What is it about?

Epilepsy is among the most prevalent serious neurological disorders, affecting over 70 million people worldwide, in Algeria, the prevalence of epilepsy was estimated to be eight times more common. Carbamazepine is frequently the first-line treatment, making early prediction of patient response essential for personalized care. This approach helps reduce adverse effects and healthcare costs, while enhancing patient outcomes. This study aims to explore the link between the ABCB1 c.3435C > T genetic variation and Carbamazepine resistance and toxicity in Algerian patients with epilepsy, with a focus on the impact of genetic variations on Carbamazepine plasma concentrations and treatment outcomes. Ninety-eight Algerian patients with epilepsy were recruited and categorized as either drug-responsive or drug-resistant based on their clinical response to CBZ treatment. Genotyping of the ABCB1 c.3435 C > T polymorphism was performed using Polymerase Chain Reaction—Restriction Fragment Length Polymorphism (PCR–RFLP) method, and CBZ plasma levels were measured to assess its effect on metabolism. Clinical data, including drug response, therapy type, and adverse drug reactions (ADRs), were collected and analyzed. For the statistical analysis we used chi-squared tests and Exact Fisher's for corrections. Our findings show no significant association between the ABCB1 c.3435C > T genotypes with carbamazepine resistance (p = 0,1) nor incidence of adverse reactions. This polymorphism also indicated no statistically significant link with Carbamazepine plasma levels. The sample size in this study might be limitation; therefore, expanded investigations on Algerian population are needed. Although this study indicates no significant correlation of the ABCB1 c.3435C > T polymorphism with influencing CBZ Pharmacoresistance and therapeutic outcomes, larger-scale-studies are required to confirm these results and assess their reliability.

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Why is it important?

Carbamazepine (CBZ) is one of the most used Anti seizure medication (ASM) in Algeria and worldwide because of it’s efficacy and affordability. Is also fully covered by medical insurance. Personalized prescriptions of ASMs would help improve patients daily life and also has an economic aspect. ABCB1 gene is important in the transport of CBZ in and out of cells. It has been the center of focus in many studies in different populations worldwide. This study is the first in Algeria to investigate the association between ABCB1 polymorphism and CBZ outcomes in a cohort of Algerian patients with epilepsy.

Perspectives

Wa aim to to investigate the influence of several gene polymorphisms ( cytochrome P450 such as CYP3A4, CYP2C8 and CYP3A5, EPHX1) on Carbamazepine outcomes in lager cohorts of Algerian patients with epilepsy to identify new molecular biomarkers with potential impact.

PhD Student Rachda Riffi
Ecole Supérieure en Sciences Biologiques d'Oran (ESSBO)

Read the Original

This page is a summary of: ABCB1 c.3435 C > T (rs1045642) as a biomarker for carbamazepine efficacy and toxicity in Algerian patients with epilepsy: initial findings report, Neurogenetics, February 2025, Springer Science + Business Media,
DOI: 10.1007/s10048-025-00807-w.
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