Revimmune, NIH National Institute of General Medical Sciences GM44118.

CYP3A activity in adults varies between individuals and it has been suggested that this has a genetic basis, possibly related to variant alleles in CYP3A4 and CYP3A5 genes. Accordingly, genotype-phenotype associations were investigated under constitutive and induced conditions. Midazolam's systemic and oral clearances, and the erythromycin breath test (ERBT) were determined in 57 healthy subjects: 23 (11 men, 12 women) European- and 34 (14 men, 20 women) African-Americans. Studies were undertaken in the basal state and after 14-15 days pretreatment with rifampin. DNA was characterized for the common polymorphisms CYP3A4*1B, CYP3A5*3, CYP3A5*6 and CYP3A5*7 by direct sequencing, and for exon 21 and exon 26 variants of MDR1 by allele-specific, real-time polymerase chain reaction. In 95% of subjects, the basal systemic clearance of midazolam was unimodally distributed and variability was less than four-fold whereas, in 98% of the study population, oral clearance varied five-fold. No population or sex-related differences were apparent. Similar findings were observed with the ERBT. Rifampin pretreatment markedly increased the systemic (two-fold) and oral clearance (16-fold) of midazolam, and the ERBT (two-fold) but the variabilities were unchanged. No associations were noted between these phenotypic measures and any of the studied genotypes, except for oral clearance and its fold-increase after rifampin. These were related to the presence of CYP3A4*1B and the inversely linked CYP3A5*3 polymorphism, with the extent of induction being approximately 50% greater in CYP3A5*3 homozygotes compared to wild-type subjects. In most healthy subjects, variability in intestinal and hepatic CYP3A activity, using midazolam as an in-vivo probe, is modest and common polymorphisms in CYP3A4 and CYP3A5 do not appear to have important functional significance.

Objective-Our aims were to evaluate the effects of polymorphisms in the hepatic drug uptake transporter organic anion transporting polypeptide 1B1 (OATP1B1, SLCO1B1) and efflux transporters multidrug resistance-associated protein 2 (MRP2, ABCC2), bile salt export pump (BSEP, ABCB11), and breast cancer-related protein (BCRP, ABCG2) on single-dose pravastatin pharmacokinetics in healthy European-and African-American participants.Methods-The pharmacokinetics of a single oral 40mg dose of pravastatin was determined in 107 participants (69 European-Americans and 38 African-Americans). Participants were genotyped for known OATP1B1, MRP2, BSEP, and BCRP polymorphisms. Baseline serum total and unconjugated plasma bilirubin concentrations were also determined.Results-OATP1B1 genotypes were ethnicity-dependent with a 521C allele frequency of ~15% in European-Americans and ~1% in African-Americans. SLCO1B1 521TC genotype was associated with significantly higher pravastatin area under the curve [AUC (0)(1)(2)(3)(4)(5) NIH-PA Author ManuscriptNIH-PA Author Manuscript NIH-PA Author Manuscript SLCO1B1*1b/*1b (P= 0.011) carriers, respectively. European-Americans had significantly higher plasma pravastatin AUC (0-5) (P =0.01) and C max values (P=0.009) than African-Americans. Neither ABCC2, ABCB11, nor ABCG2 genotypes were associated with differences in pravastatin pharmacokinetics. We did not observe an effect of SLCO1B1 genotype on baseline total or unconjugated bilirubin levels.Conclusion-SLCO1B1 genotype, in particular the 521C allele, had a significant effect on the pharmacokinetics of pravastatin. Even when adjusted for the presence of the SLCO1B1 521C or 388G variant allele, European-Americans demonstrated significantly higher pravastatin AUC and C max values than African-Americans.

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Background Polymorphisms in CYP2B6 affect steady-state plasma concentrations of nevirapine and efavirenz. In many resource-limited countries, single-dose nevirapine has been widely prescribed to pregnant women at delivery to reduce mother-to-child transmission. We characterized relationships between genetic polymorphisms and the pharmacokinetics of single doses of nevirapine and efavirenz. Methods Plasma drug concentrations were determined over 13 days following a 200-mg oral dose of nevirapine administered to non-pregnant, HIV-negative African Americans. A 600-mg oral dose of efavirenz was subsequently administered and pharmacokinetic sampling repeated. Pharmacokinetic parameters were estimated using a non-compartmental approach. Primary analyses involved two CYP2B6 polymorphisms (516G>T and 983T>C) known to predict increased steady-state plasma nevirapine and efavirenz exposure. Exploratory analyses involved another 51 polymorphisms in CYP2B6, ABCB1, CYP3A4 and CYP3A5. Results Based on composite CYP2B6 516/983 genotype, the 34 participants comprised 10 extensive, 17 intermediate, and 7 slow metabolizer genotypes. Composite CYP2B6 516/983 genotype was significantly associated with plasma drug exposure and clearance for efavirenz but not for nevirapine. Exploratory analyses suggested possible associations between additional CYP2B6 polymorphisms and pharmacokinetics for nevirapine and efavirenz. Conclusions Selective pressure for drug-resistant HIV-1 following single-dose nevirapine may not differ substantially by CYP2B6 516/983 genotype. Additional polymorphisms, genes and populations warrant further study.