1 Introduction
Oral direct thrombin inhibitor (DTI), a new type of direct oral anticoagulants (DOACs), has been increasingly used in recent years for the prevention of stroke and systemic embolism in cases of non-valvular atrial fibrillation (NVAF) and are currently recommended as the first line of medication-based treatment for this condition, according to American CHEST Guidelines (Lip et al., 2018). Dabigatran, which is converted by liver esterase carboxylesterase 1 (CES1) from the oral prodrug dabigatran etexilate, is the sole reversible and active DTI (Stangier and Clemens, 2009). It was first approved by the United States (US) Food and Drug Administration (FDA) in 2010 for stroke prevention in patients with NVAF, and subsequently launched in China in 2013 (Li et al., 2020). With the advantages of rapid absorption, high bioavailability, fixed-dose regimens, requiring no coagulation monitoring, and having no food and few drug interactions, dabigatran is becoming more widely used in clinical application (Kanuri and Kreutz, 2019; Wieland and Shipkova, 2019).
Although the above characteristics of dabigatran are either equivalent or superior to Vitamin k Antagonists (Connolly et al., 2009), more attention should be given to its relative high risk for bleeding. In the US, dabigatran was the 10th most implicated drug for adverse drug events in emergency department visits among older adults in 2013–2014 (Shehab et al., 2016). However, the risk that dabigatran poses for bleeding may depend on inter-individual (as opposed to intra-individual) and ethnic variations. Extensive clinical experiences and studies have already demonstrated that inter-individual variations regarding pharmacokinetics (PK) and pharmacodynamics (PD) do exist. For example, Stangier et al. (2007) reported that the inter-individual coefficient of variation (CV) in PK parameters of dabigatran was approximately 30%, and that the CV in PD parameters was <10%. Besides, Chan et al. (2015) demonstrated that inter-patient variability in dabigatran level (geometric CV: 51–64%) was greater than intra-patient variability (geometric CV: 32–40%). Many factors, including renal function, age, weight, sex, and food consumption, may influence the PK parameters of dabigatran (Reilly et al., 2014). Yet these factors alone do not fully explain inter-individual variation, whether in the case of healthy volunteers or enrolled patients (Fawzy and Lip, 2019; Wieland and Shipkova, 2019).
The Framingham heart study (O'Donnell et al., 2001) would suggest that genetic factors play a major role in determining coagulation function. Dabigatran etexilate is a substrate of p-glycoprotein (P-gp), which is encoded by the ABCB1 gene and generally not metabolized by cytochrome oxidase P450 (CYP450), except at supra-therapeutic concentrations (Raymond et al., 2021). Besides activation by the CES1 enzyme as previously mentioned, dabigatran is also metabolized to four active metabolites by UDP-glucuronyltransferase (UGT) isoforms 1A9, 2B7, and 2B15 (<10%) (Raymond et al., 2021). So far, there have indeed been several previous pharmacogenomics studies of dabigatran that explore the effects of genetic variation on its PK/PD parameters and clinical outcomes (Supplementary 1, Supplementary Table S1). However, these studies were mainly focused on genetic polymorphisms of ABCB1 (rs1045642, rs1128503, rs2032582, and rs4148738) and CES1 (rs2244613, rs8192935, and rs7164787). Only two studies (Lähteenmäki et al., 2021; Liu et al., 2021) have explored the influences of other genes, such as CYP2D6, CYP3A5, SLC22A1, and so on. Furthermore, the results of previous studies have not been totally consistent (Ašić et al., 2018; Cullell et al., 2018; Xie et al., 2018; Kanuri and Kreutz, 2019; Raymond et al., 2021; Shnayder et al., 2021). Most analytical methods involved a candidate gene approach, and only one study applied genome-wide association (GWA) analysis (Paré et al., 2013). As stated in the GWA study (GWAS), the frequency of the C allele in CES1 rs2244613 varied from 15% in Europeans to 60% in Asians according to data from the 1000 Genomes Project (accessed July 2012), which has been verified in a recent Asian study (Ji et al., 2021). Finally, of all previous studies, only three have investigated Asian populations (Chinese and Japanese) (Tomita et al., 2016; Ji et al., 2021; Liu et al., 2021), where only one analyzed PD parameters (Ji et al., 2021) and none performed GWA.
With this information in mind, the current fixed doses of dabigatran may not be applicable to all real-world subjects. Additionally, data on genetic polymorphisms in Chinese populations is insufficient, and their potential roles in influencing PK/PD and clinical outcomes of dabigatran application remain unclear. Our study carried out whole-exome sequencing and genome-wide association analyses in healthy Chinese subjects, thus aiming to explore the potential metabolic pathways of dabigatran. Through studying the associations between various biomarkers and PK/PD outcomes in a separate cohort of healthy volunteers, we attempted to discover novel genetic marks and their respective values of influence on individual anticoagulation therapy with dabigatran.
Materials and Methods
Study Design
This genome-wide association study was based on a bioequivalence (BE) trial conducted in China, which was mainly performed to assess the BE of domestic generic dabigatran etexilate capsules, with reference to the original product (brand name: Pradaxa®), in healthy subjects under fasting and fed conditions (Li et al., 2020). Enrolled subjects with unknown genotypes were required to be 18–65 years old, have a BMI ranging from 19 to 26 kg/m2, and meet all other inclusion and exclusion criteria following screening visits. This BE trial followed an open-label, single-center, randomized, single-dose, four-period crossover design. Eligible healthy participants were randomly divided into either a test-reference-test-reference sequence group or a reference-test-reference-test sequence group. Subjects received a single dose of dabigatran etexilate capsule (150 mg) with 240 ml of warm water after either being fed a standard high-fat meal (Li et al., 2020) within 30 min or fasting overnight for at least 10 h. Then, they were discharged 48 h after drug administration. Based on the BE trial, we added genotype and PD parameter tests that were conducted during any one of the two reference periods. Additionally, PK parameters used for subsequent matching analysis were also obtained during this time.
This protocol was approved by an independent ethics committee and the Institutional Review Board of Peking University First Hospital (Protocol Code: 2016[1236]; date of approval: 11 October 2017) and the Third Hospital of Changsha (Protocol Code: 2018-KL-012; date of approval: 5 July 2018). The ClinicalTrial.org registration number was NCT03161496. This study was conducted in accordance with both the Good Clinical Practice guidelines and the Declaration of Helsinki. Prior to the beginning of the study, all involved subjects were briefed on the purpose, duration, and potential risks of the study and provided written informed consent.
Sample Collection
Serial blood samples used for PK parameter analysis were collected from the BE trial. Venous blood samples (4 ml) were collected before dosing and then at 17–18 time points after drug administration (Li et al., 2020). We also collected 2 ml blood samples for genotyping before dosing, and 2.7 ml blood samples for PD parameter tests at 0 and 2 h after administration.
For PK analysis, blood samples were collected in EDTA-K2 tubes and centrifuged for 10 min at 4°C and 1700 g within 1 hour of sampling. Plasma samples were transferred to cryovials and stored at −80°C until PK analysis. For PD analysis, blood samples were collected in sodium citrate (3.2% v/v) tubes and centrifuged for 15 min at room temperature and 2500 g within 1 hour of sampling. Plasma samples were transferred to cryovials that were stored at −80°C, and were subjected to PD analysis within 6 months of sampling. For genetic polymorphism testing, blood samples were collected in EDTA-K2 tubes, transferred to cryovials, and stored at below −60°C until genotype testing.
Pharmacokinetic Evaluations
Plasma concentrations of total and free (nonconjugated) dabigatran from BE trial center samples were determined by a home-validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, which has been previously published (Li et al., 2020). PK parameters for total and free dabigatran were determined by standard noncompartmental methods using a WinNonlin 7.0 (Pharsight Corporation, California, United States). Maximum concentration (Cmax) and the time to Cmax (Tmax) were recorded from the observed data. Values for the terminal half-life (t1/2) and area under the curve (AUC) for plasma concentration at time zero versus the last measurable time point (AUC0-t) were calculated. AUC0-t(total), Cmax(total), Tmax(total), and t1/2(total) reflected the PK parameters of total dabigatran, while AUC0-t(free), Cmax(free), Tmax(free), and t1/2(free) represented that of free dabigatran. No significant matrix effect was observed. All samples were analyzed within their established storage stability periods.
Pharmacodynamic Evaluations
The prothrombin time (PT), activated partial thromboplastin time (APTT), and levels of anti-FIIa activity were assessed using the Sysmex® CS-2100i fully automated multiparameter hemostasis analyzer (Sysmex, Kobe, Japan) at Peking University First Hospital. PT and APTT were measured by validated Coagulation Method Assay Kits (Thromborel-S® and Actin®, Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany). During the 2018 International Council for Standardization in Hematology (ICSH) (Gosselin et al., 2018), anti-FIIa activity was recommended as a marker for the qualitative assessment of dabigatran–furthermore, the correlation between anti-FIIA activity and drug concentration (p < 0.001) was demonstrated in our previous study of Chinese patients (Liu et al., 2020). Anti-FIIa activity was measured using a validated Chromogenic Method Anti-FIIa Kit (HEMOCLOT Thrombin Inhibitors®, HYPHEN BioMed, Neuville sur Oise, France). Specific calibrators and controls were used for dabigatran (BIOPHEN dabigatran® Calibrator and Control, HYPHEN BioMed, Neuville sur Oise, France). The results of the anti-FIIa assay were reported in dabigatran units (with limits of detection for dabigatran of 0–550 ng/ml). The two QC sample concentrations used were 24 and 399 ng/ml. The inter- and intra-day precision (RSD%) were measured as < 6.76% and 7.53%, whereas inter- and intra-day accuracy were determined to be 97.71% and 86.69%. Relative changes in PT and APTT were also used for PD assessments, which involved taking the ratio after administration to before administration (i.e., ∆PT2h = PT2h/PT0h).
Whole-Exome Sequencing
For DNA preparation, the quality of isolated genomic DNA was assessed by using the following three methods in combination: 1) DNA degradation and contamination were monitored on 0.8% agarose gels; 2) DNA purity was checked using the NanoPhotometer® Spectrophotometer (IMPLEN, CA, United States); 3) DNA concentration was measured using a Qubit® DNA Assay Kit in a Qubit® 3.0 Flurometer (Invitrogen, United States).
For library preparation and sequencing, the whole exome library was prepared using the Agilent SureSelectXT Human All Exon V6 Kit (Agilent Technologies Inc., United States) according to the manufacturer’s standard protocol. Briefly, qualified genomic DNA was fragmented to an average size of 200bp. The ends of the DNA fragments were subjected to end repair processes, followed by A-tailing and adapter ligation. DNA fragments with adapters ligated on both ends were selectively enriched by polymerase chain reaction (PCR). After PCR, library hybridization and exome capture were performed using biotin labeled probes and magnetic bead selection. Captured libraries were enriched and tagged by PCR to prepare for sequencing. The final libraries were quantified using a KAPA Library Quantification Kit (KAPA Biosystems, South Africa) and an Agilent 2100 Bioanalyzer. Paired-end sequencing (2 × 150 bp) was performed on an Illumina NovaSeq 6000 sequencer (Illumina, United States).
Variant filtering and prediction were performed on 347,010 single-nucleotide polymorphisms (SNPs) detected in exons, with 200 bp extensions on either end. SNPs were retained for association analysis when the missing rate was <10%, minor allele frequency was >5%, and Hardy-Weinberg equilibrium p-value was >10–6. Based on the high-quality data obtained after quality control, PCA conducted in PLINK 1.09 was used for stratified population assessment to remove outlier samples. Finally, 75,348 SNPs were tested for association with PK and PD parameters of dabigatran.
Statistical Analysis
Genome-wide analyses of PK and PD parameters pertaining to dabigatran were performed by linear regression, assuming an additive genetic model, in PLINK 1.09. To account for possible population stratification, all analyses were adjusted for the first four genetic principal components. Covariates of PK and PD indexes were also further adjusted for age, sex, food, and high-density lipoprotein (HDL) to correct for residual population stratification (the effect of sex and food on metabolism is shown in Supplementary 1, Supplementary Table S2). These variables were chosen because they were associated with PK and PD parameters of dabigatran in univariate analyses. Analyses of non-imputed data were performed using the Gen ABEL package in R, whereas imputed data were analyzed using the Prob ABEL package. According to our original plan, the genome-wide p-value significance threshold was set at the Bonferroni limit of 6.6 × 10–7 in the discovery phase–SNPs reaching this threshold were taken forward for replication. The significance level for successful replication was set at p = 0.05/75,348 of SNPs for which replication was attempted. Following the genome-wide analyses of the merged and imputed discovery and replication phase data, follow-up analyses were performed by adding each top hit SNP as an additional covariate in GWA. This procedure was performed in a sequential manner until no significant genome-wide signals remained. Regional plots were generated with LocusZoom (Pruim et al., 2010) and all other figures were created in R. Continuous variables are presented as mean ± standard deviation (SD), and two-sided p-values < 0.05 were considered statistically significant.
Candidate Gene Association Analysis
To extensively investigate the influences of previously reported candidate genes on PK and PD parameters of dabigatran in our study population, we also identified related genes and made detailed analyses of these genes. According to previous pharmacogenomic studies (Supplementary 1, Supplementary Table S1) and reviews (Raymond et al., 2021; Shnayder et al., 2021), the following 22 genes were selected: ABCB1, ABCC2, ABCG2, CES1, CES1P2, CYP1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2J2, CYP2D6, CYP3A4, CYP3A5, CYP4F2, SLCO1B1, SLC22A1, UGT1A1, UGT1A9, UGT2B7, and UGT2B15. According to the number of independent variables and whether the data were normally distributed, we used the Student’s t-test or one-way analysis of variance (ANOVA) and the Mann-Whitney or nonparametric Kruskal–Wallis H test to analyze the data. Age, sex, food, and HDL were adjusted for by multivariate linear regression. Two-sided p-values < 0.05 were considered statistically significant.
Discussion
To the best of our knowledge, this was the first genome-wide association study to investigate genetic variations associated with pharmacokinetic and pharmacodynamic characteristics of dabigatran metabolism among healthy Chinese individuals. We performed whole-exome sequencing and candidate gene analysis to extensively explore and verify both novel and reported SNPs that may impact PK/PD parameters. First, we identified three suggestive SNPs (SLC4A4 rs138389345, FRAS1 rs6835769, and SULT1A1 rs9282862) that were associated with the metabolism of dabigatran. AUC0–t(total), AUC0–t(free), Cmax(total), Cmax(free), and IIa2h values in the minor alleles of SLC4A4 rs138389345 and SULT1A1 rs9282862 were significantly lower compared to in their wild type counterparts. Conversely, these values were significantly higher in FRAS1 SNP rs6835769. Additionally, SLC4A4 rs138389345 and SULT1A1 rs9282862 were found to have significant influences on APTT and PT, respectively. Moreover, through correlation analyses of reported candidate genes, we found inconsistencies in the results for three previously reported SNPs (ABCC2 rs2273697, SLCO1B1 rs4149056, and ABCB1 rs1045642) regarding their associations with AUC0–t, Cmax, and PD indexes. Furthermore, we identified 30 new potential SNPs of 13 reported candidate genes in our study. ABCB1, ABCC2, ABCG2, CYP2B6, CYP1A2, CES1, SLCO1B1, UGT1A1, UGT1A9, and UGT2B7 might influence PK parameters, while ABCG2, CYP1A2, CYP2B6, CYP2C19, CYP3A5, SLCO1B1, and SLC22A1 might influence PD characteristics. Since our study was based on an original BE trial in healthy subjects, the accuracy of the PK/PD results was high and no known diseases or other factors affected drug metabolism. These same advantages of the previous study, which followed a similar experimental design (Liu et al., 2021), increased the quality and reliability of our results for determining the impact of various genetic polymorphisms on PK and PD parameters of dabigatran metabolism.
The major pharmacokinetic features of dabigatran etexilate include having a rapid absorption, low bioavailability (3–7%), variable peak concentration, steady state concentration attainment within two to 3 days, bi-exponential distribution phase, volume of distribution (50–70 L), 35% bind rate to plasma proteins, hepatic conjugation with glucuronide, and ability for renal elimination (80%) (Kanuri and Kreutz, 2019). As a BCS Class IIb drug, dabigatran etexilate exhibits high solubility at acidic pHs, but tends to precipitate after emptying from the stomach into the small intestine, leading to low bioavailability (Tsume et al., 2014). As previous reported, dabigatran is mainly eliminated in a non-metabolized form by urine (80%), and approximately 20% is conjugated to form dabigatran acylglucuronide eliminated in stools (Blech et al., 2008). While recent research by Park et al. (2021) with a new direct measurement method revealed that the portion of dabigatran conjugated to form dabigatran acylglucuronide would be much higher than previous results by the old indirect method. As renal excretion is the predominant elimination pathway for dabigatran, the medication is avoided in patients with impaired kidney function–especially those with end-stage renal disease (Ašić et al., 2018). Compared with the negligible role of phase I metabolic reactions, the formation of 1-O-acylglucuronide in phase II is the predominant route of dabigatran metabolism in humans (Blech et al., 2008). After conjugation with activated glucuronic acid, dabigatran acylglucuronide as the main metabolite possess the similar or even weaker anticoagulant effects to prolong APTT, PT, and TT compared with dabigatran (Blech et al., 2008; Kim et al., 2022).
Drug transporters, including members of the ATP-binding cassette (ABC) and solute carrier (SLC) superfamilies, are recognized as important determinants for governing the therapeutic response of many drugs (César-Razquin et al., 2015). SLC4A4, located in chromosome 4q13.3, encodes an anion exchange protein named electrogenic sodium bicarbonate cotransporter 1 (NBCe1) (Demirci et al., 2006). NBCe1 is involved in the regulation of bicarbonate secretion and absorption, as well as intracellular pH. Mutations in this gene are associated with proximal renal tubular acidosis, an extremely rare autosomal recessive syndrome involving ocular abnormalities and developmental delay (Dinour et al., 2004). SLC4A4 SNP rs138389345 is a variant of SLC4A4 in which a single G base is deleted (G > -). From the HPA RNA-seq normal tissue data, the SLC4A4 gene is most expressed in the kidney. NBCe1 plays a major role in renal bicarbonate absorption via the proximal tubules and maintaining normal blood pH (Demirci et al., 2006). Abnormal function of NBCe1 can cause severe HCO3- reabsorption and decrease blood HCO3- concentration, resulting in acidic pH. Due to the strong pH-dependent solubility of dabigatran etexilate, with decreased solubility at basic pH values (Chai et al., 2016), it is reasonable to speculate the influence of SLC4A4 genetic variance on dabigatran metabolism. In our study, SLC4A4 SNP rs138389345 showed a significantly higher AUC0-t(total) (TGTG 1018.11 ± 269.56, TGT 1231.16 ± 429.25, TT 1451.17 ± 471.41, ngh/ml). Additionally, this SNP resulted in increased values for AUC0-t(free), Cmax(total), Cmax(free), IIa2h, and APTT2h.
The FRAS1 gene, also known as KIAA1500, is located in chromosome 4q21.21, encodes the extracellular matrix (ECM) proteins, and regulates epidermal-basement membrane adhesion and organogenesis during development (Hoefele et al., 2013). FRAS1 SNP rs6835769 involves the mutation of a C base to a T base (C > T) within the gene, which can lead to the A817V mutation at the protein level. FRAS1 mutations have been confirmed to cause an extremely rare autosomal recessive genetic disorder named Fraser Syndrome (FRASRS), and seem to be responsible for non-syndromic unilateral renal agenesis (Hoefele et al., 2013). Furthermore, FRAS1 mutations are associated with bone metabolism, where FRAS1 may be involved in the metabolism of calcium and phosphorous (Reyer et al., 2019). While most studies of FRAS1 mutation have focused on its role in the pathogenesis and prognosis of diseases (Zhan et al., 2014), there has only been one GWAS (Fridley et al., 2016) that investigated drug related variations. From a study of 74 invasive epithelial ovarian cancer patients observed at the Mayo Clinic, it was found that some genes including FRAS1 may explain inter-patient variation in clinical response to platinum-taxane therapies. In our study, FRAS1 SNP rs6835769 was associated with the PK parameters of AUC0-t and Cmax, and followed the same trend of SLC4A4 mutations. Perhaps the reasoning behind this is as follows: the FRAS1 gene is secondarily expressed in the kidney, including in the glomerular podocytes and podocyte precursors (Pitera et al., 2008), while dabigatran is primarily excreted via the kidney. While this may provide preliminary insight into how FRAS1 impacts dabigatran metabolism, the detailed mechanism must be further explored and investigated through in vivo and in vitro studies.
Drugs usually undergo two phases of metabolism in the body. The main purpose of phase II metabolic reactions is to combine reactions, increase drug polarity, and facilitate drug exclusion from the body. The most common phase II biotransformation enzymes include sulfotransferases (SULTs), N-acetyltransferases (NATs), and methyltransferases (MTs). SULTs utilizes 3′-phospho-5′-adenylyl sulfate (PAPS) as a sulfonate donor to catalyze the sulfate conjugation of a wide variety of acceptor molecules that bear a hydroxyl or an amine group (Daniels and Kadlubar, 2014). Sulfonation increases the water solubility of most compounds, and therefore their potential for renal excretion, but it can also result in bioactivation to form active metabolites. The SULT1A1 gene locates in chromosome 16q11.2, and rs9282862 is a mutation of a T base to C base within a SULT1A1 intron. Proteins encoded by SULT1A1 are present in many human tissues, including the liver, kidney, and platelets (Raftogianis et al., 1997). The two most common SULT1A1 variant alleles are 638G > A (formerly named rs9282861, now named rs1042028, SULT1A1*2) and 667A > G (rs1801030, SULT1A1*3). Previous reports have confirmed that these alleles have significantly different frequencies depending on race (Carlini et al., 2001). SULT1A1 mutations could explain the wide range of individual differences in tamoxifen efficacy (Gjerde et al., 2008), and have also been shown to be involved in the heparan sulfate and heparin metabolism pathway (Jiang et al., 2011). Although no study (Shnayder et al., 2021) has investigated the impact of SULT1A1 gene variants on the efficacy or toxicity of apixaban, another DOAC, SULT1A1 is indeed involved in the conversion of approximately one fourth of the absorbed amount of Apixaban to inactive metabolites (Raymond et al., 2021). For the metabolism of Apixaban (leading to O-desmethyl-apixaban sulfate), SULT1A1 and SULT1A2 account for a quarter of its conversion to inactive metabolites (Kanuri and Kreutz, 2019). Several SNPs in linkage disequilibrium with each other and with SULT1A1*1 have also been identified in both the distal and proximal promoter region of SULT1A1, and are associated with platelet enzymatic activity (Ning et al., 2005; Lin et al., 2012). SNP rs9282862 is also in strong linkage disequilibrium with SULT1A1*1 (r
2 = 1.00, D´= 1.00), as seen in data from the Gambian Genome Variation Project (GGVP). SLC4A4 SNP rs138389345 showed a significantly decreased AUC0-t(total) (TT 1382.89 ± 476.91, TC 1097.46 ± 337.20, ng h/ml), with similar trends observed in AUC0-t(free), Cmax(total), Cmax(free), IIa2h, PT2h, and ∆PT2h. Although this linkage disequilibrium needs to be verified in Asian populations, and UGTs were the main phase II enzymes involved, SULT1A1 variation may have the potential to be a new biomarker for antithrombotic therapy–it would certainly be worthy to conduct more detailed studies to investigate this possibility.
For the reported candidate genes, 13 genes (ABCB1, ABCC2, ABCG2, CYP2B6, CYP1A2, CYP2C19, CYP3A5, CES1, SLCO1B1, SLC22A1, UGT1A1, UGT1A9, and UGT2B7) were found to have significant effects on drug metabolism. The most commonly reported SNPs, including ABCB1 rs1045642 and CES1 rs2244613, had no influence on any PK or PD parameters in our study, which was a finding consistent with Ji Q’s research (Ji et al., 2021) but not totally with Liu Y’s study of Chinese participants (Liu et al., 2021). As we know, UGTs are involved in the production of active metabolites in a small proportion of dabigatran (Ishiguro et al., 2014). Besides, polymorphisms of CYP450 for isoenzymes 1A2, 2C8, 2C9, 2C19, and 2J2 have been shown to affect the pharmacokinetics of dabigatran, and especially the co-administration of DOACs with other drugs (Shnayder et al., 2021). Outside of the ABCB1 and CES1 genes, almost no study to date has focused on the associations between carriers of the UGT (including UGT1A9, 2B7, and 2B15), CYP, and SLC gene families and dabigatran metabolism in humans (Raymond et al., 2021; Shnayder et al., 2021). Zubiaur et al. (2020) investigated the influence of genetic polymorphisms in UGT and CYP, which encode for enzymes, and SLC, which encodes for transporters, on the pharmacokinetics and safety of dabigatran. In 107 healthy Caucasian and Latin-American volunteers, UGT1A1 rs887829, SLCO1B1, and most CYP polymorphisms were found to have no influence in this regard. On the other hand, while CYP2D6 poor metabolizers, SLC22A1 haplotype, and CYP3A5-expressing subjects (*1/*1) had positive change. Lähteenmäki et al. (2021) investigated the effects of ABCG2 and CYP3A5 variants on bleeding and thromboembolic events in Finnish patients who were given dabigatran, where the results were all negative. In our study, the positive SNPs which had the most effects on PK or PD parameters included SLCO1B1 rs11045748 (AUC0-t, Cmax, APTT2h, PT2h, and ∆PT2h), SLCO1B1 rs2291075 & rs4149056 (AUC0-t and Cmax), UGT1A9 rs7586110 (AUC0-t, Cmax, and Tmax), UGT1A1 rs4148323 & rs4148327, ABCC2 rs2273697 & rs4148395 (AUC0-t and Cmax), CYP2B6 rs56156262 (AUC0-t and Cmax), and CYP2B6 rs34433978 (IIa2h, APTT2h, PT2h, and ∆PT2h). The reported positive SNPs of CYP2D6, SLC22A1, CYP3A5, and ABCG2 were not consistent with previous studies (Zubiaur et al., 2020; Lähteenmäki et al., 2021). Accordingly, the impacts of all aforementioned SNPs should be verified in studies with larger sample sizes and that investigate other ethnicities.
There were a few key limitations to our study worth discussing. First, as the sample size was limited, no SNP was found to meet the genome-wide significance threshold. Therefore, future multi-center studies with larger sample sizes should be conducted. Second, not all potential SNPs could be detected by our genotyping method, such as the reported SNPs of ABCB1, CES1, SULT1A1 rs9282861, and UGT2B15 (Shnayder et al., 2021). Supplementary genome-wide detection or other forms of exploration should be performed to account for this. Third, as our study was only performed in healthy Chinese subjects, it should be replicated in another population–especially among patients and other ethnicities. As mentioned in the background, many factors may influence the metabolism of dabigatran and these indexes have different characteristics of distribution between healthy subjects and patients. Recent pharmacogenetic studies also showed different results between these two groups (Supplementary 1, Supplementary Table S1). Our findings Whether our findings can be replicated in patients or other ethnicities is worth exploring further. Finally, explorations into the functions of our newfound suggestive genes were mostly insufficient. More identification studies (both in vivo and in vitro) should be performed to document their detailed pathways in drug metabolism.