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Cytochrome P450 2B6 (CYP2B6) metabolizes efavirenz and nevirapine, the major core antiretroviral drugs for HIV in Thailand. Rifampicin, a critical component of tuberculosis (TB) therapy is a potent inducer of CYP enzyme activity. Polymorphisms of CYP2B6 and CYP3A4 are associated with altered activity of hepatic enzyme in the liver and pharmacokinetics resulting in treatment efficacy. This study aimed to investigate whether CYP2B6 or CYP3A4 polymorphisms had effects on plasma efavirenz and nevirapine concentrations when co-administered with rifampicin in HIV/TB co-infected Thai adults.
We studied 124 rifampicin recipients with concurrent HIV-1/TB coinfection, receiving efavirenz (600 mg/day) (n = 65) or nevirapine (400 mg/day) (n = 59) based antiretroviral therapy (ART). The frequencies of GG, GT and TT genotypes of CYP2B6-G516T were 38.46%, 47.69% and 13.85% in efavirenz group and 44.07%, 52.54% and 3.39% in nevirapine group, respectively. The mean 12-hour post-dose plasma efavirenz concentration in patients with TT genotype at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation (10.97 ± 2.32, 13.62 ± 4.21 and 8.48 ± 1.30 mg/L, respectively) were significantly higher than those with GT (3.43 ± 0.29, 3.35 ± 0.27 and 3.21 ± 0.22 mg/L, respectively) (p < 0.0001) or GG genotypes (2.88 ± 0.33, 2.45 ± 0.26 and 2.08 ± 0.16 mg/L, respectively) (p < 0.0001). Likewise, the mean 12-hour post-dose plasma nevirapine concentration in patients carrying TT genotype at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation (14.09 ± 9.49, 7.94 ± 2.76 and 9.44 ± 0.17 mg/L, respectively) tended to be higher than those carrying GT (5.65 ± 0.54, 5.58 ± 0.48 and 7.03 ± 0.64 mg/L, respectively) or GG genotypes (5.42 ± 0.48, 5.34 ± 0.50 and 6.43 ± 0.64 mg/L, respectively) (p = 0.003, p = 0.409 and p = 0.448, respectively). Compared with the effects of CYP2B6-516TT genotype, we could observe only small effects of rifampicin on plasma efavirenz and nevirapine levels. After 12 weeks of both drug regimens, there was a trend towards higher percentage of patients with CYP2B6-TT genotype who achieved HIV-1 RNA levels <50 copies/mL compared to those with GT or GG genotypes. This is the first report to demonstrate the effects of CYP2B6 G516T polymorphisms on plasma efavirenz and nevirapine concentrations when co-administered with rifampicin in HIV/TB co-infected Thai adults.
CYP2B6-TT genotype had impact on plasma efavirenz and nevirapine concentrations, while rifampicin co-administration had only small effects.
Tuberculosis (TB) is the most common opportunistic infections in human immunodeficiency virus (HIV) infected individuals, accounting for more than 30% in Thailand, and up to 50% of them die during treatment . The mortality is reduced in HIV-TB co-infected patients who have started the combination antiretroviral therapy after diagnosis of TB . Concomitant administration of highly active antiretroviral therapy (HAART) and anti-TB medications is often complicated due to the drug-drug interaction and the adverse effect profile. Efavirenz and nevirapine based HAART regimens have mostly recommended to use as components of first-line antiretroviral drug regimens worldwide . As efavirenz and nevirapine are potent non-nucleoside reverse transcriptase inhibitors (NNRTIs), they are the preferable option for initial antiretroviral treatments (ART) in HIV/TB co-infection. Rifampicin is a critical component of TB therapy while it is a potent inducer of cytochrome P450 (CYP) enzyme activity . The available pharmacokinetic data showed that rifampicin reduced the plasma concentration of efavirenz and nevirapine of 13-25% and 40%, respectively [5-7]. Recently, efavirenz was shown in vitro to be primarily metabolized by hepatic CYP2B6, with minor contributions from CYP3A4 and CYP2A6 [4,8]. While rifampicin is an inducer of CYP3A4, nevirapine induces more CYP2B6 than CYP3A4 . Nevirapine was also shown to be principally metabolized by CYP3A4 and CYP2B6 . CYP2B6 and CYP3A4 genotypes are evidenced to be associated with altered activity of hepatic enzyme in the liver and pharmacokinetics that may influence efficacy of treatment, since rifampicin causes decrease in efavirenz and nevirapine concentrations [11-13].
The CYP2B6 and CYP3A4 genes are highly polymorphic  and are subject to pronounce interindividual variability in expression and activity. A single nucleotide polymorphism (SNP) at position 516 on the CYP2B6 gene has been widely reported to play an important role in the metabolism of antiretroviral drugs [15-18]. This CYP2B6 genetic variant affects the efavirenz and nevirapine pharmacokinetics [16,19,20] and associated with clinical response to nevirapine-containing regimens in children . Significant advances have led to a greater understanding of interactions between genetic and host factors that influence the efficacy and toxicity of efavirenz [19,21]. However, the findings from one population may not be generalised to other populations due to the ethnic differences in drug effect and body weight of the patients. In Thailand, it has been recently reported that CYP2B6-G516T polymorphism significantly affected the drug metabolism of efavirenz in HIV-infected Thai children , while its impact on nevirapine concentrations was less pronounced after intra-partum single-dose nevirapine in HIV-infected mothers . As efavirenz or nevirapine-based HAART is being used as the main therapy in Thailand, however, limited information was obtained so far among various Thai population regarding the influence of host genetic polymorphism on these drug levels especially nevirapine when co-administered with rifampicin which is essential for optimization of ARV dosage or drug-drug interaction. Therefore, the main objective of the present study is to investigate whether CYP2B6 and CYP3A4 polymorphisms could influence the plasma efavirenz and nevirapine levels when co-administered with rifampicin in HIV/TB infected Thai adults. The evaluation of clinical and immunological outcomes was also aimed.
One hundred and twenty four rifampicin recipients with concurrent HIV-1/TB coinfection were studied. Sixty-five of them received efavirenz (600 mg/day) based ART while 59 received nevirapine (400 mg/day) based ART. Initially, 142 patients were recruited for the study on a randomized control trial to compare the efficacy of efavirenz and nevirapine among HIV-infected patients receiving rifampicin at Bamrasnaradura Infectious Diseases Institute (BIDI), Nonthaburi since December 2006 . They are ARV naïve with active tuberculosis and received rifampicin containing anti-TB regimens for 4-6 weeks prior to enrolment. The patients received oral lamivudine (150 mg) and stavudine (30 mg for those who weighed ≤ 60 kg and 40 mg for those who weighed >60 kg) every 12 hours. They were randomized to receive either efavirenz 600 mg at bedtime while fasting or nevirapine 200 mg every 12 hours after 2 weeks at a starting dose of 200 mg every 24 hours. The dosage of rifampicin was 450 mg/day for patients who weighed ≤ 50 kg and 600 mg/day for those who weighed >50 kg. The anti-TB drug regimen was isoniazid, rifampicin, ethambutol and pyrazinamide for the first two months, followed by isoniazid and rifampicin for the subsequent 4-7 months. Among 142 patients recruited, 25 patients (9 in the efavirenz group and 16 in the nevirapine group) failed to continue the study because of hepatitis (2 cases in the nevirapine group), skin rash (3 in the efavirenz group and 2 in the nevirapine group), death (2 in the efavirenz group and 6 in the nevirapine group), transfer to the other hospital (1 in the nevirapine group), or lost to follow up (4 in the efavirenz group and 5 in the nevirapine group). In the present study, we analyzed 124 patients who have a complete data set of plasma drug levels at week 6 and 12 of ART and 1 month after rifampicin discontinuation. The study was approved by Institutional Ethics Committees of Bamrasnaradura Infectious Diseases Institute and the Ministry of Public Health, Thailand and the written informed consents were obtained from all participants.
EDTA bloods were collected from patients for SNP genotyping, CD4 T cell counts and HIV-1 viral load. Lithium heparinized bloods were collected after 12 hours of drug administration (C12) at weeks 6 and 12 of ART and after rifampicin discontinuation for 1 month for analysis of plasma efavirenz and nevirapine concentrations. The plasma were separated by centrifugation at 1800 g for 20 minutes and stored at -20°C.
The genomic DNA was extracted by using QIAamp DNA blood Mini kit (QIAGEN, Hilden, Germany) and stored at -20°C for SNP genotyping. Genotyping of allelic variants in CYP2B6 and CYP3A4 were carried out by real-time PCR using the allelic-specific fluorogenic 5' nuclease chain reaction assay by ABI PRISM 7500 sequence detection system (Applied Biosystems, Foster City, CA) as described previously . Seven SNPs were genotyped: 4 SNPs of CYP2B6-G516T, -C777A, -A415G and -C1459T and 3 SNPs of CYP3A4-T566C, -T878C and C1088T. Each 25 μl PCR mixture contained 20 ng of genomic DNA, 900 nM primers, 200 nM TaqMan minor groove binder (MGB) probes and 12.5 μl TaqMan universal PCR master mix. The thermal cycler program was set up at 95°C for 10 minutes, and then repeated 40 cycles with 95°C for 15 seconds and 60°C for 1 minute. The plate was read by the allelic discrimination settings. The SNP assay was set up using SDS, version 1.3.0 as an absolute quantification assay. Post-assay analysis was done by using SDS software.
Plasma efavirenz and nevirapine concentrations were measured by reverse phase high performance liquid chromatography (HPLC) method at the HIV-Netherlands-Australia-Thailand (HIV-NAT) Research Pharmacokinetic Laboratory, Chulalongkorn Medical Research Center (Bangkok, Thailand). HPLC was performed in accordance with the protocol developed by Department of Clinical Pharmacology, University Medical Center Nijmegan (Nijmegan, the Netherlands) .
The CD4 T lymphocyte counts were done at baseline and every 12 weeks after initiation of antiretroviral treatment by flow cytometry using monoclonal antibodies with three colors reagent (TriTEST, Becton Dickinson BioSciences, USA) and analyzed by FACScan flow cytometer (Becton Dickinson BioSciences, USA.). Plasma HIV-1 RNA was determined by RT-PCR at baseline and every 12 weeks after initiation of ART and quantified using the COBAS Amplicor, version 1.5 (Roche Diagnostics, USA). The lower detection limit for HIV-1 RNA level is 50 copies/mL.
The different genotypes in relation to plasma drug levels were analysed by SPSS software version 14.0 (ID 5038562) (SPSS Inc., Chicago, IL, USA). If unpaired one-way analysis of variance (ANOVA) was significant (p < 0.05), then post hoc Scheffe's F test was applied for multiple comparison. When plasma drug levels of different time points were compared, paired T test was used. The CD4 T cell counts and HIV-1 viral load in patients carrying different genotypes were compared by Kruskal-Wallis test. A difference in proportion of patients who achieved plasma HIV-1 RNA < 50 copies/ml at week 12 of ART was evaluated by Chi square or Fisher's exact test. A p value of < 0.05 was considered statistically significant.
The baseline characteristics of patients are shown in Table Table1.1. All 124 patients were ethnically Thai and among these, 64.6% and 67.8% were male in efavirenz and nevirapine groups, respectively. The patients had the mean ages of 35.89 ± 8.17 and 38.03 ± 8.60 years and the mean body weights of 53.30 ± 9.79 and 54.39 ± 9.39 kg in efavirenz and nevirapine groups, respectively. Similar levels of laboratory parameters including alkaline phosphatase, aspartate aminotransferase, alanine aminotransferase, total bilirubin and direct bilirubin were seen in both patient groups. However, the levels of alkaline phosphatase among patients carrying TT genotype in efavirenz group were higher than those carrying GG or GT genotypes, but this difference was not statistically significant (p = 0.085). The median (interquartile range, IQR) CD4 T lymphocyte counts were similar in both groups. In nevirapine treatment group, the log number of plasma HIV-1 viral load among patients carrying GG, GT and TT genotypes seem to be significantly different (p = 0.041).
Seven SNPs: 4 SNPs of CYP2B6- G516T, -C777A, -A415G and -C1459T and 3 SNPs of CYP3A4-T566C, -T878C and -C1088T were genotyped. For CYP2B6-G516T, 38.46% (25/65) of GG genotype (wild-type), 47.69% (31/65) of GT genotype (heterozygous mutant) and 13.85% (9/65) of TT genotype (homozygous mutant) were found among patients in efavirenz group, while in nevirapine group, there were 44.07% (26/59) of CYP2B6-516GG genotype, 52.54% (31/59) of GT genotype and 3.39% (2/59) of TT genotype. The genotype frequencies of CYP2B6-C777A and -A415G in efavirenz and nevirapine groups were 100% of homozygous mutant AA and 100% of homozygous wild-type AA, respectively. For CYP2B6-C1459T, there were 98.5% (64/65) of CC homozygous wild-type and 1.5% (1/65) of CT heterozygous mutant in efavirenz group, and 91.5% (54/59) of CC homozygous wild-type, 6.8% (4/59) of CT heterozygous mutant and 1.7% (1/59) homozygous mutant in nevirapine group. Likewise, the genotype frequencies in CYP3A4-T566C and -C1088T were 100% of homozygous wild-type TT and homozygous mutant TT, respectively, in both efavirenz and nevirapine groups. For CYP3A4-T878C, there were 95.4% (62/65) of homozygous TT and 4.6% (3/65) of heterozygous TC, and 98.3% (58/59) of homozygous TT and 1.69% (1/59) of heterozygous TC in efavirenz and nevirapine groups, respectively.
Among 4 SNPs of CYP2B6-G516T, -C777A, -A415G and -C1459T being evaluated, the frequencies of wild-type, heterozygous mutant and homozygous mutant were well distributed only in CYP2B6-G516T polymorphism, therefore, the analysis of this gene polymorphism was further done in relation to plasma efavirenz and nevirapine levels. The mean plasma efavirenz concentration in patients with homozygous TT genotype at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation (10.97 ± 2.32, 13.62 ± 4.21 mg/L and 8.48 ± 1.30 mg/L, respectively) were significantly higher than those with GT genotype (3.43 ± 0.29, 3.35 ± 0.27 mg/L and 3.21 ± 0.22 mg/L, respectively) or GG genotype (2.88 ± 0.33, 2.45 ± 0.26 and 2.08 ± 0.16 mg/L, respectively) (p < 0.0001) (Figure 1a, b, c). Similar results were found in nevirapine group (Figure 1d, e, f) in that the mean plasma drug concentration of patients with TT genotype at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation (14.09 ± 9.49, 7.94 ± 2.76 and 9.44 ± 0.17 mg/L, respectively) tended to be higher than those with GT genotype (5.65 ± 0.54, 5.58 ± 0.48 and 7.03 ± 0.64 mg/L, respectively) or GG genotype (5.42 ± 0.48, 5.34 ± 0.50 and 6.43 ± 0.64 mg/L, respectively) (p = 0.003, p = 0.409 and p = 0.448, respectively).
One month after rifampicin discontinuation, there was a clear trend towards lower plasma efavirenz levels than those during concomitant rifampicin at week 6 and 12 of ART regardless of CYP2B6 G516T genotypes. In fact, when we evaluated effects of rifampicin on plasma efavirenz levels without stratifying CYP2B6 G516T polymorphisms, the plasma efavirenz levels after rifampicin discontinuation (3.5 ± 2.67 mg/L) were significantly lower than those at week 6 (4.26 ± 3.96 mg/L) (p = 0.043) and tended to be lower than those at week 12 (4.42 ± 5.97 mg/L) (p = 0.133). In contrast, plasma nevirapine levels at 1 month after rifampicin discontinuation (6.84 ± 3.4 mg/L) were significantly higher than those at week 6 (5.83 ± 3.6 mg/L, p = 0.034) and those at week 12 (5.56 ± 2.63 mg/L, p < 0.001). The reason for these discrepant results on effects of rifampicin on plasma efavirenz and nevirapine levels is not clear at present. Further studies including evaluation of plasma drug levels at time points other than 12-hour post-dose would be thus necessary. Nevertheless, we at least can conclude that the magnitude of effects on plasma efavirenz and nevirapine levels by rifampicin was much smaller than that by CYP2B6 516 TT genotype.
With respect to CYP3A4, the analysis was done in only CYP3A4-T878C, since there was no variation at the CYP3A4-T878C and -C1088T in our study subjects. The results showed that the mean plasma efavirenz concentration at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation were 4.00 ± 0.42, 4.20 ± 0.72 and 3.48 ± 0.34 mg/L, respectively, in patients with homozygous TT genotype and 9.62 ± 6.35, 8.97 ± 6.33 and 3.87 ± 1.69 mg/L, respectively, in those with heterozygous TC genotype. Similarly, the mean plasma nevirapine concentration at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation were 5.85 ± 0.48, 5.50 ± 0.34 and 6.80 ± 0.45 mg/L, respectively, in patients with homozygous TT genotype, and 4.8, 8.69 and 9.12 mg/L, respectively, in one patient with heterozygous mutant TC genotype. Although there was a trend towards higher plasma drug levels in patients with heterozygous mutant TC genotype, appropriate statistical evaluation of this difference was difficult due to small numbers of heterozygous mutant TC.
The CD4 T cell counts among patients carrying different CYP2B6 genotypes in efavirenz and nevirapine groups are shown in Figure Figure2.2. The number of CD4 T cells in patients with TT, GT and GG genotypes increased in a similar manner at all time points at weeks 12, 24, 36 and 48 of ART compared to the baseline in both efavirenz and nevirapine groups. No significant difference in median CD4 T cell counts of each genotype at different time points was seen in efavirenz group (p = 0.818, 0.838, 0.783, 0.753 and 0.587 for baseline, weeks 12, 24, 36 and 48 of ART, respectively), whereas, in nevirapine group, the median CD4 T cell counts of patients with TT genotype seem to be lower than those with the other two genotypes at different time points, although this difference did not reach statistical significance (p = 0.595, 0.182, 0.554, 0.573 and 0.494, respectively) (Figure 2a, b).
As shown in Table Table2,2, when the proportion of patients with HIV-1 RNA level <50 copies/mL (log 1.69) were compared among CYP2B6-G516T genotypes at week 12 of ART, 88.89% (8/9) of patients with TT genotype in efavirenz group could achieve the HIV-1 RNA levels <50 copies/mL, which were higher than those with GT genotype (77.42%, 24/31) and GG genotype (68%, 17/25), although this difference was not statistically significant (p = 0.430). Similarly, in nevirapine group, 100% (2/2) of those with TT genotype, 70.97% (23/31) of those with GT genotype and 60% (15/26) of those with GG genotype could achieve the HIV-1 RNA levels <50 copies/mL, but this difference also did not reach statistical significance (p = 0.288) due to small numbers of patients with homozygous TT genotype in this study. At weeks 24, 36 and 48 of ART, nearly all the patients achieved undetectable viral load, since viral load were not detected in 95.38% (62/65), 93.65% (59/63) and 87.9% (54/62), respectively, of efavirenz group and 96.55% (56/58), 94.64% (53/56) and 94.64% (53/56), respectively, of nevirapine group.
This is the first report to demonstrate the effects of CYP2B6-G516T and CYP3A4-T878C polymorphisms on plasma efavirenz and nevirapine concentrations in rifampicin-treated HIV/TB co-infected Thai adults. The results indicated that the wide interindividual variability of efavirenz concentrations is strongly influenced by CYP2B6-516TT genotype by the finding of significantly higher plasma efavirenz concentration at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation compared to those with GT or GG genotype. Likewise, it seems to be that this CYP2B6-516TT would also influence nevirapine concentrations, although it was less pronounced probably due to the small samples size of homozygous mutant TT in our sample set. The present results were in line with the previous report on efavirenz pharmacokinetics when co-administration with rifampicin in HIV/TB co-infected Indian [26,27] and Ghana patients  in that plasma efavirenz was highest in patients with CYP2B6-516TT genotype when compared to those with GT or GG genotypes. While the heterozygous TC mutant in CYP3A4-T878C in this study seems to have some effects on plasma drug concentrations in patients at weeks 6 and 12 of ART and 1 month after rifampicin discontinuation in both efavirenz and nevirapine groups, further statistical analysis was not done due to the relatively less variation of CYP3A4 among Thai adults in this study. Further investigation should include a larger sample size with varying genotypes in order to draw a definite conclusion on the effect of CYP3A4 variations.
In this study, the frequency of CYP2B6-G516T among 124 Thai adults was 8.9%, which was close to that of our recent study on 237 HIV-infected Thai adults with different rate of CD4 T cell recovery after ARV treatment (9.7%) (submitted for publication) and slightly lower than what has been reported in Thai children (11%) . Comparing to the other ethnic groups, it was higher than those of Japanese (3.3%)  and Caucasian (6%) , but lower than that of African-American (20%)  or African population (23%) [28,29]. Although the frequencies of CYP2B6-G516T were different among populations or ethnicity, the pharmacogenetic studies reported so far in HIV patients demonstrated that CYP2B6 516TT was definitely associated with plasma efavirenz concentration [15,19,21,29,30]. The findings of CYP2B6 516TT genotype in the present study support its effect on plasma efavirenz concentration in different ethnic group and gave additional information of this SNP on nevirapine based-ART when co-administered with rifampicin. The recent pharmacogenetic study in HIV patients co-administrated with efavirenz and rifampicin demonstrated that patients carrying TT genotype had significantly higher mean plasma efavirenz but lower oral clearance , indicating that rifampicin does not fully reverse the poor metabolizer phenotype and that TT genotype can be used to identify poor metabolizers of efavirenz even in patients co-administrated with rifampicin. Consistently, the present results also indicated that rifampicin coadministration in HIV/TB infected patients did not significantly alter plasma efavirenz and nevirapine levels in patients with TT genotype (p > 0.05). Other possible factors that might affect the plasma drug levels could be excluded since they were carefully controlled.
Although rifampicin can cause the decrease in NNRTI concentrations, the mean plasma efavirenz and nevirapine concentrations in all studied patients with TT, GT and GG genotypes had plasma drug levels above the minimum recommendation (1 mg/L for efavirenz and 3.4 mg/L for nevirapine). One important conclusion from our recent prospective and randomized clinical trial in patients with concurrent HIV/TB receiving rifampicin  is that the standard dosage of efavirenz 600 mg or nevirapine 400 mg per day and co-administration with rifampicin was adequate for HIV-1 suppression, however, variation in the plasma drug levels in some patients were found, which might be due to the genetic variations among individuals. Although we reported recently that high body weights of the patients were associated with a low efavirenz C12 at weeks 6 and 12 of ART , the present results demonstrated that the body weights did not differ among patients with different genotypes of CYP2B6 G516T polymorphism. The present results thus demonstrated that rifampicin has very small effects on efavirenz and nevirapine plasma drug. The advantage of our present study over previous studies is that plasma efavirenz and nevirapine concentrations during co-administration of rifampicin could be compared with those without rifampicin after completing TB drug treatment.
In general, the high plasma efavirenz and nevirapine levels could lead to the adverse effect such as rash, hepatitis, and neuropsychological toxicity [32,33]. In order to reduce such adverse effects, several studies attempted to test the feasibility of genotype-based dose reduction of efavirenz in African-American  and Japanese HIV infected patients  and showed that efavirenz dose reduction is feasible and can reduce efavirenz-associated central nervous system symptoms in homozygotes of CYP2B6-G516T. Although patients with CYP2B6-516TT in our cohort had obviously high plasma efavirenz levels at all time points and certain degree of central nervous system and psychiatric manifestations, they were all well tolerated with the adverse effects. The adverse drug events have not recorded in nevirapine based treatment probably due to the limited number of patients with homozygous TT. Since there were 7 cases who could not complete the study due to side effects  it is necessary to determine CYP2B6 G516T genotypes of these individuals in order to know whether CYP2B6-516TT homozygote in Thailand were all well tolerated with the adverse effects of efavirenz and nevirapine.
With respect to possible correlation of the variations in plasma efavirenz and nevirapine levels with the treatment outcome, our results indicated that the patients with CYP2B6 516TT genotype had a higher frequency of viral load suppression at week 12 of ART than those with GT and GG genotype. The CD4 T cell counts increased after treatment at all time points which were correlated with HIV-1 viral load reduction. When the effect of different CYP2B6-G516T genotypes was analysed, no difference was observed among patients with TT, GT and GG genotypes in both efavirenz and nevirapine groups. Collectively, it is indicated that the efavirenz and nevirapine-based ART co-administered with rifampicin are well correlated with virological and immunological outcomes in patients undergoing treatment for HIV and TB.
In summary, the CYP2B6 and CYP3A4 polymorphisms were analysed, for the first time, in HIV/TB co-infected Thai adults receiving efavirenz and nevirapine based-ART co-administered with rifampicin and the results indicated that only 516G>T in CYP2B6 gene, but not CYP3A4 gene polymorphism, gave the significant effects on plasma drug levels. Only small effects of rifampicin on efavirenz and nevirapine plasma concentration were observed. However, for further investigation, other SNPs such as CYP2B6 T983C or TGATC-CYP2B6 haplotypes which were shown to influence the NNRTI plasma drug levels [23,36,37] should be taken into account and larger sample size with varying genotypes should be included.
CYP2B6-TT genotype had effects on both the plasma efavirenz and nevirapine concentrations in HIV/TB patients when co-administered with rifampicin. The information might be useful for better treatment of patients with HIV or HIV/TB.
The authors declare that they have no competing interests.
SU, SL, WM, NW, TK, SK participated in the study design. SU performed genotyping, CD4 counts and HIV-1 viral load determination, analysed the data and drafted the manuscript. EEN and NW took part in genotyping. SL and WM coordinated the study. TS and SK revised and finalised the manuscript. All authors read and approved the final manuscript.
SU is a Ph.D. candidate at the Faculty of Tropical Medicine, Mahidol University, Bangkok and deputy chief of Immunology and Virology Laboratory, Bamrasnaradura Infectious Diseases Institute (BIDI), Nonthaburi, Thailand. SL is a chief of Immunology and Virology Laboratory, BIDI. WM is a clinician who is taking care of HIV-1 infected patients and a principle investigator of a randomized control trial of efavirenz-based versus nevirapine-based antiretroviral therapy among HIV-infected patients receiving rifampicin. NW is the chief of Genetic Research Laboratory, National Institute of Health. TK is an assistant professor of Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University. EEN is an assistant professor of Osaka University, Japan. TS is a professor of Osaka University and works on HIV-1 infection and host genome. SK is a professor of Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University who does the research on malaria, TB and HIV and the supervisor of SU.
We thank the patients for their kind participation in the study. This study was supported by the Royal Golden Jubilee Ph.D. Program (Grant No. PHD/0094/2551) of the Thailand Research Fund; Faculty of Graduate Studies in the academic year 2008-2009 and Faculty of Tropical Medicine, Mahidol University; the Health Sciences foundation and the Ministry of Education, Culture, Sports, Sciences and Technology, Japan and Bamrasnaradura Infectious Diseases Institute (BIDI), Thailand. We thank Dr. Kiat Ruxrungtham, the HIV-Netherlands-Australia-Thailand (HIV-NAT) Research Pharmacokinetic Laboratory for determining plasma drug levels, Dr. Surakameth Mahasirimongkol, Department of Medical Sciences, Ministry of Public Health for advice on SNP analysis, Dr. Jaranit Kaewkungwal and Mr. Irwin Chavez for advice on statistical analysis, Ms. Tippawan Rattanatham, Ms. Samruay Nilkamhang, and Ms. Supeda Tongyen, BIDI for their help in recruiting patients.