vigabatrin has been researched along with Inborn Errors of Metabolism in 14 studies
Excerpt | Relevance | Reference |
---|---|---|
"His younger brother had mild axial hypotonia when 5 months old." | 1.36 | [Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]. ( Escalera, GI; Ferrer, I; Jakobs, C; Marina, LC; Pérez-Cerdá, C; Sala, PR; Salomons, GS, 2010) |
"Epilepsy was characterized by status epilepticus or a cluster of seizures." | 1.31 | Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance. ( Bellet, H; Echenne, B; Humbertclaude, V; Morin, D; Rivier, F; Roubertie, A; Vallat, C, 2001) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (14.29) | 18.7374 |
1990's | 7 (50.00) | 18.2507 |
2000's | 3 (21.43) | 29.6817 |
2010's | 1 (7.14) | 24.3611 |
2020's | 1 (7.14) | 2.80 |
Authors | Studies |
---|---|
Mir, A | 1 |
Hadab, S | 1 |
Sammak, M | 1 |
Alhazmi, R | 1 |
Housawi, Y | 1 |
Bashir, S | 1 |
Escalera, GI | 1 |
Ferrer, I | 1 |
Marina, LC | 1 |
Sala, PR | 1 |
Salomons, GS | 1 |
Jakobs, C | 5 |
Pérez-Cerdá, C | 1 |
Ergezinger, K | 1 |
Jeschke, R | 1 |
Frauendienst-Egger, G | 1 |
Korall, H | 1 |
Gibson, KM | 5 |
Schuster, VH | 1 |
Ogier, H | 1 |
Hagenfeldt, L | 1 |
Eeg-Olofsson, KE | 1 |
Eeg-Olofsson, O | 1 |
Aksu, F | 2 |
Weber, HP | 2 |
Rossier, E | 2 |
Vollmer, B | 2 |
Uziel, G | 1 |
Bardelli, P | 1 |
Pantaleoni, C | 1 |
Rimoldi, M | 1 |
Savoiardo, M | 1 |
Rahbeeni, Z | 1 |
Ozand, PT | 2 |
Rashed, M | 1 |
Gascon, GG | 1 |
al Nasser, M | 1 |
al Odaib, A | 1 |
Amoudi, M | 1 |
Nester, M | 1 |
al Garawi, S | 1 |
Brismar, J | 1 |
Preece, MA | 1 |
Sewell, IJ | 1 |
Taylor, JA | 1 |
Green, A | 1 |
Christensen, E | 1 |
Fowler, B | 1 |
Clarke, MA | 1 |
Hammersen, G | 1 |
Raab, K | 1 |
Kobori, J | 1 |
Moosa, A | 1 |
Iafolla, AK | 1 |
Matern, D | 1 |
Brouwer, OF | 1 |
Finkelstein, J | 1 |
Bakkeren, JA | 1 |
Gabreels, FJ | 1 |
Bluestone, D | 1 |
Barron, TF | 1 |
Beauvais, P | 1 |
Rabier, D | 1 |
Santos, C | 1 |
Lehnert, W | 1 |
Hoffmann, GF | 1 |
Hodson, AK | 1 |
Bottiglieri, T | 1 |
Rite Gracia, S | 1 |
Guallarte Alias, MP | 1 |
Martínez Moral, M | 1 |
Baldellou Vázquez, A | 1 |
Rite Montañés, S | 1 |
Ruiz-Echarri Zalaya, MP | 1 |
Marco Tello, A | 1 |
Rebage Moisés, V | 1 |
Al-Essa, MA | 1 |
Bakheet, SM | 1 |
Patay, ZJ | 1 |
Powe, JE | 1 |
Humbertclaude, V | 1 |
Rivier, F | 1 |
Roubertie, A | 1 |
Echenne, B | 1 |
Bellet, H | 1 |
Vallat, C | 1 |
Morin, D | 1 |
Jaeken, J | 1 |
Casaer, P | 1 |
de Cock, P | 1 |
Francois, B | 1 |
DeVivo, DC | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
PET Imaging of GABA Receptors in Succinic Semialdehyde Dehydrogenase Deficiency[NCT00246870] | 42 participants (Actual) | Observational | 2005-10-24 | Completed | |||
Succinic Semialdehyde Dehydrogenase Deficiency: Physiological Markers of Taurine Therapy[NCT01608178] | 7 participants (Actual) | Observational | 2012-04-27 | Completed | |||
Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency[NCT02019667] | Phase 2 | 19 participants (Actual) | Interventional | 2014-03-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Transcranial Magnetic Stimulation (TMS) is a non-invasive technique which applies magnetic pulses to the brain via a coil inducing an electrical current in the brain. Stimulation is typically applied at a sufficient intensity to trigger action potentials in nearby neurons. Intracortical facilitation (ICF) and inhibition (ICI) were studied using a paired stimulus paradigm. The motor threshold (MT) was first established. The conditioning stimulus (70% MT) followed by the test stimulus (120% MT) was delivered at an interstimulus interval (ISI) of 10 ms for ICF. Each run consisted of 10 trials, and the amplitude ratio of the mean conditioned Motor Evoked Potential (MEP) to control MEP was determined. A larger amplitude ratio indicates greater cortical excitability. The differences between Placebo and Baseline, and SGS and Baseline were obtained. These values were averaged across individuals to report a mean. (NCT02019667)
Timeframe: Baseline and Six months
Intervention | ratio of MEP amplitude (Mean) |
---|---|
Placebo | 49.9 |
Study Drug | 40.5 |
Transcranial Magnetic Stimulation (TMS) is a non-invasive technique which applies magnetic pulses to the brain via a coil inducing an electrical current in the brain. Stimulation is typically applied at a sufficient intensity to trigger action potentials in nearby neurons.Intracortical facilitation and inhibition were studied using a paired stimulus paradigm. The motor threshold (MT) was first established. The conditioning stimulus (70% MT) followed by the test stimulus (120% MT) was delivered at 100 ms for long ICI. Each run consisted of 10 trials, and the amplitude ratio of the mean conditioned Motor Evoked Potential (MEP) to control MEP was determined. A larger amplitude ratio indicates greater cortical excitability. The differences between Placebo and Baseline, and SGS and Baseline were obtained. These values were averaged across individuals to report a mean. (NCT02019667)
Timeframe: Baseline and Six months
Intervention | ratio of MEP amplitude (Mean) |
---|---|
Placebo | -9.3 |
Study Drug | 0.3 |
Transcranial Magnetic Stimulation (TMS) is a non-invasive technique which applies magnetic pulses to the brain via a coil inducing an electrical current in the brain. Stimulation is typically applied at a sufficient intensity to trigger action potentials in nearby neurons. The motor threshold is defined as the minimum percentage of the stimulator output that evoked a motor evoked potential of more than 50µV in at least 5 out of 10 trials. Motor threshold was measured at the end of the study drug period and the end of the Placebo period. The differences between Placebo and Baseline, and SGS and Baseline were obtained. A decrease from baseline value indicates increased cortical excitability and an increase from baseline value indicates reduced cortical excitability. These values were averaged across individuals to report a mean and standard deviation of this baseline-to-treatment period change. The mean for each treatment can be compared to have a baseline-adjusted treatment effect. (NCT02019667)
Timeframe: Baseline and Six months
Intervention | percentage of stimulator output (Mean) |
---|---|
Placebo | -2 |
Study Drug | -0.5 |
Transcranial Magnetic Stimulation (TMS) is a non-invasive technique which applies magnetic pulses to the brain via a coil inducing an electrical current in the brain. Stimulation is typically applied at a sufficient intensity to trigger action potentials in nearby neurons. Intracortical facilitation and inhibition were studied using a paired stimulus paradigm. The motor threshold (MT) was first established. The conditioning stimulus (70% MT) followed by the test stimulus (120% MT) was delivered at an interstimulus interval (ISI) of 2 ms for short ICI. Each run consisted of 10 trials, and the amplitude ratio of the mean conditioned Motor Evoked Potential (MEP) to control MEP was determined. A larger amplitude ratio indicates greater cortical excitability. The differences between Placebo and Baseline, and SGS and Baseline were obtained. These values were averaged across individuals to report a mean. (NCT02019667)
Timeframe: Baseline and Six months
Intervention | ratio of MEP amplitude (Mean) |
---|---|
Placebo | 35.5 |
Study Drug | -11.0 |
The ABAS questionnaire was completed by the participant's parent or caregiver at the end of each six month treatment period.The ABAS provides a comprehensive picture of adaptive skills across the lifespan. The questionnaire addresses Conceptual, Social and Practical skills including communication, self-direction, use of leisure time, health, safety and self-care. The General Adaptive Composite score ranges from <40 to >160 with a lower score representing lower adaptive behavior. The difference between Placebo and Baseline and Study Drug and Baseline were obtained. These values were averaged across individuals to report a mean and a standard deviation of the baseline-to-treatment period change. The means for each treatment can be compared to have a baseline-adjusted treatment effect interpretation. A positive change represents an improvement in adaptive skills compared with baseline and a negative change represents a decline in adaptive skills compared with baseline. (NCT02019667)
Timeframe: baseline and six months
Intervention | scores on a scale (Mean) |
---|---|
Placebo | 5.2 |
Study Drug | 4.5 |
A physical examination was administered by a physician to subjects at the end of each six month treatment period, i.e., following completion of a six month period on SGS-742 or Placebo. Results of the examination ranged from 0-4 with scores defined as follows: 0=No observation; 1=Stable baseline findings; 2=New asymptomatic finding; 3=Patient reports some worsening of a baseline daily function associated with new finding; 4=Patient unable to carry out a baseline daily function associated with new finding (NCT02019667)
Timeframe: Six months
Intervention | Participants (Count of Participants) | ||||
---|---|---|---|---|---|
0 | 1 | 2 | 3 | 4 | |
Placebo | 0 | 14 | 4 | 0 | 0 |
Study Drug | 0 | 15 | 3 | 0 | 0 |
1 review available for vigabatrin and Inborn Errors of Metabolism
Article | Year |
---|---|
4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism.
Topics: Aldehyde Oxidoreductases; Animals; Anticonvulsants; Child; Developmental Disabilities; Disease Model | 1998 |
13 other studies available for vigabatrin and Inborn Errors of Metabolism
Article | Year |
---|---|
Complete resolution of epileptic spasms with vigabatrin in a patient with 3-methylglutaconic aciduria caused by TIMM50 gene mutation.
Topics: Female; Humans; Infant; Membrane Transport Proteins; Metabolism, Inborn Errors; Mitochondrial Precur | 2020 |
[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin].
Topics: Adult; Dose-Response Relationship, Drug; Female; GABA Agents; gamma-Aminobutyric Acid; Humans; Infan | 2010 |
Monitoring of 4-hydroxybutyric acid levels in body fluids during vigabatrin treatment in succinic semialdehyde dehydrogenase deficiency.
Topics: Aldehyde Oxidoreductases; Child; Developmental Disabilities; Enzyme Inhibitors; Female; Humans; Hydr | 2003 |
Vigabatrin therapy in six patients with succinic semialdehyde dehydrogenase deficiency.
Topics: 4-Aminobutyrate Transaminase; Aldehyde Oxidoreductases; Brain Diseases, Metabolic; GABA Antagonists; | 1995 |
4-Hydroxybutyric aciduria: clinical findings and vigabatrin therapy.
Topics: Aldehyde Oxidoreductases; Anticonvulsants; Child; Female; gamma-Aminobutyric Acid; Gas Chromatograph | 1993 |
4-Hydroxybutyric aciduria.
Topics: Adult; Anticonvulsants; Brain; Child; Child, Preschool; Dextromethorphan; Female; gamma-Aminobutyric | 1994 |
Vigabatrin--interference with urinary amino acid analysis.
Topics: 4-Aminobutyrate Transaminase; Adult; Amino Acids; Aminocaproates; Anticonvulsants; Child; Child, Pre | 1993 |
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.
Topics: Adolescent; Adult; Aldehyde Oxidoreductases; Child; Child, Preschool; Developmental Disabilities; Di | 1997 |
[Non-ketotic hyperglycinemia: clinical and therapeutic course in three patients].
Topics: Dextromethorphan; Enzyme Inhibitors; Excitatory Amino Acid Antagonists; Female; Food Preservatives; | 1999 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic disease.
Topics: Brain; Child, Preschool; Dextromethorphan; Fluorodeoxyglucose F18; Humans; Hydroxybutyrates; Magneti | 2000 |
Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance.
Topics: Anticonvulsants; Brain; Cerebral Ventricles; Epilepsy; Humans; Infant; Male; Metabolism, Inborn Erro | 2001 |
Vigabatrin in GABA metabolism disorders.
Topics: Aminocaproates; Anticonvulsants; Child; Child, Preschool; Female; gamma-Aminobutyric Acid; Humans; M | 1989 |
Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency.
Topics: Aldehyde Oxidoreductases; Aminocaproates; Anticonvulsants; Child, Preschool; Humans; Male; Metabolis | 1989 |