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Frequencies of Cytochrome P450 2B6 and 2C8 Allelic Variants in the Mozambican Population

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Specialty General Medicine
Date 2013 Sep 18
PMID 24043992
Citations 15
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Abstract

Background: The cytochrome P450 enzymes (CYP) play an important role in the metabolism of many therapeutic agents. The activities of different enzymes exhibit variability in different populations, which causes variations in drug response or toxicity. The CYP2B6 and CYP2C8 enzymes are encoded by polymorphic genes characterised by different single nucleotide polymorphisms (SNPs). Several of these CYP variants are often associated with slow metabolism phenotypes. This study aimed to analyse the frequencies of allelic variants of CYP2B6 and CYP2C8 in the Mozambican population.

Methods: Using a polymerase chain reaction and restriction fragment length polymorphism assay (PCR-RFLP), the frequencies of the allelic variants of CYP2B6 (c.64C>T, c.516G>T, c.777C>A, c.785A>G, c.1459C>T) and CYP2C8 (c.805A>T, c.416G>A, c.1196A>G, c.792C>G) were determined in 360 Mozambican blood donors.

Results: The frequencies of the allelic variants of the CYP2B6 gene were 0.057, 0.426, 0.0, 0.410, and 0.004. For the CYP2C8 gene, the frequencies of the allelic variants were 0.160, 0.048, 0.0, and 0.005. No significant differences were observed between the gender and geographic distribution of volunteers around the country.

Conclusion: The frequencies of the allelic variants of the CYP2B6 and CYP2C8 genes were found to be homogeneously distributed in the Mozambican population and were comparable to other African populations. Further studies are required to explore the impact of these variants on the clinical response (efficacy and toxicity) of drugs, including antimalarials.

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References
1.
Krishna S, Planche T, Agbenyega T, Woodrow C, Agranoff D, Bedu-Addo G . Bioavailability and preliminary clinical efficacy of intrarectal artesunate in Ghanaian children with moderate malaria. Antimicrob Agents Chemother. 2001; 45(2):509-16. PMC: 90320. DOI: 10.1128/AAC.45.2.509-516.2001. View

2.
Miksys S, Lerman C, Shields P, Mash D, Tyndale R . Smoking, alcoholism and genetic polymorphisms alter CYP2B6 levels in human brain. Neuropharmacology. 2003; 45(1):122-32. DOI: 10.1016/s0028-3908(03)00136-9. View

3.
Svensson U, Ashton M . Identification of the human cytochrome P450 enzymes involved in the in vitro metabolism of artemisinin. Br J Clin Pharmacol. 1999; 48(4):528-35. PMC: 2014388. DOI: 10.1046/j.1365-2125.1999.00044.x. View

4.
Li X, Bjorkman A, Andersson T, Gustafsson L, Masimirembwa C . Identification of human cytochrome P(450)s that metabolise anti-parasitic drugs and predictions of in vivo drug hepatic clearance from in vitro data. Eur J Clin Pharmacol. 2003; 59(5-6):429-42. DOI: 10.1007/s00228-003-0636-9. View

5.
Hofmann M, Blievernicht J, Klein K, Saussele T, Schaeffeler E, Schwab M . Aberrant splicing caused by single nucleotide polymorphism c.516G>T [Q172H], a marker of CYP2B6*6, is responsible for decreased expression and activity of CYP2B6 in liver. J Pharmacol Exp Ther. 2008; 325(1):284-92. DOI: 10.1124/jpet.107.133306. View