generalized epilepsy with febrile seizures plus (GEFS+)
Nota:
mutations alter channel activity
patients with GEFS+ demonstrate febrile seizures that persist beyond 6 years of age and are associated with generalized or partial epilepsies, such as absence epilepsy, myoclonic seizures, atonic seizures, and myoclonic–astatic epilepsy (Scheffer & Berkovic, 1997; Singh et al., 1999). Affected individuals within GEFS+ families often display a wide variety of epilepsy subtypes, with markedly different ages of onset and severity, suggesting the action of genetic and/or environmental modifiers.
Overall- Decreases inhibition
SCN1B gene
Nota:
encoding the sodium channel β1 subunit and two GABAA receptor genes: GABRG2 encoding the γ2 subunit
Na b1 subunit
GABARG2
SCN1A
10% of cases
missense mutations (amino acid
substitutions) that mutation alter,
but not abolish SCN1A activity
Animal models
BAC transgene with R1648H mutation
Nota:
Increased seizure susceptibility to kainic acid
Decreased sodium current density in inhibitory bipolar neurons
Delayed recovery from inactivation and increased use-dependent inactivation of mutant sodium channels in inhibitory bipolar neuronsHyperpolarizing shift in the voltage dependence of inactivation of mutant sodium channels in excitatory pyramidal neurons
Tang et al (2009)
Knock-in of R1648H mutation
Nota:
Spontaneous seizures and death between P16 and P26 in homozygous mice
Infrequent spontaneous seizures, reduced seizure thresholds, and accelerated propagation of febrile seizures in heterozygous mice
Slower recovery from inactivation, greater use-dependent inactivation, reduced sodium current density, and decreased action potential firing in bipolar inhibitory neurons
Martin et al (2012)
Other genetic influences/ evironmental
Nota:
often display a wide range of seizure types and severities, suggesting that additional environmental or genetic factors likely influence clinical presentation
Dravet syndrome (DS)
Nota:
severe myoclonic epilepsy of infancy
>>Most of the mutations that cause DS result in loss of function
SCN1A
Nota:
main cause
85% of cases
result from frameshift, nonsense, and splice-site mutations
Nota:
Several of these mutations occur very early in the sequence of SCN1A, strongly suggesting that expression of the mutant allele is reduced or that a nonfunctional protein product is generated from the mutant allele, demonstrating haploinsufficiency of SCN1A
Some are missense mutations
Nota:
also abolish channel function, possibly by altering the properties of the channel, trafficking or subcellular localization, or interactions with other molecules
De novo mutation
Nota:
An alteration in a gene that is present for the first time in one family member as a result of a mutation in a germ cell
Animal models
Knockout
Nota:
Spontaneous seizures, febrile seizures, ataxia, and death at P15 in homozygous mice
Spontaneous seizures, febrile seizures, and impaired coordination in heterozygous mice
Decreased sodium current density in inhibitory interneurons and cerebellar Purkinje neurons, but not in excitatory pyramidal neuronsDecreased action potential firing in inhibitory interneuronsUpregulation of Nav1.3 in hippocampal interneurons
Knock-in of R1407X nonsense mutation
Nota:
Spontaneous seizures, unstable gait, and death by P20 in homozygous mice
Spontaneous seizures in heterozygous mice
Spike amplitude decrements in parvalbumin-positive interneurons from heterozygous mice
Nav1.1 was clustered at the axon initial segments of parvalbumin-positive interneurons
Ogiwara et al., 2007
SCN2A
Nota:
some cases
Early life
disorder
Nota:
DS is a catastrophic early life epilepsy disorder in which the seizures are usually refractory to treatment and are associated with intellectual disability
characterized by febrile hemiclonic seizures or generalized status epilepticus starting at approximately 6 months of age, with other seizure types including partial, absence, atonic, and myoclonic seizures occurring after 1 year.
genetic modifiers
SCN9A
Nota:
might be a genetic modifier
Singh et al. (2009)
Nota:
six DS patients who harbored missense or splice-site mutations in SCN1Awere also found to carry SCN9A variants. This raises the possibility that alterations in SCN9A may exacerbate the impact of otherwise less deleterious SCN1A mutations on neuronal excitability.
Scn8a
Martin et al (2007)
Nota:
mice with mutations in Scn8a display elevated thresholds to chemically induced seizures when compared with wild-type littermates
in the presence of an Scn8a mutation, normal seizure thresholds and life spans were restored in heterozygous Scn1aknockout mice, which serve as a model of DS
voltage-gated calcium channel β4 subunit
Ohmori et al. (2008)
Nota:
In DS-positive patients screening- The amino acid substitution R468Q in CACNB4
link with SCN1A
Nota:
Increased calcium currents were seen when R468Q mutant channels were examined in BHK cells. Therefore, this mutation may result in increased neurotransmitter release from excitatory cells, which when combined with reduced inhibition as a result of the SCN1A mutation, may cause a more severe clinical presentation
adult CNS, Nav1.1 is the
predominant channel in
the caudal regions and
the spinal cord
modulates excitatibility of networks
Nota:
Nav1.1 is clustered at the axon initial segments of parvalbumin-positive basket cells, which project their terminal axonal arbors around the soma and proximal dendrites of excitatory neurons, it may play an important role in modulating excitability of the network.