Skip to main content

ORIGINAL RESEARCH article

Front. Neurosci., 21 August 2020
Sec. Brain Imaging Methods

Transcutaneous Spinal Cord Direct-Current Stimulation Modulates Functional Activity and Integration in Idiopathic Restless Legs Syndrome

\r\nMin Zeng&#x;Min Zeng1†Li Wang,&#x;Li Wang2,3†Bochao Cheng&#x;Bochao Cheng4†Guiqiang QiGuiqiang Qi1Junwei HeJunwei He1Zhexue Xu,Zhexue Xu2,3Tao Han,Tao Han2,3Chunyan Liu,*Chunyan Liu2,3*Yuping Wang,*Yuping Wang2,3*
  • 1Department of Radiology, Pidu District People’s Hospital, Chengdu, China
  • 2Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China
  • 3Beijing Key Laboratory of Neuromodulation, Beijing, China
  • 4Department of Radiology, West China Second University Hospital of Sichuan University, Chengdu, China

Idiopathic restless legs syndrome (RLS) is a sensorimotor disorder and is suggested to be caused by central nervous system abnormalities. Non-invasive transcutaneous spinal direct-current stimulation (tsDCS) was recently used for RLS therapy. However, the neurophysiological basis of tsDCS treatment is still unknown. In this study, we explored the neural basis of tsDCS in 15 RLS patients and 20 gender- and age-matched healthy controls using resting-state functional magnetic resonance imaging. We calculated the whole-brain voxel-wise fractional amplitude of low-frequency fluctuations (fALFF), regional homogeneity (ReHo), and weighted degree centrality (DC) to characterize the intrinsic functional activities and the local and global functional integration. We found that tsDCS can effectively improve the sleep and RLS symptoms in RLS patients. Moreover, after tsDCS therapy, the RLS patients showed decreased fALFF in the right anterior insula/temporal pole, decreased ReHo in the supplementary motor area, increased weighted DC in the left primary visual cortex, and decreased weighted DC in the right posterior cerebellum. The changed patterns were consistent with that found between RLS patients and healthy controls. The weighted DC in the left primary visual cortex after treatment and the fALFF in the right anterior insula/temporal pole before treatment were significantly and marginally correlated with sleep and RLS symptom scores, respectively. These results revealed that tsDCS can normalize the functional patterns of RLS patients and is an effective way for RLS therapy. Our findings provide the neurophysiological basis for tsDCS treatment and may facilitate understanding the neuropathology of RLS and directing other neuromodulation treatments.

Introduction

The restless legs syndrome (RLS) is a common sensorimotor disorder, and the prevalence of the syndrome is between 3 and 9% in the general population (Phillips et al., 2000; Rothdach et al., 2000). The main characteristic of RLS is an unpleasant sensation in the lower limbs, especially during nighttime. RLS is primarily associated with the underlying genetics, iron deficiency, uremia, pregnancy, or end-stage renal disease (Trenkwalder et al., 2005). Dopaminergic medication is the main therapeutic approach for RLS, but given augmentation and the side effects of medication (Paulus and Trenkwalder, 2006; Earley and Silber, 2010; Allen et al., 2011; García-Borreguero and Williams, 2011), currently, non-pharmacological neuromodulation therapy has become a more and more popular approach for brain disorder treatment as it has less side effects.

A few previous studies have revealed that central nervous system overactivity may be the underlying mechanism of RLS (Bucher et al., 1997; Trenkwalder et al., 2005; Spiegelhalder et al., 2008; Margariti et al., 2012; Liu et al., 2015, 2018). A recent study using the non-invasive and painless transcutaneous spinal direct-current stimulation (tsDCS) technique demonstrated that tsDCS can reduce spinal cord excitability and can effectively alleviate the symptoms of RLS patients (Heide et al., 2014). This finding indicated that tsDCS may open a new avenue for RLS therapy. However, the neurophysiological basis of tsDCS therapy for RLS remains unclear.

Resting-state functional magnetic resonance imaging (rs-fMRI) mainly characterizes the spontaneous low-frequency fluctuations of brain activities as measured by blood oxygen level-dependent signals (Fox and Raichle, 2007). rs-fMRI has been widely used to detect the intrinsic functional organization and functional couplings in healthy subjects and in diseases (Fox et al., 2006; Wang et al., 2015, 2016b,2019b; Wang C. et al., 2017; Wang J. et al., 2017; Sun et al., 2018; Xu et al., 2019; Gao et al., 2020). Therefore, rs-fMRI is a particularly effective way to explore the neurophysiological basis of neuromodulation treatment for brain disorders (Liu et al., 2015; Wang et al., 2016a, 2018, 2020). To characterize the functional activity and the interaction patterns during resting, the amplitude of low-frequency fluctuations (ALFF), functional signals regional homogeneity (ReHo), and weighted degree centrality (DC) were proposed to delineate the functional oscillation (Zang et al., 2007), local information integration (Zang et al., 2004), and global functional integration (Wu et al., 2016; Liu et al., 2018; Song et al., 2019), respectively. Therefore, ALFF, ReHo as well as DC can provide a comprehensive and complementary evidence for the neurophysiological basis of tsDCS treatment.

In this study, we aimed to identify the neurophysiological basis of tsDCS treatment for RLS using rs-fMRI in 15 RLS patients before and after tsDCS and in 20 age- and gender-matched healthy controls. First, voxel-wise fALFF, ReHo, and weighted DC maps for each subject were calculated. Then, paired t-tests were used to identify the changed functional activity and local and global information integration in RLS patients after tsDCS. Finally, correlation analyses were performed to reveal the relationships between changed neural measurements and clinical performances.

Materials and Methods

Participants

Thirty idiopathic RLS patients (23 females and seven males; mean age: 62.1 ± 8.04 years) and 20 gender- and age-matched healthy controls (17 females and 3 males; mean age: 60.1 ± 7.9 years) were used in our current study. The RLS patients were diagnosed based on the International Criteria of the International Restless Legs Syndrome Study Group. Patients with anemia, renal disease, a history of alcohol or drug abuse, spinal cord injury, pregnancy, or other neuropathies were excluded. All patients were randomly divided into the tsDCS stimulation group and the sham stimulation group, with 15 patients in each group. The severity of RLS was characterized using the International RLS Rating Scale (IRLS-RS) and Pittsburgh Sleep Quality Index (PSQI). Both IRLS-RS and PSQI were measured at baseline (before treatment) and at 2 weeks after treatment. The 20 right-handed healthy controls were recruited from the community and did not have any neurological disorders nor were taking medication and did not have a family history of RLS. The written informed consents were provided and obtained from all subjects. The study was approved by the ethics committee of the Xuan Wu Hospital of Capital Medical University and was in accordance with the Helsinki Declaration and its later amendments or comparable ethical standards.

The tsDCS Procedures

The tsDCS protocol was performed according to that reported in a previous study (Heide et al., 2014). Anodal stimulation with a constant direct current was conducted. The subjects were placed in prone position. The center of the stimulation electrode was placed over the 10th thoracic vertebra and the return electrode was placed above the right shoulder. Both equally sized rectangular electrodes (5 × 7 × 6 cm) were applied. The stimulation current strength was 2 mA for 20 min. A current density of 0.057 mA/cm2 and a total delivered charge of 51.3 mC/cm2, which is far below the threshold for tissue damage, were applied (Nitsche et al., 2003; Liebetanz et al., 2009). The treatment was applied daily for 14 consecutive days for all the patients. Sham stimulation was delivered by turning off the stimulator after 30 s, and the subjects experienced the same tingling sensation at the beginning of the stimulus.

Resting-State fMRI Data Collection

The resting-state fMRI data were collected using a Siemens Trio 3-Tesla (Siemens, Erlangen, Germany) head MRI scanner. All the RLS patients were scanned twice, i.e., before and after treatment, and the healthy controls were only scanned once. All the subjects were asked not to move as much as possible and to relax their minds and to keep their eyes closed without falling asleep. Foam pads and headphones were used to reduce head movement and scanner noise. The resting-state fMRI data were collected with the following parameters: repetition time/echo time ratio = 2,000/30 ms, flip angle = 90°, acquisition matrix size = 64 × 64, voxel size = 3.75 mm × 3.75 mm × 4 mm with 1-mm gap, 33 slices, and 240 volumes.

Resting-State fMRI Data Preprocessing

The resting-state fMRI data for each subject were preprocessed using SPM8 software with DPARSF, version 2.31. The first 10 volumes were discarded to facilitate magnetization equilibrium effects; the remaining images were realigned to the first volume to correct head motion; the fMRI images were then normalized to EPI template in standard MNI space and resampled to 3-mm isotropic voxels; Friston 24-parameter model of head motion, white matter, cerebrospinal fluid, and global mean signals were regressed out and filtered with a temporal band-path of 0.01–0.1 Hz. To further exclude the head motion effects, first, if the head motion exceeds 3 mm or 3°, the subject was excluded. Under this criterion, no subjects were excluded. Second, a scrubbing method was conducted to censor each subject’s bad images with the mean frame displacement (FD) above 0.5 mm, and one volume before and two volumes after the bad volume were discarded (Power et al., 2012). The voxel-wise fALFF was calculated for each subject before the preprocessing of filtering, and the ReHo and weighted degree centrality were calculated with the scrubbed fMRI data.

The fALFF, ReHo, and Weighted DC Calculation

The fALFF was used to characterize the resting-state functional activity of each brain voxel since fALFF is more robust to white matter and cerebrospinal fluid noises and can better exclude individual variations compared with ALFF (Zou et al., 2008). To calculate fALFF, the time series for each voxel was transformed to the frequency domain and the power spectrum was obtained. fALFF is defined as the power within the low-frequency range (0.01–0.1 Hz) divided by the total power in the entire detectable frequency range. To characterize the local functional integration, voxel-wise ReHo was mapped for each participant by calculating the Kendall’s coefficient of concordance for the time series of a given voxel with those of its nearest 26 neighbors (Zang et al., 2004). The global functional integration defined by weighted DC was also calculated for each subject at voxel-wise level. To calculate the weighted DC, functional connections of a given voxel and all other voxels constrained within a binary gray matter mask, created by thresholding the gray matter probability template with 0.2 in the brain, were first calculated (Wang et al., 2014; Wu et al., 2016; Liu et al., 2018). Then, the weighted DC for each voxel was obtained by averaging the functional connectivity strengths higher than a threshold of 0.25 over the whole brain (Wang et al., 2014; Wu et al., 2016; Liu et al., 2018). Finally, the fALFF, ReHo, and weighted DC maps were transformed to Z scores to improve normality. For statistical analyses, all these measurements were spatially smoothed with a 6-mm Gaussian kernel. Paired t-tests were performed to compare the fALFF, ReHo, and weighted DC maps between RLS patients before and after tsDCS. The significance was determined using a Gaussian random field correction method with p < 0.05. Moreover, the regional mean fALFF, ReHo, and weighted DC in RLS patients before and after tsDCS and in healthy controls were calculated. Two-sample t-tests were conducted between healthy controls and RLS patients before and after tsDCS was performed. The significant level was set at p < 0.05 with Bonferroni correction.

Correlation Analyses

To explore the relationship between the resting-state fMRI indices and the clinical characteristics, correlation analyses were performed between the mean fALFF, ReHo, weighted DC, and PSQI and IRLS-RS scores in RLS patients before, after, and after-minus-before. The significance was set at p < 0.05.

Results

Clinical Characteristics

A chi-square test and two-sample t-test were performed for gender and age, respectively. There were no significant differences in gender (p = 0.15), and age (p = 0.64) between RLS patients and healthy controls (Table 1). Paired t-tests were performed for clinical characteristics, and it was found that the RLS patients showed significantly decreased IRLS-RS (p < 10–6) and PSQI (p < 10–4) scores after tsDCS compared with before treatment (Table 1). In the sham tsDCS group, no significant changes in IRLS-RS (p = 0.22) and PSQI (p = 0.50) scores were found after treatment (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Demographics and clinical characteristics of the subjects used in present study.

Changed fALFF After tsDCS

Statistical analyses identified a significant difference in functional activity, characterized using fALFF in RLS patients before and after tsDCS. Significantly reduced fALFF in the right anterior insula/temporal pole (INS/TP) was identified in RLS patients after tsDCS compared to before tsDCS treatment (Table 2 and Figure 1). Compared with healthy controls, the RLS patients also showed elevated fALFF in the right INS/TP (Figure 1). There was no significant difference in fALFF between healthy controls and RLS patients after tsDCS treatment (Figure 1).

TABLE 2
www.frontiersin.org

Table 2. Regions with changed fALFF, ReHo, and weighted DC in RLS patients after tsDCS treatment.

FIGURE 1
www.frontiersin.org

Figure 1. Decreased fractional amplitude of low-frequency fluctuation (fALFF) in restless leg symptom (RLS) patients after transcutaneous spinal cord direct current stimulation (tsDCS). Paired t-test was performed and identified significantly decreased fALFF in right anterior insula (INS)/temporal pole (TP) in RLS patients after tsDCS compared to that before tsDCS. Regional mean fALFF values in the right anterior INS/TP were calculated in healthy controls (HC) and RLS patients before and after tsDCS, and two-sample t-tests were performed between HC and RLS patients before and after tsDCS and found decreased fALFF in HC compared to RLS patients before tsDCS treatment. No significant difference in fALFF between HC and RLS patients after tsDCS was found. *p < 0.05.

Changed ReHo After tsDCS

We used ReHo measurement to characterize local functional integration and found decreased ReHo in supplementary motor area (SMA) in RLS patients after tsDCS treatment (Table 2 and Figure 2). A similar pattern was also found between healthy controls and RLS patients before tsDCS treatment, but no significant difference was found (Figure 2). Furthermore, we found a significant difference in ReHo between healthy controls and RLS patients after tsDCS (Figure 2).

FIGURE 2
www.frontiersin.org

Figure 2. Decreased regional homogeneity (ReHo) in restless leg symptom (RLS) patients after transcutaneous spinal cord direct current stimulation (tsDCS) treatment. Paired t-test found significantly decreased ReHo in supplementary motor area (SMA) in RLS patients after tsDCS compared to that before tsDCS. Regional mean ReHo values in SMA were calculated in healthy controls (HC) and RLS patients before and after tsDCS. Two-sample t-tests also found significantly decreased ReHo in RLS patients after tsDCS treatment compared to HC. No significant difference in ReHo between HC and RLS patients before tsDCS was found. *p < 0.05.

Changed Weighted DC After tsDCS

The global integration was characterized using weighted DC in this study. In RLS patients after tsDCS, increased weighted DC was shown in the left primary visual cortex (V1) and decreased weighted DC was shown in the posterior cerebellum (pCereb) (Table 2 and Figure 3). The increased weighted DC in the left V1 was also found in healthy controls compared to RLS patients before tsDCS (Figure 3). In RLS patients after tsDCS, the increased and the decreased weighted DC patterns were similar with that in healthy controls, but no differences were found between healthy controls and RLS patients after tsDCS (Figure 3).

FIGURE 3
www.frontiersin.org

Figure 3. Changed weighted degree centrality (DC) in restless leg symptom (RLS) patients after transcutaneous spinal cord direct current stimulation (tsDCS) treatment. Paired t-test found significantly decreased weighted DC in posterior cerebellum (pCereb) and significantly increased weighted DC in primary visual cortex (V1) in RLS patients after tsDCS compared to that before tsDCS. Regional mean weighted DC values in pCereb and V1 were calculated in healthy controls (HC) and RLS patients before and after tsDCS. Two-sample t-tests only found significantly increased weighted DC of V1 in HC compared to RLS patients before tsDCS. No other significant differences in weighted DC between HC and RLS patients before or after tsDCS were found. *p < 0.05.

Correlation Analyses

Correlation analyses revealed that the weighted DC values of the left V1 in RLS patients after tsDCS treatment were significantly correlated with the PSQI scores (r = 0.58, p = 0.025) (Figure 4). Moreover, a marginal correlation between the fALFF values in the right anterior INS/TP and the IRLS-RS scores in RLS patients before tsDCS treatment was found (r = 0.49, p = 0.064) (Figure 4).

FIGURE 4
www.frontiersin.org

Figure 4. Correlation analyses between neuroimaging indices and clinical characteristics. A significant correlation was found between the weighted DC values of V1 in restless leg symptom (RLS) patients after transcutaneous spinal cord direct current stimulation (tsDCS) treatment and Pittsburgh Sleep Quality Index scores. A marginal correlation between the fractional amplitude of low-frequency fluctuation values of the right anterior insula/temporal pole in RLS patients before tsDCS treatment and the international RLS Rating Scale scores was found.

Discussion

In this study, we revealed that tsDCS can effectively alleviate RLS symptoms by modulating the low-frequency oscillation and the local and global information integration. We found decreased fALFF in the right anterior INS/TP, decreased ReHo in SMA, and increased weighted DC in the left V1 as well as decreased weighted DC in the posterior cerebellum in RLS patients after tsDCS treatment. Moreover, the weighted DC values in the left V1 and the fALFF values in the right anterior INS/TP were significantly or marginally correlated with the PSQI and the IRLS-RS scores, respectively. Our findings demonstrate that tsDCS can normalize the neuronal activities for effective treatment of RLS, which provide the preliminary evidence for the neurophysiological basis of tsDCS treatment for RLS.

Using resting-state fMRI, we found that tsDCS treatment reduced the low-frequency functional oscillation in the right anterior INS/TP. The insula serves as an interface between internal and extra-personal stimuli and thus plays an important role in integrating emotion, cognitive, and homeostatic information (Craig, 2011; Simmons et al., 2013). The anterior INS primarily participates in cognitive control, decision making, and emotion and pain processing through connections with the dorsal anterior and posterior cingulate cortex (Dosenbach et al., 2007; Thielscher and Pessoa, 2007; Kelly et al., 2012). A large number of recent studies have revealed that the functional disruption of the anterior INS results in depression and the functional remodeling is closely related to depression remission (Wang C. et al., 2017; Wang et al., 2019a, b). Moreover, the previous functional mapping of TP also identified the emotion processing of this area (Olson et al., 2007; Fan et al., 2014). Thus, decreased fALFF in the anterior INS/TP may contribute to the cognitive and emotional recovery in RLS patients after tsDCS treatment. Given the correlation result between the fALFF of the anterior INS/TP and the IRLS-RS scores and the role of pain processing in the anterior INS (Kong et al., 2006), the decreased fALFF in the anterior INS suggested that tsDCS may alleviate the RLS symptoms by reducing the sensitivity of pain threshold.

We also found decreased ReHo in SMA and decreased weighted DC in the posterior cerebellum in RLS patients after tsDCS treatment. These findings suggested that tsDCS treatment can reduce the local and global functional integration in RLS patients. SMA and cerebellum are the main parts of the sensorimotor circuit in the brain (Goldberg, 2010; Buckner, 2013). Previous fMRI studies have identified an overactivity of the cerebellum during sensory discomfort and periodic limb movements (Bucher et al., 1997; Spiegelhalder et al., 2008; Margariti et al., 2012). Our recent study using resting-state fMRI also identified an increased functional connectivity between the cerebellum and the thalamus in RLS patients (Liu et al., 2018). The SMA plays an important role in the planning of complex movements (Goldberg, 2010). Liu et al. (2015) found that RLS patients showed a lower ALFF value in SMA, and repetitive transcranial magnetic stimulation induced an increase in the functional activity of this area. In our study, we found that effective tsDCS treatment can decrease the local and global functional integration of SMA and the cerebellum, which indicated that the functional segregation of SMA and the reduced excessive activity of the cerebellum are important for alleviating the RLS symptoms and may be the neuropathology of RLS. Notably, we found that the ReHo in SMA is lower in RLS patients after treatment compared to both in healthy controls and in RLS patients before treatment. This finding indicated that lower ReHo in SMA may be a biomarker for remission of RLS symptoms. However, no significant differences in the ReHo of SMA between RLS patients before treatment and healthy controls were observed, which may mainly result from the small sample of RLS patients and thus with low statistical power.

Finally, we found that tsDCS treatment increased the global functional integration of V1 in RLS patients. V1 is important for visual information processing. Recent functional MRI and lesion-related studies in humans have revealed that V1 is involved in visuospatial attention and conscious visual awareness (Silvanto et al., 2005; Fang et al., 2008; Wang et al., 2016a). Since motor responses are closely linked to visual stimuli, thus, visual information processing in V1 is an important part of the sensorimotor network. Moreover, a previous study reported that stimulation of the occipital cortex has an antinociceptive effect by activating the descending inhibitory pathway (Zhang et al., 2007). In our study, besides the increased global functional integration, we also found that the weighted DC in V1 is closely associated with the PSQI scores. Our findings, together with previous results, indicated that the increased global information integration of V1 after tsDCS may serve as an effective biomarker of treatment response.

Several limitations of the present study are worth mentioning. First, only 15 RLS patients were used to investigate the changes of functional activity and local and global information integration. Thus, these findings should be further validated with a larger sample. Second, our study only focused on voxel-wise functional characterization; how tsDCS modulates the topological architecture of the functional network should be explored in future studies.

Conclusion

The present study revealed the voxel-wise functional changes in low-frequency oscillation and local and global information integration in RLS patients after tsDCS treatment. These results showed that the sensorimotor areas and the visual cortex are important biomarkers for response of RLS treatment. Our findings provide a comprehensive evidence for the neurophysiological basis of tsDCS treatment for RLS patients from different aspects and will facilitate the future understanding of the neuropathology of RLS and the direction of therapy for RLS patients.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by Xuan Wu Hospital of Capital Medical University. The patients/participants provided their written informed consent to participate in this study.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

Funding

This work was supported by grants from the National Key R&D Program (No. 2018YFC1314500) and the National Natural Science Foundation of China (No. 81701297).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

  1. ^ www.restfmri.net/forum/DPARSF

References

Allen, R. P., Ondo, W. G., Ball, E., Calloway, M. O., Manjunath, R., Higbie, R. L., et al. (2011). Restless legs syndrome (RLS) augmentation associated with dopamine agonist and levodopa usage in a community sample. Sleep Med. 12, 431–439. doi: 10.1016/j.sleep.2011.03.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Bucher, S. F., Seelos, K. C., Oertel, W. H., Reiser, M., and Trenkwalder, C. (1997). Cerebral generators involved in the pathogenesis of the restless legs syndrome. Ann. Neurol. 41, 639–645. doi: 10.1002/ana.410410513

PubMed Abstract | CrossRef Full Text | Google Scholar

Buckner, R. L. (2013). The cerebellum and cognitive function: 25 years of insight from anatomy and neuroimaging. Neuron 80, 807–815. doi: 10.1016/j.neuron.2013.10.044

PubMed Abstract | CrossRef Full Text | Google Scholar

Craig, A. D. (2011). Significance of the insula for the evolution of human awareness of feelings from the body. Ann. N. Y. Acad. Sci. 1225, 72–82. doi: 10.1111/j.1749-6632.2011.05990.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Dosenbach, N. U., Fair, D. A., Miezin, F. M., Cohen, A. L., Wenger, K. K., Dosenbach, R. A., et al. (2007). Distinct brain networks for adaptive and stable task control in humans. Proc. Natl. Acad. Sci. U.S.A. 104, 11073–11078. doi: 10.1073/pnas.0704320104

PubMed Abstract | CrossRef Full Text | Google Scholar

Earley, C. J., and Silber, M. H. (2010). Restless legs syndrome: understanding its consequences and the need for better treatment. Sleep Med. 11, 807–815. doi: 10.1016/j.sleep.2010.07.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Fan, L., Wang, J., Zhang, Y., Han, W., Yu, C., and Jiang, T. (2014). Connectivity-based parcellation of the human temporal pole using diffusion tensor imaging. Cereb. Cortex 24, 3365–3378. doi: 10.1093/cercor/bht196

PubMed Abstract | CrossRef Full Text | Google Scholar

Fang, F., Boyaci, H., Kersten, D., and Murray, S. O. (2008). Attention-dependent representation of a size illusion in human V1. Curr. Biol. 18, 1707–1712. doi: 10.1016/j.cub.2008.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., and Raichle, M. E. (2006). Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems. Proc. Natl. Acad. Sci. U.S.A. 103, 10046–10051. doi: 10.1073/pnas.0604187103

PubMed Abstract | CrossRef Full Text | Google Scholar

Fox, M. D., and Raichle, M. E. (2007). Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nat. Rev. Neurosci. 8, 700–711. doi: 10.1038/nrn2201

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, Z., Guo, X., Liu, C., Mo, Y., and Wang, J. (2020). Right inferior frontal gyrus: an integrative hub in tonal bilinguals. Hum. Brain Mapp. 41, 2152–2159. doi: 10.1002/hbm.24936

PubMed Abstract | CrossRef Full Text | Google Scholar

García-Borreguero, D., and Williams, A.-M. (2011). Dopaminergic augmentation of restless legs syndrome: the scope of the problem. Sleep Med. 12, 425–426. doi: 10.1016/j.sleep.2011.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Goldberg, G. (2010). Supplementary motor area structure and function: review and hypotheses. Behav. Brain Sci. 8, 567–588. doi: 10.1017/s0140525x00045167

CrossRef Full Text | Google Scholar

Heide, A. C., Winkler, T., Helms, H. J., Nitsche, M. A., Trenkwalder, C., Paulus, W., et al. (2014). Effects of transcutaneous spinal direct current stimulation in idiopathic restless legs patients. Brain Stimul. 7, 636–642. doi: 10.1016/j.brs.2014.06.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Kelly, C., Toro, R., Di Martino, A., Cox, C. L., Bellec, P., Castellanos, F. X., et al. (2012). A convergent functional architecture of the insula emerges across imaging modalities. Neuroimage 61, 1129–1142. doi: 10.1016/j.neuroimage.2012.03.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Kong, J., White, N. S., Kwong, K. K., Vangel, M. G., Rosman, I. S., Gracely, R. H., et al. (2006). Using fMRI to dissociate sensory encoding from cognitive evaluation of heat pain intensity. Hum. Brain Mapp. 27, 715–721. doi: 10.1002/hbm.20213

PubMed Abstract | CrossRef Full Text | Google Scholar

Liebetanz, D., Koch, R., Mayenfels, S., Konig, F., Paulus, W., and Nitsche, M. A. (2009). Safety limits of cathodal transcranial direct current stimulation in rats. Clin. Neurophysiol. 120, 1161–1167. doi: 10.1016/j.clinph.2009.01.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, C., Dai, Z., Zhang, R., Zhang, M., Hou, Y., Qi, Z., et al. (2015). Mapping intrinsic functional brain changes and repetitive transcranial magnetic stimulation neuromodulation in idiopathic restless legs syndrome: a resting-state functional magnetic resonance imaging study. Sleep Med. 16, 785–791. doi: 10.1016/j.sleep.2014.12.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, C., Wang, J., Hou, Y., Qi, Z., Wang, L., Zhan, S., et al. (2018). Mapping the changed hubs and corresponding functional connectivity in idiopathic restless legs syndrome. Sleep Med. 45, 132–139. doi: 10.1016/j.sleep.2017.12.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Margariti, P. N., Astrakas, L. G., Tsouli, S. G., Hadjigeorgiou, G. M., Konitsiotis, S., and Argyropoulou, M. I. (2012). Investigation of unmedicated early onset restless legs syndrome by voxel-based morphometry, T2 relaxometry, and functional MR imaging during the night-time hours. Am. J. Neuroradiol. 33, 667–672. doi: 10.3174/ajnr.a2829

PubMed Abstract | CrossRef Full Text | Google Scholar

Nitsche, M. A., Liebetanz, D., Lang, N., Antal, A., Tergau, F., and Paulus, W. (2003). Safety criteria for transcranial direct current stimulation (tDCS) in humans. Clin. Neurophysiol. 114, 2220–2222. doi: 10.1016/s1388-2457(03)00235-9

CrossRef Full Text | Google Scholar

Olson, I. R., Plotzker, A., and Ezzyat, Y. (2007). The Enigmatic temporal pole: a review of findings on social and emotional processing. Brain 130, 1718–1731. doi: 10.1093/brain/awm052

PubMed Abstract | CrossRef Full Text | Google Scholar

Paulus, W., and Trenkwalder, C. (2006). Less is more: pathophysiology of dopaminergic-therapy-related augmentation in restless legs syndrome. Lancet Neurol. 5, 878–886. doi: 10.1016/s1474-4422(06)70576-2

CrossRef Full Text | Google Scholar

Phillips, B., Young, T., Finn, L., Asher, K., Hening, W. A., and Purvis, C. (2000). Epidemiology of restless legs symptoms in adults. Arch. Intern. Med. 160, 2137–2141.

Google Scholar

Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., and Petersen, S. E. (2012). Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 59, 2142–2154. doi: 10.1016/j.neuroimage.2011.10.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Rothdach, A. J., Trenkwalder, C., Haberstock, J., Keil, U., and Berger, K. (2000). Prevalence and risk factors of RLS in an elderly population: the MEMO study. Memory and Morbidity in Augsburg Elderly. Neurology 54, 1064–1068. doi: 10.1212/wnl.54.5.1064

PubMed Abstract | CrossRef Full Text | Google Scholar

Silvanto, J., Lavie, N., and Walsh, V. (2005). Double dissociation of V1 and V5/MT activity in visual awareness. Cereb. Cortex 15, 1736–1741. doi: 10.1093/cercor/bhi050

PubMed Abstract | CrossRef Full Text | Google Scholar

Simmons, W. K., Avery, J. A., Barcalow, J. C., Bodurka, J., Drevets, W. C., and Bellgowan, P. (2013). Keeping the body in mind: insula functional organization and functional connectivity integrate interoceptive, exteroceptive, and emotional awareness. Hum. Brain Mapp. 34, 2944–2958. doi: 10.1002/hbm.22113

PubMed Abstract | CrossRef Full Text | Google Scholar

Song, L., Peng, Q., Liu, S., and Wang, J. (2019). Changed hub and functional connectivity patterns of the posterior fusiform gyrus in chess experts. Brain Imaging Behav. 14, 797–805. doi: 10.1007/s11682-018-0020-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Spiegelhalder, K., Feige, B., Paul, D., Riemann, D., van Elst, L. T., Seifritz, E., et al. (2008). Cerebral correlates of muscle tone fluctuations in restless legs syndrome: a pilot study with combined functional magnetic resonance imaging and anterior tibial muscle electromyography. Sleep Med. 9, 177–183. doi: 10.1016/j.sleep.2007.03.021

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, H., Luo, L., Yuan, X., Zhang, L., He, Y., Yao, S., et al. (2018). Regional homogeneity and functional connectivity patterns in major depressive disorder, cognitive vulnerability to depression and healthy subjects. J. Affect. Disord. 235, 229–235. doi: 10.1016/j.jad.2018.04.061

PubMed Abstract | CrossRef Full Text | Google Scholar

Thielscher, A., and Pessoa, L. (2007). Neural correlates of perceptual choice and decision making during fear-disgust discrimination. J. Neurosci. 27, 2908–2917. doi: 10.1523/jneurosci.3024-06.2007

PubMed Abstract | CrossRef Full Text | Google Scholar

Trenkwalder, C., Paulus, W., and Walters, A. S. (2005). The restless legs syndrome. Lancet Neurol. 4, 465–475.

Google Scholar

Wang, C., Wu, H., Chen, F., Xu, J., Li, H., Li, H., et al. (2017). Disrupted functional connectivity patterns of the insula subregions in drug-free major depressive disorder. J. Affect. Disord. 234, 297–304. doi: 10.1016/j.jad.2017.12.033

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Ji, Y., Li, X., He, Z., Wei, Q., Bai, T., et al. (2020). Improved and residual functional abnormalities in major depressive disorder after electroconvulsive therapy. Prog. Neuropsychopharmacol. Biol. Psychiatry 100:109888. doi: 10.1016/j.pnpbp.2020.109888

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Tian, Y., Wang, M., Cao, L., Wu, H., Zhang, Y., et al. (2016a). A lateralized top-down network for visuospatial attention and neglect. Brain Imaging Behav. 10, 1029–1037. doi: 10.1007/s11682-015-9460-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Xie, S., Guo, X., Becker, B., Fox, P. T., Eickhoff, S. B., et al. (2017). Correspondent functional topography of the human left inferior parietal lobule at rest and under task revealed using resting-state fmri and coactivation based parcellation. Hum. Brain Mapp. 38, 1659–1675. doi: 10.1002/hbm.23488

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Wei, Q., Wang, L., Zhang, H., Bai, T., Cheng, L., et al. (2018). Functional reorganization of intra- and internetwork connectivity in major depressive disorder after electroconvulsive therapy. Hum. Brain Mapp. 39, 1403–1411. doi: 10.1002/hbm.23928

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Yang, Y., Fan, L., Xu, J., Li, C., Liu, Y., et al. (2015). Convergent functional architecture of the superior parietal lobule unraveled with multimodal neuroimaging approaches. Hum. Brain Mapp. 36, 238–257. doi: 10.1002/hbm.22626

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Zhang, J., Rong, M., Wei, X., Zheng, D., Fox, P. T., et al. (2016b). Functional topography of the right inferior parietal lobule structured by anatomical connectivity profiles. Hum. Brain Mapp. 37, 4316–4332. doi: 10.1002/hbm.23311

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Dai, Z., Peng, H., Tan, L., Ding, Y., He, Z., et al. (2014). Overlapping and segregated resting-state functional connectivity in patients with major depressive disorder with and without childhood neglect. Hum. Brain Mapp. 35, 1154–1166. doi: 10.1002/hbm.22241

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Wei, Q., Wang, C., Xu, J., Wang, K., Tian, Y., et al. (2019a). Altered functional connectivity patterns of insular subregions in major depressive disorder after electroconvulsive therapy. Brain Imaging Behav. 14, 753–761. doi: 10.1007/s11682-018-0013-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Yu, L., Wu, F., Wu, H., and Wang, J. (2019b). Altered whole brain functional connectivity pattern homogeneity in medication-free major depressive disorder. J. Affect. Disord. 253, 18–25. doi: 10.1016/j.jad.2019.04.040

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, H., Sun, H., Xu, J., Wu, Y., Wang, C., Xiao, J., et al. (2016). Changed hub and corresponding functional connectivity of subgenual anterior cingulate cortex in major depressive disorder. Front. Neuroanat. 10:120. doi: 10.3389/fnana.2016.00120

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, J., Lyu, H., Li, T., Xu, Z., Fu, X., Jia, F., et al. (2019). Delineating functional segregations of the human middle temporal gyrus with resting-state functional connectivity and coactivation patterns. Hum. Brain Mapp. 40, 5159–5171. doi: 10.1002/hbm.24763

PubMed Abstract | CrossRef Full Text | Google Scholar

Zang, Y., Jiang, T., Lu, Y., He, Y., and Tian, L. (2004). Regional homogeneity approach to fMRI data analysis. Neuroimage 22, 394–400. doi: 10.1016/j.neuroimage.2003.12.030

PubMed Abstract | CrossRef Full Text | Google Scholar

Zang, Y. F., He, Y., Zhu, C. Z., Cao, Q. J., Sui, M. Q., Liang, M., et al. (2007). Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. Brain Dev. 29, 83–91. doi: 10.1016/j.braindev.2006.07.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J.-H., Cao, X.-D., Li, J., Tang, W.-J., Liu, H.-Q., and Feng, X.-Y. (2007). Neuronal specificity of needling acupoints at same meridian: a control functional magnetic resonance imaging study with electroacupuncture. Acupuncture Electro Ther. Res. 32, 179–193. doi: 10.3727/036012907815844075

CrossRef Full Text | Google Scholar

Zou, Q. H., Zhu, C. Z., Yang, Y., Zuo, X. N., Long, X. Y., Cao, Q. J., et al. (2008). An improved approach to detection of amplitude of low-frequency fluctuation (ALFF) for resting-state fMRI: fractional ALFF. J. Neurosci. Methods 172, 137–141. doi: 10.1016/j.jneumeth.2008.04.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: idiopathic RLS, tsDCS, resting state, fMRI, therapy

Citation: Zeng M, Wang L, Cheng B, Qi G, He J, Xu Z, Han T, Liu C and Wang Y (2020) Transcutaneous Spinal Cord Direct-Current Stimulation Modulates Functional Activity and Integration in Idiopathic Restless Legs Syndrome. Front. Neurosci. 14:873. doi: 10.3389/fnins.2020.00873

Received: 25 May 2020; Accepted: 27 July 2020;
Published: 21 August 2020.

Edited by:

Jiaojian Wang, University of Electronic Science and Technology of China, China

Reviewed by:

Chao Wang, Shenzhen University, China
Sangma Xie, Hangzhou Dianzi University, China

Copyright © 2020 Zeng, Wang, Cheng, Qi, He, Xu, Han, Liu and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Chunyan Liu, lcy_e_mail@163.com; Yuping Wang, wangyuping01@sina.cn

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.