Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?

Mol Genet Metab. 2016 Jan;117(1):42-8. doi: 10.1016/j.ymgme.2015.11.008. Epub 2015 Nov 17.

Abstract

We describe neurotransmitter abnormalities in two patients with drug-resistant epilepsy resulting from deleterious de novo mutations in sodium channel genes. Whole exome sequencing identified a de novo SCN2A splice-site mutation (c.2379+1G>A, p.Glu717Gly.fs*30) resulting in deletion of exon 14, in a 10-year old male with early onset global developmental delay, intermittent ataxia, autism, hypotonia, epileptic encephalopathy and cerebral/cerebellar atrophy. In the cerebrospinal fluid both homovanillic acid and 5-hydroxyindoleacetic acid were significantly decreased; extensive biochemical and genetic investigations ruled out primary neurotransmitter deficiencies and other known inborn errors of metabolism. In an 8-year old female with an early onset intractable epileptic encephalopathy, developmental regression, and progressive cerebellar atrophy, a previously unreported de novo missense mutation was identified in SCN8A (c.5615G>A; p.Arg1872Gln), affecting a highly conserved residue located in the C-terminal of the Nav1.6 protein. Aside from decreased homovanillic acid and 5-hydroxyindoleacetic acid, 5-methyltetrahydrofolate was also found to be low. We hypothesize that these channelopathies cause abnormal synaptic mono-amine metabolite secretion/uptake via impaired vesicular release and imbalance in electrochemical ion gradients, which in turn aggravate the seizures. Treatment with oral 5-hydroxytryptophan, l-Dopa/Carbidopa, and a dopa agonist resulted in mild improvement of seizure control in the male case, most likely via dopamine and serotonin receptor activated signal transduction and modulation of glutamatergic, GABA-ergic and glycinergic neurotransmission. Neurotransmitter analysis in other sodium channelopathy patients will help validate our findings, potentially yielding novel treatment opportunities.

Keywords: Channelopathy; Dopamine; Na(v)1.2; Na(v)1.6; SCN2A; SCN8A; Seizures; Serotonin; Therapy.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autistic Disorder / etiology
  • Autistic Disorder / genetics
  • Channelopathies / drug therapy
  • Channelopathies / metabolism*
  • Child
  • Drug Resistant Epilepsy / drug therapy
  • Drug Resistant Epilepsy / metabolism*
  • Epilepsy / drug therapy
  • Epilepsy / genetics
  • Epilepsy / metabolism*
  • Exome
  • Female
  • Homovanillic Acid / cerebrospinal fluid
  • Humans
  • Hydroxyindoleacetic Acid / cerebrospinal fluid
  • Male
  • Muscle Hypotonia / etiology
  • Muscle Hypotonia / genetics
  • Mutation, Missense*
  • NAV1.2 Voltage-Gated Sodium Channel / genetics
  • NAV1.6 Voltage-Gated Sodium Channel / genetics
  • Neurotransmitter Agents / deficiency*
  • Neurotransmitter Agents / metabolism
  • Receptors, Dopamine / metabolism
  • Seizures / etiology*
  • Seizures / genetics
  • Sequence Analysis, DNA
  • Sodium Channels / deficiency
  • Sodium Channels / genetics
  • Tetrahydrofolates / cerebrospinal fluid

Substances

  • NAV1.2 Voltage-Gated Sodium Channel
  • NAV1.6 Voltage-Gated Sodium Channel
  • Neurotransmitter Agents
  • Receptors, Dopamine
  • SCN2A protein, human
  • SCN8A protein, human
  • Sodium Channels
  • Tetrahydrofolates
  • Hydroxyindoleacetic Acid
  • 5-methyltetrahydrofolate
  • Homovanillic Acid