- Oral presentation
- Open Access
Inter-ethnic differences in efavirenz CNS toxicity – role of cytochrome P450 2B6 polymorphisms
BMC Infectious Diseases volume 12, Article number: O17 (2012)
Highly active antiretroviral therapy regimens that include efavirenz are effective, but adverse events are common, especially central nervous system (CNS) toxicities. We previously showed increased discontinuation rates of efavirenz due to CNS toxicities in Malay and Chinese patients in our Treat Asia HIV Observational Database (TAHOD) database. We postulate that these differences may be due to genetic differences.
We performed genome wide genotyping with the Illumina 1M and the Affymetrix 6.0 microarrays in healthy volunteers from the 3 major ethnic groups in Singapore, consisting of Chinese (mainly of southern Chinese origin), Malays and Indians (mainly of southern Indian origin). Genetic information was available from 95 Chinese, 89 Malays and 82 Indians.
Allele frequencies were obtained for the rs3745274 single nucleotide polymorphism coding for the cytochrome P450 2B6 (CYP2B6) 516 G>T mutation. The allele frequency of the mutant gene was found in 22.1% in Chinese, 37.6% in Malays and 37.8% in Indians. Homozygous TT mutations were found in 4.2% in Chinese, 12.4% in Malays and 12.2% in Indians. This homozygous TT mutation frequency is higher than that found in the European American HIV-infected population, which was reported to be 3%.
Our study showed significant ethnic differences in CYP2B6 516 G>T mutations in Singapore. The frequencies of these mutations are significantly higher than in Caucasian populations. This finding may explain the higher discontinuation rate of efavirenz due to CNS side effects. Further studies with studying the association of CYP2B6 genotype with CNS toxicities and efavirenz concentrations are indicated.
About this article
Cite this article
Lee, L.S., Soon, G.H. & Teo, Y.Y. Inter-ethnic differences in efavirenz CNS toxicity – role of cytochrome P450 2B6 polymorphisms. BMC Infect Dis 12, O17 (2012). https://doi.org/10.1186/1471-2334-12-S1-O17
- Discontinuation Rate
- Rs3745274 Single Nucleotide Polymorphism
- Central Nervous System Toxicity
- Genome Wide Genotyping