<abstract xmlns="http://www.w3.org/1999/xhtml"><p><bold>Introduction.</bold> Epilepsy is one of the most common neurological disorders worldwide. In most cases, epilepsy can be well managed. However, there is a number of patients who do not respond well enough to common medical treatments; a situation known as pharmacoresistant epilepsy. It can be caused by mechanisms that may involve environmental and genetic factors, as well as disease or drug related factors. <bold>Case presentation.</bold> Herein we present a case report of a six-year-old girl who has been diagnosed with pharmacoresistant epilepsy, characterized by generalized and focal seizures while she was on two antiepileptic drugs. Molecular testing, with Next Generation Sequencing (NGS) technique, revealed mutations at KCNB1 and RELN genes.</p></abstract>

Introduction. Epilepsy is one of the most common neurological disorders worldwide. In most cases, epilepsy can be well managed. However, there is a number of patients who do not respond well enough to common medical treatments; a situation known as pharmacoresistant epilepsy. It can be caused by mechanisms that may involve environmental and genetic factors, as well as disease or drug related factors. Case presentation. Herein we present a case report of a six-year-old girl who has been diagnosed with pharmacoresistant epilepsy, characterized by generalized and focal seizures while she was on two antiepileptic drugs. Molecular testing, with Next Generation Sequencing (NGS) technique, revealed mutations at KCNB1 and RELN genes.


<div xmlns="http://www.w3.org/1999/xhtml"><sec id="j_joepi-2020-006_s_001" sec-type="introduction"><div>INTRODUCTION</div><p>Epilepsy is one of the most common neurological diseases worldwide and is considered a major public health problem, with socioeconomic problems (<a ref-type="bibr" href="#j_joepi-2020-006_ref_002">Camfield and Camfield, 2015</a>; <a ref-type="bibr" href="#j_joepi-2020-006_ref_014">López González et al., 2015</a>). Generally, this disease can be successfully treated in most cases. However, there is a high percent of patients that does not respond favorably to common antiepileptic drugs (AED) despite the continued development of new AED the last two decades, resulting in pharmacoresistance (<a ref-type="bibr" href="#j_joepi-2020-006_ref_012">Kwan and Brodie, 2000</a>). It is considered that via biochemical and biological sciences new AED can be developed and perhaps with different mechanisms of action compared to the AED currently on the market.</p><p>Pharmacoresistant epilepsy is defined as an epilepsy that does not respond to at least two AED, used either in monotherapy or in combination therapy (bi- or polytherapy) and failed to control seizures for a sufficient period of time (<a ref-type="bibr" href="#j_joepi-2020-006_ref_013">Kwan et al., 2010</a>). However, in 2011, the International League Against Epilepsy (ILAE) modified the definition of drug-resistant epilepsy to the presence of seizures for a period of 6 months, even under suitable treatment (either monotherapy or combination therapy) (<a ref-type="bibr" href="#j_joepi-2020-006_ref_013">Kwan et al., 2010</a>).</p><p>Various prognostic factors, associated with the development of drug resistance, have been investigated in various studies. Special abnormalities at electroencephalogram (EEG) such as asymmetric generalized spike-wave discharges (<a ref-type="bibr" href="#j_joepi-2020-006_ref_020">Szaflarski et al., 2010</a>) or generalized polyspikes during sleep (<a ref-type="bibr" href="#j_joepi-2020-006_ref_019">Sun et al., 2018</a>), status epilepticus, febrile seizures, neurological disorders and mental retardation were identified as factors associated with worse outcomes (<a ref-type="bibr" href="#j_joepi-2020-006_ref_008">Kalilani et al., 2018</a>). Other factors which have been analyzed in multivariate studies, and are associated with poor prognosis, are the pre-treatment seizure frequency, the recreational drug use and the family history of epilepsy in 1st degree relatives (<a ref-type="bibr" href="#j_joepi-2020-006_ref_021">Téllez-Zenteno et al., 2014</a>; <a ref-type="bibr" href="#j_joepi-2020-006_ref_007">Fiest et al., 2017</a>), as well as the failure of previous AED and the duration of epilepsy (<a ref-type="bibr" href="#j_joepi-2020-006_ref_015">Luciano et al., 2007</a>). Moreover, another prospective incident study of newly diagnosed drug-resistant patients found that the largest percentage of patients with bad prognosis was those with temporal onset compared to occipital or unclear onset (<a ref-type="bibr" href="#j_joepi-2020-006_ref_004">Choi et at., 2016</a>).</p><p>Regarding the biological basis of AED pharmacoresistance, the data is poorly understood. Epilepsy is a heterogeneous condition with multiple etiologies, and it is considered that the pathogenesis of AED pharmacoresistance is multifactorial and may involve both genetic and environmental factors (<a ref-type="bibr" href="#j_joepi-2020-006_ref_003">Cárdenas-Rodríguez et al., 2020</a>).</p></sec><sec id="j_joepi-2020-006_s_002" sec-type="case"><div>CASE PRESENTATION</div><p>We report a case of a six-year-old female who was referred to our Neurology Department at the age of three because of frequent episodes of altered level of consciousness. Perinatal history was normal; she was term and her delivery was vaginal and an APGAR score of 9–10. She had a birth weight of 2840 gram and a head circumference of 36.1 cm. However, from the patient’s personal history it is described that at the age of 9 months she had further developed complex febrile seizures, while at the age of three-years-old she developed the first afebrile seizures, with disturbance of the level of consciousness and lip-smacking/chewing movements, without the episode developing into generalized tonic-clonic seizures, lasting up to 5 minutes. From her family history, her father described episodes of convulsions in infancy which were self-resolved without any treatment requirement. All her family members are healthy.</p><p>On the first physical examination, neither pathological findings nor dysmorphic facial features were noticed. EEG was compatible with focal epilepsy. Especially, the main characteristic of EEG is the recording of sharp waves, spikes and spike-and-wave complexes at the centrotemporal regions (Figure <a ref-type="fig" href="#j_joepi-2020-006_fig_001">1</a>). Polyspikes have been recorded to a lesser extent. Brain magnetic resonance imaging (MRI) did not reveal any pathological findings. Therefore, she was commenced on levetiracetam. Moreover, in the future, on follow up, significant speech delay was also reported, which required speech and language therapy sessions. A developmental assessment was also recommended to parents and performed which revealed a mild developmental disorder.</p><figure id="j_joepi-2020-006_fig_001" position="float" fig-type="figure"><h2>Figure 1.</h2><figCaption><p>EEG trace showing sharp waves, spikes and spike-and-wave complexes in the frontal and centrotemporal regions.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_joepi-2020-006_fig_001.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64721fd7215d2f6c89dbcb47/j_joepi-2020-006_fig_001.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240616T220108Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240616%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=9d56e487bd6dcf90750f7acb986d38f1e5bc5b7b7ae47174ced13d86aef6fcef" class="mw-100"/></figure><p>For the next two and a half years, she continued to present with similar episodes of seizures, which partially treated AED dosage adjustments. Thus, levetiracetam was discontinued and oxcarbazepine with sodium valproate were added to her treatment plan, without any improvement. At that time, different type of seizures, with tonic-clonic movements, occurred.</p><p>Due to the combination of speech delay and pharmacoresistant epilepsy, Next Generation Sequencing (NGS) technique with DNA isolation from the patient was performed. Oligonucleotide-based target capture analysis and nucleotide sequencing were undertaken using the Blueprint Genetics (BpG) Beyond Pediatric Epilepsy Panel Plus and the NGS (Illumina NextSeq), respectively, examining 283 disease-causing genes. The Burrows-Wheeler Aligner (BWA-MEM) software was used for the data analysis [reference genome UCSC hg19 and reference database Human Gene Mutation Database (HGMD v.2017.1)]. Two nucleotide changes were detected. The first one c.1234A> G, p. (Ile412Val) in the KCNB1 gene, in heterozygous state (NM_004975.3), (Figure <a ref-type="fig" href="#j_joepi-2020-006_fig_002">2</a>) and the second one, c.6770C> G, p. (Ser-2257Trp) in the RELN gene, in heterozygous state (NM_005045.3) (Figure <a ref-type="fig" href="#j_joepi-2020-006_fig_003">3</a>).</p><figure id="j_joepi-2020-006_fig_002" position="float" fig-type="figure"><h2>Figure 2.</h2><figCaption><p>Molecular testing with Next Generation Sequencing technique revealed mutations at KCNB1 gene.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_joepi-2020-006_fig_002.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64721fd7215d2f6c89dbcb47/j_joepi-2020-006_fig_002.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240616T220108Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240616%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=5a508dd4c816874b092e156cd7d4b5975e5e11f1615e2e75659c3ba76706304d" class="mw-100"/></figure><figure id="j_joepi-2020-006_fig_003" position="float" fig-type="figure"><h2>Figure 3.</h2><figCaption><p>Molecular testing with Next Generation Sequencing technique revealed mutations a tRELN gene.</p></figCaption><img xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/j_joepi-2020-006_fig_003.jpg" src="https://sciendo-parsed.s3.eu-central-1.amazonaws.com/64721fd7215d2f6c89dbcb47/j_joepi-2020-006_fig_003.jpg?X-Amz-Algorithm=AWS4-HMAC-SHA256&amp;X-Amz-Date=20240616T220108Z&amp;X-Amz-SignedHeaders=host&amp;X-Amz-Expires=18000&amp;X-Amz-Credential=AKIA6AP2G7AKP25APDM2%2F20240616%2Feu-central-1%2Fs3%2Faws4_request&amp;X-Amz-Signature=35f4a2716675320e1ad4ef050d77076f35de243e7a98321e9945395692296087" class="mw-100"/></figure><p>Nucleotide change c.1234A> G to KCNB1 gene leads to replacement of the amino acid isoleucine by valine at 412 position of amino acid chain and the c.6770C> G change in RELN gene causes the replacement of the amino acid serine by tryptophan at 2257 position of the amino acid chain. These result in disruption of the protein’s structure and function.</p><p>We believe that the above genetic changes have not been previously reported in the scientific literature or in the ClinVar and HGMD databases.</p><p>However, it should be noted that it remains unknown whether these mutations have been inherited from the parent or were de novo, because the parents did not agree to undergo genetic testing themselves.</p><p>At her most recent re-evaluation (at the age of 6 years old), she was seen more sociable and smiley. However, deficits in speech perception still persist, while she is still under speech and language therapy. The likelihood of borderline mental retardation is increased but no mental quotient measurement has been performed yet. Presently, she is on two AED (sodium valproate and lacosamide) and is free of seizures.</p></sec><sec id="j_joepi-2020-006_s_003" sec-type="discussion"><div>DISCUSSION</div><p>This case report highlights the difficulties that neurologists often face when managing patients with the drug-resistant epilepsy. The developing genomic technologies have dramatically increased the understanding of the genetic background in epilepsy (<a ref-type="bibr" href="#j_joepi-2020-006_ref_018">Myers, Mefford, 2015</a>). However, underlying mechanisms about pharmacological resistance, have not yet been fully exemplified (<a ref-type="bibr" href="#j_joepi-2020-006_ref_005">Depondt, 2006</a>).</p><p>The first mutation in our patient’s DNA is at the KCNB1 gene which is located on the chromosomal region 20q13.13. This encodes the KV2.1-ion channel which contributes to the exit of potassium (K) from the cell and plays an important role in the cell’s ability to generate and transmit electrical signals. Because KCNB1 is a voltage gated potassium channel, its function is based on the charge around it. A change (variant/mutation) at the one copy of the KCNB1 gene stops it from working properly (<a ref-type="bibr" href="#j_joepi-2020-006_ref_022">Torkamani et al., 2014</a>; <a ref-type="bibr" href="#j_joepi-2020-006_ref_011">de Kovel et al., 2017</a>).</p><p>Patients have developmental delay starting in infancy or early childhood, often with prominent language impairment. Most children develop multiple types of seizures that can be frequent and hard to control with standard treatments. However, a few patients do not have seizures but may still have abnormal patterns on their EEG. Some other children may have features of autism or Rett syndrome or have a diagnosis of Lennox-Gastaut syndrome. Generally, patients with KCNB1 gene mutations may be classified as having a developmental and epileptic encephalopathy since features of developmental delay and epilepsy are the most common (<a ref-type="bibr" href="#j_joepi-2020-006_ref_016">Marini et al., 2017</a>).</p><p>In the literature, KCNB1 mutations are commonly associated with diffuse brain dysfunction combining seizures, motor, and cognitive impairment (<a ref-type="bibr" href="#j_joepi-2020-006_ref_016">Marini et al., 2017</a>; <a ref-type="bibr" href="#j_joepi-2020-006_ref_010">Kang et al., 2019</a>).</p><p>The second mutation is at the RELN gene which encodes the protein reelin. It is located on human chromosome 7q22 and is considered as a potential gene for childhood epilepsy (<a ref-type="bibr" href="#j_joepi-2020-006_ref_006">Dutta et al., 2011</a>). Reelin is a protein that plays a crucial role in regulating the processes of neuronal migration and their installation in the developing brain along with the adult brain (<a ref-type="bibr" href="#j_joepi-2020-006_ref_001">Bosch et al., 2016</a>).</p><p>Unfortunately, there are not many studies linking epilepsy with mutations in the RELN gene. However, homozygous RELN mutations have been reported in three families, causing lissencephaly and cerebellar hypoplasia, which led to epilepsy and severe cognitive defect. Moreover, in other studies, heterozygous mutations of RELN gene are associated with the onset of autosomal dominant lateral temporal lobe epilepsy (<a ref-type="bibr" href="#j_joepi-2020-006_ref_017">Michelucci et al., 2017</a>). Thus, as in other genetic epilepsy syndromes, RELN mutations might result in different clinical phenotypes, depending on the mode of inheritance. Heterozygous mutations might cause autosomal dominant lateral temporal epilepsy (ADLTE) and homozygous mutations might result in more severe disorder, as lissencephaly with cerebellar hypoplasia (<a ref-type="bibr" href="#j_joepi-2020-006_ref_009">Hong et al., 2000</a>).</p><p>In our case, the patient certainly has the features described above such as speech delay, mild mental retardation and seizures. However, we cannot be certain if both described mutations are pathogenic or not because, as highlighted above, there are no genetic examinations of the parents. Thus, at this stage, the genetic epidemiology of our patient is only a suspicion.</p></sec><sec id="j_joepi-2020-006_s_004" sec-type="conclusion"><div>CONCLUSION</div><p>In this case report we describe a six-year-old girl with speech delay and drug resistant epilepsy, with mutations in two different genes associated with epilepsy. New genetic techniques are very useful in clinical practice and may help clinicians to explain the clinical presentation of drug resistant epilepsy. In addition, this will probably help us understand the impact of pharmacological treatment on epilepsy. That is why cooperation with clinical geneticists is important.</p></sec></div>

Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report

Journal of Epileptology

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Introduction. Epilepsy is one of the most common neurological disorders worldwide. In most cases, epilepsy can be well managed. However, there is a number of...

Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report

Article Category: case-report

Publié en ligne: 25 nov. 2020

Pages: 73 - 77

Reçu: 31 juil. 2020

Accepté: 15 oct. 2020

DOI: https://doi.org/10.21307/joepi-2020-006

Mots clés
pharmacoresistant epilepsy, KCNB1 gene, RELN gene, delayed speech

© 2020 Adamantios Katerelos et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Figure 1.

Figure 2.

Figure 3.

Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report

Article Category: case-report

Publié en ligne: 25 nov. 2020

Pages: 73 - 77

Reçu: 31 juil. 2020

Accepté: 15 oct. 2020

DOI: https://doi.org/10.21307/joepi-2020-006

Mots cléspharmacoresistant epilepsy, KCNB1 gene, RELN gene, delayed speech

© 2020 Adamantios Katerelos et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Figure 1.

Figure 2.

Figure 3.

Mots clés
pharmacoresistant epilepsy, KCNB1 gene, RELN gene, delayed speech