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The effect of simvastatin on warfarin anticoagulation: a Swedish register-based nationwide cohort study

  • Marine L. Andersson
  • Buster MannheimerEmail author
  • Jonatan D. Lindh
Open Access
Pharmacokinetics and Disposition

Abstract

Purpose

Some data indicate that simvastatin may increase the anticoagulative effect in patients treated with warfarin, but the evidence is scarce. The aim of the present study was to investigate how the anticoagulative effect of warfarin is affected by the initiation of simvastatin in a very large patient sample.

Methods

In a retrospective cohort study, we included 5637 individuals on warfarin treatment initiating simvastatin. INR values and warfarin doses were calculated week-by-week during co-treatment. Data were obtained from two large Swedish warfarin registers and from the Swedish Prescribed Drug Register.

Results

INR increased from 2.43 at baseline to 2.58, 4 weeks after simvastatin initiation, and did not stabilize until the last quarter of the year studied. Consequently, the proportion of patients with an INR above 3 increased from around 8 to 15%.

Conclusions

In conclusion, initiation of simvastatin resulted in moderately increased INR values and subsequent dose decreases in patients already on warfarin. In order to avoid the increased risk of bleeding, the initiation of simvastatin may be accompanied by closer INR monitoring.

Keywords

Simvastatin Cytochrome P-450 CYP2C9 Drug interactions International normalized ratio Warfarin 

Introduction

Warfarin is the world-leading oral anticoagulant used for the treatment and prevention of thromboembolic disease. The therapeutic interval of warfarin is narrow, and the dose needed for sufficient anticoagulation is close to that which may cause bleeding [1]. The effect of warfarin is influenced by genetic factors, for example, vitamin K epoxide reductase complex (VKORC1) and cytochrome P450 2C9 (CYP2C9) genotypes, but also exogenic factors such as dietary vitamin K intake and drug interactions [2]. There are many examples of clinically relevant drug-drug interactions, such as increased warfarin effect due to amiodarone co-treatment [3, 4] and induction of CYP2C9 by carbamazepine [5] leading to subtherapeutic international normalized ratio (INR) levels.

Simvastatin is one of the most prescribed drugs and is often used by individuals also dispensed anticoagulants. In Sweden alone, about 50,000 individuals (428 per 100,000 inhabitants) are treated with simvastatin in combination with warfarin [6]. Some data indicate that simvastatin may increase the anticoagulative effect in patients treated with warfarin [3, 7, 8, 9]. We have previously studied the influence of the CYP2C9 genotype on the magnitude of the interaction between warfarin and simvastatin. In carriers of the CYP2C9*3 allele, simvastatin reduced warfarin dose requirements by 29%, compared with 5% in non-carriers, suggesting that the mechanism may be due to selective inhibition of the inhibition of the CYP2C9*3 allele [10]. The main aim of the present study was to investigate how the anticoagulative effect of warfarin is affected by the initiation of simvastatin in a very large patient sample.

Methods

In this retrospective cohort study, we hypothesized firstly that simvastatin would enhance the anticoagulative effect of warfarin and, secondly, that the effect would be more pronounced in patients with low maintenance doses, a group where CYP2C9*3 carriers are more common.

We investigated the change in warfarin dose and INR during simvastatin therapy in patients with ongoing warfarin anticoagulation, by comparing warfarin doses before and after initiation of co-treatment with simvastatin. Data on daily warfarin dose and results from INR measurements were retrieved from two anticoagulation registers, Journalia and Auricula [11, 12]. These systems are used in more than 300 anticoagulation clinics in Sweden and contain information about warfarin doses, INR, sex, and personal identification numbers for patients using warfarin for atrial fibrillation as well as for other indications. Information on the use of other medications was retrieved from the Swedish Prescribed Drug Register [13]. This register includes data on all dispensed prescriptions in Sweden. By linking and matching these registers, we could analyze warfarin doses and INR in patients initiating simvastatin therapy.

All adult patients (age 18 or above) dispensed warfarin and starting simvastatin therapy were available for inclusion. The index date for the start of simvastatin therapy was defined as the date of the first simvastatin dispensing. To make sure simvastatin therapy was initiated, this period should have been preceded by a period of at least 12 months during which no simvastatin had been dispensed. Ongoing warfarin anticoagulation was defined by at least one dispensing of warfarin within 4 to 20 weeks before the index date and warfarin doses documented in Journalia or Auricula during the baseline period (4–20 weeks prior to the index date). To avoid including patients ending simvastatin therapy within a year, we also required three additional simvastatin dispensings after the index date, the first within 55–145 days after the index date, the second within 155–245 days, and the third within 255–345 days after the index date. In Sweden, each dispensing of simvastatin usually covers 3 months.

Patients were excluded if they were using other drugs known to influence warfarin pharmacokinetics, causing a more than 10% change in warfarin doses. Hence, patients were excluded if they had been dispensed any of the following drugs: amiodarone, bosentan, capecitabine, carbamazepine, cimetidine, clofibrate, co-trimoxazole, dabrafenib, darunavir, dasabuvir, disulfiram, dronedarone, enzalutamide, eslicarbazepine, erythromycin, fluconazole, fluorouracil, lopinavir, metronidazole, miconazole, paritaprevir, phenobarbital, primidone, propafenone, rifampicin, ritonavir, sitaxentan, ombitasvir, oritavancin, vemurafenib, voriconazole, or zafirlukast.

In the main analysis, we compared the mean daily warfarin dose 1–28 days prior to the index date (initiation of simvastatin) with the mean daily warfarin dose 337–364 days after the index date. In subjects ending warfarin therapy during the follow-up period, all available doses within the period were included in the analysis. The two periods were compared by calculation of the change in log-transformed dose in each patient, and the mean difference was compared with no change (zero) using a two-sided paired t test. The relative dose decrease was calculated by retransformation of the mean difference.

A multiple regression model was used to investigate the effect of sex and age on the proposed drug-drug interaction. The dependent variable in the model was the change in log-transformed warfarin dose, and age was analyzed in groups that ranged 18–49, 50–59, 60–69, 70–79, 80–89, and 90–100 years. The dose at baseline was plotted against the dose at week 49–52 in each patient to visualize the changes within the whole study population.

To study the interaction effect over time, we calculated the week-by-week normalized dose (by dividing dose by baseline dose) for each patient. Normalization was performed since we assumed that the relative effect (the percent dose change) would be more uniform than the change in dose/week in milligrams. We also calculated the fraction of patients with a decrease in warfarin dose by > 10%, > 25%, and > 50% compared with baseline. The fraction was calculated separately for each week and not cumulatively. To investigate the theoretical possibility of time-dependent covariates reducing the correlation with baseline values over time, we also analyzed the proportion of patients with different levels of increases of warfarin doses after the index date. For symmetry reasons, a 10% decrease was contrasted against an 11% decrease, a 25% decrease against a 33% increase, and a 50% decrease against a 100% increase.

The effect on INR was investigated by interpolation of INR values by the method of Rosendaal [14]. All values were log-transformed and the mean INR value with 95% CI was calculated week by week until 52 weeks after the index date. We also calculated the fraction of patients having an INR above 3 and above 4.

To investigate the effect of initial warfarin dose requirements, as a rough marker for the CYP2C9*3 genotype, we divided the patients into 4 subgroups based on the baseline dose (quartiles). All analyses described above were then repeated separately for each of these subgroups. In addition, we performed subgroup analyses based on the simvastatin dose. In this case, we divided patients into those receiving 10–20 mg simvastatin and those receiving 40–80 mg.

p values below 0.05 were considered statistically significant. All analyses were performed using R version 3.3.2 [15].

Results

We identified 7305 patients during the period July 1, 2005, until December 31, 2012, who had started simvastatin therapy and who had been dispensed simvastatin three times after the index date according to the inclusion criteria and who had not received any interacting drugs. After further exclusions due to missing warfarin dosage data or lack of warfarin exposure 90 days or more before starting simvastatin, 5637 patients were included in the analysis (Fig. 1).
Fig. 1

Patient flow diagram

The median age of the included patients was 72 years (interquartile range (IQR) 65–78 years), and 34% were female. The median warfarin dose per week during the baseline period was 32.5 mg (IQR 23.8–42.5).

INR increased from 2.43 at baseline to 2.58, 4 weeks after simvastatin initiation, and did not stabilize until the last quarter of the year studied. Even then, the mean INR level had not returned to its baseline value slightly above 2.4 (Fig. 2). Figure 3 shows the fraction of patients with INR above 3 and above 4. Fifteen percent of patients reached an INR above 3 and less than 1% an INR above 4.
Fig. 2

Weekly mean INR during co-treatment with warfarin and simvastatin. The INR was interpolated to allow inclusion of weekly values for all patients. Brackets denote 95% confidence intervals

Fig. 3

Fraction of patients with an INR over 3.0 and 4.0 following simvastatin initiation. The numbers at the bottom of the graph indicate the number of patients remaining in the study (i.e., still co-treated with warfarin and simvastatin) at different time points

When comparing warfarin doses before simvastatin initiation with doses during a 4-week period (337–364 days) after simvastatin initiation, we found a decrease in warfarin doses by 6.8%. In a multivariable regression model, we did not find a significant effect of age or gender on the decrease in warfarin dose. The relative warfarin doses decreased slowly during the whole year studied (Fig. 4). The fraction of patients with a > 10 decrease, > 25% decrease, and > 50% decrease in warfarin dose is presented in Fig. 5. Up to 35% of patients experienced dose decreases by at least 10%, and in approximately 5%, the dose was decreased by 25% or more.
Fig. 4

Changes in dispensed warfarin dose during concomitant simvastatin treatment (means and 95% confidence intervals)

Fig. 5

Fraction of patients with warfarin dose decreases of 10, 25, and 50% during co-treatment with simvastatin. The numbers at the bottom of the graph indicate the number of patients remaining in study (i.e., still co-treated with warfarin and simvastatin) at different time points

In addition, we performed subgroup analysis in patients with different simvastatin doses and baseline doses of warfarin. Simvastatin in doses 20 mg and above was associated with a significant attenuated decreased warfarin dose (− 6.1%, p < 0.01). The decreased warfarin dose associated with simvastatin doses of 40 mg or above was more attenuated (− 8.1%, p < 0.001).

Analysis of the effect in individuals with different baseline doses of warfarin revealed a mean decrease by 5.6% in the subjects whose baseline dose was within the first quantile, by 6.9% in the second quantile, by 7.0% in the third quantile, and by 7.9% in those in the fourth quantile.

Discussion

In this study, including data from 5637 patients with warfarin, we found that the proportion of patients with an INR above 3 increased from around 8 to 15% during the first 7 weeks after initiating simvastatin. Warfarin dose requirements were subsequently decreased by 6.8%.

According to the present study, INR was increased by on average 6%. Previous evidence with regard to effects on anticoagulation is limited to two rather small studies by Hickmott et al. and Lin et al. including 29 and 46 patients, respectively. The results indicated an increase in INR by 27% [9] and 13% [7]. Lin et al. reported that the number of patients with an INR > 3.0 increased from 22 to 35% during simvastatin co-administration. Thus, the effect on anticoagulation was a bit more modest in the present study indicating an increase in INR of 6%. In the present study, initiation of simvastatin decreased warfarin weekly doses by 7%. The results are in line with previous studies indicating a modest decreased requirement of warfarin doses ranging from 3.4 to 9% [3, 7, 8, 9, 10].

In a previous study, we found a significant effect of simvastatin on warfarin doses exclusively in patients with the CYP2C9*3 allele. Unfortunately, we did not have information on the included patients’ CYP2C9 genotypes. As patients with the *3 allele are known to have substantially lower warfarin maintenance doses, we instead used the baseline dose of warfarin as a proxy for this variant. However, we could not demonstrate a more pronounced interaction effect in individuals with low baseline doses of warfarin, and the trend was indeed opposite to our hypothesis. A weakness of this approach may have been that subjects with the *3 genotype are more prone to have difficulties having a stabile INR and may have changed anticoagulant therapy due to this. In addition, it should be acknowledged that warfarin dose requirements are also influenced by the VKORC1 genotype and a range of other factors unrelated to the CYP2C9 genotype. Consequently, the validity of warfarin dose as a proxy for CYP2C9 enzymatic activity could be questioned.

One possible pharmacokinetic mechanism other than a selective inhibition of the CYP2C*3 variant includes interaction due to competition of CYP3A4-mediated metabolism of R-warfarin [10]. Pharmacodynamic effects have also been suggested to cause the interaction. Several, but not all, studies have shown that the risk of thrombosis is lower in statin users than in non-users. Hence, simvastatin may have an antithrombotic effect on its own. Simvastatin has been shown to decrease the levels of fibrinogen, factor VII, and plasminogen factor [16] and to decrease platelet aggregation [17].

Using three nationwide registries, we have developed a methodology that previously have proven useful to study drugs that decrease [5] and increase [4] the effect of warfarin anticoagulation. The approach has several strengths especially the high number of subjects and the possibility to study the longitudinal effect of the interaction. One limitation of the present study is that we lack information about the patients’ compliance to simvastatin treatment. However, the rather strict inclusion criteria in the present study requiring three additional simvastatin dispensings after the index date may have decreased the influence of non-compliance. Another limitation is that patients with a pronounced interaction effect may have been switched to other anticoagulation and consequently excluded from the analysis. Finally, we did not have access to data on adverse events in the cohort and could not analyze the clinical impact of the interaction effect. However, substantial evidence shows that an INR of 3.0 increases the risk of cerebral hemorrhage and other severe bleeding [18, 19].

In Fig. 5, we present the proportion of patients with different levels of decreases in warfarin doses. Importantly, the changes are calculated separately for each week and not cumulatively. Nevertheless, these changes may theoretically still increase with time due to changes in different time-dependent covariates. To picture this potential statistical bias, we also analyzed the proportions of individuals with different levels of increases in warfarin doses after 1 year after the index date. The proportion of patients with warfarin doses increased by > 11% was only a sixth (7%) of that with doses decreased by > 10% (35%) indicating that such statistical effect was small.

Simvastatin is one of the most extensively used drugs and is often used in individuals also dispensed anticoagulants. The results of the present study therefore have important implications. Although the average effect on warfarin requirements and anticoagulation was modest, the proportion of patients exposed at supratherapeutic INR levels was almost doubled which may have serious consequences with regard to the risk of bleeding. Prescribers should include this information when facing a patient initiating treatment with simvastatin.

In conclusion, initiation of simvastatin resulted in moderately increased INR values and subsequent dose decreases in patients already on warfarin. In order to avoid the increased risk of bleeding, the initiation of simvastatin may be accompanied by closer INR monitoring.

Notes

Authors’ contribution

MLA, JDL, and BM designed the study, interpreted the data, wrote the paper, and approved the final version and have agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work have been appropriately investigated and resolved. JDL performed the statistical analysis.

Funding information

The study was supported by Bengt Ihres fond, Karolinska Institutet.

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Copyright information

© The Author(s) 2019

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Karolinska Institutet, Department of Laboratory Medicine, Division of Clinical PharmacologyKarolinska University Hospital HuddingeStockholmSweden
  2. 2.Department of Clinical Science and Education at SödersjukhusetKarolinska InstitutetStockholmSweden
  3. 3.Section of Diabetes and Endocrinology, Department of Internal MedicineSödersjukhusetStockholmSweden

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