Vigabatrin is an anticonvulsant that inhibits the catabolism of GABA. It is an analog of GABA, but it is not a receptor agonist.[Long, Phillip W. "Vigabatrin." Internet Mental Health. 1995-2003.]
Mechanism of action
Vigabatrin is an irreversible inhibitor of gamma-aminobutyric acid
transaminase (GABA-T), the
enzyme responsible for the catabolism of GABA, which increases the level of GABA in the
synapses.
Vigabatrin is a racemic compound, and its *-enantiomer is pharmacologically active.[}}],
Pharmacokinetics
With most drugs, elimination half-life is a useful predictor of dosing schedules and the time needed to reach
steady state concentrations. In the case of vigabatrin, however, it has been found that the half-life of biologic activity is far longer than the elimination half-life.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=9818917&dopt=ExternalLink}}]
For vigabatrin, there is no range of target concentrations because researchers found no difference between the serum concentration levels of responders and those of non-responders. Instead, the duration of action is believed to be more a function of the GABA-T resynthesis rate; levels of GABA-T do not usually return to their normal state until six days after stopping the medication.
Uses
Approved/clinically proven
Canada
In Canada, vigabatrin is approved for use as an adjunctive treatment (with other drugs) in treatment resistant
epilepsy,
complex partial seizures,
secondary generalized seizures, and for monotherapy use in
infantile spasms in
West syndrome.
Mexico
As of 2003, vigabatrin is approved in Mexico for the treatment of epilepsy that is not satisfactorily controlled by conventional therapy (adjunctive or monotherapy) or in recently diagnosed patients who have not tried other agents (monotherapy).
[DEF MEXICO: SABRIL Diccionario de Especialdades Farmaceuticas. Edicion 49, 2003.]
Vigabatrin is also indicated for monotherapy use in secondarily generalized tonic-clonic seizures, partial seizures, and in infantile spasms due to West syndrome.
Unapproved/Investigational
In November of 2001, a team of scientists lead by Peter Zwanzger of the University of Munich reported that vigabatrin reduced
cholecystokinin tetrapeptide-induced symptoms of
panic disorder, in addition to elevated
cortisol and
ACTH levels, in healthy volunteers.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=11682253&dopt=ExternalLink}}]
In 1994, Feucht and Brantner-Inthaler reported that vigabatrin reduced seizures by 50-100% in 85% of children with Lennox-Gastaut syndrome who had poor results with a valproate.[ | url=http://www.blackwell-synergy.com/doi/pdf/10.1111/j.1528-1157.1994.tb02544.x| format=PDF| accessdate=2006-05-25}}]
In 1984, a double-blind crossover-study of six Huntington's disease patients—five of them on antipsychotics—reported that vigabatrin did little, if anything, to improve hyperkinetic movements, the ability to carry out daily activities, or normalize motor function.[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=6228746&dopt=ExternalLink}}]
Adverse effects
Central nervous system
Common
Out of 2,081 subjects,
somnolence (12.5%),
headache (3.8%), dizziness (3.8%), nervousness (2.7%),
depression (2.5%), memory disturbances (2.3%),
diplopia (2.2%), aggression (2.0%),
ataxia (1.9%),
vertigo (1.9%),
hyperactivity (1.8%), vision abnormalities (1.6%),
confusion (1.4%),
insomnia (1.3%), impaired concentration (1.2%),
personality disorder (1.1%).
Out of 299 children, 33 (11%) became hyperactive.
Rare
Some patients develop
psychosis during the course of vigabatrin therapy,
which is more common in adults than in children.
[ in Italian PMID 7885961] This can happen even in patients with no prior history of psychosis.
[}}] Other rare CNS side effects include anxiety,
emotional lability, irritability, tremor, abnormal
gait, and
speech disorder.
Gastrointestinal
Common
Abdominal pain (1.6%), constipation (1.4%), vomiting (1.4%), and nausea (1.4%).
Rare
Dyspepsia and increased appetite occurred in less than 1% of subjects in clinical trials.
Body as a Whole
Common
Fatigue (9.2%), weight gain (5.0%),
asthenia (1.1%).
Teratogenicity
A
teratology study conducted in rabbits found that a dose of 150mg/kg/day caused
cleft palate in 2% of pups and a dose of 200 mg/kg/day caused it in 9%.
This may be due to a decrease in
methionine levels, according to a study published in March of 2001.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=11283969&dopt=ExternalLink}}] In 2005, a study conducted at the University of Catania was published stating that rats whose mothers had consumed 250-1000 mg/kg/day had poorer performance in the
water maze and
open-field tasks, rats in the 750-mg group were underweight at birth and did not catch up to the control group, and rats in the 1000 mg group did not survive pregnancy.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=15995825&dopt=ExternalLink}}]
There is no controlled teratology data in humans to date.
More on "abnormal vision"
In 2003, vigabatrin was shown by Frisén and Malmgren to cause irreversible diffuse
atrophy of the
retinal
nerve fiber layer in a
retrospective study of 25 patients.
[ |url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=14510793&dopt=ExternalLink}}] This has the most effect on the outer area (as opposed to the
macular, or central area) of the retina.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=15465561&dopt=ExternalLink}}]
Drug interactions
A study published in 2002 found that vigabatrin causes a
statistically significant increase in
plasma clearance of
carbamazepine.
[ | url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&list_uids=12472982&dopt=ExternalLink}}]
In 1984, Drs Rimmer and Richens at the University of Wales reported that administering vigabatrin with phenytoin lowered the serum phenytoin concentration in patients with treatment-resistant epilepsy.[}}] The concentration of phenytoin falls to 23% within five weeks, according to an experiment published in 1989 by the same two scientists that tried and failed to elucidate the mechanism behind this interaction.[}}]
Brand names
Vigabatrin is sold as
Sabril® in Canada,
[drugs.com Vigabatrin Drug Information] Mexico,
and the United Kingdom.
[Treatments for Epilepsy - Vigabatrin Norfolk and Waveney Mental Health Partnership NHS Trust]
References and end notes
Anticonvulsants | Vigabatrin