Young children with multidrug-resistant epilepsy and vagus nerve stimulation res

lNTRODUCTlON

About 10% of children with epilepsy have drug-resistant epilepsy[1]. The treatment of drug-resistant epilepsy can be challenging, including resective surgery, ketogenic diet, vagus nerve stimulation (VNS),and new antiepileptic drugs (AEDs). The anticonvulsant perampanel (PER), a selective and noncompetitive α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist, is a newly developed third-generation AED, possessing the completely different antiepileptic mechanisms with previous AEDs. Currently, PER is recommended by the American Academy of Neurology guideline as add-on therapy in treatment-resistant adult focal epilepsy to reduce epilepsy frequency (level A)[2].However, only a few studies have reported the efficacy and safety of PER in children younger than 12 years old with drug-resistant epilepsy. In this paper, we present a 4-year-old child with multidrugresistant epilepsy in whom the seizures were not well controlled after VNS implantation, and PER administration significantly reduced seizure frequency in a dose-dependent manner. We aimed to describe our experience about reducing the seizures in multidrug-resistant young children with PER.

CASE PRESENTATlON

Chief complaints

A 19-mo-old boy presented with ictal seizures since age 14 mo, and was brought to our pediatric neurology department because of gradually increased seizure attack.

History of present illness

The history taken from the parents revealed that the patient began to have ictal seizures after age 14 mo,with jerky movement of four limbs and head nodding, and he experienced one seizure per week lasting for 1-2 s. His seizure frequency increased gradually, and when he was admitted to our department, he was experiencing 10-15 seizures per day lasting for 1-3 min each time, with hand raising and head nodding. The patient could speak only simple words, and could not communicate with others and understand instructions.

History of past illness

The patient had a free previous medical history.

Personal and family history

His parents reported that there was no consanguinity, and the patient was born at full termvaginal delivery with a birth weight of 3100 g. He had no perinatal asphyxia, and his Apgar scores were 10 at 1,5 and 10 min of life. He had no family history of epilepsy and other familial diseases.

Physical examination

Physical examination showed that the patient had normal consciousness but could not communicate with others and understand instructions. He showed normal appearance, and there was no abnormal skin mass or depigmentation. The muscle tension, strength and mobility of the limbs were normal.

Laboratory examinations

PER is a selective, noncompetitive antagonist of ionotropic AMPA glutamate receptor (AMPAR) that mediates the fast excitatory synaptic neurotransmission in the central nervous system (CNS). The AMPARs are expressed throughout the CNS, and are tetrameric complexes of four different types of subunits, including GluA1, GluA2, GluA3 and GluA4. The AMPAR subunits bind in pairs to form a variety of symmetric dimers, which next form functional ionic glutamate receptors surrounding a permeable cation channel of sodium (Na), potassium (K), and calcium (Ca). Following the binding of glutamate to AMPARs, Na, Kand Caions rapidly flow into the neurons, and depolarize the postsynaptic membranes from the resting potential[4]. The normal function of the human brain depends on the balance of excitatory and inhibitory activities of neural networks. Neurons antagonize excitatory activities by upregulating the aggregation of inhibitory -aminobutyric acid receptors (GABARs) on the postsynaptic membrane, so as to prevent excessive excitability of the neural network[5]. Abnormal changes in the composition, function and dynamic characteristics of AMPAR subunits lead to a large amount of Cainflux into dendritic cells to overactivate the downstream pathway, inhibit the inhibitory GABARs function, and over-increase the excitability of neuronal networks, leading to the excitation/inhibition imbalance in brain, which may be the etiology and mechanism of epilepsy[6]. Up to now,there are only two AMPAR antagonists, talampanel and PER, which have entered clinical trials.However, development of talampanel was discontinued due to its short half-life, poor antiepileptic efficacy and serious adverse reactions in clinical trials. PER is the second AMPAR antagonist and is the only one approved for clinical use[6].

Imaging examinations

The cranial fluid-attenuated inversion recovery images showed patchy high-signal areas in the posterior part of bilateral lateral ventricle, and in the subcortical white matter of left occipital and temporal lobes(Figure 1).

FURTHER DlAGNOSTlC WORK-UP

Video-electroencephalography (vEEG) recordings showed irregular and slow background activity, as well as multifocal generalized sharp and (multi-) spike wave discharge (Figure 2A). The high-amplitude slow waves with high-frequency discharges were recorded in vEEG during a seizure (Figure 2B). To determine the underlying cause of epilepsy, we performed whole exome sequencing for the patient and his parents, however, no pathogenic mutation was found.

We thank the patient and his parents.

FlNAL DlAGNOSlS

This patient had both focal and generalized seizures, and was later diagnosed as idiopathic multidrugresistant epilepsy.

TREATMENT

Several AEDs were applied to this patient sequentially. Valproate sodium (VPA, maximum dose 50 mg/kg/d) was started at age 19 mo after hospitalization; however, it was ineffective at reducing seizure frequency. Levetiracetam (LEV, maximum dose 50 mg/kg/d) was add 1 mo later, and the seizures were reduced by 60% after the add-on of LEV. When he was aged 32 and 33 mo, topiramate (TPM, maximum dose 5 mg/kg/d) and oxcarbazepine (OXC, maximum dose 60 mg/kg/d) were added, and the seizure frequency was decreased gradually to five or six times per day. VPA was replaced with clonazepam(CLZ, maximum dose 0.1 mg/kg/d) at 3 years old; however, CLZ was discontinued after 3 mo due to ineffectiveness.

To further decrease seizure frequency, left VNS implantation was performed at age 39 mo, and the seizures were reduced by 50% to two per day, and he became responsive to calling. LEV, TPM and OXC were continued for 7 mo after the insertion of VNS, and OXC was gradually replaced with lacosamide(LCM, maximum dose 125 mg/d) in 3 mo after no improvement of seizure frequency. However, the seizures were still two per day and LCM was discontinued. PER was started at age 4 years and 3 mo at an initial dose of 2 mg/d (0.1 mg/kg/d, body weight 20 kg), and the seizures were significantly reduced to one every 1-2 d. Three months later his PER was up-titrated to 4 mg/d (0.2 mg/kg/d) and his seizure frequency was one seizure every 2-3 d. After 2 mo, PER was added to current dose of 6 mg/d (0.3 mg/kg/d), which improved his seizure frequency to one seizure every 3-4 d lasting for 1-2 min each time (Figure 3).

OUTCOME AND FOLLOW-UP

At the last follow-up visit, 7 mo after the add-on of PER, the follow-up vEEG showed a decrease in the frequency of multifocal discharges, and no seizure was observed during the monitoring (Figure 2C).Therefore, the improvements after the use of PER were both clinical and electrophysiological. The patient was responsive to calling, and could communicate with others and follow simple instructions,showing improved cognitive skills and language according to our observation and his parents’ records.In addition, the adverse reactions of anger and aggressive behavior were noticed after the use of PER.Although the seizure-free status was not achieved in this patient after 7 mo treatment with PER, he was closely followed up to assess the long-term effect of PER oral treatment.

DlSCUSSlON

PER is the first AED targeting AMPA receptors, which was approved by the United States Food and Drug Administration (FDA) to treat partial-onset seizures with or without secondarily generalized seizures for adult patients with epilepsy in September 2018[2,3]. Its great cognitive profile, ease of use of the titration scheme and the once-daily oral regimen give it advantages over other AEDs. Although the FDA approved the use of PER in persons ≥ 4 years of age, according to the strategy that allows extrapolation of efficacy across populations[2], reports about the efficacy and safety of PER in children under 12 years old with drug-resistant epilepsy are still limited. In the present case, after the sequential use of six AEDs and left VNS implantation, the 4-year-old patient still had frequent seizure attacks,while seizures were significantly reduced by ＞ 80% after adding PER in a dose-dependent manner.Hence, we believe that PER may be an effective and important add-on drug for treatment of multidrugresistant epilepsy, especially in young children, which may be attributed to the novel antiepileptic mechanism of PER.

His laboratory examinations revealed nothing notable.

VNS is an adjuvant treatment approved by the FDA for patients ≥ 12 years of age with drug-resistant epilepsy, and was further approved for use in patients ＞ 4 years of age in 2017. Nowadays, much evidence supports that VNS implantation as adjuvant therapy is possibly effective in pediatric (≤ 18 years old) drug-resistant epilepsy. The pooled prevalence estimates for 50% responder rate and seizure freedom at last follow-up (mean 2.54 years) were 56.4% and 11.6%, respectively[7], and VNS may have improved efficacy over time[8]. Davis Jones[9] reported that PER could further reduce the seizure frequency in some adult patients with drug-resistant epilepsy who still had seizures after their previous VNS implantation or resective surgery. However, no report was found about the use of PER in young children with drug-resistant epilepsy after VNS implantation. Our patient was a 4-year-old boy with multidrug-resistant epilepsy who still had frequent seizures after VNS implantation as adjuvant therapy, and he showed significant response to PER as add-on in a dose-dependent manner, with seizures reduced by ＞ 80% after 7 mo treatment. Therefore, we propose that for young children with drug-resistant epilepsy who still have frequent seizures after VNS implantation, the use of PER as addon could further reduce the seizure frequency.

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In addition, we also searched the National Library of Medicine and the China National Knowledge Infrastructure between January 10 and 15, 2020, with the following keywords perampanel AND children. Only papers on the administration of PER for multidrug-resistant epilepsy were selected. We identified the data about the efficacy and safety profile of PER in children under 12 years old with drugresistant epilepsy (summarized in Supplementary Table 1). From most previous researches, after 3-12 mo of treatment, nearly 40%-50% or more young children showed responses to PER, and some patients could reach seizure-free status using PER. For patients with various genetic causes, significant seizure reduction was also reached with treatment of PER. In children under 12 years old, the incidence of AEs ranged from 20% to 50%, including somnolence, behavioral deterioration, and emotional change, while no obvious AEs were demonstrated in most case reports. Furthermore, in most reported cohorts, PER possessed similar efficacy and safety profiles in children under 12 years old as in older people[15,16].Together with this case, these results suggest that PER is an effective and broad-spectrum AED for children under 12 years old, who suffer from multidrug-resistant epilepsy, with acceptable safety profile.

Some studies have shown that PER may improve cognitive function in children patients. In a phase II randomized, double-blind, placebo-controlled study of 133 adolescent patients with uncontrolled partial-onset seizures, the systematic analysis of the Cognitive Drug Study revealed that PER may have favorable cognitive profile for adolescent population[10]. The increase of β-band in quantitative electroencephalogram (QEEG) is related to the improvement of attention and cognitive function, and the increase of α-band is related to the impairment of cognitive function[11]. In a QEEG study on patients treated with PER, PER increased the β-band in the occipital lobe region, without increasing the α-band,confirming the beneficial effect of PER on cognitive function, which may be mediated by its direct effect on the neurotransmission of glutamate[11]. In our case, although the quantitative scales were not evaluated in this patient before and after treatment with PER, he showed improved cognitive skills and language according to our observation and his parents’ records, which suggested the favorable cognitive profile of PER in young children.

CONCLUSlON

In this study, we presented a 4-year-old boy with multidrug-resistant epilepsy who still had frequent seizures after VNS implantation, and he showed significant response to PER as add-on in a dosedependent manner. We proposed that the use of PER as add-on could further reduce the seizure frequency for young children with drug-resistant epilepsy and even after VNS implantation, which may be attributed to its novel antiepileptic mechanism. Considering the similar efficacy and safety profile of PER in children ＜ 12 years old as in older people, as well as its potential favorable cognitive profile and convenience of use, PER should be considered as an effective and important treatment for young children with multidrug-resistant epilepsy. Adverse reactions like irritability and aggressive behavior should be monitored during use.

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Yang H wrote the manuscript; Yang H and Yu D collected the data and participated in patient care; Yu D reviewed and edited the manuscript.

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The adverse events (AEs) of AEDs are the key factors affecting drug selection, patients’ quality of life and long-term drug retention. The AEs of PER mainly include dizziness, irritability, fatigue, aggressiveness, suicide, nausea and weight gain[2]. Dizziness and somnolence are the most common AEs[3].Because of some severe mental and behavioral adverse reactions, including aggressiveness, irritability,homicidal behavior, and threats, PER was given a black box warning by the FDA when it was first approved[12]. The patient in our case developed irritability and aggressive behavior after treatment with PER, which were considered to be its adverse reactions. Irritability is the most common psychotic adverse reaction, with an incidence of 2.1%-17.9%[13]. Although the mechanism behind irritability and related aggressive behavior is unclear, serotonin, GABA, and especially glutamate (the AMPAR)seems to play an important role[13]. The effects of glutamate on behavior are complex, and some animal studies have shown that blocking AMPARs can lead to increases or decreases in aggressive behavior.This indicates that the AMPAR blockage may contribute to the emotion-related adverse reactions of PER[13]. The AEs of PER are dose-dependent, and may disappear after dose adjustment or drug withdrawal[14].It is recommended to start PER with a low dose and titrate slowly,generally adding 2 mg every 2-4 wk. Slow titration can improve the long-term tolerance of PER and reduce the incidence and severity of AEs, including psychiatric symptoms. Adverse reactions of PER can be alleviated by taking the drug before bedtime[10].

Informed written consent was obtained from the patient for publication of this report and any accompanying images.

The authors declare that they have no conflict of interest.

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The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).

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Hua Yang 0000-0001-5418-3605; Dan Yu 0000-0003-2859-5897.

Wang JJ

Kerr C

Wang JJ