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Vigabatrin-associated reversible MRI signal changes in patients with infantile spasms
Aphrodite Dracopoulos1, Elysa Widjaja, Charles Raybaud
1Department of Ophthalmology & Vision Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada. aphrodite.dracopoulos@gmail.com
Insights
Vigabatrin (VGB) treatment for infantile spasms (IS) can cause reversible MRI changes in the brain, particularly in younger infants and those with cryptogenic IS.
Area of Science:
- Pediatric Neurology
- Neuroimaging
- Pharmacology
Background:
- Infantile spasms (IS) are a severe form of epilepsy in infants.
- Vigabatrin (VGB) is a common treatment for IS.
- The neuroimaging effects of VGB in pediatric patients are not fully understood.
Purpose of the Study:
- To evaluate magnetic resonance imaging (MRI) findings in pediatric patients with IS treated with VGB.
- To investigate potential brain alterations induced by VGB therapy.
Main Methods:
- Retrospective analysis of MRI and diffusion-weighted imaging (DWI) in 107 pediatric patients with IS.
- Patients were categorized based on VGB treatment (>=120 mg/kg/day) or no VGB treatment.
- Comparison of imaging before, during, and after VGB treatment.
Main Results:
- 30.9% of patients (n=81) on VGB showed abnormal MRI signal or restricted DWI in deep gray nuclei and brainstem.
- These changes were reversible in 15 of 25 patients upon VGB withdrawal.
- Younger infants (<12 months) and those with cryptogenic IS had a higher likelihood of developing these MRI changes.
Conclusions:
- VGB induces reversible MRI signal and diffusion restriction changes in specific brain regions (globi pallidi, thalami, brainstem, dentate nuclei).
- These VGB-induced neuroimaging findings are reversible.
- Risk factors for these changes include younger age and cryptogenic IS.
Purpose:
To evaluate the magnetic resonance imaging (MRI) of pediatric patients with infantile spasms (IS) treated with vigabatrin (VGB) in order to investigate whether VGB affects the brain.
Methods:
One hundred seven pediatric patients diagnosed with IS and treated with (n = 95) >or=120 mg/kg/day VGB or without (n = 12) VGB were included. MRI and diffusion-weighted imaging (DWI) were retrospectively analyzed.
Results:
Of the patients who had MRI scans during, but not before, VGB treatment (n = 81), 25 (30.9%) exhibited abnormal MRI signal intensity and/or restricted DWI in the deep gray nuclei and brainstem. Follow-up scans (performed in 15 of the 25 patients) revealed that these changes were reversible upon withdrawal of the medication. Analysis of patients undergoing scans before, during, and after VGB treatment (n = 14) revealed that four patients had abnormal MRI signal during treatment with VBG, two of whom reversed with cessation of VGB, one reversed without cessation of VGB, and another had persistent abnormal signal while being weaned from the VGB. Patients who had not received VGB treatment (n = 12) displayed normal imaging. Younger infants (
Discussion:
In pediatric patients, VGB induces reversible MRI signal changes and reversible diffusion restriction in the globi pallidi, thalami, brainstem, and dentate nuclei. The risk for this phenomenon was greater in younger infants and patients with cryptogenic IS.
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