Zhi-Chun Gu
Xiao-Wei Ma
Xiao-Yuan Zheng
Long Shen
Fang-Hong Shi
Hao Li- 1Department of Pharmacy, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China
- 2Department of Clinical Laboratory, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China
- 3Department of Pharmacy, Affiliated Hospital of Jiangnan University, Wuxi, China
- 4Department of Cardiology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China
- 5Department of Pharmacy, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiaotong University, Shanghai, China
Dabigatran, directly targeting thrombin, is widely used for the prevention of stroke in nonvalvular atrial fibrillation (NVAF). We reported a rare case of left atrial appendage thrombus formation in a persistent NVAF patient despite the 31 months uninterrupted treatment with dabigatran 110 mg twice daily. The patient is a carrier of ABCB1 variant alleles with 7 heterozygote single nucleotide polymorphisms (SNPs: rs4148738, rs2235046, rs1128503, rs10276036, rs1202169, rs1202168, rs1202167) as well as CES-1 variant alleles with 2 homozygote SNPs (rs2244613 and rs4122238) and 2 heterozygote SNPs (rs8192935 and rs4580160), which may contribute to the changes of dabigatran plasma concentration. In addition, Drug-drug interaction with atorvastatin may also play a role to decrease dabigatran plasma concentration. There are only four such cases till date, of which had thrombus in the left atrium, reported in the literature. We firstly reported the documented case in a Chinese patient carrying multiple alleles of ABCB1 and CES-1, who suffered from thrombus in the left atrial appendage despite long-term anticoagulation with dabigatran. More clinical data are required to elucidate the impact of CES-1 and ABCB1 polymorphism on dabigatran pharmacokinetics, especially for Asian.
Introduction
Warfarin, one of the vitamin K-dependent antagonists (VKAs), is the most commonly used oral anticoagulant (Mega and Simon, 2015). Although warfarin has been used clinically for more than 60 years, several challenges including bleeding complications have been noted, which are one of the primacy causes of severe adverse drug events (Crowther et al., 2000; Wysowski et al., 2007). The inherent limitations of warfarin, comprising narrow therapeutic window, intra-patient variability, and numerous food-drug interaction and drug-drug interaction, lead to a need for more elaborative anticoagulation monitoring (Johnson et al., 2011; Pirmohamed et al., 2013). Different from warfarin, non-VKA oral anticoagulants (NOACs), which directly target thrombin or Xa factor, have been approved for the prevention of stroke and systemic embolism in non-valvular atrial fibrillation without necessary of routine blood monitoring (López-López et al., 2017). Dabigatran etexilate, the prodrug of dabigatran, has the lowest bioavailability of present NOACs of 3~7% (Mega and Simon, 2015), which is rapidly converted by esterases-1 (CES-1) to dabigatran after administration (Stangier and Clemens, 2009; Laizure et al., 2014). In addation, dabigatran etexilate is a substrate of the P-glycoprotein intestinal efflux transporter (P-gp), which also known as ATP-binding cassette sub-family B member 1 (ABCB1) (Paré et al., 2013). P-gp is one of the drug transporters expressed in gastrointestinal tract which involves in the efflux of various kinds of drugs into lumen (Ambudkar et al., 2003). Thus, strong P-gp inhibitors can increase dabigatran bioavailability by 12–23% (Liesenfeld et al., 2011; Paré et al., 2013; Kishimoto et al., 2014). Unlike Xa factor inhibitors, oxidoreductases or cytochrome P450 enzymes are not involved in the metabolism of dabigatran (Blech et al., 2008). As the renal clearance of dabigatran is 80%, renal function should be monitored regularly in patients taking dabigatran (Mega and Simon, 2015). Accordingly, changes in the process of absorption or elimination could have a great effect on dabigatran plasma concentrations (Antonijevic et al., 2017; Favaloro et al., 2017). We reported a dabigatran-treated patient who presented with severe left atrial appendage thrombus formation, of whom ABCB1 and CES1 genetic polymorphism and drug-drug interaction may have been the contributing factors. The patient gave his written informed consent for publication of this report.
Case Presentation
The present patient is a 70-year-old Chinese male with paroxysmal atrial fibrillation, complicating hypertension, type 2 diabetes mellitus, coronary heart disease, cerebral infarction, and lost binocular vision. The patient had received dabigatran etexilate 110 mg twice daily since April 30th, 2015 for the prevention of stroke and systemic embolism. Before the introduction of dabigatran, several drugs, including atorvastatin, have been taking for years (Table 1). The patient was admitted to the department of cardiology on November 9th 2017 due to the recurrence of cardio-embolic stroke. Vital signs were normal with blood pressure of 133/73 mmHg and heart rate of 73 rates per minute. Transesophageal echocardiography on admission showed a large thrombus in the left atrial appendage (Figure 1, Video 1), the enlarged left atrial diameter of 46 mm (reference: 30–40 mm) as well as depressed left ventricular function with left ventricular ejection fraction of 52% (reference: 55%) (Table 2). Laboratory data on admission were within normal limits expect for serum creatinine of 115 umol/L (reference: 45–104 umol/L) and B type natriuretic peptide (BNP) of 188 pg/mL (reference: 0.0~100 pg/mL) (Table 2). Dabigatran was stopped at admission, and enoxaparin was administrated with the combination of warfarin since November 8th, 2017 for 20 days till November 28th, 2017. Finally, the patient was treated with coronary artery bypass grafting (CABG), atrial fibrillation ablation, left atrial appendage excision and pericardial drainage plus cardiac temporary pacemaker implantation in November 29th, 2017. He was discharged day 15 post-operation on treatment with warfarin 2.5 mg daily. At 3 months follow up, the patient has been doing well without any evidence of recurrent thrombotic events.
Table 1. Drugs administration during 3 years.
Figure 1. Transesophageal echocardiogram showed the large left atrial thrombus.
Table 2. Results of main laboratory test.
Investigations
Clinical investigations were performed to assess the causes of potential decreased dabigatran effects at therapeutic doses. They included patient's characteristic, co-administrated drugs, and genotyping of ABCB1 and CES1.
ABCB1 and CES1 Genotyping
Genomic DNA was extracted from whole blood (200 μl) using the QIAamp DNA blood mini kit (QIAGEN, Hombrechtikon, Switzerland). ABCB1 (rs4148738, rs2235046, rs1128503, rs10276036, rs1202169, rs1202168, and rs1202167) and CES1 (rs8192935, rs2244613, and rs4122238) and CES1P2 (rs4580160 and rs4784563) polymorphisms were determined by Sanger sequencing. The polymerase chain reaction primers were presented in Table 3. Sequencing was performed on 1 μl of the purified mixture using the BigDye Terminator v1.1 Cycle Sequencing kit (Life Technologies, Warsaw, Poland) and an ABI 3130 Automatic Capillary DNA Sequencer.
Table 3. The polymerase chain reaction primers of ABCB1 and CES1.
Results
Several reasons that contributed to treatment failure with dabigatran should be considered in this case: (1) the patient is a 70-year-old Chinese male and had a moderate renal insufficiency (estimated glomerular filtration rate of 55 mL/min); (2) the drug-drug interaction between dabigatran and atorvastatin was present; (3) as shown in Table 4, The patient is a heterozygote carrier of ABCB1 variant alleles with 7 heterozygote single nucleotide polymorphisms (SNPs: rs4148738, rs2235046, rs1128503, rs10276036, rs1202169, rs1202168, rs1202167) as well as CES-1 variant alleles with 2 homozygote SNPs (rs2244613 and rs4122238) and 2 heterozygote SNPs (rs8192935 and rs4580160).
Table 4. The results of ABCB1 and CES1 Genotyping.
Discussion
We described the case of an old dabigatran-treated patient who presented with left atrial appendage thrombus formation despite the 31 months uninterrupted dabigatran therapy. Laboratory investigations showed a serum creatinine of 115 μmol/L and estimated glomerular filtration rate of 55 mL/min, which indicated a moderate renal insufficiency. Given that more than 80% of dabigatran is eliminated via urine, renal insufficiency was probably a contributing factor to increase the susceptibility of dabigatran. Furthermore, dabigatran may not suitable for elderly person due to insufficient renal function and correspondingly increased risk of bleeding. However, the mutation of both ABCB1 and CES-1 alleles may lead to a significant decrease of dabigatran blood concentration. The ABCB1 gene encodes for P-gp, and P-gp is an ATP-dependent drug efflux pump (Verhalen et al., 2017). Dabigatran etexilate, but not dabigatran, is a P-gp substrate. P-gp inhibitors increase dabigatran bioavailability by 10–20% (Stangier and Clemens, 2009). As compared to the homozygotes for ABCB1 SNP rs4148738 (G allele), patients carrying 1 or 2 A alleles showed 5% lower trough concentration (Dimatteo et al., 2016). CES-1 gene, which encodes for the liver carboxylesterase 1 enzyme, is responsible for the biotransformation of dabigatran etexilate into the active metabolite, namely, dabigatran (Wadkins et al., 2001; Redinbo et al., 2003). Paré et al. (2013) conducted a genome-wide association study, and found that the association of ABCB1 and CES-1 SNPs was consistent with its effect on dabigatran blood concentration. Of which, CES-1 SNP rs2244613 is associated at genome-wide significance with trough concentration, while rs8192935 and rs4148738 are associated with peak concentration modestly (Paré et al., 2013; Ross and Paré, 2013). The minor allele of the CES-1 SNP rs8192935 is associated with a 12% decrease in adjusted peak concentration (Paré et al., 2013). The CES-1 SNP rs2244613 is associated with a 15% decrease in adjusted trough concentration per minor allele (Paré et al., 2013). Thus, the subject carrying 2 minor alleles of rs2244613 are expected to have 28% lower concentration than no-carriers (Paré et al., 2013). In agreement with genome-wide association study, Gouin-Thibault I et al. (Gouin-Thibault et al., 2016) indicated that the heterozygous and homozygous of rs2244613 (CES-1) mutated groups had 14 and 26% lower AUC values as well as 13 and 43% lower Cmax values than the wild-type groups. Of note, the frequency of the T allele of rs2244613 (CES-1) is 33% in overall populations, but affects up to over 60% in Asians. Also, the frequency of the A allele of rs8192935 affects up to 76% in Asians while that is 42% in overall populations (Table 3). Therefore, the impacts on dabigatran concentrations related to rs2244613 and rs8192935 may be greater than previously postulated especially in Asians. Regretfully, no studies that focused on the relationship between CES-1 SNP and ischemic events have been carried out. The present case indicated the presence of ABCB1 heterozygotes in all tested allele. Meanwhile, there is a homozygous mutation of CES-1 rs2244613 and rs4122238 as well as heterozygote mutation of CES-1 rs8192935 and rs4580160. Presumably, patient carrying all these alleles may bring about the relatively low dabigatran blood concentration, subsequently leading to thrombus in the left atrial appendage. In addition, the presence of drug interaction with atorvastatin was probably another contributing factor to increase the risk of thrombosis. Atorvastatin is known as a moderate inhibitors of P-gp, which leads to an approximate 20% decrease in dabigatran concentrations (Wessler et al., 2013; Stöllberger and Finsterer, 2015). According to a large retrospective cohort study of 91,330 Taiwanese patients with non-valvular atrial fibrillation who were treated with dabigatran (49.65% of subjects) or another NOACs, concurrent use of atorvastatin was associated with a 29% decrease in the incidence rate ratio of major bleeding (Chang et al., 2017).
At present, there are limited data on the thrombosis in atrial fibrillation with the management of dabigatran. Luis et al. (2013) firstly reported the images which demonstrated the documented case of thrombosis in atrial fibrillation with coexistent valvular heart disease after 4 months anticoagulation with dabigatran. Sharma et al. (2014) report 2 cases of development of large left atrial thrombus in spite of the continuous treatment with dabigatran. Shah et al. (2015) reported another patient with thrombus formation in the left atrium. In all four cases, the formation of thrombus were in the left atrium but not in the left atrial appendage (Shah et al., 2015). Several proposed mechanisms might explain the reason of left atrial thrombus formation on dabigatran therapy. Firstly, dabigatran therapy is a single level downstream inhibition of thrombin, which could lead to a compensatory increase in upstream clotting factors. Secondly, incomplete inhibition of all available coagulation factors leaves some thrombin activity uninhibited or active. Thirdly, potential drug-drug interactions or inadequate absorption may lead to the unachieved therapeutic levels. Currently, the best strategy of anticoagulation in patients who develop thrombus on dabigatran therapy is uncertain, and a tried therapy with warfarin or left atrial appendage closure should be considered in such patients.
Our report had a few potential limitations. Firstly, our study was underpowered to detect the dabigatran plasma concentration. Secondly, we did not investigate ABCB2 gene polymorphism, which may also impact the blood concentration of dabigatran. Moreover, we did not evaluate P-gp and CES activity in vivo.
Concluding Remarks
We suggest that the presence of ABCB1 variant alleles and CES-1 variant alleles and drug-drug interaction with atorvastatin are possibly contributing factors for dabigatran therapy failure in this case. Indeed, dabigatran may not suitable for elderly person owing to insufficient renal function and potential drug-drug interaction. Regarding optimal strategy, the treatment with warfarin or left atrial appendage closure may be the viable regimens in such patients suffering dabigatran therapy failure.
More clinical data are required to elucidate the impact of genetic polymorphism on dabigatran pharmacokinetics and thrombosis formation in atrial atrium or left atrial appendage. The impact of ABCB1 and CES-1 gene polymorphism on dabigatran pharmacokinetics should be investigated in a phase 1 clinical study in healthy volunteers based on different races.
Author Contributions
LS was in charge of the treatment of patient. X-YZ was responsible for collecting the patient's information. X-WM was performed the phenotyping test of ABCB1 and CES-1 gene. Z-CG was involved in the care of the patient and interpreted the results, and wrote the manuscript. HL supervised the investigations and interpreted the results, and wrote the manuscript. F-HS was redacted of the manuscript. All authors read and approved the manuscript.
Funding
This work was supported by the Science Fund of Hospital Pharmacy of Shanghai Jiaotong University School of Medicine (JDYX2016ZD003), Program for Key Discipline of Clinical Pharmacy of Shanghai (2016-40044-002), Program for Key but Weak Discipline of Shanghai Municipal Commission of Health and Family Planning (2016ZB0304), and the Fundamental Research Funds for the Central Universities (No.17JCYB11).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
The authors would like to thank the patient for allowing publication of this case.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2018.00491/full#supplementary-material
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Keywords: dabigatran, left atrial appendage thrombus, genetic polymorphism, ABCB1, CES-1, drug-drug interaction
Citation: Gu Z-C, Ma X-W, Zheng X-Y, Shen L, Shi F-H and Li H (2018) Left Atrial Appendage Thrombus Formation in a Patient on Dabigatran Therapy Associated With ABCB1 and CES-1 Genetic Defect. Front. Pharmacol. 9:491. doi: 10.3389/fphar.2018.00491
Received: 09 March 2018; Accepted: 25 April 2018;
Published: 15 May 2018.
Edited by:
Colin H. Macphee, GlaxoSmithKline (United States), United StatesReviewed by:
Milica S. Prostran, University of Belgrade, SerbiaClaudio de Lucia, Temple University, United States
Copyright © 2018 Gu, Ma, Zheng, Shen, Shi and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Hao Li, bGloYW8xOTg4MDgxMEBob3RtYWlsLmNvbQ==
†These authors have contributed equally to this work as first authors.