding, and consolidation [13–15].

Although the slow-2 and slow-3 bands were typically discarded as physiological noises [14], they were still adopted in the correlation analysis for objective and comprehensive comparison in this study. In these two bands, a significant difference was found in several areas. However, further analysis failed to show significant correlation between Sunnybrook scores and ALFF values in facial synkinesis patients in the most significantly different cluster between the two groups (the right insula in the slow-2 band and the left thalamus in the slow-3 band).

Of note, the slow-4 and slow-5 bands were thought to be linked with neurophysiological processes, which were typically utilized in resting-state fMRI studies (below 0.1 Hz) [20, 21]. In the results of the slow-4 and slow-5 bands, we observed decreased ALFF values for neuronal activity in facial synkinesis patients in the right superior frontal cortex and right hippocampus and increased ALFF values predominantly in areas acting sensorimotor integration functions. Similar with the pattern of ALFF alternations in these two bands, the data analysis in the slow-6 band showed that facial synkinesis patients exhibited significantly increased ALFF values in areas of sensorimotor integration and bilateral temporal lobe, whereas it was decreased in the left right hippocampus and left cerebellum. Based on the results of post hoc two-sample -test, ALFF values of the left insula showed the most significant difference between the two groups in these three frequency bands. And the ALFF value in the slow-6 band was most significantly correlated with Sunnybrook scores. Previous studies demonstrated that the slow-6 band was ascribed to low-frequency drifts [14, 19]. Although a few studies have addressed the indicative utilization of fluctuations in the slow-6 band, our data demonstrated its potential role of neurophysiological biomarker in the functional assessment of facial synkinesis patients.

4.3. Insula and Motor Control

This study demonstrated that facial synkinesis was mostly affected in areas of higher order processing sensorimotor information, including the postcentral cortex, insula, thalamus, ACC, hippocampus, and cerebellum. However, the patterns of ALFF alteration in the ACC or cerebellum areas were not fixed. It suggested that these changes were very likely to be caused by the motor-sensory mismatch due to the substantial prediction error. Among those heterogeneous results, it was interesting to find significant difference of ALFF in the insula between the two groups in each frequency band. Moreover, the ALFF values of the left insula in facial synkinesis patients in the slow-6 band were found to correlate with the improvement of facial nerve function significantly. The insula was demonstrated to contribute to hand and eye motor movement in motor control [22, 23]. The result indicated the motor control deficits in facial synkinesis. Recent neuroimaging studies have showed that the insula was associated with higher cognitive processing [24], pain, and sensorimotor processing [25, 26]. The insula participates in higher order processing of somatosensory input and has the most connections with other regions in the brain network, including the thalamus, hippocampus, and ACC [27–29]. In addition to pain, electrical stimulation of the human insula cortex elicits auditory, vestibular, vegetative, olfactory, and gustatory responses, thereby implying a multimodal role for the insula [30]. In the present study, the increased ALFF value in the insula ipsilateral to the lesioned side is considered to be in an abnormal state of hypercompensation in motor control of facial synkinesis patients.

4.4. Possible Source of Artifacts

Many studies paid attention to physiological signals arising from cardiac- and respiratory-related processes, for example, heart rate, respiration sources, and blood pressure, which could impact regional measures of ALFF [31–34]. These physiological factors that are closely related with the quality of BOLD signals raise great concerns regarding test-retest reliability [35]. However, Zuo et al. have confirmed test-retest reliability of ALFF [14]. Baria et al. also demonstrated that it showed little difference from uncorrected ones when regressing out cardiac and respiration signal in each subject per voxel [36]. Besides, the noise was generally assumed a random factor in both groups. Thus, there should not be significant differences between the two groups, even when comparing the noise effect among the five frequency bands.

4.5. Limitations

This study was an explorative neuroimaging study, and several limitations should be noted. Firstly, the sample size was relatively small, which might have limited the power of persuasion. Secondly, it might be better to compare patients who have recovered from facial paralysis and those who suffered from facial synkinesis to investigate alterations of spontaneous activity caused by facial synkinesis only, although the functional activities in the related brain regions gradually recovered to the normal level with the gradual recovery of facial nerve function [37–39]. Considering unavailability of people recovered from facial paralysis, we recruited healthy normal control instead. Thirdly, the gender and age in the healthy controls did not match the patients perfectly. Finally, the variety of the disease duration was not well controlled, which could bring negative impact on homogeneity within the patient group.

5. Conclusion

We reported multiple changes of band-specific ALFF in facial synkinesis patients. The increased ALFF value in the slow-6 band in the ipsilateral insula was positively related with facial nerve function (Sunnybrook scores). This study revealed frequency-specific changes in local spontaneous neuronal activity for severity correlation in facial synkinesis, which could be a potential indicator of disease progression. It also provided valuable spatial information about the functionally aberrant regions, which implied the possible involvement of motor control system in facial synkinesis. Although it is with limitation, this study may broaden our vision of the neural mechanism of facial synkinesis.

Data Availability

The data that support the findings of this study are available from the corresponding author, Jian-guang Xu, upon reasonable request.

Conflicts of Interest

We have no financial or personal conflicts of interest to disclose.

Acknowledgments

This study was financially supported by the Shanghai Jiaotong University Multidisciplinary Research Fund of Medicine and Engineering (YG 2016QN13).

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