Figures
Abstract
Background
Genetic determinants of drug response remain stable throughout life and offer great promise to patient-tailored drug therapy. The adoption of pharmacogenetic (PGx) testing in patient care requires accurate, cost effective and rapid genotyping with clear guidance on the use of the results. Hence, we evaluated a 32 SNPs panel for implementing PGx testing in clinical laboratories.
Methods
We designed a 32-SNP panel for PGx testing in clinical laboratories. The variants were selected using the clinical annotations of the Pharmacogenomics Knowledgebase (PharmGKB) and include polymorphisms of CYP2C9, CYP2C19, CYP2D6, CYP3A5 and VKORC1 genes. The CYP2D6 gene allele quantification was determined simultaneously with TaqMan copy number assays targeting intron 2 and exon 9 regions. The genotyping results showed high call rate accuracy according to concordance with genotypes identified by independent analyses on Sequenome massarray and droplet digital PCR. Furthermore, 506 genomic samples across three major ethnic groups of Singapore (Malay, Indian and Chinese) were analysed on our workflow.
Results
We found that 98% of our study subjects carry one or more CPIC actionable variants. The major alleles detected include CYP2C9*3, CYP2C19*2, CYP2D6*10, CYP2D6*36, CYP2D6*41, CYP3A5*3 and VKORC1*2. These translate into a high percentage of intermediate (IM) and poor metabolizer (PM) phenotypes for these genes in our population.
Citation: Goh LL, Lim CW, Sim WC, Toh LX, Leong KP (2017) Analysis of Genetic Variation in CYP450 Genes for Clinical Implementation. PLoS ONE 12(1): e0169233. https://doi.org/10.1371/journal.pone.0169233
Editor: Aamir Ahmad, University of South Alabama Mitchell Cancer Institute, UNITED STATES
Received: September 23, 2016; Accepted: December 13, 2016; Published: January 3, 2017
Copyright: © 2017 Goh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work is supported by the research fund from the Singapore National Medical Research Council (NMRC/CG/017/2013). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
There is significant variability in drug response with regard to efficacy, optimal dose and adverse drug reactions (ADRs) [1–3]. Genetic variations have been estimated to contribute between 20–30% to variability in response to drugs [4]. Implementing PGx in routine clinical care has the potential to reduce adverse drug reactions and maximise drug efficacy based on the genetic profile of individual patients [5]. Approximately 18% of prescribed drugs carry actionable pharmacogenetic labels in the USA, demonstrating the increasing importance of genetic testing for clinical practice [6]. The incorporation of PGx into clinical practice requires accurate genotyping and correct prediction of genetic variants contributing to inter-individual differences in drug response.
The cytochrome P450 (CYP) enzymes are the major system that catalyse phase I drug metabolism, encompassing most of the clinically prescribed drugs [7]. The activity of each enzyme encoded by the combination of CYP450 star alleles is categorized as poor metabolizer (PM), intermediate metabolizer (IM), extensive metabolizer (EM) and ultra-rapid metabolizer (UM). Some of these genes are highly polymorphic with multiple alleles and the prediction of phenotypes by detecting polymorphisms of CYP genes that are important for drug metabolism is instrumental in drug therapy [8]. The genetic polymorphisms affecting activities of clinically relevant drug-metabolizing enzymes are found in CYP2C9, CYP2C19, CYP3A5 and CYP2D6. Genotyping CYP2C9 and VKORC1 aid in the management of patients receiving warfarin therapy [9,10]. CYP2C19 is important for the metabolism of a number of drugs including clopidogrel, omeprazole and phenytoin [11–13]. CYP3A5 is associated with the metabolism of tacrolimus [14]. Although CYP3A4 has overlapping substrate specificity as CYP3A5, no functional variant forms of CYP3A4 have been observed in Asians and Caucasians [15,16]. CYP2D6 is estimated to metabolize approximately 25% of all clinically used drugs, including codeine, fluoxetine and amitriptyline [17–19].
CYP2D6 is highly polymorphic and represents one of the most difficult enzymes to genotype. It spans a 4.3 Kb region on chromosome 22q13.1 and forms a cluster with two pseudogenes, CYP2D7 and CYP2D8 [20]. At present, more than 100 allelic variants and sub variants have been described [21]. Its genetic complexities are due to SNPs, duplications and multiplications, deletions and recombination events with the highly homologous CYP2D7 pseudogene. The frequency of CYP2D6 gene multiplication is as high as 45% in Asian [22]. It is important to accurately measure the exact copy number of functional CYP2D6 genes as not all copy number variations (CNVs) are functionally similar. The presence of different genetic variations mandates the use of more than one assay to determine the CYP2D6 genotypes. For example, the CYP2D6-CYP2D7 fusion genes, such as CYP2D6*36, cannot be discriminated from CYP2D6*10 that shares the same SNP (100C>T) without the identification of the sequence of each copy. Hence, it is important to identify which of the two alleles carries the duplication or multiplication in order to predict the phenotype accurately in a clinical setting. This piece of information serves as a guide for individualization of drug therapy.
The pharmacogenetic testing of CYP polymorphisms in a clinical laboratory needs to be rapid, robust and cost-effective. Available methods for CYP genotyping include restriction fragment length polymorphism analysis, allele-specific PCR or Sanger sequencing which are time consuming. Some of the available commercial kits are limited in coverage, omitting significant variations relevant for Asian populations. In this study, we explored the use of a 32-SNP panel with TaqMan genotyping assays coated in 384-well plate format and 2 copy number assays for the detection of significant variations in CYP2C9, CYP2C19, CYP3A5 and CYP2D6. We genotyped 506 subjects from our population and defined the allele frequencies and phenotypic consequences in different ethnic groups. The results are used to assess the associations of pharmacogenetics and drug response; and to assess the feasibility of implementing PGx testing in different ethnic groups. Our study contributed to the overall knowledge of the Singapore prevalence of CYP450 genotypes. Alongside with the simplicity and specificity of the TaqMan genotyping assays, this test is highly applicable in a clinical laboratory.
Methods
Sample collection and processing
In this study, we used 10 HapMap samples for assay validation. All HapMap samples were purchased from Coriell Cell Biorepositories. We tested 506 healthy individual samples from the three major ethnic groups (126 Malays, 179 Indians and 201 Chinese) in Singapore provided by TTSH BioBank. All subjects provided written consent. The study was approved by the institutional ethics review board. DNA was extracted from peripheral blood collected with EDTA blood tubes using the QIAamp® DNA Blood Mini QIAcube Kit (QIAGEN, P/N: 51126). The automated process was performed on the QIAcube® system according to manufacturer’s recommended protocols. Extracted DNA samples were quantified by NanoDrop 2000c Spectrophotometer and normalised to 5ng/μl for use in genotyping and copy number variation experiments.
32 SNP genotyping experiments
Genotyping was performed using TaqMan-based real-time PCR with TaqMan assays from Applied Biosystems™ (Table 1). Pre-coated 384-well TaqMan® Custom Plating (Applied Biosystems™, P/N: 4462783) which contains 32 pharmacogenomics assays was used. Up to 11 samples plus one no-template control were included in each run. A final volume of 5 μl consisting of 2.5 μl TaqMan® Genotyping Master Mix (Applied Biosystems™, P/N: 4371355) and 2.5 μl genomic DNA was dispensed to each well by epMotion M5073 automated pipetting system (Eppendorf). The TaqMan® Genotyping Master Mix (Applied Biosystems™, P/N: 4371355) contains ROX dye which serves as a passive reference dye to normalize signal and ensure data integrity. The qPCR was run on QuantStudio™ 6 Flex Real-Time PCR System (Applied Biosystems™) with the following thermal cycling condition: pre-PCR hold at 60°C for 30 seconds, initiation at 95°C for 10 minutes for initial denaturation and enzyme activation, followed by 50 cycles of 95°C for 15 seconds and 60°C for 90 seconds.
CYP2D6 copy number variation analysis
CYP2D6 gene copy number was determined using Applied Biosystems’ commercially available TaqMan Copy Number Assays, Exon 9 (Assay ID: Hs00010001_cn) and Intron 2 (Assay ID: Hs04083572_cn). Exon 9 copy number assay was used to quantify all non-CYP2D6*36 alleles and identify CYP2D6 gene deletion (*5) in the samples. Intron 2 copy number assay was used to quantify all alleles including CYP2D6*36 alleles. The total copy number variation difference between the two copy number assays were used to identify the actual copy number of CYP2D6*10 and CYP2D6*36 alleles. All assays were run together with a reference gene, the commercially available TaqMan Copy Number Reference Assay RNaseP (Assay ID: 4403326, Applied Biosystems™). All samples were prepared in quadruplicates in a 384-well format with the TaqMan Genotyping Master Mix (Applied Biosystems™, P/N: 4371355) using 10ng of genomic DNA in a 10 μl reaction. The qPCR was carried out using the QuantStudio™ 6 Flex Real-Time PCR System with the following thermal cycling conditions: initiation at 95°C for 10 minutes for initial denaturation and enzyme activation, followed by 40 cycles of 95°C for 15 seconds and 60°C for 1 minute.
Data analysis
The TaqMan genotyping analysis was performed according to the manufacturer's recommendations and published protocol. The run (.eds) files were first analysed using the QuantStudio™ Real-Time PCR Software v1.2 to check for the overall quality of the amplification of all 32 assays. The end-point data files were then imported into Applied Biosystems® TaqMan® Genotyper Software v1.3.1 to verify the genotype calls and clustering patterns. The analysis was done by Autocalling with pre-defined algorithmic approach and information from imported Assay Information File (AIF). Manual calling was done to overwrite the auto-calling if necessary. The analysed genotype results were exported into a tab-delimited (.txt) file using the “Advanced’ settings before being incorporated into AlleleTyper™ Software v1.0.7-I0B01 (Applied Biosystems™) to determine the haplotypes.
For CYP2D6 gene copy number analysis, relative quantitation (RQ) analysis was performed using CopyCaller™ Software (Applied Biosystems™). The raw results were first analysed using the QuantStudio™ Real-Time PCR Software v1.2 with a manual CT threshold level of 0.2 and auto baseline settings to determine CT values. The results were exported to tab-delimited (.txt) files, before being imported into the CopyCaller® Software to determine the copy number using the comparative CT (ΔΔCT) method. The HapMap DNA sample, NA18558 (Coriell Institute), was used as the calibrator sample, with a known copy number value of 2 for both Exon 9 and Intron 2 assays. Copy number results were then exported to tab-delimited (.txt) files to be used in the AlleleTyper™ Software.
The results of the genotype calls and the copy number variations were incorporated into AlleleTyper™ Software v1.0.7-I0B01 to determine the haplotypes of the samples. The star-allele calls were performed based on the pre-set translation tables.
Phenotype translation
The genotyping data were used to assign PGx phenotypes based on current understanding of the roles of these genes in drug metabolism and the functional consequences of the identified sequence alterations. Star allele assignments and genotype to phenotype correlation were adapted from information available at the human Cytochrome P450 Allele Nomenclature Committee website (http://www.cypalleles.ki.se). The phenotype algorithms were derived from the Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines at Pharmacogenomics Knowledgebase (PharmGKB) website (https://www.pharmgkb.org). The method used to predict drug metabolizer phenotype for CYP2D6 included intermediate phenotype categories (EM to UM, IM to EM and PM to IM) according to a recent paper and was summarized in S1 Fig. [23].
Alternative molecular tests for validation
Ten HapMap samples were tested on an alternative platform to verify our genotype calls and copy number variation results. Results of the 28 SNPs or INDEL assays and CYP2D6 intron 2 copy number assay in our panel were compared with the results interrogated by iPLEX® PGx 68 Panel (Agena Bioscience) using MALDI-TOF mass spectrometry. Multiplex PCR was performed followed by dephosphorylation with alkaline phosphatase and primer extension reactions. The products were spotted onto MassArray SpectroCHIP and analysed using the MassARRAY® system. The concordance of our CYP2D6 exon 9 copy number assay results were validated by running the 10 HapMap samples on QX200™ Droplet Digital™ PCR (ddPCR) System (Bio-Rad Laboratories Inc, P/N: 1864001). In this system, PCR reaction occurs independently in individual droplets, which are subjected to fluorescence reading after amplification. The same Taqman probe was used according to published protocol [24].
Statistical analysis
The chi-squared test with one degree of freedom was used to test the departure from Hardy-Weinberg equilibrium (HWE) for each variant allele in different ethnic group. All the genotypes were in Hardy-Weinberg Equilibrium (HWE). Wright’s fixation index (Fst) was calculated to assess the variance in SNPs across the three ethnicities (Malay, Indian, and Chinese) in the Singapore population. Fst values range from 0 to 1; values less than 0.05 indicate little differentiation and those greater than 0.15 show substantial differentiation.
Results
Assay verification
The major genetic polymorphisms of CYPP450s drug metabolism are caused by variations in CYP2D6, CYP2C9, CYP2C19 and CYP3A5 genes. A customized panel that allows for detection of 32 gene variations from a single run on 384-well plate format was evaluated for clinical use (Table 1). Key variants of CYP2C9, CYP2C19, CYP2D6, CYP3A5 and VKORC1 were interrogated by TaqMan assays. These 32 variants were identified from literature, CYP allele website and selected based on the curated pharmacogenetics data and PharmGKB. Their clinical evidence and prevalence in Asians are the basis of selection. DNA samples from 10 Coriell Cell Repository with known genotypes in rs1057910, rs28399504, rs776746 and rs9923231 were used to assess the performance of the genotyping assays. The assays performed well with 31 assays having unambiguous genotypes, yielding 96.8% call rate. Only CYP2C9*6 required manual calling due to high background of the VIC-dye labelled Taqman probe (data not shown). The haplotypes of the Coriell samples were shown in Table 2. As most of the alleles examined in this study were absent in these samples, an alternative test method based on MALDI-TOF mass spectrometry was included for validation. The PGx68 panel (Agena Biosciences) was used to analyse 28 alleles in our current study. The 10 Coriell samples were run in duplicates and the results were in concordance with the known genotypes and between the 2 platforms (S2 Fig). There were 4 alleles that were interrogated by only one assay and have not been confirmed by a separate method. These included rs28399507 and rs6413438 of CYP2C19 and rs1080985 and rs769258 of CYP2D6. We compared their allele frequencies with those in ExAC database and published literatures. The similar allelic frequencies suggested that our assays for these variants were valid.
The genotypes for CYP2D6 was determined with CNVs using 2 TaqMan assays targeting exon 9 and intron 2 [25]. As shown in Table 2, the use of two different assays enabled the differentiation of *36 from *10. The accuracy of exon 9 and intron 2 CNV assays were evaluated by alternate platforms using mass array and ddPCR, respectively. There was good concordance between our assays and the alternative assays (S3 Fig).
Allele frequencies
The assays were applied to samples from 506 healthy Singapore individuals. The individual allele frequencies for the 5 genes were summarized in Table 3. The frequencies of the various alleles were highly similar between the Chinese and Malay ethnic groups. A greater differentiation was observed between the Indian and Chinese/Malay populations. Overall, the allelic frequencies were similar to those reported in the ExAC database (East Asian—Chinese and Malay; South Asian—Indian). Five different alleles of CYP2C9 were examined and the frequencies of the defective alleles *2 and *3 found in our study were comparable with published data [26]. The *3 allele was more common in our population whereas *2 allele is only observed in the Indians with a frequency of 0.042. The other deficient alleles for CYP2C9 (*4, *5 and *6) were not observed in the study population.
For CYP2C19, *2 allele was the most common allele in our population, followed by *3 and *17 alleles [27,28]. The *3 allele frequency was higher in Chinese (0.037) and Malay (0.028) subjects, compared to the Indian subjects (0.011). By contrast, the *17 allele was more prevalent among the Indians subjects (0.151), compared to the Chinese (0.01) and Malay (0.024) subjects. The *6 allele was rare and the other deficient alleles for CYP2C19 (*4, *5, *7, *8, *9 and *10) were not observed in the study population.
The polymorphisms in CYP2D6 *2 (rs16947, rs1135840), *2A (rs1080985), *10 (rs1065852) and *41 (rs28371725) are common in our population [29]. The Chinese and Malay subjects exhibited approximately five-fold higher allele frequencies of *10 (rs1065852) compared with the Indian subjects. Similarly, the *2 (rs1135840) allele frequencies was approximately 2-fold higher in Chinese and Malay subjects than the Indians subjects. By contrast, the variant frequencies of *2 (rs16947), *2A (rs1080985), *4 (rs3892097) and *41 (rs28371725) were higher in the Indian subjects compared with the Chinese and Malay subjects. The *7 (rs5030867), *9 (rs5030656) and *35 (rs769258) alleles were rare and only observed in the Indian subjects. The *14 (rs5030865) allele was also rare and only observed in the Chinese subjects. The other deficient alleles, *3 (rs35742686), *6 (rs72552267), *8 (rs5030865), *17 (rs28371706) and *29 (rs59421388) were not detected in this study.
In line with previous findings, CYP3A5*3 is prevalent in our population with allele frequencies ranging from 0.587 to 0.734 [26]. VKORC1*2 differed by approximately 5 folds within our population. Notable difference was observed for rs9923231 with Fst 0.382. It was more common in the Chinese and Malay subjects than the Indian subjects.
Diplotypes frequencies and phenotype consequences
Table 4 shows the distribution of diplotypes among Chinese, Malay and Indian subjects. Phenotypes were inferred as described in S1 Fig and the frequencies of the various combinations of phenotype classes are depicted in Fig 1. CYP2C9*2 and *3 alleles are present in our population and both conferred reduced activity. The *3 allele is known to be prevalent in Asians and accounts for approximately 11.8% (60/506) of IM and 1% (5/506) of PM in our population. We noted a higher proportion of IM and PM among the Indian subjects, followed by the Malay subjects and the Chinese subjects (Fig 1A).
(A) CYP2C9 (B) CYP2C19 and (C) CYP2D6.
Among the CYP2C19 variants, *2 and *3 alleles are prevalent in our population. Both confer loss of function such that *1/2 and *1/3 heterozygous are assigned as IMs, and combinations of *2 and *3 alleles as PMs (Table 4). Due to the high frequency of *2 and *3 alleles in our population, there was subsequently a high proportion of IMs (about 45%). Fig 1B showed a higher proportion of PMs among the Indian and Chinese subjects (16%) compared to the Malay subjects (9%). In contrast, UMs were only prevalent among the Indian subjects (17%) and were less frequent among the Chinese (1%) and Malay (4%) subjects.
Several diplotypes observed in CYP2D6 (Table 4) were represented by 10 different alleles. Some alleles could not be unambiguously detected because their SNP combination did not match any known CYP2D6 alleles. The common alleles included *10, *36 and *41 alleles with reduced function that accounted for the IMs and PMs observed in our population. The gene allele quantification of CYP2D6 had to be determined simultaneously with its genotype in order to assign the correct phenotype. Some alleles (*1, *2 and *2A) were duplicated and accounted for the UMs in our study subjects. The frequencies of individuals with more than 2 copies ranged from 2.8% to 37%, based on the assays targeting exon 9 and intron 2, respectively (Table 5). The two copy number assays were concordant in only 62% of the 506 samples tested. This was not unanticipated as exon 9 assay did not detect CYP2D6*36 allele which was common among Asians while intron 2 assay detected all alleles. The use of these two assays targeting different regions of CYP2D6 helped to distinguish *10 and *36 alleles. The CYP2D6*36 allele is a gene conversion from CYP2D6 to CYP2D7 in exon 9. Detection of this allele was problematic and most commercial assays are not designed to detect *36, which is often misinterpreted as *10. The distinction of these 2 alleles is important as *36 is a non-functional allele whereas *10 is a decreased functional allele. This will have an impact on the risk of treatment failure or toxicity of drugs metabolized by CYP2D6. The observed diplotypes were classified into 6 phenotypes as depicted in Fig 1C. The diplotype frequencies predicting PM were the highest in the Indian subjects, followed by the Malay subjects and were absent in the Chinese subjects. Conversely, diplotypes predicting UM were highest in the Chinese, followed by the Indian and Malay subjects.
CYP3A5 and CYP3A4 have overlapping substrates specificity. We only included CYP3A5 in our panel as no functional variant forms of the CYP3A4 gene has been observed in Asians and Caucasian. A substantial proportion of CYP3A5 diplotypes in our population were *1/*3 and *3/*3 with intermediate and low activities, respectively (Table 4).
Clinically relevant variants
We determined the expected rates of actionable PGx variants in each CYP450 gene examined in our population. The proportions of individuals carrying an actionable variant were 14.2%, 16%, 67.8% and 84.4% in CYP3A5, CYP2C9, CYP2C19 and CYP2D6, respectively. Considering all four CYP450 genes together, 98% of the subjects carried an actionable PGx variant in at least one gene. We next determined the proportion of individuals carrying actionable genotypes for four drugs with evidence level 1A in CPIC (Fig 2 and Table 5). We noted a high proportion of individuals (approximately 50%) carrying actionable genotypes for warfarin and tacrolimus. It was noted that the CYP3A5*1 genotype codes for functional CYP3A5 enzyme but standard dosing recommendations for tacrolimus are based on individuals with the CYP3A5*3 (non-functional) genotype. Approximately 25% and 35% of individuals carried actionable genotypes for codeine and clopidogrel, respectively.
The definition of actionable diplotypes is defined as follows: (i) warfarin, CYP2C9 *2 or *3 heterozygote or homozygote with VKORC1 GA or AA genotype and CYP2C9*1 with VKORC1 AA genotype; (ii) clopidogrel, CYP2C19*2, *3 and *6; (iii) codeine, CYP2D6 poor and intermediate metabolizers; (iv) tacrolimus, CYP3A5*1 heterozygote or homozygote.
Discussion
In this study, we developed an appropriate panel relevant to the prescription patterns and genotype prevalence in this country. Several factors, including cost, ease of workflow, turnaround time and the flexibility of the assay were considered in when choosing the genotyping approach. We built the panel utilizing the Life technologies TaqMan assays for both genotyping and copy number analyses. The panel in a 384-well format can detect 32 genetic variants in CYP450 genes simultaneously and CYP2D6 copy number assays were performed separately in the same platform. Data analysis tools were provided by Life technologies to facilitate the translation of individual’s genotypes into star allele haplotypes. To access the quality of the panel, we measured concordance of genotypes determined by independent platforms. The results showed a high call rate (96.8%) with 1 out of 32 SNPs requiring manual calling (CYP2C9*6) and 100% concordance for 28 SNPs with known genotypes or verified on alternative platform. To test the workflow for clinical use, we attempted to predict the phenotypes from the genotype data using guidelines from CPIC which provides information on allele frequencies and instructions to translate diplotypes into predicted phenotypes.
There is considerable diversity in the frequency of PGx variants that contribute to inter-population differences in drug response. Hence, 506 subjects from three distinct Asian ethnic groups in our population were analysed on our panel. Most of the data generated in this study corroborated data previously reported for the 3 major ethnic groups in our population. For example, CYP2C19*3, which is virtually absent in Caucasians, is common among East Asians [27]. Similarly, our subjects showed high prevalence of CYP2C19*2 and *3 loss of function alleles, implying that a large proportion of individuals in our population have poor response to clopidogrel; hence testing for CYP2C19 variants in our population may be useful. Clopidogrel has been identified as a high-priority drug for clinical implementation of PGx testing [30]. Individuals with reduced function phenotypes have reduced conversion of clopidogrel to its active metabolite and an increased risk for stent thrombosis after percutaneous coronary interventions. Pharmacogenomic implementation guidelines recommend that carriers of the CYP2C19 loss-of-function alleles *2 and *3 receive an alternative antiplatelet drug such as prasugrel or ticagrelor (Table 6).
There was an overall high similarity in the allele frequencies among the Chinese and Malay populations. The Indian subjects exhibited greater genetic differences in specific variants of CYP2C9, CYP2C19, CYP2D6 and VKORC1 genes from the Chinese/Malay populations. One of the potential useful findings concerns the CYP2C9 and VKORC1 genes. We examined the genotype combinations of CYP2C9 and VKORC1 variants and noted that about 68.2% of Indians harboured the VKORC1 *1/*1 (GG) diplotype, implying that a substantial proportion of Indians require a higher starting dose of warfarin (Table 6) [10].
To our knowledge, this is the most comprehensive study of variation at the CYP2D6 locus in the Singapore population. A total of 17 alleles and duplication/multiplication were examined. CYP2D6*5 and *10 were previously shown to be prevalent in our population [29]. Our results are generally consistent with previous reports in that CYP2D6*2, *2A, *10 and *36 are found to be common and *5 and *41 to be relatively common in East Asians. We noted that CYP2D6*10 was mostly represented by *36 which are common in Asians. In this study, we tried to provide an exact copy number of functional CYP2D6 genes as accurate determination of the functional gene dosage is essential for detailed pharmacogenetic analysis of CYP2D6. The use of two assays targeting different regions of CYP2D6 serves to distinguish between *10 and *36 alleles [25]. In our population, EM was the most common phenotype for CYP2D6 followed by the IM. The prevalence of PM ranged from 0.7% to 3.4% and this phenotype was not observed in the Chinese subjects. We noted the highest proportion of UMs among the Chinese subjects (11%) followed by the Indian (5%) and Malay subjects (4.8%). Both PMs and UMs have an altered capacity to metabolize CYP2D6 substrates and could potentially benefit from genotyping. The typical substrates for CYP2D6 include codeine, some anti-depressants and antipsychotics. We predicted the response to codeine based on our results using CPIC guidelines [31]. Individuals who are UMs are at increased risk for toxicity due to increased formation of morphine following codeine administration (Table 6). By contrast, those carrying no functional alleles are at increased risk of insufficient pain relief due to lack of efficacy.
In conclusion, we described the potential use of a PGx panel in clinical testing. 506 subjects from our population were analysed on the panel and the knowledge of allele distribution and frequency is required to effectively translate pharmacogenetics to the clinics. Our study also showed that the vast majority of individuals (98%) have at least one actionable genotype even among the small range of drug gene rules. These findings have implications for warfarin, clopidogrel, codeine and anti-psychotics pharmacogenomics and provide impetus to incorporate PGx genotyping in our population.
Supporting Information
S1 Fig. Prediction of drug metabolizer phenotype.
https://doi.org/10.1371/journal.pone.0169233.s001
(DOCX)
S2 Fig. Concordance between Taqman SNP genotyping assays and iPLEX PGx 68 Panel.
https://doi.org/10.1371/journal.pone.0169233.s002
(DOCX)
S3 Fig. Quantitation of CYP2D6 gene copy numbers in 10 HapMap samples.
(A) Quantitative real-time PCR results in CopyCaller software (in quadruplicates) with intron 2 and exon 9 assays in green and blue, respectively; (B) mass spectrometry analysis of CN based on intron 2 (in singleplex) and (C) absolute quantitaion based on exon 9 using ddPCR (in duplicates).
https://doi.org/10.1371/journal.pone.0169233.s003
(TIF)
Acknowledgments
This work is supported by the research fund from the Singapore National Medical Research Council (NMRC/CG/017/2013) and the authors appreciate the team for recruiting the healthy control samples for this study.
Author Contributions
- Conceptualization: LLG.
- Data curation: CWL.
- Formal analysis: LLG CWL.
- Funding acquisition: KPL.
- Investigation: WCS CWL LXT.
- Methodology: WCS LXT.
- Writing – original draft: LLG.
- Writing – review & editing: LLG KPL.
References
- 1. Weinshilboum RM, Wang L (2006) Pharmacogenetics and pharmacogenomics: development, science, and translation. Annu Rev Genomics Hum Genet 7: 223–245. pmid:16948615
- 2. Wang L, McLeod HL, Weinshilboum RM (2011) Genomics and drug response. N Engl J Med 364: 1144–1153. pmid:21428770
- 3. Green ED, Guyer MS, National Human Genome Research I (2011) Charting a course for genomic medicine from base pairs to bedside. Nature 470: 204–213. pmid:21307933
- 4. Sim SC, Kacevska M, Ingelman-Sundberg M (2013) Pharmacogenomics of drug-metabolizing enzymes: a recent update on clinical implications and endogenous effects. Pharmacogenomics J 13: 1–11. pmid:23089672
- 5. Wu AC, Fuhlbrigge AL (2008) Economic evaluation of pharmacogenetic tests. Clin Pharmacol Ther 84: 272–274. pmid:18580869
- 6. Relling MV, Evans WE (2015) Pharmacogenomics in the clinic. Nature 526: 343–350. pmid:26469045
- 7. Furge LL, Guengerich FP (2006) Cytochrome P450 enzymes in drug metabolism and chemical toxicology: An introduction. Biochem Mol Biol Educ 34: 66–74. pmid:21638641
- 8. van der Weide J, Steijns LS (1999) Cytochrome P450 enzyme system: genetic polymorphisms and impact on clinical pharmacology. Ann Clin Biochem 36 (Pt 6): 722–729.
- 9. Wadelius M, Pirmohamed M (2007) Pharmacogenetics of warfarin: current status and future challenges. Pharmacogenomics J 7: 99–111. pmid:16983400
- 10. Johnson JA, Gong L, Whirl-Carrillo M, Gage BF, Scott SA, Stein CM, et al. (2011) Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C9 and VKORC1 genotypes and warfarin dosing. Clin Pharmacol Ther 90: 625–629. pmid:21900891
- 11. Gurbel PA, Bliden KP, Antonino MJ, Stephens G, Gretler DD, Jurek MM, et al. (2010) The effect of elinogrel on high platelet reactivity during dual antiplatelet therapy and the relation to CYP2C19*2 genotype: first experience in patients. J Thromb Haemost 8: 43–53. pmid:19817997
- 12. Furuta T, Shirai N, Sugimoto M, Nakamura A, Hishida A, Ishizaki T (2005) Influence of CYP2C19 pharmacogenetic polymorphism on proton pump inhibitor-based therapies. Drug Metab Pharmacokinet 20: 153–167. pmid:15988117
- 13. Thorn CF, Whirl-Carrillo M, Leeder JS, Klein TE, Altman RB (2012) PharmGKB summary: phenytoin pathway. Pharmacogenet Genomics 22: 466–470. pmid:22569204
- 14. Birdwell KA, Decker B, Barbarino JM, Peterson JF, Stein CM, Sadee W, et al. (2015) Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for CYP3A5 Genotype and Tacrolimus Dosing. Clin Pharmacol Ther 98: 19–24. pmid:25801146
- 15. Lamba JK, Lin YS, Schuetz EG, Thummel KE (2002) Genetic contribution to variable human CYP3A-mediated metabolism. Adv Drug Deliv Rev 54: 1271–1294. pmid:12406645
- 16. Ingelman-Sundberg M (2004) Pharmacogenetics of cytochrome P450 and its applications in drug therapy: the past, present and future. Trends Pharmacol Sci 25: 193–200. pmid:15063083
- 17. Crews KR, Caudle KE, Dunnenberger HM, Sadhasivam S, Skaar TC (2015) Considerations for the Utility of the CPIC Guideline for CYP2D6 Genotype and Codeine Therapy. Clin Chem 61: 775–776. pmid:25770140
- 18. Hicks JK, Bishop JR, Sangkuhl K, Muller DJ, Ji Y, Leckband SG, et al. (2015) Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2D6 and CYP2C19 Genotypes and Dosing of Selective Serotonin Reuptake Inhibitors. Clin Pharmacol Ther 98: 127–134. pmid:25974703
- 19. Zhou SF (2009) Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I. Clin Pharmacokinet 48: 689–723. pmid:19817501
- 20. Kimura S, Umeno M, Skoda RC, Meyer UA, Gonzalez FJ (1989) The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene. Am J Hum Genet 45: 889–904. pmid:2574001
- 21. Sim SC, Ingelman-Sundberg M (2013) Update on allele nomenclature for human cytochromes P450 and the Human Cytochrome P450 Allele (CYP-allele) Nomenclature Database. Methods Mol Biol 987: 251–259. pmid:23475683
- 22. Sistonen J, Fuselli S, Levo A, Sajantila A (2005) CYP2D6 genotyping by a multiplex primer extension reaction. Clin Chem 51: 1291–1295. pmid:15905314
- 23. Ji Y, Skierka JM, Blommel JH, Moore BE, VanCuyk DL, Bruflat JK, et al. (2016) Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade. J Mol Diagn 18: 438–445. pmid:26947514
- 24. Hindson BJ, Ness KD, Masquelier DA, Belgrader P, Heredia NJ, Makarewicz AJ, et al. (2011) High-throughput droplet digital PCR system for absolute quantitation of DNA copy number. Anal Chem 83: 8604–8610. pmid:22035192
- 25. Ramamoorthy A, Flockhart DA, Hosono N, Kubo M, Nakamura Y, Skaar TC (2010) Differential quantification of CYP2D6 gene copy number by four different quantitative real-time PCR assays. Pharmacogenet Genomics 20: 451–454. pmid:20421845
- 26. Brunham LR, Chan SL, Li R, Aminkeng F, Liu X, Saw WY, et al. (2014) Pharmacogenomic diversity in Singaporean populations and Europeans. Pharmacogenomics J 14: 555–563. pmid:24861855
- 27. Chan MY, Tan K, Tan HC, Huan PT, Li B, Phua QH, et al. (2012) CYP2C19 and PON1 polymorphisms regulating clopidogrel bioactivation in Chinese, Malay and Indian subjects. Pharmacogenomics 13: 533–542. pmid:22462746
- 28. Tan DS, Yeo AH, Ho HK, Wee HL, Ong HY (2014) Asian study of clopidogrel (ASCLOP) responsiveness: the contributions of genetic and non-genetic factors. Int J Cardiol 171: e21–23. pmid:24377711
- 29. Lim JS, Chen XA, Singh O, Yap YS, Ng RC, Wong NS, et al. (2011) Impact of CYP2D6, CYP3A5, CYP2C9 and CYP2C19 polymorphisms on tamoxifen pharmacokinetics in Asian breast cancer patients. Br J Clin Pharmacol 71: 737–750. pmid:21480951
- 30. Scott SA, Sangkuhl K, Stein CM, Hulot JS, Mega JL, Roden DM, et al. (2013) Clinical Pharmacogenetics Implementation Consortium guidelines for CYP2C19 genotype and clopidogrel therapy: 2013 update. Clin Pharmacol Ther 94: 317–323. pmid:23698643
- 31. Crews KR, Gaedigk A, Dunnenberger HM, Klein TE, Shen DD, Callaghan JT, et al. (2012) Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for codeine therapy in the context of cytochrome P450 2D6 (CYP2D6) genotype. Clin Pharmacol Ther 91: 321–326. pmid:22205192