Pyridoxine for treatment of levetiracetam-induced behavioral adverse events: A randomized double-blind placebo-controlled trial.


Journal

Epilepsy & behavior : E&B
ISSN: 1525-5069
Titre abrégé: Epilepsy Behav
Pays: United States
ID NLM: 100892858

Informations de publication

Date de publication:
11 2022
Historique:
received: 05 05 2022
revised: 27 09 2022
accepted: 27 09 2022
pubmed: 14 10 2022
medline: 8 11 2022
entrez: 13 10 2022
Statut: ppublish

Résumé

Levetiracetam is a broad-spectrum antiseizure medication with known behavioral side effects. The possible beneficial effect of pyridoxine on improvement of these psychiatric problems has been suggested in few previous studies. This clinical trial aimed to investigate the effect of pyridoxine on behavioral side effects of levetiracetam in adult patients with epilepsy. This study was a randomized double-blind placebo-controlled clinical trial on 53 adult patients with epilepsy with behavioral side effects after treatment by levetiracetam. Patients who met the study criteria were randomized to receive 40 mg/day pyridoxine or placebo. Their psychiatric state was surveyed by SCL-90-R questionnaire before and three weeks after initiation of treatment. There were no statistically significant differences in the behavioral adverse effects between the pyridoxine-treated group and the placebo group. Although this study showed no statistically significant beneficial effects of pyridoxine on the behavioral adverse effects of levetiracetam, placebo-controlled trials with a larger size and higher doses are needed to determine whether it is effective or not.

Sections du résumé

BACKGROUND
Levetiracetam is a broad-spectrum antiseizure medication with known behavioral side effects. The possible beneficial effect of pyridoxine on improvement of these psychiatric problems has been suggested in few previous studies. This clinical trial aimed to investigate the effect of pyridoxine on behavioral side effects of levetiracetam in adult patients with epilepsy.
METHODS
This study was a randomized double-blind placebo-controlled clinical trial on 53 adult patients with epilepsy with behavioral side effects after treatment by levetiracetam. Patients who met the study criteria were randomized to receive 40 mg/day pyridoxine or placebo. Their psychiatric state was surveyed by SCL-90-R questionnaire before and three weeks after initiation of treatment.
RESULTS
There were no statistically significant differences in the behavioral adverse effects between the pyridoxine-treated group and the placebo group.
CONCLUSION
Although this study showed no statistically significant beneficial effects of pyridoxine on the behavioral adverse effects of levetiracetam, placebo-controlled trials with a larger size and higher doses are needed to determine whether it is effective or not.

Identifiants

pubmed: 36228485
pii: S1525-5050(22)00387-0
doi: 10.1016/j.yebeh.2022.108938
pii:
doi:

Substances chimiques

Levetiracetam 44YRR34555
Piracetam ZH516LNZ10
Pyridoxine KV2JZ1BI6Z
Anticonvulsants 0

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108938

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Hamed Cheraghmakani (H)

Neurology Department, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Maryam Rezapour (M)

Psychiatry and Behavioural Sciences Research Center, Addiction Institute, Department of Psychiatry, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Faezeh Asghari (F)

Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Reza Alizadeh-Navaei (R)

Gastrointestinal Cancer Research Center, Non-communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.

Monireh Ghazaeian (M)

Pharmaceutical Research Center, Department of Clinical Pharmacy, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Nasim Tabrizi (N)

Neurology Department, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran. Electronic address: n.tabrizi@mazums.ac.ir.

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Classifications MeSH