Lennox–Gastaut syndrome

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Lennox–Gastaut syndrome
SpecialtyNeurology

Lennox–Gastaut syndrome (LGS) is a complex, rare, and severe childhood-onset epilepsy. It is characterized by multiple and concurrent seizure types, cognitive dysfunction, and slow spike waves on electroencephalogram (EEG). Typically, it presents in children aged 3–5 years and can persist into adulthood.[1][2] It has been associated with several gene mutations, perinatal insults, congenital infections, brain tumors/malformations, and genetic disorders such as tuberous sclerosis and West syndrome. The prognosis for LGS is poor with a 5% mortality in childhood and persistent seizures into adulthood (80%–90%).[3]

LGS was named for neurologists William G. Lennox (Boston, USA) and Henri Gastaut (Marseille, France).[4] The international LGS Awareness Day is on November 1st.[5]

Signs and symptoms[edit]

The symptoms vary and progress with age. The symptoms are characterized by a triad of seizures, cognitive dysfunction, and EEG findings. The triad may not fully emerge until 1–2 years after first seizure episode.

Seizures[edit]

The peak age of onset of seizures is typically between 3 and 5 years of age.[6] The mainstay symptoms is seizures that are frequent – occurring daily – and difficult to treat with antiseizure medications. An estimated 30% of patients with infantile spasms (West syndrome) have been reported to progress to LGS.[7][8]

The seizures are most commonly tonic seizures. They occur most frequently during non-REM sleep (90%). The seizures initially last only a few seconds and are activated by sleep. The presentation can be subtle The present often as tonic eyelid opening with some changes in breathing coupled with pupillary dilation, urinary incontinence, increased heart rate, and flushing can occur

Nonconvulsive status epilepticus occurs in about 50% of patients. The seizures can cause sudden falling often leading to injury. These "drop attacks" are typically first manifestation of LGS. These drop attacks are characterized by single, generalized monoclonic jerk that precedes tonic contraction of axial muscles.

EEG findings[edit]

Findings that strongly suggest LGS include consistent slow spike-wave (< 3 hertz [Hz]) on awake EEG. The complexes typically consist of a spike (duration < 70 milliseconds) or a sharp wave (70-200 milliseconds), followed first by a positive deep trough, then a negative wave (350-400 milliseconds). Not every wave is preceded by a spike. Bursts increase and decrease without clear onset and offset. Slow spike waves may occur during seizure or between seizures, or may occur in absence of any observable clinical changes which helps distinguish pattern from extended 3-Hz spike-wave discharges.

Ocular abnormality[edit]

Ocular abnormalities affect around 90% of children. They can present as refractive error, strabismus, cortical visual impairment, and premature retinopathy.[9]

Causes[edit]

The disease pathophysiology is mostly unknown, but some evidence implicates cortical hyperexcitability occurring at critical periods of brain development.

There are two types of LGS: idiopathic and secondary. Idiopathic is unknown origin. Secondary is when an identifiable underlying pathology is responsible. The most common type of LGS (70–78%) is secondary.[10] These patients tend to have a worse prognosis than those with idiopathic LGS.[11] In up to one-third of cases no cause can be found.[11]

Brain injury[edit]

Lennox Gastaut most often occurs secondary to brain damage. The brain damage can occur from perinatal insults, encephalitis, meningitis, tumor, and brain malformation.

Genetic mutations[edit]

Other identified disorders include genetic disorders such as tuberous sclerosis and inherited deficiency of methylene tetrahydrofolate reductase. Some of these cases once thought to be of unknown cause may have definitive etiology by modern genetic testing.[11]

Progress in genome and exome sequencing is revealing that some individuals diagnosed with Lennox Gastaut Syndrome have de novo mutations in a variety of genes, including CHD2, GABRB3, ALG13 and SCN2A[12][13] The Epi4K study consortium (2013) observed de novo mutations in at least 15% of a study cohort of 165 patients with LGS and infantile spasms using whole exome sequencing.[14] A 2013 study found a high frequency of rare copy-number variation (CNV's) in adult patients with LGS or LGS-like epilepsy[15]

Diagnosis[edit]

The diagnosis of LGS should be suspected in children less than 8 years old with seizures of multiple types that cannot be treated with antiseizure medications. Because of high risk of irreversible brain damage in early stages of syndrome (particularly in infants and young children), early diagnosis is essential. It may take 1–2 years after first initial seizure for all criteria for diagnosis to emerge, so LGS should be considered if there are suggestive signs and symptoms without presence of complete triad.

To confirm diagnosis, awake and asleep EEG and magnetic resonance imaging (MRI) are performed. MRI is used to detect focal brain lesions.

Ruling out other diagnosis[edit]

Certain diagnosis must be ruled out before diagnosing LGS. These diagnosis are:

LGS is more easily distinguished from LGS by seizure type after the syndrome has progressed. Doose syndrome has more myoclonic seizures and LGS has more tonic seizures. The Doose syndromes is less likely to have cognitive disabilities.

The Dravet syndrome has a strong family history of epilepsy, unlike LGS. Also, many children with Dravet syndrome have seizures triggered by light.

Pseudo-Lennox-Gastaut syndrome can be distinguished from LGS because pseudo-LGS has different spike-and-wave patterns on EEG.

Treatment[edit]

There are several treatment options, including medications, surgery, and diet.

Medications[edit]

In most patients with LGS, the treatment does not end seizure recurrence. The goals of treatment are to lower frequency and severity of seizures to greatest extent possible. The appropriate treatment varies depending on individual.[16]

The treatments for LGS has evolved over the years. Various treatments have been shown to have some degree of efficacy. In 1997-1999, lamotrigine was found to be effective and approved by the Food and Drug Administration and Health Canada.[17][18][19] In 1999, topiramate trials showed that topiramate decreased seizure occurrence by more than 50%.[20][21]

Felbamate is the treatment of last resort in the event that everything else fails,[22] and was found to be superior to placebo in controlling treatment resistant partial seizures and atonic seizures.[23][24] However, it has been known to cause aplastic anemia and liver toxicity.[25]

First-line drugs[edit]

Second-line drugs[edit]

Third-line drugs

Treatment of last resort

Adjuvant drugs[edit]

Surgery[edit]

In the past, LGS patients were not eligible for surgery, as the medical community thought the LGS involved the whole brain as a generalized epilepsy in all cases. Since 2010, this assumption has been challenged.[27] Two studies on LGS patients series who underwent curative surgery in Korea[28] and China,[29] showed very good results, up to seizure freedom for 80% of these patients below 5 years old, and 40% above 5 years old. Like all epilepsy curative surgeries, seizures may recur in the years following surgery, but surgery allows the child to have better brain development during the seizure free period.

There are several procedures that have shown efficacy:

Diet[edit]

A ketogenic diet is a diet that causes ketosis, a state in which there is an increased amount of ketones in the body. Adopting and maintaining rigid diet may be difficult for some families. Short-term ketogenic diet might be associated with nonsignificant decreases in frequency of parent-reported seizures in children with LGS.[30] A case series study showed 50% seizure reduction reported in almost half of children with LGS after 1 year of ketogenic diet. However, the strength of the study is challenged because it represents reports rather than scientific analysis of the clinical outcomes such as in a randomized controlled trial.[31]

Prognosis[edit]

The mortality rate ranges from 3–7% in a mean follow up period of 8.5 to 9.7 years. Death is often related to accidents.[32]

Epidemiology[edit]

LGS is seen in approximately 4% of children with epilepsy, and is more common in males than in females.[10] Usual onset is between the ages of three and five.[6] Children can have no neurological problems prior diagnosis, or have other forms of epilepsy. West syndrome is diagnosed in 20% of patients before it evolves into LGS at about 2 years old.[11]

Finland[edit]

According to a 1997 community-based retrospective study in the Helsinki metropolitan area and the province of Uusimaa, the annual incidence of Lennox–Gastaut was 2 in 100,000 (0.002%) from 1975 to 1985.[33]

United States[edit]

0.026% of all children in the Atlanta, Georgia metropolitan area were estimated to have LGS in 1997, which was defined as, "onset of multiple seizure types before age 11 years, with at least one seizure type resulting in falls, and an EEG demonstrating slow spike-wave complexes (<2.5 Hz)." The study concluded that LGS accounts for 4% of childhood epilepsies.[10]

Research[edit]

Vigabatrin was found by Feucht et al. to be an effective add-on in patients whose seizures were not satisfactorily controlled by valproate. Out of 20 children, only 1 experienced a serious side effect (dyskinesia).[34]

Zonisamide showed promise in an overview of controlled and uncontrolled trials conducted in Japan.[35] However, in a physician survey conducted December 2004, only 28% of Lennox–Gastaut and West syndrome patients improved on zonisamide.[36]

One yet to be published study from 2017 supported the use of cannabidiol.[37]

Another article published in the New England Journal of Medicine has also shown a significant reduction of seizures of patients taking 10 and 20 mg/kg a day compared to placebo. [36]

References[edit]

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