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Cytochrome 2B6 polymorphism and efavirenz-induced central nervous system symptoms : a substudy of the ANRS ALIZE trial
- Source :
- HIV Medicine, HIV Medicine, Wiley, 2017, 18 (8), pp.537-545. ⟨10.1111/hiv.12488⟩
- Publication Year :
- 2017
- Publisher :
- HAL CCSD, 2017.
-
Abstract
- International audience; OBJECTIVES:Single nucleotide polymorphisms in the cytochrome P450 (CYP) 2B6 gene have been associated with high interindividual variation in efavirenz pharmacokinetics. However, clinical data on the relationship of CYP2B6 polymorphisms with the occurrence of efavirenz-induced central nervous system (CNS) symptoms are limited.METHODS:We analysed four polymorphisms in the CYP2B6 (516 G>T), CYP3A5 (6986 A>G) and ATP-binding cassette, sub-family B, member 1 (ABCB1) (2677 G>T/A and 3435 C>T) genes in HIV-infected adults virologically suppressed on a protease inhibitor-based regimen who switched to a regimen containing emtricitabine, didanosine and efavirenz in the setting of the ANRS ALIZE trial. Kaplan-Meier methods and Cox regression analysis were used to investigate their association with efavirenz plasma levels and CNS events up to 48 months after switching.RESULTS:In total, 191 patients with a median age of 41 years, who were 87% male and 85% Caucasian, were enrolled in the study. Variant allelic frequencies were 0.49, 0.93, 0.59 and 0.63 for CYP2B6 516, CYP3A5 392, ABCB1 2677 and ABCB1 3435, respectively. The median efavirenz plasma concentration (MEPC) was 2.2 mg/L [interquartile range (IQR) 1.7-2.8 mg/L] and was significantly higher in patients with the deficient CYP2B6 516T. Overall, 242 CNS events were reported in 104 individuals (54%). No correlation was found between MEPC and CNS events. The occurrence of a first CNS event was lower in patients with the CYP2B6 516 G/G genotype vs. CYP2B6 516 T genotypes [50% (IQR: 40-60%) vs. 66% (IQR: 56-75%), respectively; P = 0.02]. In an adjusted Cox regression model, there was a tendency towards a higher risk of a first CNS event among carriers of the variant CYP2B6 516 T allele (relative risk 1.4 [95% CI, 0.99-2.1]; P?=?.06), compared with noncarriers.CONCLUSIONS:The deficient CYP2B6 516 T allele is associated with higher efavirenz plasma drug levels and more frequent CNS-related symptoms.
- Subjects :
- Cyclopropanes
Male
HIV Infections
Pharmacology
030226 pharmacology & pharmacy
Gastroenterology
chemistry.chemical_compound
Plasma
0302 clinical medicine
Interquartile range
Central Nervous System Diseases
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Antiretroviral Therapy, Highly Active
Pharmacology (medical)
030212 general & internal medicine
Didanosine
cytochrome P450 2B6 (CYP2B6)
pharmacogenetics
Health Policy
efavirenz
Middle Aged
3. Good health
Infectious Diseases
Alkynes
Female
medicine.drug
Adult
medicine.medical_specialty
Efavirenz
Drug-Related Side Effects and Adverse Reactions
Anti-HIV Agents
Single-nucleotide polymorphism
Emtricitabine
Polymorphism, Single Nucleotide
03 medical and health sciences
Internal medicine
medicine
Humans
Genetic Predisposition to Disease
CYP3A5
business.industry
toxicity
central nervous system
Benzoxazines
Cytochrome P-450 CYP2B6
chemistry
Relative risk
business
Pharmacogenetics
Follow-Up Studies
Subjects
Details
- Language :
- English
- ISSN :
- 14642662 and 14681293
- Database :
- OpenAIRE
- Journal :
- HIV Medicine, HIV Medicine, Wiley, 2017, 18 (8), pp.537-545. ⟨10.1111/hiv.12488⟩
- Accession number :
- edsair.doi.dedup.....dc280f718b05f81d5e7707d1f4afe277