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Ticagrelor improves blood viscosity-dependent microcirculatory flow in patients with lower extremity arterial disease: the Hema-kinesis clinical trial



Microvascular blood flow (MBF) impairment in patients with lower extremity arterial disease (LEAD) is associated with more severe major adverse limb events (MALE). The contribution of ticagrelor, a P2Y12 antagonist and an adenosine enhancer, on blood viscosity (BV) and BV-dependent MBF in LEAD is unknown. The aim of the trial is to investigate the effects of ticagrelor on BV, and explore the association of BV-dependent MBF in participants with LEAD and type 2 diabetes (T2DM).


Randomized, double-blind, double-dummy, crossover trial design that compares treatment with aspirin 81 mg/ticagrelor placebo, aspirin 81 mg/ticagrelor 90 mg twice daily and aspirin placebo/ticagrelor 90 mg twice daily on high-shear (300 s−1) and low-shear (5 s−1) BV, and laser Doppler flowmetry (LDF) in the dorsum of the feet of participants with T2DM.


We randomized 70 (45% female) participants aged (mean ± SD) 72 ± 9 years. The duration of LEAD was 12.3 ± 10.3 years, and 96.9% reported intermittent claudication symptoms. Use of statins was 93% (high-intensity 43%, moderate intensity 49%), renin–angiotensin–aldosterone system inhibitors (75%) and beta-blockers (61%). Treatment with ticagrelor with or without aspirin reduced high-shear BV by 5%, in both cases, while aspirin monotherapy increased high-shear BV by 3.4% (p < 0.0001). Ticagrelor with or without aspirin reduced low-shear BV by 14.2% and 13.9% respectively, while aspirin monotherapy increased low-shear BV by 9.3% (p < 0.0001). The combination of ticagrelor and aspirin increased MBF in the left foot compared to the other two treatments (p = 0.02), but not in the right foot (p = 0.25).


Ticagrelor should be considered in the treatment of microvascular disease in patients with LEAD and T2DM.

Trial registration Registration number: NCT02325466, registration date: December 25, 2014


Lower extremity arterial disease (LEAD) occurs more often in patients with diabetes than in patients without diabetes [1]. Microvascular disease in patients with diabetes and LEAD is associated with more severe major adverse limb events (MALE) [2]. As compared with non-diabetes patients with LEAD, patients with diabetes have higher rates of severe below-the-knee disease, lower limb amputations and critical ischemia resulting in less effective and durable percutaneous and surgical revascularization rates [3,4,5,6].

Multiple studies have shown higher blood viscosity values in patients with type 2 diabetes than controls [7]. Elevated blood viscosity is more common in patients with claudication than controls resulting in shorter mean claudication distance [8, 9]. This phenomenon termed “rheological claudication” was reported in about 25% of patients with moderate to severe claudication and blood hyperviscosity. Low shear blood viscosity influences microcirculatory flow in patients with LEAD [10, 11].

Certain pharmacological therapies recommended for the treatment of intermittent claudication in patients with LEAD reduce blood viscosity including clopidogrel [12] and pentoxifylline [13, 14]. In contrast, other commonly used therapies such as cilostazol or ticlopidine improve pain-free walking distance, but do not alter blood rheology [15]. Ticagrelor is potent a P2Y12 receptor antagonist that also inhibits adenosine uptake via the equilibrative nucleoside transporter 1 (ENT1) transporter and increases adenosine concentrations in acute coronary syndrome patients [16, 17]. In addition ticagrelor stimulates the rapid release of adenosine triphosphate from red blood cells in vitro [18]. The administration of ticagrelor increases adenosine-induced coronary blood flow velocity and improves vascular reactivity compared with clopidogrel [19, 20]. Agents that increase adenosine have been shown to lower blood viscosity [21].

The clinical relevance of reducing blood viscosity on microcirculatory perfusion in patients with LEAD remains unknown. The aim of this clinical trial is to investigate the effects of ticagrelor on high-shear and low-shear blood viscosity, and explore the effect of ticagrelor on microvascular blood flow in patients with LEAD and type 2 diabetes.


This study was approved by the institutional review board at the Icahn School of Medicine at Mount Sinai. Written informed consent was obtained from all participants.

Study design

Details of the trial design have been reported previously. Hema-kinesis is a randomized, double-blind, double-dummy, crossover trial design that compares treatment with aspirin 81 mg/ticagrelor placebo, aspirin 81 mg/ticagrelor 90 mg twice daily and aspirin placebo/ticagrelor 90 mg twice daily on high-shear (300 s−1) and low-shear (5 s−1) blood viscosity (NCT02325466) [22]. The inclusion and exclusion criteria are provided in Table 1. Study participants were recruited from the outpatient cardiology practice and the Cardiac Catheterization database at the Mount Sinai Hospital, New York, NY, USA. An exploratory endpoint was measurement of microvascular blood flow in the dorsum of the feet of participants with type 2 diabetes.

Table 1 Inclusion and exclusion criteria

Study participants were randomized into three groups. Each group received each of three treatments in the crossover study. Block randomization is used in block sizes of six to create groups designed to have equal and balanced sample sizes.

Study medications

Ticagrelor and matching ticagrelor placebo were provided by AstraZeneca (Wilmington, DE). Aspirin and matching placebo were obtained from the University of Iowa Pharmaceuticals (Iowa City, IA). Ticagrelor and matching placebo, as well as aspirin and matching placebo, were compounded then over-encapsulated to maintain double-blind conditions. Stability and antimicrobial quality assurance tests were performed prior to and post over-encapsulation [22]. The Clinical Materials Services Unit of the University of Rochester Medical Center (Rochester, NY) prepared study medication kits. Non-enteric-coated aspirin 81 mg (Bayer, Inc, Pittsburgh, PA) was provided to subjects for the aspirin lead-in prior to screening and washout periods between treatment arms.

Study procedures

Blood viscosity measurements

Blood viscosity is measured in vitro using a Hemathix scanning capillary viscometer (King of Prussia, PA). Whole blood samples are collected by venipuncture, anti-coagulated using ethylenediaminetetraacetic acid (EDTA) and stored between 2 and 8 °C for a maximum of 4 days prior to analysis. Temperature of blood specimens are raised to 37 °C by the viscometer for 30 min and subjected to a range of shear rates through a U-shaped capillary in a single decelerating scan for complete viscosity assessment [23, 24]. High-shear BV is reported at a shear rate of 300 s−1 and low-shear BV at a shear rate of 5 s−1.

Laser Doppler flowmetry

Laser Doppler flowmetry, TBI and ABI are measured using the PeriFlux 5000 (Stockholm, Sweden) as previously described [22, 25]. Both feet were examined except in the setting of unilateral amputation. Measurements were made from the hallux and the four webs and following by TBI and ABI. A sum of flow measurements was calculated for each foot.

Safety assessments

Study participants had measurements of the complete blood count, electrolytes and liver function tests. At the time of each study encounter, potential adverse events of special interest, including bleeding complications, were reviewed [22].

Statistical analyses

The data were analyzed using a general linear model to account for the crossover nature of the study design, but incorporated the repeated-measure nature of the data. The variance–covariance matrix was initially assumed to have had compound symmetry, but other assumptions were considered. The main effects of the model include treatment period, sequence and the corresponding interactions. Analyses were conducted at the 5% significance level. All statistical analyses were performed using NCSS 12 Statistical Software (2018) (NCSS, LLC. Kaysville, Utah, USA,

Pre-planned contrasts comparing aspirin-ticagrelor with both ticagrelor and aspirin alone were used to evaluate the blood viscosity outcomes. These contrasts were evaluated using an experiment-wide multiple comparison procedure. Statistical considerations assumed that there was no carryover effect between treatments. In order to verify this assumption, evaluation of the treatment by period interactions was statistically tested.

The scanning capillary viscometer used in the proposed study was employed in an earlier study of 47 patients with hyperhomocysteinemia in addition to stable CVD or high CVD risk factors based on a Framingham score of > 20% [15]. In this prior CVD population, mean blood viscosity levels at a low shear rate of 5 s−1 were reported to be 9.98 ± 2.42 cP in the control group at baseline. A standard deviation of 2.42 cP for low-shear (5 s−1) blood viscosity was used throughout our sample size calculations. Separately, treatment by clopidogrel 75 mg daily for 3 weeks was reported to reduce viscosity levels by 0.6 cP and 5.0 cP at shear rates of 94.5 s−1 and 0.94 s−1, respectively [12]. Using this data, blood viscosity reduction of 2.0 cP by clopidogrel was interpolated for a shear rate of 5 s−1. This study was powered to detect a 2.0 cP difference in low-shear blood viscosity at a shear rate of 5 s−1, relative to aspirin 81 mg, with 90% power using a type I error rate of 5%. Combination aspirin-ticagrelor and low-dose aspirin control and separately, ticagrelor monotherapy and low-dose aspirin control were to be compared. This required about 72 patients in total.

The Institutional Review Board at the Icahn School of Medicine at Mount Sinai in New York, NY approved this study.


Baseline characteristics

A total of 70 participants with LEAD and type 2 diabetes were included in the final analysis population. The patient disposition throughout the trial is shown in Fig. 1. Baseline characteristics of the study population are presented in Table 2. Overall, the mean age was 72 years and 45% were women. The population was racially diverse with 58.6% Hispanic and 31.4% African American. T2DM was diagnosed for a mean 12.3 ± 10.1 years before study enrollment, 71.4% had a history of peripheral artery revascularization and 97.1% reported intermittent claudication symptoms (Additional file 1: Table S1). There was a significant burden of comorbidities in this population including 100% with diabetes including 40% on insulin, 91.4% with hypertension, 48.6% with current or former tobacco use. Most of the participants received guideline-recommended medications including 93% with statins (high-intensity 43%, moderate intensity 49%), 75% with angiotensin converting enzyme inhibitors/angiotensin receptor blockers (ACE-I/ARB) and 61% with beta-blockers. Anti-diabetic medications included 53% with metformin, 20% with sulfonylurea, 34% with DP4 inhibitor and 40% with insulin.

Fig. 1
figure 1

Flow of patients throughout the trial

Table 2 Baseline characteristics of study participants

Effect of trial regimen on blood viscosity

At baseline, mean low shear BV was 11.1 ± 2.1 cP and high shear BV was 4.0 ± 0.6 cP (Table 2). When compared with aspirin monotherapy, treatment with ticagrelor either with or without aspirin reduced low shear BV by 14.2% and 13.9%, respectively, and reduced high shear BV by 5% in either case, while aspirin monotherapy increased low shear BV by 9.3% and high shear BV by 3.4% (p < 0.0001 for either high or low hear BV comparisons) (Fig. 2). There were no significant differences in BV between the groups treated with ticagrelor and ticagrelor with aspirin. There also were no significant interactions between the assignment to treatment arm and change in blood viscosity (Additional file 1: Table S2).

Fig. 2
figure 2

Mean levels of blood viscosity measured at low shear and high shear rate in patients treated with aspirin monotherapy, ticagrelor monotherapy and combined aspirin and ticagrelor therapy

Effect of trial regimen on microvascular blood flow

Combined therapy with ticagrelor and aspirin increased MBF in the left foot compared to the other two treatments (p = 0.02). Changes in MBF in the right foot were not significant (p = 0.25). The use of temperature change to assess microvascular blood vessel recruitment was not significant in either the left or right foot (Additional file 1: Table S2). In this trial, baseline blood viscosity was not associated with a change in MBF (Additional file 1: Table S2). The change in blood viscosity did not correlate with change in MBF.

The overall coefficient of variation for MBF measurements was on the order of 70%. This calculation was made on the baseline MBF measurements in the left and right feet at the time of randomization into each of the three treatment arms.


One study participant developed dyspnea on treatment with aspirin and ticagrelor. These symptoms resolved within 24 h after discontinuing study medication. There were no major or minor hemorrhagic complications or differences in hemorrhagic complications in the treatment groups.


Among patients with symptomatic LEAD and long-standing type 2 diabetes, blood viscosity was lower when treated with ticagrelor alone or the combination of ticagrelor and aspirin than treatment with aspirin alone. MBF tended to be higher with combined treatment of ticagrelor and aspirin. These benefits were observed in the context of background care that included extensive use of evidence based treatments. The absolute benefit of ticagrelor with respect to the primary end point was not influenced by baseline blood viscosity.

Over the duration of this three-arm crossover trial, one patient discontinued therapy due to dyspnea. After unblinding of the trial, this subject was assigned to ticagrelor monotherapy. A total of eight participants did not complete the trial, including two patients who had urgent peripheral artery revascularization that required a prescription for P2Y12 antagonist, and six persons who were unable to complete the study schedule timelines.

The overall findings of Hema-kinesis should be placed in the context of advanced disease of the study population. Nearly three-fourths of participants had prior peripheral artery revascularization and nearly all study participants reported intermittent claudication. After peripheral artery revascularization, many patients with LEAD have repeat outpatient endovascular revascularization procedures or limb-related and cardiovascular hospitalizations within the subsequent year [26]. The most important comorbidities associated with 1-year hospitalization in the Premier Healthcare Database included diabetes, current/former smoking, hypertension and renal insufficiency. The current study includes 71.4% patients with prior revascularization who had many high-risk characteristics for MALE and cardiovascular events. Hema-kinesis selected patients with diabetes, and included 48.6% current/former smokers, 91.4% with hypertension, 31.4% with human immunodeficiency virus infection and 14.3% with renal insufficiency.

Microvascular disease is influenced by perturbations in blood rheology, endothelial dysfunction, impaired angiogenesis, hypofibrinolysis and systemic inflammation [27,28,29]. Although we did not measure fibrinolytic biomarkers, blood viscosity is an integrated measure of thrombosis [10]. In Hema-kinesis, blood viscosity at low shear rates was significantly reduced in ticagrelor-treated patients. Comorbidities and risk factors for LEAD have varying influence on blood viscosity and microvascular disease. Cigarette smokers have higher blood viscosity, calculated from plasma viscosity and hematocrit, than ex-smokers or former smokers. Active cigarette smoking reduced blood fluidity, an effect reversed 3 months after smoking cessation [30]. Among patients with diabetes, microvascular disease may cause neuropathy and neuropathic ulcers [27, 31] (Table 3).

Table 3 Baseline laboratory values of study participants

Elevations in blood viscosity > 4.5 cP measured at a rate of 230 s−1 were reported in 25–30% of patients with LEAD [25]. LEAD patients with hyperviscosity had shorter mean claudication distance and worse prognosis than claudicants with lower blood viscosity [25]. This study sought to explore the relationship between reductions in BV and MBF with ticagrelor in patients with diabetes and LEAD. An increase in MBF was observed with ticagrelor treatment. In order to explore whether there was a threshold of elevated blood viscosity that might identify higher risk subjects as proposed by Dormandy [9], we report that treatment with ticagrelor and aspirin lowered high shear blood viscosity to less than 4.5 cPs in about 50%; however, the improvement in MBF was statistically significant in the left foot and trended lower in the right foot. Changes in MBF were not different in patients stratified by tertiles of low shear or high shear blood viscosity. We acknowledge the large variability in LDF measurements may have influenced a meaningful treatment effect.

We compared the effects of ticagrelor with aspirin, an agent that has no effect on blood viscosity [24]. The reduction in blood viscosity with ticagrelor may be partially mediated by adenosine-mediated actions [16]. In an open-label study of 45 participants with coronary artery disease, the use of ticagrelor improved microvascular endothelial function as assessed by the reactive hyperemia index measured by plethysmography on the index finger of the hand. The improvement in reactive hyperemia was observed at the peak (2 h) concentration of ticagrelor and not at trough (12 h) levels. Another open-label study of 72 participants with coronary artery disease showed that 21 days treatment with ticagrelor was more effective than clopidogrel for improving microvascular endothelial function [19]. In patients with COPD undergoing coronary PCI, ticagrelor, but not clopidogrel reduced circulating epidermal growth factor levels and release of endothelial nitric oxide synthase (eNOS) from cultured human umbilical vein endothelial cells [32]. The authors suggest that by lowering EGF levels, ticagrelor improves endothelial function by activation of eNOS.

Anti-platelet therapy has been considered a mainstay of treatment for LEAD [33, 34]. The Examining Use of Ticagrelor in Peripheral Artery Disease (EUCLID) trial reported no difference in cardiovascular outcomes or acute ischemic limb events in patients without and with diabetes. In EUCLID, the cardiovascular event rate was higher in the 38.5% of patients with versus without diabetes 15.9% versus 10.4%, adjusted hazard ratio 1.56 [95% CI 1.41 to 1.72] [35]. Subsequently, THEMIS (The Effect of Ticagrelor on Health Outcomes in diabEtes Mellitus patients Intervention Study) investigated the efficacy of aspirin and ticagrelor 60 mg twice daily versus aspirin alone on major adverse cardiovascular events in patients with coronary artery disease and type 2 diabetes who had no prior myocardial infarction or stroke [36]. In a press announcement, the trial sponsor reported a significant reduction in major adverse cardiovascular events (Brilinta reduced cardiovascular events in patients with no prior heart attack or stroke. Press release AstraZeneca 25 February 2019 07:00 GMT). The use of vorapaxar, a protease-activated receptor antagonist, added to background treatment with aspirin, P2Y12 inhibitors or both, reduced acute limb ischemia and limb revascularization [37]. Low-dose rivaroxaban and aspirin was more effective than aspirin alone for reducing major adverse limb events including ischemia within 30 days or ischemic amputation [38].

Strengths and limitations

Several strengths of this trial include the use of a randomized, double-blind, double-dummy, controlled crossover trial design in which all study participants received each treatment. A crossover design was a crucial aspect of mechanistic trial that eliminates differences in patient characteristics. Due to the effects of cigarette smoking on blood viscosity and blood fluidity, none of the study participants changed their smoking behavior during the course of the trial. Limitations of a crossover trial requires a longer time commitment from study participants. During the course of the trial, two participants required urgent revascularization for ischemic ulcers. A total of 12 participants did not meet study timelines, and were not exposed to all three treatments. Microvascular blood flow was measured by laser Doppler flowmetry; however, we found this method highly variable. The variability in microvascular blood flow measurements reduced the ability to consistently ascertain the effects of blood viscosity reductions on this functional parameter. Mahe et al. reported a coefficient of variation of 40% for the local thermal hyperemia peaks using the laser speckle contrast imager and LDF.


This trial supports the use of targeted anti-platelet therapy with ticagrelor in patients with LEAD. Further research is needed to investigate the contribution of ticagrelor as therapy for the prevention of microvascular complications of diabetes. More robust methods for the assessment of microvascular blood flow in the lower extremities are needed for evaluation of microvascular complications.

Availability of data and materials

The data are available for review by external regulatory agencies by prior written consent.



ankle brachial index


blood viscosity


equilibrative nucleoside transporter 1


laser Doppler flowmetry


lower extremity arterial disease


major adverse limb events


microvascular blood flow


type 2 diabetes mellitus


toe-brachial index


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This investigator-initiated trial was funded by an unrestricted grant to the Icahn School of Medicine from AstraZeneca (Grant Number ISSBRIL0174/D5130L00060).

Author information

Authors and Affiliations



RSR designed the trial, analyzed the data and wrote the manuscript. QC performed the study procedures, analyzed the data and wrote the manuscript. SDN and DJC designed the trial, analyzed the data and contributed to the writing of the manuscript. PK participated in study recruitment, analyzed the data and contributed to writing of the manuscript. MLL analyzed the data and contributed to writing of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Robert S. Rosenson.

Ethics declarations

Ethics approval and consent to participant

The Institutional Review Board at the Icahn School of Medicine at Mount Sinai in New York, NY approved this study.

Consent for publication

The manuscript was submitted to the sponsor for review before submission. The analysis of data and decision to publish these data were the sole decision of the investigators.

Competing interests

Dr. Rosenson receives grant funding from Akcea, Amgen, AstraZeneca, Medicines Company and Regeneron. At the time of funding for this trial, he attended an Advisory Board for AstraZeneca. He receives consulting fees and honoraria from Amgen, C5, CVS Caremark and Kowa; royalties from UpToDate, Inc. and holds stock in MediMergent LLC. Dr. Chen and Mr. Najera report no relevant conflicts of interest. Dr. Krishnan receives consultanting fees Medtronic and Abbott. Dr. Lee and Mr. Cho receive consulting fees from Rheovector LLC.

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Additional file

Additional file 1: Table S1.

Characteristics of peripheral artery disease in study participants. Table S2. Results of ABI, TBI and LBF in study participants.

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Rosenson, R.S., Chen, Q., Najera, S.D. et al. Ticagrelor improves blood viscosity-dependent microcirculatory flow in patients with lower extremity arterial disease: the Hema-kinesis clinical trial. Cardiovasc Diabetol 18, 77 (2019).

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  • Lower extremity arterial disease
  • Microvascular disease
  • Blood viscosity
  • Type 2 diabetes
  • Ticagrelor