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Serum Homocysteine, Folate, and Vitamin B12 Levels in Carbamazepine Treated Epileptic Children
Insights
Carbamazepine monotherapy in children with epilepsy significantly increases homocysteine levels and decreases folate and vitamin B12. Monitoring these levels is crucial for potentially preventing atherosclerosis.
Area of Science:
- Pediatric Neurology
- Clinical Biochemistry
- Pharmacology
Background:
- Antiepileptic drugs (AEDs) are linked to metabolic issues, increasing atherosclerosis risk in epilepsy patients.
- Carbamazepine (CBZ) is a common AED, necessitating investigation into its specific metabolic effects.
Purpose of the Study:
- To investigate alterations in homocysteine, folate, and vitamin B12 levels in children on carbamazepine monotherapy.
- To assess early metabolic changes associated with carbamazepine treatment in pediatric epilepsy.
Main Methods:
- Study included 50 newly diagnosed epileptic children (ages 2-15) after 3-month follow-up.
- Serum homocysteine measured via enzyme immunoassay.
- Serum folate and vitamin B12 analyzed using Competitive Chemiluminescent Enzyme Immunoassay.
Main Results:
- Carbamazepine monotherapy significantly elevated serum homocysteine levels in epileptic children.
- A highly significant decrease in serum folate and vitamin B12 levels was observed post-carbamazepine therapy.
Conclusions:
- Carbamazepine monotherapy can lead to early, significant increases in homocysteine and decreases in folate and vitamin B12 in pediatric epilepsy.
- Monitoring these biomarkers is recommended to mitigate potential atherogenic risks associated with carbamazepine treatment.
Background:
Antiepileptic drugs (AEDs) have been associated with metabolic consequences that lead to an increase in risk of atherosclerosis in patients with epilepsy. Therefore, we evaluated whether differences exist in homocysteine, folate, and vitamin B12 levels in children receiving carbamazepine (CBZ) monotherapy.
Methods:
A total of 58 newly diagnosed epileptic children with ages ranging from 2 to 15 years were enrolled at the start of study. However, after 3 months follow up, the final total sample size was only 50 epileptic children. Eight children dropped out of the study due to poor follow up. Serum homocysteine levels were measured by enzyme immunoassay method. Serum folate and vitamin B12 levels were estimated by Competitive Chemiluminescent Enzyme Immunoassay method.
Results:
The serum homocysteine level in epileptic children was found to be significantly increased after carbamazepine (CBZ) monotherapy as compared to before therapy. Moreover, a highly significant decrease was observed in the serum folate and vitamin B12 levels, after carbamazepine monotherapy as compared to before therapy in epileptic children.
Conclusions:
Carbamazepine monotherapy may cause a significant increase in the levels of homocysteine and a significant decrease in the levels of serum folate and vitamin B12 in children with epilepsy, significant changes in above mentioned parameters occurring early in the course of treatment. The atherogenic effect of increased serum homocysteine level is well established, and patients under carbamazepine monotherapy should be monitored for possible atherogenic effects. Therefore, it may be useful to measure serum homocysteine, folate, and vitamin B12 concentrations routinely in children with epilepsy taking carbamazepine monotherapy and be treated when their levels are found to be disturbed.
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