Jiangwei Ding1,2†
Lei Wang1,3†
Wenchao Li1,3
Yangyang Wang1,3
Shucai Jiang1,2
Lifei Xiao1,2
Changliang Zhu1,2Xiaoyan Hao4Jiali Zhao1Xuerui Kong1Ziqin Wang1Guangyuan Lu1*
Feng Wang1,5*
Tao Sun1,2*- 1Ningxia Key Laboratory of Cerebrocranial Disease, The Incubation Base of National Key Laboratory, Ningxia Medical University, Yinchuan, China
- 2Department of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China
- 3Department of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, Weihui, China
- 4Department of Neurology, First Affiliated Hospital of Zhengzhou University, Academy of Medical Sciences of Zhengzhou University, Zhengzhou, China
- 5Department of Neurosurgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Background: Dravet syndrome (DS) is a refractory developmental and epileptic encephalopathy (EE) with a variety of comorbidities, including cognitive impairment, autism-like behavior, speech dysfunction, and ataxia, which can seriously affect the quality of life of patients and impose a great burden on society and their families. Currently, the pharmacological therapy is patient dependent and may work or not. Neuromodulation techniques, including vagus nerve stimulation (VNS), deep brain stimulation (DBS), transcranial magnetic stimulation (TMS), responsive neurostimulation (RNS), and chronic subthreshold cortical stimulation (CSCS), have become common adjuvant therapies for neurological diseases, but their efficacy in the treatment of DS is unknown.
Methods: We searched Web of Science, PubMed, and SpringerLink for all published cases related to the neuromodulation techniques of DS until January 15, 2022. The systematic review was supplemented with relevant articles from the references. The results reported by each study were summarized narratively.
Results: The Web of science, PubMed and SpringerLink search yielded 258 items. A total of 16 studies published between 2016 and 2021 met the final inclusion criteria. Overall, 16 articles (109 cases) were included in this study, among which fifteen (107 patients) were involved VNS, and one (2 patients) was involved DBS. After VNS implantation, seizures were reduced to ≥50% in 60 cases (56%), seizure free were found in 8 cases (7.5%). Only two DS patients received DBS treatment, and the initial outcomes of DBS implantation were unsatisfactory. The seizures significantly improved over time for both DBS patients after the addition of antiepileptic drugs.
Conclusion: More than half of the DS patients benefited from VNS, and VNS may be effective in the treatment of DS. However, it is important to note that VNS does not guarantee improvement of seizures, and there is a risk of infection and subsequent device failure. Although DBS is a safe and effective strategy for the treatment of refractory epilepsy, the role of DBS in DS needs further study, as the sample size was small. Thus far, there is no strong evidence for the role of DBS in DS.
Introduction
Epileptic encephalopathy (EE) generally refers to severe cognitive and behavioral impairments resulting from epileptic activity. Such impairments can worsen over time, and the extent of these impairments often exceeds what would be expected from the underlying pathology alone (1). Dravet syndrome (DS), also known as severe infantile myoclonic epilepsy, is a severe EE primarily caused by haploinsufficiency of the SCN1A gene, which encodes the brain voltage-gated sodium channel NaV1.1 (2, 3). Similarly, gene missense or point mutation mutations in SCN2A, SCN8A, SCN1B, PCDH19, GABRA1, GABRG2, STXBP1, HCN1, CHD2, and KCNA2 can also cause DS or DS-like symptoms (4).
Febrile seizure is a typical feature of the early stage (“febrile” phase) of DS. Patients usually have seizures (mostly clonic generalized and unilateral motor seizures) after a fever, vaccination, or warm bath in the first year of life (usually between 4 and 8 months) and often progress to status epilepticus (5–7). This phase is followed by the “worsening” phase at the age of 1–4 years, characterized by the presence of additional seizure types (such as generalized motor, atypical, myoclonic, and absence seizures) with cognitive, behavioral, and motor impairments in which thermogenic factors can still induce seizures (5–8). Finally, the “worsening” phase is followed by the “stabilization” phase, in which the frequency of seizures is reduced compared with the febrile stage (generalized tonic–clonic seizures and tonic seizures are still observed), but cognitive and psychomotor disorders and ataxia are significantly aggravated in the previous phase (5, 7–9). In addition to difficult-to-control epilepsy, DS is often associated with some serious comorbidities, including cognitive impairment, premature death, autism, sleep disorders, hyperactivity, ataxia, and sudden unexpected death in epilepsy (SUDEP) (Figure 1) (9–12), which seriously affect the quality of life of affected children and impose heavy burdens on society and family.
Figure 1. Multiple genetic mutations cause DS or DS-like phenotypes and lead to epilepsy and its comorbidities including cognitive dysfunction (motor, language, and intellectual deficits), autistic behavior, ataxia, sleep disorders, SUDEP and premature death.
Neuromodulation, including vagus nerve stimulation (VNS), deep brain stimulation (DBS), and transcranial magnetic stimulation (TMS), responsive neurostimulation (RNS), and chronic subthreshold cortical stimulation (CSCS) (Figure 2), has been widely used in drug-resistant epilepsy (DRE), drug-resistant depression, Parkinson's disease, and other neurologic diseases (Figure 2) (13–19), VNS is the most commonly used of these neuromodulation techniques. Currently, approximately 1,00,000 patients worldwide have received VNS implants (20), but the effectiveness of neuromodulation in DS has rarely been evaluated.
Figure 2. Brief schematic diagram of three neuromodulation techniques commonly used in Dravet syndrome. (A) Vagus nerve stimulation (VNS); (B) Deep brain stimulation (DBS); (C) Transcranial magnetic stimulation (TMS). (A) Vagus nerve technique (VNS); (B) Deep brain stimulation (DBS); (C) Repetitive transcranial magnetic stimulation (rTMS) (13); (D) Responsive neurostimulation (RNS) (18); (E) and chronic subthreshold cortical stimulation (CSCS) (20).
Methods
Literature Search
A systematic search was performed in Web of science, PubMed and SpringerLink. The most recent search was performed on January 15, 2022, using the term (Dravet Syndrome) AND [(VNS) OR (DBS) OR (TMS) OR (RNS) OR (CSCS)]. We also screened references from the published review papers on VNS and Dravet syndrome. References from relevant articles were used to supplement the systematic review (Figure 3).
Figure 3. Flow diagram depicting search process and study selection.
Data Extraction
We excluded articles not written in English or Chinese, if any. Non-original work that has nothing to do with people, such as reviews, meta-analysis, animals or cells, experimental articles not adding information to the question posed in this review, and papers that could not be retrieved via PubMed or SCOPUS. The records were screened by JD and evaluated by LW with respect to the inclusion and exclusion criteria. Disagreements were resolved through a discussion between the two review authors.
Study Selection Criteria
Inclusion criteria: (i) all neuromodulation techniques related to DS, (ii) effective data between DS and neuromodulation techniques that can be extracted independently, and (iii) not only must the neuromodulation techniques be applied, but also the purpose of epilepsy improvement in DS.
Exclusion criteria: (i) non-neuromodulation techniques, such as antiepileptic drugs, and resection; (ii) DS mixed with other refractory epilepsy disease so that data cannot be summarized for the treatment effect of DS; (iii) only neuromodulation techniques applied but no focus on therapeutic effects for epilepsy; and (iv) unpublished studies, case reports, comments, practice guidelines, reviews, or letters.
Results
After the elimination of duplicates (20 articles), the literature search yielded 238 articles (Figure 1). After screening all the abstracts, 179 records were excluded. Thus, 59 articles were included in the full-text analysis. Of these, 49 full-text articles were excluded. Six records were identified and supplemented by references to other articles.
Finally, 16 studies met the inclusion and did not meet the exclusion criteria (Figure 1).
Summary of Findings
According to the previous description, in this study, we still defined the improvement of epilepsy control (responder) as a reduction of more than 50% in generalized tonic-clonic or secondarily generalized tonic-clonic seizures. Patients were followed up for at least 6 months after implantation, otherwise, there was no improvement (responder) (21).
Sixteen articles were eligible in the study, among which 15 (107 patients) were involved in the treatment of DS by VNS (21–35), and one (2 patients) was involved in the treatment of DS by DBS (36) and a total of 107 patients with DS were implanted with VNS, of which 60 (56%) had good epileptic control reduced to more than 50%, and the remaining 47(44%) patients had unsatisfactory epileptic control (Table 1). Eight of the patients were seizure-free, and although most of the adverse effects of VNS implantation were not reported, hoarser was the major side effect and weight loss was reported in one case. The clinical experience of DBS in DS is limited. Two patients with anterior thalamic nucleus stimulation had good epileptic control over time, and their seizures were reduced by more than 90% (Table 2).
Table 1. Clinical data of DS patients with VNS implantation.
Table 2. Clinical data of DS patients with DBS implantation.
Discussion
DS is a special type of DRE. Despite the emergence of new antiseizure medications (ASMs; such as cannabidiol, CBD; stiripentol, STP; and fenfluramine, FFA) in recent years, the treatment of DS is still challenging (38). Neuromodulation techniques as a minimally invasive or non-invasive approach is a promising treatment for neurologic disorders. Our objective in this review was to demonstrate the efficacy of neuromodulation techniques, especially VNS, in DS and to provide a treatment option for patients with DS.
Effect of ASMs on Dravet Syndrome
Conventional ASMs Therapy
The treatment of DS follows an individualized treatment regimen, but medication is only partially effective for DS seizures. Commonly used sodium channel blockers such as carbamazepine and lamotrigine may exacerbate seizures or even cause epileptic status, and may also cause further deterioration of cognitive function. Control of seizures often requires a combination of antiepileptic drugs (AEDs), of which valproate and clobazam are considered first-line treatments for DS (38–41). Ketogenic diet (KD) have shown promise in the treatment of DS and have been effective in animal models of DS (41, 42).
Novel ASMs Therapy
Cannabidiol
CBD is one of the most abundant plant-derived cannabinoids. CBD, as a non-psychoactive agent, has pharmacological properties of anti-epilepsy (43–45). The United States Food and Drug Administration (FDA) has approved CBD for two childhood-onset EE: DS and Lennox-Gastaut syndrome (LGS) (46, 47). In 2017,Devinsky et al. conducted a double-blind controlled trial of 120 patients with DS and found that 43% of the patients in the CBD group (oral, 20 mg/kg/day) had at least a 50% reduction in seizures compared with a 27% reduction in the placebo control group (48). Miller et al.'s double-blind evaluation of the efficacy of different doses of CBD for DS showed that the oral administration of 10 and 20 mg/kg/day resulted in seizure control rates of 48.7% and 45.7%, respectively (49). Recently, seizures were reduced to 50 in 71% of patients a long-term open-label extension trial (50). Although CBD has been a great success for patients with DS (45, 51), it still fails in 29% to 57% of patients (48, 50). In addition, in a retrospective analysis, CBD was found to be effective in only 3/17 patients and reduced seizures by only >30% (52). Some objective factors, such as CBD is illegal in some countries including mainland China, which also limits the use of CBD to a certain extent (53). Adverse reactions to CBD include diarrhea, vomiting, fatigue, fever, drowsiness, and abnormal liver function (45, 48) (Table 3).
Table 3. Representative studies of novel ASMs for DS.
Stiripentol
STP is a novel antiepileptic drug with oral activity and unique structure (59, 60). In the European Union and Canada, STP is approved for use in combination with clobacan and valproate as an adjunct treatment for refractory generalized tonic-clonic seizures in patients with DS (infancy). In Japan, STP is approved in combination with clobazam and valproate for the treatment of clonic or tonic-clonic seizures in DS patients with poor response to clobazam and valproate. The United States approved indication for STP is for the treatment of DS related seizures in patients 2 years of age and older taking clobazine (61). Unlike the European Union, Canada and Japan, the United States has an age limit on the use of STP for DS patients and does not specify valproic acid as a required combination drug. STP reduces the frequency of epileptic seizures in DS patients. Compared with other antiepileptic drugs, it acts as an allosteric modulator of GABAAR, and may increase the inhibitory effect of GABA on neurotransmission and enhance the effect of BZ. The initial dose of the drug is 15–20 mg/(kg·d) and the target dose is 50 mg/(kg·d) in 2–4 weeks, with the maximum dose of 100 mg/(kg·d) available for children (56). In a recent study, STP was shown to respond to only 54% of patients (57). Adverse effects commonly observed with STP are dose-dependent and include somnolence, fidgety, irritability, low IOP, nausea, vomiting, loss of appetite and weight. There are also reported risks of elevated γ-glutamyltransferase and neutropenia, so routine tests of liver function and blood are also necessary. Since some of these side effects may be associated with an accompanying increase in valproate or clobazam levels, it is recommended to reduce the dose of the latter two drugs at the onset of STP (Table 3).
Fenfluramine
Sullivan et al. administered FFA to 232 DS patients (initial dose 0.2 mg/kg/d, 4 weeks later, the dose of fenfluramine can be adjusted according to efficacy and tolerability, with a maximum dose of 0.7 mg/kg/d, a maximum dose of 0.4 mg/kg/d when combined with STP), which has been shown to reduce the frequency of seizures in patients (62). Specchio et al. (58) enrolled 52 patients with DS with a median age of 8.6 years and found that FFA reduced the median incidence of DS seizures by 77.4%. 32 patients (71.1%) had a ≥50% reduction in seizures, and 24 patients (53.3%) had a ≥75% reduction in seizures, among which 5 patients (11.1%) had good control without seizures (58). The most common adverse reactions included fever (21.6%), nasopharyngitis (19.4%) and loss of appetite (15.9%), without valvular disease or pulmonary hypertension (62) (Table 3).
Surgery and Ketogenic Diet
Surgical Operation
Epilepsy lesions removal is the preferred treatment for intractable focal epilepsy, such as focal cortical dysplasia and hippocampal sclerosis (63–65). However, DS is mainly caused by SCN1A gene mutation, which belongs to “whole brain” epilepsy (66), resulting in over-excitability of the whole brain region without obvious focal lesions, and does not belong to the surgical indication for focal resection. The corpus callosotomy is a palliative surgical treatment and used as an adjunct treatment for refractory epilepsy. Dlouhy et al. (22). made a retrospective analysis of 7 DS patients, in which 5 patients only received VNS implantation, 1 patient only received corpus callosotomy, and 1 patient only received corpus callosotomy after VNS due to poor epileptic control. However, it is important to note that corpus callosotomy is not currently recommended for the treatment of Dravet syndrome (38–41).
Ketogenic Diet
KD is a diet with a high proportion of fat intake, a moderate proportion of protein intake and a low proportion of carbohydrate intake, which is commonly used as an adjutant non-drug therapy for the treatment of epilepsy in children (67, 68). Although the mechanism of KD is not fully understood, it has benefits in anti-epilepsy and in improving cognitive function and behavior. Caraballo et al. (42) found that epilepsy was significantly controlled in 76.9% of DS patients with a continuous KD for more than 1 year, in which 2 patients (15.4%) had seizure free, and 8 patients (61.5%) had a 75–99% decrease in seizures. A study of 60 Chinese patients with DS also found that KD had a good antiepileptic effect, and with the prolongation of KD use time, the benefits of DS patients increased. Most of the patients had KD effect within 2 weeks. At 12 weeks, 58.3% of the patients had >50% seizure reduction. At 24 weeks and 48 weeks, the percentage of DS patients with >50% reduction in seizures increased to 61.1 and 77.3%, respectively. In addition to epilepsy control, cognitive function improved in 22 patients, language progression in 14 patients, and motor function improved in 13 patients (69). A recent meta-analysis also concluded that 63, 60, and 47% of DS patients had a ≥50% reduction in seizures at 3, 6, and 12 months after KD, and the seizure control rates at 6 and 12 months were 78 and 49%, respectively (37). The KD not only effectively controlled seizures, but also improved cognitive, motor and other behaviors. Even in patients with unreduced seizures, the quality of life was improved, and the number of AEDs reduced to one or two on the ketogenic diet (37, 42). Caraballo et al. (42) believed that KD treatment should be considered immediately after three failed AEDs.
Neurostimulation Techniques
VNS
VNS is the most commonly used neuromodulation for DRE. To date, VNS has been implanted in at least 1,00,000 patients worldwide (20, 70). In addition to DRE, VNS has been approved by the FDA for the treatment of refractory depression, migraine (15, 71, 72), and other central nervous system diseases, such as schizophrenia, addiction, Parkinson's disease (73–75), and non-psychiatric diseases such as rheumatoid arthritis, inflammatory bowel disease, and asthma (76–78).
In 2006, a 165-month-old child with DS received VNS implantation, which may be the first reported case of a child with DS receiving VNS treatment (31). Although seizures were not well controlled in this patient, with only a 25% seizure rate reduction, this has provided new ideas for the treatment of DS. In 2017, the FDA approved VNS for the treatment of DRE in children (79). Since then, an increasing number of DS patients have also received VNS treatment (Table 1). The number of DS patients who received VNS implants after 2017 (62/107, 58%) is significantly more than those receiving them before 2017 (45/107, 42%) (Figure 4A).
Figure 4. (A), Percentage of DS patients receiving VNS before and after 2017; (B), 15 articles on the epilepsy control rate of VNS in the treatment of DS; (C), Percentage of responders and non-responders to DS receiving VNS.
The efficacy of VNS for DRE has been widely established. A recent meta-analysis of 101 studies showed that the 50% response rate and seizure freedom were 56.4 and 11.6%, respectively (14). Another study showed that VNS was effective in 54.6% of patients with LGS (80). Obviously, VNS is effective for non-DS refractory epilepsy, but its efficacy against DS, a genetic refractory epilepsy, is our main concern. Dibue-Adjei et al. reported that about 52.9% of patients with VNS had a >50% reduction in seizure rates (81).
Currently, we have included 15 studies involving 107 patients, of which 60 (56%) saw their seizures reduce by ≥50% and eight (7.5%) became seizure-free, indicating that patients with DS can benefit from VNS (Figures 4B,C, Table 1). These results suggest that VNS is equally effective for both DS and non-DS refractory epilepsy.
Similar findings were reported in a meta-analysis by Dibue-Adjei et al. (81), who reported that 52.9% of patients experienced a 50% reduction of seizures. However, since they included only 68 patients in their study, this is slightly lower than our results (56% reduction of seizures), which may be more reliable than Dibue-Adjei et al.'s (81) results since we systematically included the latest studies (30, 32). Although some studies reported hoarseness, coughing, and weight loss in DS patients treated with VNS (31–35) (Table 1), most of them did not describe side effects, and hence we still cannot draw conclusions on tolerability. But despite this, we think these side effects may be insignificant for good seizure improvement. Currently, only VNS has been included in the third-line treatment of DS, and other surgical options, including callosotomy, are not recommended for DS (53).
DBS
DBS, which is commonly used to treat movement disorders such as Parkinson's disease, has also been shown to improve the treatment of refractory epilepsy (82–84).
DBS implantation in patients with DS is currently rare, but in two current patients (36). DBS has been shown to significantly reduce epileptic status and appears to be beneficial. In one patient, after ANT-DBS implantation, the frequency of seizures was reduced to 11 generalized tonic-clonic seizures per month (81% reduction). Nine and a half years after DBS implantation, the patient experienced 0.5–1 secondarily generalized tonic-clonic seizures per month. Another DS patient underwent callosotomy at the age of 19 and received ANT-DBS at the age of 36. Levetiracetam and lamotrigine therapy were added in the third and 8 years after the operation, but the seizure frequency changed only slightly. Ten years after DBS implantation, the patient's seizure frequency decreased from 15 seizures per month before DBS to 1–5 seizures per month (Table 2).
Conclusion
Neuromodulation techniques are a common adjuvant therapy for neurologic diseases. DS is a rare and catastrophic EE. VNS appears to have a positive effect on DS. DBS has been shown to be effective in DRE, but its role in DS is unclear; therefore, a large number of samples and high-quality controlled studies are required.
Author Contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This study was supported by the National Natural Science Foundation of China, Grant/Award Number: 81971085 and the Advantages Discipline Group Project of Ningxia Medical University, Grant/Award Number: XY201511.
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.
Publisher's Note
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Keywords: Dravet syndrome, drug-resistant epilepsy, neuromodulation, vagus nerve stimulation, deep brain stimulation, transcranial magnetic stimulation
Citation: Ding J, Wang L, Li W, Wang Y, Jiang S, Xiao L, Zhu C, Hao X, Zhao J, Kong X, Wang Z, Lu G, Wang F and Sun T (2022) Up to What Extent Does Dravet Syndrome Benefit From Neurostimulation Techniques? Front. Neurol. 13:843975. doi: 10.3389/fneur.2022.843975
Received: 27 December 2021; Accepted: 14 February 2022;
Published: 13 April 2022.
Edited by:
Yvonne Höller, University of Akureyri, IcelandReviewed by:
Ricardo Zavala-Yoé, Monterrey Institute of Technology and Higher Education (ITESM), MexicoFlavia Venetucci Gouveia, University of Toronto, Canada
Copyright © 2022 Ding, Wang, Li, Wang, Jiang, Xiao, Zhu, Hao, Zhao, Kong, Wang, Lu, Wang and Sun. 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: Guangyuan Lu, gylulifescience@163.com; Tao Sun, suntao_nxmu@163.com; Feng Wang, nxwwang@163.com
†These authors have contributed equally to this work