Direct oral anticoagulant treatment of deep vein thrombosis reduces IL-6 expression in peripheral mono-nuclear blood cells

Abstract

Multiple factors play a pathophysiologic role for the venous thromboembolism (VTE) as a multi-factorial disease. Inflammation might play a peculiar role in shifting towards a pro-thrombotic state. Anticoagulant drugs are the first cure line for VTE. The low-molecular-weight heparins (LMWH) show anti-coagulant capability as well as reducing levels of inflammatory factors, including interleukin (IL)-6. The direct oral anticoagulants (DOACs) have shown efficacy in threating VTE, additionally to the anti-activated factor X these drugs seem able to reduce the abnormal release of pro-inflammatory agents. The present study evaluated the capability of DOACs in reducing plasma level of IL-6 in patients suffered from deep vein thrombosis (DVT) of the lower limbs. Our results showed reduced IL-6 expression levels in the peripheral lymphocytes of DVT compared to controls (fold-change, 2.8; P<0.05). We postulate that lowered IL-6 expression in the lymphocytes of DVT patients may mediate the anti-inflammatory action of DOACs. The present study is the first evidence concerning the anti-inflammatory properties of DOACs in specific setting of VTE patients such as DVT.

Introduction

Venous thromboembolism (VTE) is a multi-factorial disease, and several findings have suggested that inflammation might play a role in shifting the hemostatic balance towards a pro-thrombotic state (1-4). Moreover, studies have demonstrated the frequency of VTE events in infected patients (5,6). The most recent studies on patients infected by SARS-CoV-2 have shown high levels of D-dimer and fibrinogen-derived peptide (FDP) (7). Patients infected by SARS-CoV-2 were affected by very serious VTE events. Thus, VTE is closely linked to most inflammatory conditions. The role played by inflammation in promoting hyper-coagulation and counteracting systemic fibrinolysis seems crucial. The so-called ‘cytokine storm’ triggers excessive inflammation due to the bloodstream release of several pro-inflammatory cytokines (8). The role of leukocytes both in thrombus generation and vein remodeling has not yet been clarified (9), whereas pleiotropic interleukin (IL)-6 and the development of thrombotic plugs in the venous circulation of the lower limbs (10) seem to play a crucial role. The hemodynamic disorders in venous circulation especially near venous valves, provoke hypoxia and oxidative stress, whereas several endogenous anticoagulants are expressed by intact endothelium (i.e., thrombomodulin, tissue factor pathway inhibitor, endothelial protein C receptor) (1). Leukocyte recruitment, adhesion receptor expression and tissue factor release initiate coagulation pathways (11-14). Therefore, activating the coagulation system is the main step in venous thrombosis, while the role of endothelium activation, as well as that of platelets, still require clarification. Concerning the role played by inflammation several studies demonstrated a key role of IL-6 in the development of deep vein thrombosis (DVT) in lower limbs (15,16). Hypercoagulation is the main mechanism to be counteracted in treating patients with VTE, both DVT and PE. Here it is noted that PE has a high mortality risk, often the consequence of progressive, under-treated or undiagnosed and untreated DVT (17). Anticoagulant drugs are the first response in combating VTE and DVT. A number of factors (obesity, recent trauma, recent surgery, reduced mobilization, solid and non-solid cancer and genetic factors) have been listed as risk factors for DVT although the mechanisms involved in VTE are still under debate (11,18,19). Low-molecular-weight heparins (LMWH) show concomitant anti-coagulant and anti-inflammatory activities reducing levels of inflammatory factors, including IL-6(20). Recently, direct oral anticoagulants (DOACs) have demonstrated favorable results in combating VTE. DOACs showed anti-inflammatory capabilities in reducing the abnormal release of pro-inflammatory factors in addition to inhibiting the activation of factor X of the coagulation cascade (21-25). Our study focuses on the capability of DOACs in reducing plasma level of IL-6 in patients having DVT of the lower limbs.

Patients and methods

The potential anti-inflammatory activity of DOACs in 20 patients hospitalized with lower limb DVT was investigated. The patients were hospitalized at the Internal Medicine Unit of the Catania University Hospital ‘Policlinico-Vittorio Emanuele’ (Catania, Italy). In diagnosing DVT, we checked for compression of one or more lower limb veins (CUS test) and any echogenic material (thrombus) inside the veins. These DVT patients were initially assigned to the conventional therapy of LMWHs (5 days) and then treated with DOACs (Dabigatran 150 mg daily, Edoxaban 60 mg daily) from the sixth day. As controls, 22 healthy blood samples were obtained from previous case-control studies. Clinic, pathologic and demographic features and routine clinical biochemistry data were retrieved for each sample (Table I). The blood samples were drawn in the morning 5 days after patients started the DOAC therapy and after 12 h of fasting. All the patients supplied a blood sample 10 days after the starting of the DOACs drugs. Buffy coats were obtained by centrifuging (2000 x g for 10 min) according to standard procedure. All the sampled patients were informed on the study and they gave their verbal consensus. Total RNA was extracted from the Buffy Coat samples using TRIzol™ LS reagent (cat. no. 10296028; Thermo Fisher Scientific, Inc.) according to the manufacturer's instructions. After treatment with DNase I RNase-free (cat. no. EN0525; Thermo Fisher Scientific, Inc.), 400 ng of treated RNA (final concentration 20 ng/µl) was converted into cDNA using the SuperScript™ IV Reverse Transcriptase kit (cat. no. 18090050; Thermo Fisher Scientific, Inc.) following the manufacturer's protocol. Then, 2.5 µl of each cDNA underwent Real-Time amplification using Luminaris Color HiGreen qPCR Master Mix, high ROX (cat. no. K0362; Thermo Fisher Scientific, Inc.). The amplification of IL-6 and the GAPDH gene for reference, was performed with the 7300 Real-Time PCR System (Applied Biosystems; Thermo Fisher Scientific, Inc.) using the primer pairs reported as follows: forward (F): 5'-CACTGGCAGAAAACAACC TGA-3' and reverse (R): 5'-AGCTCTGGCTTGTTCCTC ACT-3' for IL-6 and F: 5'-AGAAGGCTGGGGCTCATTTG-3' and R: 5'-AGGGGCCATCCACAGTCTTC-3' for GAPDH. Thermal conditions: 50˚C for 2 min, followed by 95˚C for 10 min, and 40 cycles of 95˚C for 15 sec, 60˚C for 30 sec and 72˚C for 30 sec. The relative expression levels of IL-6 were obtained by the 2^-ΔΔCq method (26).

Table I.

Demographic and clinicopathological characteristics of the samples.

Characteristics	CTRL	DVT	P-value
Age (years), median (range)	48 (41.7-62)	56 (46-71)	0.2392b
Sex, no. (%)
Male	12 (54.5)	12 (63.15)	0.76a
Female	10 (45.5)	7 (36.85)
CRP, median (range)	2.062 (0.79-6.96)	6 (3-11)	0.04b

^aFisher's exact test,

^bMann-Whitney test. CTRL, control; DVT, deep vein thrombosis; CRP, C-reactive protein.

The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the Ethics Committee of the Garibaldi Hospital (Catania, Italy; resolution n.23/2016/CECT2). Patients were informed about the objective of the study and were asked to give verbal informed consent to participate in it and to withdraw blood samples. All subjects gave their informed consent for inclusion before participating in the study.

Statistical analysis

Differential analyses were performed using the non-parametric Mann-Whitney test. Fisher's exact test was used to analyze the contingency table of the demographic and clinical-pathological characteristics. The analyses were performed using GraphPad Prism (GraphPad Software, Inc.). All experiments were performed in triplicate.

Results

Results of the study showed that IL-6 expression levels were statistically reduced in the peripheral lymphocytes of DVT patients compared to controls (fold-change, 2.8; P<0.05) (Fig. 1). Despite C-reactive protein (CRP) levels being in the normal range (<15 mg/ml) for almost all samples, DVT patients showed higher CRP levels compared to normal samples (P<0.05; Table I).

Figure 1.

Expression levels of IL-6 in DVT samples and CTRL. IL, interleukin; DVT, deep vein thrombosis; CTRL, control

Discussion

Traditional knowledge on the pathophysiology of VTE consists of the three elements of Virchow's triad: endothelial injury, venous stasis and hypercoagulability (27). More data has been gathered on extending the pathophysiology of VTE (11). Damaged endothelium expresses adhesion receptors favoring the recruitment of leukocytes and platelets. Both bloodstream cell types seem to play a role in VTE (12,28). Derived leukocyte products are able to activate coagulative cascade factors (factor X, XII) promoting intrinsic coagulative pathways. Inflammation correlates with activated coagulation because it influences the initiation and propagation of coagulation, it down-regulates physiological anticoagulant pathways and it inhibits fibrin removal (13). Activated coagulative factors via protease-activated receptors (PARs) may contribute to endothelial stress and exposure to adhesion molecules on the disarranged endothelial barrier leading to inflammation (29).

On VTE pathways, an interesting concept progressively emerged related to white blood cells (leukocytes and neutrophils) being rapidly attracted, and retained at the thrombosis site. Immuno-thrombosis is an interesting interaction between the innate immune system with the procoagulative condition (30). In particular, neutrophils can promote thrombosis by releasing neutrophil extracellular traps (NETs). NETs show several coagulative properties such as platelet activation, and fibrin string generation (31), whereas NETs are resistant to systemic fibrinolysis so they impair thrombus resolution (32,33). In severe clinical conditions (i.e., acute sepsis), there is abundant expression of the ILs (e.g., IL-6) with high surface expression of the tissue factor. The relationship between inflammation and anti-coagulant balance is well known i.e. that combined tissue-factor activated factor VII converts factor X to activated factor, in turn activated factor X generates the activated factor II (thrombin) of coagulation. Reported evidence on the relationship between inflammation and the pro-coagulative activated pathway leads us to the conviction that inflammation must be considered as one of the most likely risk factors for VTE. Current approved guidelines for VTE (including DVT) therapy cite LMWH usage as first line (34). DOACs were initially approved for VTE prophylaxis in patients with favorable clinical conditions, to prevent the risk of deterioration in patients with VTE. Subsequently, DOACs have been also suggested in treating VTE. To date, DOAC therapy is currently assigned to VTE patients after discharge in preventing clinical worsening during follow-up. On the anti-inflammatory response caused by anti-thrombotic drugs, the anti-inflammatory effects of LMWHs were recently confirmed by reducing IL-6 and by the increased lymphocyte percentage found in patients infected by the COVID-19 virus (35). No specific anti-inflammatory effects have been reported for DOACs however, it could be reasonably expected that their potential anti-inflammatory effects could help in counteracting thrombin generation. In post-thrombotic syndrome, lower fibrinogen and inflammatory biomarkers were found in patients assigned to an anti-Xa activated oral drug (Rivaroxiban) compared to 5-7 days conventional treatment with LMWH and VKA (36). In conclusion, our results show lower levels of IL-6 in DVT patients assigned to DOACs compared to controls. Reduced IL-6 expression in the lymphocytes of DVT patients may mediate the anti-inflammatory action of DOACs. Anti-inflammatory activity has yet to be demonstrated in the LMWHs of patients with high inflammatory levels affected by acute dramatic thrombotic venous diseases as the consequence of SARS-CoV-2 infection. To the best of our knowledge, our study shows the first evidence concerning the anti-inflammatory properties of DOACs in DVT patients.

In conclusion, anticoagulant drugs such as LMWHs have demonstrated the direct potential of their anti-inflammatory capabilities in addition to their anticoagulant properties (37). Moreover, the involvement of inflammation in the pathophysiology of the venous thrombotic process has been clearly established (38). Inflammation is a very interesting tool for evaluating the potential of the new anti-thrombotic drugs (DOACs) targeted to inhibite or reduce inflammatory pathways. Overall, we are confident that these observations will contribute to clarifying the potential role of DOACs against the high inflammatory activity that is greatly responsible for favoring hyper-coagulation and in determining the clinical outcomes for DVT patients.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

SC, GL, GB, DV, ET, IP, EF, GP, CI, AG and SSS: substantial contributions to conception and design, acquisition of data, analysis, and interpretation of data. Drafting the article, and revising it critically for important intellectual content. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The study was conducted in accordance with the Declaration of Helsinki and was approved by the Ethics Committee of the Garibaldi Hospital (Catania, Italy; resolution n.23/2016/CECT2). All subjects gave their informed consent for inclusion before participating in the study.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.