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Research Article: Observational Study

Altered functional and effective connectivity in anticorrelated intrinsic networks in children with benign childhood epilepsy with centrotemporal spikes

Luo, Cheng PhDa,*; Yang, Fei MSb; Deng, Jiayan MSa; Zhang, Yaodan MSb; Hou, Changyue MSa; Huang, Yue MDc; Cao, Weifang PhDa; Wang, Jianjun MSc; Xiao, Ruhui MSd; Zeng, Nanlin MSd; Wang, Xiaoming MDb,*; Yao, Dezhong PhDa,*

Editor(s): Yong., Li

Author Information
doi: 10.1097/MD.0000000000003831


1 Introduction

Benign childhood epilepsy with centrotemporal spikes (BECTS) is the most common type of idiopathic epilepsy in children. The onset of this disorder ranges from 1 to 14 years old. Electroencephalography (EEG) has revealed that epileptiform discharges are localized to the centrotemporal region (Rolandic region).[1] This syndrome remits spontaneously after adolescence and does not result in structural brain damage or cognitive deficits. However, recent studies have shown that children with BECTS exhibit the following symptoms that strongly influence their daily lives: an increased frequency of partial motor seizures during sleep, the daytime appearance of atypical absence seizures, negative myoclonus, and loss of tension.[2] Additionally, BECTS is thought to be associated with abnormal development, psychiatric disorders associated with reduced IQ, dyscalculia, dyslexia, spatial perception and orientation problems, and visuomotor impairments.[3] Selective language deficits have been observed during the active phase of the syndrome.[4] These behavioral abnormalities may be associated with disturbed cerebral organization in children with BECTS.

Spontaneous low-frequency blood oxygenation level-dependent (BOLD) signals can reflect the synchronization of remote brain regions in the resting state, and are suggestive of many inherent networks in the human brain.[5,6] Research has shown that the BOLD signals are synchronized between brain regions that are connected anatomically or functionally.[7,8] Human brain is intrinsically organized into dynamic, anticorrelated systems that include the task negative network and the task positive network (TPN).[7] The TPN, which is mainly responsible for the processing of external stimuli, including the transfer of information and spatial attention, consists of the bilateral frontal eye fields, the dorsolateral prefrontal cortex, the inferior parietal lobule, the intraparietal sulcus, the supplementary motor area, and the insula. The task negative network, also known as the default mode network (DMN), includes the posterior cingulate cortex (PCC), ventral mesial prefrontal cortex, lateral parietal cortex, bilateral superior frontal cortex, and superior temporal gyrus, and deactivation is often observed in this network during the performance of specific tasks.[7] In resting state functional magnetic resonance imaging (fMRI), the 2 functional networks exhibit significant negative correlations, that is, antagonism,[9–11] in which the nodes were positively (13 typical nodes in DMN)[7] or negatively (16 typical nodes[7] in TPN) correlated with the special region PCC.[7,12] This antagonism might indicate dynamic competition between the 2 networks when multiple types of information are simultaneously processed. One hypothesis is that the reciprocal relationship might reflect a low-frequency toggling between the extrospective states and the self-referential introspective states (task independent). The extrospective states represent a preparedness to ensures that an individual is attentive to novel or unexpected environmental events.[9] The potential degree of antagonism between the 2 systems might be associated with the binding mechanism that the brain utilizes to process multiple threads while simultaneously performing psychophysiological functions. Some researchers have suggested that this antagonism may be of more scientific interest than the default mode activity.[7] In addition, the resting state functional connectivity (FC) between and among the 2 networks is also influenced by the prior brain states.[13,14]

Recently, many studies have reported altered anticorrelations between the 2 networks in patients with autism,[15] schizophrenia,[16] and attention deficit hyperactivity disorder[17] based on resting state fMRI. A proper neural machinery is important for maintaining normal neurocognitive and neuropsychological states, and the lack of a proper neural machinery has been considered to be associated with altered antagonism in these patients.[15,17] Furthermore, research has found that children with BECTS exhibit less activation in the DMN compared with control children during resting states and less deactivation in the DMN compared with control children when the subjects are asked to perform language tasks.[18] Thus, the dynamic interactions within and between the DMN and TPN might provide some evidence that will aid the understanding of the behavioral abnormalities in patients with BECTS. Granger causal analysis is often used to assess effective connectivity in the human brain based on resting state fMRI data.[19–21] These analyses may help to predict neuronal activity levels and FC dynamics in the human brain.[22] The dynamic features of the DMN have been evaluated in healthy controls and patients with Alzheimer disease.[23,24] Therefore, the alterations in the functional and effective connectivities between the TPN and DMN in patients with BECTS might be associated with disturbed neurocognitive function and abnormal development.

The purpose of this study was to test the functional and effective connectivities between and within the 2 antagonistic networks in patients with BECTS. First, using FC analysis between regions of interest (ROI) within the network, we reconstructed the functional connections within and between the ROIs in the TPN and DMN in the patient and control groups. We then assessed the effective connectivities using conditional Granger causality analysis. The effective and functional connections between each pair of ROIs were compared between 2 patients and healthy controls.

2 Materials and Methods

2.1 Subjects

Twenty-one BECTS patients (all right handed, 13 girls, age range: 6–11.5 years, 4 cases with right discharges, 7 cases with left discharges, and 10 cases with bilateral discharges) participated in the current study. These patients were recruited at the Affiliated Hospital of the North Sichuan Medical College. All of the patients underwent a comprehensive clinical evaluation for the diagnoses of BECTS according to the epilepsy classification of the International League Against Epilepsy.[25] The exclusion criteria were as follows: brain lesions on routine brain MRI scans, developmental disabilities, and other accompanying neurologic disorders. Twelve patients were newly diagnosed with epilepsy and did not receive antiepileptic drugs, and 9 patients received monotherapy with valproic acid or levetiracetam. Twenty healthy volunteers (all right handed, 10 girls, age range 6–12) were recruited as the healthy control group. The controls had no neurological or psychiatric disorders. There was no difference in the ages or genders between the 2 groups (2-sample t test of age P > 0.05 and Pearson Chi-square test of gender P > 0.05). The demographic information of the subjects is shown in Table 1. This research was approved by the Ethics Committee of the affiliated hospital of North Sichuan Medical College. All subjects and parents provided the written informed consent before any study procedure was initiated. All subjects were also included in our previous study.[26]

Table 1
Table 1:
Demographic, clinical characteristics of patients with BECTS and HC.

2.2 Neuropsychological assessment

The verbal intelligence quotient (IQ), performance IQ, and full-scale IQ based on the Chinese version of the Wechsler Intelligence Scale for Children (WISC-III) were assessed in both BECTS and control participants. The verbal IQ includes common sense, classification, arithmetic, vocabulary, and intelligence. The Performance IQ includes charting, picture arrangement, building blocks, picture mosaics, and coding.

2.3 fMRI data acquisition

All images were acquired on a 3T GE MRI scanner (EXCITE, GE, Milwaukee, WI) using a standard GE whole-head coil with eight-channel phased array. Functional images were acquired with a single shot, gradient-recalled echo-planar imaging sequence. The sequence parameters were as follows: repetition time = 2000 milliseconds, echo time = 30 milliseconds, flip angle = 90°, slice thickness = 4 milliseconds (no gap), data matrix = 64 × 64, field of view = 24 cm × 24 cm, and 32 axial slices in each volume. Two hundred five volumes were acquired in a single run. The first 5 volumes were discarded to ensure stabilization of the major magnetic field. Subjects were asked to close their eyes and to remain awake during the scanning. Anatomical T1-weighted images were acquired using a 3-dimensional fast spoiled gradient recalled sequence. The parameters were as follows: thickness = 1 mm (no gap), repetition time = 8.2 milliseconds, echo time = 3.2 milliseconds, field of view = 25.6 cm × 25.6 cm, flip angle = 12°, data matrix = 256 × 256. There were 136 axial slices for each subject.

2.4 fMRI data preprocessing

Image preprocessing was performed using the statistical parametric mapping (SPM8, software package implemented in MATLAB 2013a. Preprocessing consisted of the following steps. First, slice timing and head-motion detection were performed for each subject's functional data. Any subject with excessive motion (translation is greater than 2 mm or head rotation greater than 1.5°) was excluded. Second, the functional data were spatially normalized to the standard Montreal Neurological Institute space and resampled to 3 × 3 × 3 mm3. Finally, spatial smoothing was applied with a Gaussian kernel of 6 mm at full width at half-maximum.

2.5 Functional connectivity of the DMN and TPN

First, based on previous study,[7] the number of ROIs in 2 networks was set as 29, including 13 ROIs in the DMN and 16 ROIs in the TPN. Then, the PCC (−1, −33, 40) was selected as a seed to identify the DMN (positivity connection map) and TPN in both groups.[27,28] The peak voxel with the most significant connection to PCC in each of 29 regions was extracted as the center of ROI. Detailed information about the ROIs is listed in Table 2. The mean time series of each ROI was obtained by averaging the time series of all voxels in the spheres with a 6-mm radius around the central coordinates (Table 2). The time series were further temporally band-pass filtered (0.01–0.1 Hz), and the 6 motion parameters obtained by rigid body correction, the white matter and the whole brain signals were regressed out. The residuals of these regressions were processed by the linear detrending. For each subject, a temporal correlation matrix (29 × 29) was obtained by calculating the Pearson correlation coefficients between each pair of ROIs. Next, the Fisher Z-transformation was applied to the correlation matrix to approximate a Gaussian distribution.

Table 2
Table 2:
The 29 ROIs in DMN and TPN.

Statistical analyses of the FC were performed within and between groups. On the one hand, the within-group FC was analyzed using 1-sample, 2-tailed t tests. On the other hand, 2-sample 2-tailed t tests were used to identify the differences in FC between the 2 groups for each pair of connections. We also performed correlation analyses between the FC based on significant differences between groups and the neuropsychological test scores and clinical features (i.e., duration of epilepsy and age of onset) while controlling for the effects of age and gender.

2.6 Granger connectivity analysis

The effective connectivity analysis was applied to 29 ROIs in the 2 networks using the Granger causal connectivity toolbox.[29] First, the preprocessed time courses were extracted for each ROI and each subject, and the conditional Granger causality was assessed for each pair of ROIs in which each ROI was chosen as the origin or target. An F test implemented in the Granger causal connectivity toolbox was used to define the causal interaction coefficients based on the null hypothesis that the conditional Granger causality was zero. Then, the nonparametric test was adopted to identify the directed causal connection as a causal flow for each group (Wilcoxon signed rank test). The causal connectivity amplitudes were required to differ from the null distribution. The bootstrap methodology (the randomly sampled number of surrogate time series was 1000) was used to construct the null distribution of causal connectivity amplitudes. Lastly, the outflow degrees which represents the amount of the number of outflows of a given nodes, and inflow degrees which sums all the inflows were calculated for each node and each subject. The difference between the inflow- and outflow degrees was defined as the out–in degrees, which were tested to quantify the differences between the 2 groups (Wilcoxon signed rank test).

3 Results

3.1 Demographic characteristics and neuropsychological tests

Four patients and three controls were excluded due to excessive motion (translation greater than 2 mm in three patients and 2 controls; head rotation greater than 1.5° in 1 patient and 1 control). Seventeen patients with BECTS and 17 controls were included in the FC analysis. Table 1 illustrates the demographic characteristics and the results of the neuropsychological tests.

3.2 Functional Connectivity analysis

There were 406

pairs of potential functional connections between the 29 nodes. The average functional correlation coefficients are illustrated in Fig. 1. Consistent with previous studies, both groups of subjects exhibited positive relationships within the TPN and DMN and negative relationships between the 2 networks. However, more obvious functional connections within and between networks were observed in the patients than in the healthy controls: the control group revealed 33 significantly positive functional connections and 35 marked negative functional connections; the patients with BECTS exhibited 53 positive functional connections and 61 negative functional connections. The significance level was set at P < 0.001 in 1 sample t test for each group (FDR corrected for the multiple comparisons).

Figure 1
Figure 1:
The functional connectivity in patients BECTS (right) and healthy controls (left). The significant connections with P < 0.001 (FDR corrected for the multiple comparisons) are illustrated. The nodes in TPN are colored in red, and the nodes in DMN are colored in blue. The red lines delineate the positive functional connections (within network), and the blue lines represent the negative functional connections (between 2 networks). BECT = benign childhood epilepsy with centro-temporal spikes, FDR = False Discover Rate, DMN = Default Mode Network, TPN = Task Positive Network.

Regarding the positive functional connections within the networks, the patients with BECTS exhibited 1 pair of increased functional connections within the DMN and 3 pairs of increased functional connections within the TPN relative to the healthy controls (Table 2), but no decreased functional connections were observed in the 2 networks. Regarding the negative functional connections between the networks, there were 2 pairs of functional connections with significantly decreased anticorrelations between the networks in the patients with BECTS compared with the healthy controls (Table 3). No increased functional connections were observed. In other words, the antagonism between the 2 networks was enhanced in the patients with BECTS.

Table 3
Table 3:
Increased functional connectivity within DMN and TPN in BECTS patients.

Additionally, the patients with BECTS also exhibited stronger connectivity between the SMA and rDLPFC; this connectivity was significantly positively correlated with the duration of epilepsy (r = 0.687, P = 0.002, Fig. 2) after controlling for the effects of gender and age. There were no significant correlations between FC and IQ scores.

Figure 2
Figure 2:
(A) The difference of functional connectivity between 2 groups. The red line represents the increased functional connections in patients compared with healthy controls, and the blue represents the decreased connections. Same as Figure 1, the red dots mean the nodes in TPN, and the blue one means the nodes in DMN. (B) The positive correlation between epilepsy duration (months) and the functional connection between SMA and right DLPFC. *Residuals after controlling for the influence of the gender, age (years), and AEDs (linear regression with covariates including gender and age). The green arrowed line between Sections A and B means that the functional connection positively correlated with the duration of epilepsy.

3.3 Granger causality analysis

The average values of the Granger causal flows in the patients and healthy controls are shown in the Supplementary Material (S_Table 1 for the patients and S_Table 2 for the healthy controls). The significant Granger causal flows were delineated with arrowed line in Fig. 3. The within-group level out–in degree is illustrated in Fig. 4. The pattern in the healthy controls was clearly distinct from that in the patients. Compared with the healthy controls, the patients exhibited decreased out–in degrees in the left ventral occipital lobe and the left superior frontal cortex. The main inflow and outflow connections of 2 nodes were showed in the Supplementary Material (S_Figure 1,

Figure 3
Figure 3:
The average Granger causality in patients with BECTS (right) and healthy controls (left). The arrows represent the direction of the effective connections. The nodes in TPN are colored in red, and the nodes in DMN are colored in blue. The arrowed line represents the direction of Granger causal connection between 2 nodes.
Figure 4
Figure 4:
The within-group level causal flow (out–in degree). The red bars show the significant difference between groups (P < 0.05).

4 Discussion

Using functional and effective connectivity analyses on the resting state fMRI data, the current study primarily investigated the intrinsic connectivity between the nodes in the DMNs and TPNs of patients with BECTS and healthy controls. Positive FC within the networks and negative connectivity between the 2 networks were observed in both groups. Compared with the healthy controls, 2 main findings were observed in the patients. First, the patients exhibited more marked increases in FC within both networks, particularly in the frontoparietal nodes, including the left superior frontal cortex, and enhanced antagonism between the 2 intrinsic networks, which suggested abnormal functional integration among the nodes of the 2 networks in the patients. Second, the effective connectivity analysis revealed a significant difference in the degree of outflow relative to inflow in the left superior frontal cortex and left ventral occipital lobe in which the main forward causal interaction (output) in the healthy controls was changed into a backward causal flow (left ventral occipital lobe) or no significant out-in flow (left superior frontal cortex). These findings indicated an altered effective connection pattern in the patients with BECTS that might be related to the some frontoparietal nodes which located the epileptogenic zones in previous studies.[30,31] In general, the alterations of the functional and effective connectivities might reflect not only the association between the abnormal information integration ability and epileptic neuropathology in BECTS but also the abnormal development of the patients with cognitive impairments.

In previous studies, decreased FC has often been reported in patients with different types of epilepsy,[26,32,33] suggesting that the epileptiform activity interrupts the functional interactions of the brain. Interestingly, more obvious FC was observed in the patients with BECTS than in the healthy controls. There are 2 possibilities that might help to interpret this unusual phenomenon. On the one hand, the potential epileptogenic zones of BECTS are thought be in the frontoparietal lobe, that is, in the postcentral gyrus,[30] which is associated with the TPN. In addition, the seizure focus and propagation were investigated by the resting state function connectivity analysis[34] and effective connectivity analysis.[35] Thus, the functional integration between nodes of the network might be enhanced because of the long-term epileptiform activity in these regions associated with epileptogenic zones. On the other hand, the essential clinical feature of BECTS, that is, the remission of seizures spontaneously after adolescence,[36] might contribute to the differences in the findings related to BECTS and other types of epilepsy with poor prognoses. Future studies are needed to confirm these speculations.

In general, the slowing or regression of development in children with epilepsy is primarily due to seizures, abnormal interictal cortical and subcortical epileptic activity, or both.[37–39] BECTS is a common type of childhood epilepsy. We presumed that the epileptic activity would contribute to the cognitive behavioral defects and abnormal neuroimaging findings in children with BECTS. The DMN, which is sensitive to development,[40,41] and its anticorrelated network, the TPN, were investigated in this study. In previous studies, the functional integration of the DMN has been found to change from sparse to cohesive during childhood.[42] Here, the patients with BECTS exhibited not only altered FC between the nodes in the DMN but also anticorrelated activity between the nodes of the DMN and TPN. The abnormal FC related to the DMN might indicate that the developmental trajectory of the default mode of the brain was interrupted in these children patients. Additionally, the patients recruited for this study also exhibited decreased IQ scores relative to the healthy controls of the same age. Because the BECTS was considered as a benign epileptic syndrome without or with slight cognitive impairments,[43,44] our BECTS group would represent a cohort of specific patients with BECTS syndrome. These cognitive impairments might be related with the interrupted development in children patients. The regressions in cognitive development are typically observed in childhood and adolescence with reductions in IQ, language impairments, and neurobehavioral disturbances.[37,45] However, the use of a longitudinal design rather than the cross-sectional analysis used in this study would provide a preferable avenue to study development. Therefore, our findings reflect the abnormal development of BECTS children with cognitive impairments to some extent. The DMN and its associated regions (including the anticorrelated regions) might provide a potential window to investigate the abnormalities of development in children with epilepsy.

Findings from studies with simultaneous EEG and fMRI have shown significant negative activations in regions of the DMN and positive activations in regions of the TPN in response to both general and local epileptic discharges.[46] These regions are considered to be associated with the origination and/or propagation of the epileptic activity. The pre- and postcentral gyri have been observed to exhibit significant activation related to the local epileptiform spikes of BECTS in simultaneous EEG and fMRI.[30] In scalp EEGs, the centrotemporal region (i.e., the frontoparietal lobe) is commonly observed to exhibit epileptiform discharges in patients with BECTS.[31] Significantly increased functional connections between the frontal (SFC, DLPFC, and FEF) and parietal nodes (IPS and vIPS) were observed in this study. The increased FC exhibited in these nodes in the frontoparietal lobe might reflect the abnormal features of the connections of these regions and their tight associations with long-term epileptic activity. Moreover, the increased FC between the DLPFC and SMA was positively correlated with the duration of epilepsy. Moreover, consistent with the increased FC with the SFC, the effective connectivity analysis also demonstrated obvious alterations and abnormal causal flow directions and magnitudes in the left SFCs of the patients compared with the healthy controls. This causality may represent physiological inhibitory and excitatory effects and elucidates the pathophysiology of severe disorders.[47,48] According to the out–in degree (Fig. 4), the patients exhibited a predominant driving (outflow) effect from the left SFC to the other nodes in which feedback (inflow) was observed in the healthy controls. Altogether, our findings derived from combined functional and efficient connectivity analyses provided further evidence that interruptions in the frontoparietal nodes of the DMN and TPN may be associated with epileptiform activity in BECTS.

With regard to the limitations of this study, it could be argued that the antiepileptic drugs might cause the altered brain connectivity. Nine in 21 patients received the antiepileptic drugs in this study. The effects of the drugs might confound our observation. Second, the side of spikes in unilateral BECTS might influence the findings showed in the current study. More patients with BECTS would be recruited in future to investigate the lateral spikes’ effect on the functional and effective connectivity among the nodes in DMN and TPN. Then, the BECTS syndrome is in general not associated with significant cognitive abnormalities. Our patients’ group showed decreased IQ compared with healthy controls, thus, the findings would represent only one aspect of typical BECTS syndrome. Finally, the patients with BECTS were just performed the clinical routine EEG in this study. It is difficult to evaluate the precise source of spikes and the relation with the findings of functional and effective connectivity showed here. The high density EEG would be recorded to noninvasively localize the epileptic focus in future.

5 Conclusion

In this study, the intrinsic functional organization of the brain was investigated with functional and effective connectivity analyses of synchronized low-frequency fluctuations of the BOLD signals in the TPN and DMN in BECTS. We found that the patients with BECTS exhibited significantly altered functional connectivities within the networks and antagonism between the networks. Additionally, the nodes in the frontoparietal lobe with altered FC exhibited abnormal effective connectivities. These findings derived from combined functional and effective connectivity analyses might indicate an association of the abnormal information integration ability of the DMN-TPN with the epileptic neuropathology of BECTS. These findings provide preliminary evidence supporting the occurrence of abnormal development in BECTS children with cognitive impairments.


1. Loiseau P, Duche B. Benign childhood epilepsy with centrotemporal spikes. Cleve Clin J Med 1989; 56:S17–22.
2. Pardoe HR, Berg AT, Archer JS, et al. A neurodevelopmental basis for BECTS: evidence from structural MRI. Epilepsy Res 2013; 105:133–9.
3. Hughes JR. Benign epilepsy of childhood with centrotemporal spikes (BECTS): to treat or not to treat, that is the question. Epilepsy Behav 2010; 19:197–203.
4. Monjauze C, Broadbent H, Boyd SG, et al. Language deficits and altered hemispheric lateralization in young people in remission from BECTS. Epilepsia 2011; 52:e79–83.
5. Fox MD, Raichle ME. Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nat Rev Neurosci 2007; 8:700–11.
6. Fransson P. Spontaneous low-frequency BOLD signal fluctuations: an fMRI investigation of the resting-state default mode of brain function hypothesis. Hum Brain Mapp 2005; 26:15–29.
7. Fox MD, Snyder AZ, Vincent JL, et al. The human brain is intrinsically organized into dynamic, anticorrelated functional networks. Proc Natl Acad Sci USA 2005; 102:9673–8.
8. Salvador R, Suckling J, Coleman MR, et al. Neurophysiological architecture of functional magnetic resonance images of human brain. Cereb Cortex 2005; 15:1332–1342.
9. Broyd SJ, Demanuele C, Debener S, et al. Default-mode brain dysfunction in mental disorders: a systematic review. Neurosci Biobehav Rev 2009; 33:279–96.
10. Uddin LQ, Kelly AM, Biswal BB, et al. Functional connectivity of default mode network components: correlation, anticorrelation, and causality. Hum Brain Mapp 2009; 30:625–37.
11. Corbetta M, Kincade JM, Shulman GL. Neural systems for visual orienting and their relationships to spatial working memory. J Cogn Neurosci 2002; 14:508–23.
12. Spreng RN, Sepulcre J, Turner GR, et al. Intrinsic architecture underlying the relations among the default, dorsal attention, and frontoparietal control networks of the human brain. J Cogn Neurosci 2013; 25:74–86.
13. Tailby C, Masterton RA, Huang JY, et al. Resting state functional connectivity changes induced by prior brain state are not network specific. NeuroImage 2015; 106:428–40.
14. Grigg O, Grady CL. Task-related effects on the temporal and spatial dynamics of resting-state functional connectivity in the default network. PLoS ONE 2010; 5:e13311.
15. Kennedy DP, Courchesne E. The intrinsic functional organization of the brain is altered in autism. NeuroImage 2008; 39:1877–1885.
16. Williamson P. Are anticorrelated networks in the brain relevant to schizophrenia?. Schizophr Bull 2007; 33:994–1003.
17. Castellanos FX, Margulies DS, Kelly C, et al. Cingulate-precuneus interactions: a new locus of dysfunction in adult attention-deficit/hyperactivity disorder. Biol Psychiatry 2008; 63:332–7.
18. Oser N, Hubacher M, Specht K, et al. Default mode network alterations during language task performance in children with benign epilepsy with centrotemporal spikes (BECTS). Epilepsy Behav 2014; 33:12–7.
19. Deshpande G, Hu X. Investigating effective brain connectivity from fMRI data: past findings and current issues with reference to Granger causality analysis. Brain Connect 2012; 2:235–45.
20. Liao W, Mantini D, Zhang Z, et al. Evaluating the effective connectivity of resting state networks using conditional Granger causality. Biol Cybern 2010; 102:57–69.
21. Luo C, Guo ZW, Lai YX, et al. Musical training induces functional plasticity in perceptual and motor networks: insights from resting-state FMRI. PLoS ONE 2012; 7:e36568.
22. Hansen EC, Battaglia D, Spiegler A, et al. Functional connectivity dynamics: modeling the switching behavior of the resting state. NeuroImage 2015; 105:525–35.
23. Jiao Q, Lu G, Zhang Z, et al. Granger causal influence predicts BOLD activity levels in the default mode network. Hum Brain Mapp 2011; 32:154–61.
24. Miao X, Wu X, Li R, et al. Altered connectivity pattern of hubs in default-mode network with Alzheimer's disease: an Granger causality modeling approach. PLoS ONE 2011; 6:e25546.
25. Engel J. A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology. Epilepsia 2001; 42:796–803.
26. Luo C, Zhang Y, Cao W, et al. Altered structural and functional feature of striato-cortical circuit in benign epilepsy with centrotemporal spikes. Int J Neural Syst 2015; 25:1550027.
27. Yang T, Luo C, Li Q, et al. Altered resting-state connectivity during interictal generalized spike-wave discharges in drug-naive childhood absence epilepsy. Hum Brain Mapp 2013; 34:1761–7.
28. Luo C, Li Q, Lai Y, et al. Altered functional connectivity in default mode network in absence epilepsy: a resting-state fMRI study. Hum Brain Mapp 2011; 32:438–49.
29. Seth AK. A MATLAB toolbox for Granger causal connectivity analysis. J Neurosci Methods 2010; 186:262–73.
30. Masterton RA, Harvey AS, Archer JS, et al. Focal epileptiform spikes do not show a canonical BOLD response in patients with benign rolandic epilepsy (BECTS). NeuroImage 2010; 51:252–60.
31. Kellaway P. The electroencephalographic features of benign centrotemporal (rolandic) epilepsy of childhood. Epilepsia 2000; 41:1053–6.
32. Zhang Z, Lu G, Zhong Y, et al. Impaired perceptual networks in temporal lobe epilepsy revealed by resting fMRI. J Neurol 2009; 256:1705–1713.
33. Sargolzaei S, Cabrerizo M, Goryawala M, et al. Scalp EEG brain functional connectivity networks in pediatric epilepsy. Comput Biol Med 2015; 56:158–66.
34. Luo C, An D, Yao D, et al. Patient-specific connectivity pattern of epileptic network in frontal lobe epilepsy. NeuroImage Clin 2014; 4:668–75.
35. Klamer S, Rona S, Elshahabi A, et al. Multimodal effective connectivity analysis reveals seizure focus and propagation in musicogenic epilepsy. NeuroImage 2015; 113:70–7.
36. Bouma PA, Bovenkerk AC, Westendorp RG, et al. The course of benign partial epilepsy of childhood with centrotemporal spikes: a meta-analysis. Neurology 1997; 48:430–7.
37. Holmes GL, Lenck-Santini PP. Role of interictal epileptiform abnormalities in cognitive impairment. Epilepsy Behav 2006; 8:504–15.
38. Xue K, Luo C, Zhang D, et al. Diffusion tensor tractography reveals disrupted structural connectivity in childhood absence epilepsy. Epilepsy Res 2014; 108:125–38.
39. Jiang S, Luo C, Liu Z, et al. Altered local spontaneous brain activity in juvenile myoclonic epilepsy: a preliminary resting-state fMRI study. Neural Plast 2016; 2016:1–7.
40. Fransson P, Skiold B, Horsch S, et al. Resting-state networks in the infant brain. Proc Natl Acad Sci USA 2007; 104:15531–6.
41. Thomason ME, Chang CE, Glover GH, et al. Default-mode function and task-induced deactivation have overlapping brain substrates in children. NeuroImage 2008; 41:1493–503.
42. Fair DA, Cohen AL, Dosenbach NU, et al. The maturing architecture of the brain's default network. Proc Natl Acad Sci USA 2008; 105:4028–4032.
43. Lopes AF, Simoes MR, Monteiro JP, et al. Intellectual functioning in children with epilepsy: frontal lobe epilepsy, childhood absence epilepsy and benign epilepsy with centro-temporal spikes. Seizure 2013; 22:886–92.
44. Datta AN, Oser N, Bauder F, et al. Cognitive impairment and cortical reorganization in children with benign epilepsy with centrotemporal spikes. Epilepsia 2013; 54:487–94.
45. Eddin AS, Wang J, Wu W, et al. The effects of pediatric epilepsy on a language connectome. Hum Brain Mapp 2014; 35:5996–6010.
46. Gotman J, Grova C, Bagshaw A, et al. Generalized epileptic discharges show thalamocortical activation and suspension of the default state of the brain. Proc Natl Acad Sci USA 2005; 102:15236.
47. Ji GJ, Zhang Z, Zhang H, et al. Disrupted causal connectivity in mesial temporal lobe epilepsy. PLoS ONE 2013; 8:e63183.
48. Palaniyappan L, Simmonite M, White TP, et al. Neural primacy of the salience processing system in schizophrenia. Neuron 2013; 79:814–28.

antagonism; benign childhood epilepsy; default mode; effective connectivity; functional connectivity; functional magnetic resonance imaging

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