, , and  genetic polymorphisms do not affect methadone maintenance treatment in HCV-positive patients

Methadone is a synthetic opioid used for detoxification and maintenance treatment of patients who are dependent on opiates, mainly heroin. In the liver it is metabolised to 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) through N-demethylation mediated by several cytochrome P450 (CYP) enzymes, including CYP3A4 and CYP2B6 (1). The CYP3A4 enzyme metabolises both (R)- and (S)-methadone enantiomers, but the (S)-enantiomer is mostly metabolised by CYP2B6 (2, 3).

Methadone kinetics is also slightly affected by ABCB1 genetic polymorphisms (4). In a study of their effects on methadone maintenance treatment (MMT) in 60 opioid-dependent patients, Coller et al. (5) reported that ABCB1 genetic variability influenced daily methadone requirements.

In addition, CYP gene variants may contribute to the risk of fatal methadone toxicity posed by high concentrations of unmetabolised methadone in plasma (6). The risk may be even greater in patients with liver damage caused by hepatitis C virus (HCV) infection, which is common in opioid dependency. Our earlier studies (7, 8) have shown that chronic overdose and liver insufficiency (damage) increase the amount of unmetabolised methadone and its toxicity, but we did not consider the influence of the ABCB1, CYP2B6, and CYP3A4 genes on methadone metabolism as one of the numerous factors that influence inter-individual variability in that respect. The aim of this study was therefore to address this gap and see if the ABCB1, CYP2B6, and CYP3A4 genetic polymorphisms affect methadone metabolism in patients on MMT.

Materials and methods

The study was conducted in accordance with the Declaration of Helsinki and was approved by the Ethics Committee of the University Hospital Split, Croatia (No. 530-01/12-01/164). All patients signed informed consent to participation in the study.

Participants

Our study participants were 35 adult men aged ≥21 years, who were in the MMT programme conducted by the Institute for Public Health of the Split-Dalmatia County, Croatia. To arrive to this number we first assessed for eligibility 74 adult male heroin addicts in the programme according to the following inclusion criteria: male, Caucasian, at least 9 months on MMT with regular attendance, no HIV or HBV co-infection or infection, negative urine tests for the presence of heroin or other pharmacological substances that could interfere with methadone metabolism, and no liver cirrhosis or history of significant alcohol abuse. HCV-positive patients were receiving interferon therapy that does not interfere with methadone metabolism (9). Thirty-nine candidates who did not meet these criteria were excluded.

The remaining 35 participants were divided in groups according to their HCV status: HCV-negative (HCV-) (N=12), HCV positive (HCV+) (N=16), and those in clinical remission (HCV CR) (N=7). Their liver damage was assessed according to the fibrosis-4 (FIB-4) index as described elsewhere (10). They were receiving different recommended doses of oral methadone based on their clinical presentation, and these doses were not modified for at least six months before the study (Table 1).

Table 1

Average FIB-4 index, methadone-to-EDDP urine concentration ratio, and methadone dose received by study groups (N=35)

Parameters	HCV-negative (n=12)	HCV-positive (n=16)	HCV clinical remission (n=7)
FIB-4 index	0.81	2.61	2.08
Methadone-to-EDDP urine concentration ratio	0.87	2.04	0.79
Methadone dose (mg)	83.2	85.0	62.5

Methadone and EDDP determination

For this study, methadone and EDDP concentrations were tested only in urine during three regular check-ups 15 days apart. We took two urine samples per check-up; one immediately before and the other 90 min after oral methadone administration, which totalled six samples per participant. The samples were stored at 4 °C and analysed within 1–4 days as described in detail in our previous reports (8, 11). Methadone and EDDP concentrations were used to calculate their ratio (Table 1).

DNA analysis

Blood samples for DNA analysis were collected at regular check-ups and stored in EDTA tubes. DNA was isolated with a commercial genomic DNA isolation kit (High Pure PCR Template Preparation Kit, Roche Diagnostics GmbH, Mannheim, Germany) according to the manufacturer’s instructions. Extracted DNA was quantified using a Qubit 4 fluorimeter (Thermo Fischer Scientific, Waltham, MA, USA).

SNP genotyping

Using the TaqMan^® SNP genotyping assay (Thermo Fischer Scientific) and an Applied Biosystems 7500 real-time polymerase chain reaction (RT-PCR) system (Applied Biosystems, Foster City, CA, USA) we genotyped for the following single-nucleotide polymorphisms (SNPs): ABCB1 rs1045642 (DME C_7586657_20), CYP2B6 SNP rs3745274 (DME C_7817765_60), CYP3A4 rs2242480 (DME C_26201900_30), and CYP3A4 rs2740574 (DME C_1837671_50). RT-PCR and allelic discrimination analyses were performed according to the manufacturer’s instructions in a 25-mL reaction volume. The temperature program for RT-PCR was 60 °C for 1 min and 95 °C for 10 min, followed by 50 cycles of 92 °C for 15 s and 60 °C for 90 s. SNP genotypes were determined using instrument software with the manual allele call option.

Statistical analysis

Statistics and differences between the samples and groups were tested by using GraphPad Prism version 8.0.0 for Mac (GraphPad Software, San Diego, CA, USA). Hardy-Weinberg equilibrium, chi-square, and the p value were calculated with an on-line calculator (12).

Results and discussion

Methadone is converted to its inactive metabolites EDDP and EMDP by hepatic CYP450 enzymes. Its pharmacokinetics is individual, not only because of differences in sex, age, body weight, and use of other drugs, but also because of different allelic frequencies of genetic polymorphisms (2). Some earlier studies have already shown that allelic variations in the ABCB1 rs1045642, CYP2B6 rs3745274, and CYP3A4 rs2242480 and rs2740574 SNPs may affect the distribution of methadone in patients undergoing MMT (6, 13, 14).

Table 2 shows the genotypes of the four investigated SNP loci in DNA obtained from blood samples. Genotype frequencies were consistent with the Hardy-Weinberg equilibrium and did not significantly differ for any of the studied SNPs (the p value ranged from 0.55 to 0.93). Minor allele frequencies (MAF) (Table 2) were consistent with those presented in a meta study by Dennis et al. (15), in which they ranged between 24.5 and 50 % for ABCB1 rs1045642 and between 24 and 39 % for CYP2B6 rs3745274.

Table 2

Genotype and allele frequencies (%) by loci for the ABCB1, CYP2B6 and CYP3A4 genes in all participants (N=35)

Gene	SNP	Genotype	n (%)	Minor allele	MAF (%)	Hardy-Weinberg equilibrium
Gene	SNP	Genotype	n (%)	Minor allele	MAF (%)	p allele frequency	χ² p-value
		GG	12 (34.3)
ABCB1	rs1045642	AG	16 (45.7)	A	42.9	0.57	0.15 0.69
		AA	7 (20)
		GG	15 (42.9)
CYP2B6	rs3745274	GT	17 (48.5)	T	32.9	0.67	0.36 0.55
		TT	3 (8.6)
		CC	30 (85.7)
CYP3A4	rs2242480	CT	5 (14.3)	T	7.1	0.93	0.21 0.65
		TT	0 (0)
		TT	34 (97.1)
CYP3A4	rs2740574	CT	1 (2.9)	C	1.4	0.99	0.007 0.93
		CC	0 (0)

In contrast to ABCB1 and CYP2B6 SNPs, no mutated alleles were found in either of the analysed CYP3A4 SNPs (Figure 1).

Methadone-to-EDDP ratio in all patients with different ABCB1, CYP2B6, CYP3A4 480 and CYP3A4_574 variants. H – heterozygotes; M – mutant; wt – wild type

We observed a small difference in wild and mutant genotypes between the ABCB1 and CYP2B6 genes. Patients with the ABCB1 AA and CYP2B6 TT genotype had a slower methadone metabolism than those with the GG genotype. In both SNPs of the CYP3A4 gene the wild genotype had a slower methadone metabolism than the heterozygous genotype.

Methadone-to-EDDP ratio in patients with different ABCB1and CYP2B6 variants by HCV status. H – heterozygotes; HCV-– HCV-negative group; HCV+ – HCV-positive group; HCV CR – group in HCV clinical remission ; M – mutant; wt – wild type

Although several studies have suggested an association between genetic variability and methadone metabolism, our results showed no significant difference in methadone-to-EDDP ratio between the SNP genotypes. For ABCB1 rs1045642 it was p=0.3772 (ANOVA F=1.005), for CYP2B6 rs3745274 p=0.6909 (F=0.374), and for CYP3A4 rs2242480 p=0.6533 (F=0.4313).

Even within the groups divided by HCV status this difference was not significant (p>0.05) (Figure 2). In the HCV+ group, the methadone-to-EDDP ratio was similar for all three ABCB1 genotypes and slightly higher in patients with the mutated CYP2B6 genotype.

The liver is the primary target organ of HCV infection and is the main organ responsible for metabolism of drugs. Wu et al. (16) reported that HCV affected methadone metabolism in MMT patients. Our results seem to confirm this finding, as the severity of liver damage (median FIB-4 index) was the highest in HCV patients, who also showed the slowest methadone metabolism (the highest methadone-to-EDDP ratio; Table 1).

Figure 3 shows FIB-4 indices relative to the ABCB1 and CYP2B6 gene polymorphisms for all 35 patients. The median FIB-4 index in both examined genes was higher in patients with the mutated genotype. However, we found no statistically significant difference in FIB-4 index between the SNP genotypes. For ABCB1 rs1045642 it was p=0.4465 (ANOVA F=0.8269) and for CYP2B6 rs3745274 p=0.1551 (F=1.977).

FIB-4 index in all patients with different ABCB1 and CYP2B6 variants. H– heterozygotes; M – mutant; wt – wild type

In conclusion, our study found no significant influence of the established genetic polymorphisms in our patients with methadone metabolism. Similar has been reported by Fonseca et. al. (17), who found negligible impact of the CYP3A5, CYP2B6, CYP2C9, CYP2C19, and ABCB1 genetic polymorphisms on S-methadone metabolite plasma concentrations (16).

The only major influence on the methadone-to-EDDP ratio in HCV+ patients we found was the stage of liver damage. HCV- and HCV+ patients were taking similar methadone doses. The FIB-4 index and the methadone-to-EDDP ratio in HCV- patients were lower, regardless of the genotype.

However, our conclusion should be taken with reserve, as this study had a small sample size. Future research should therefore involve more MMT patients.

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ABCB1, CYP2B6, and CYP3A4 genetic polymorphisms do not affect methadone maintenance treatment in HCV-positive patients

Article Category: Original article

Published Online: Dec 31, 2020

Page range: 353 - 358

Received: Dec 01, 2019

Accepted: Nov 01, 2020

DOI: https://doi.org/10.2478/aiht-2020-71-3378

© 2020 Davorka Sutlović et al., published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

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