Abstract

BackgroundArterial and venous thrombosis may share common pathophysiology involving the activation of platelets and inflammatory mediators. A growing body of evidence suggests prothrombotic effect of renin angiotensin system (RAS) including vascular inflammation and platelet activation. We hypothesized that the use of angiotensin converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) plays a role in protecting against venous thromboembolism (VTE) in patients atherosclerosis.MethodsWe conducted a retrospective study, reviewing 1,100 consecutive patients admitted to a teaching hospital with a diagnosis of either myocardial infarction or ischemic stroke from 2005 to 2010. Patients who had been treated with anticoagulation therapy before or after the first visit were excluded. The occurrence of VTE during the follow up period, risk factors for VTE on admission, and the use of ACEIs or ARBs during the follow up period were recorded.ResultsThe mean age of the entire study population was 68.1 years. 52.0% of the patients were female and 76.5% were African American. 67.3% were on RAS inhibitorsThe overall incidence of VTE was 9.7% (n = 107). Among the RAS inhibitor users, the incidence of VTE events was 9.0% (54/603) for the ACEI only users, 7.1% (8/113) for the ARB only users, and 0% (0/24) for the patients taking combination of ACEI and ARB. Among patients on RAS inhibitors, 8.4% (62/740) developed a VTE, compared with 12.5% (45/360) in the nonuser group [HR (hazard ratio), 0.58; 95% CI (confidence interval), 0.39–0.84; P<0.01]. Even after controlling for factors related to VTE (smoking, history of cancer, and immobilization, hormone use) and diabetes, the use of RAS inhibitors was still associated with a significantly lower risk of developing VTE (AHR, 0.59; 95% CI, 0.40–0.88; P = 0.01).ConclusionsThe use of RAS inhibitors appears to be associated with a reduction in the risk of VTE.

Highlights

  • Venous thromboembolism (VTE) is a serious condition affecting approximately 2 persons per 1000 each year [1,2]

  • Internleukin-6 (IL-6), IL-8 and tumor necrosis factor alpha (TNF-a) released by the inflammatory cells present in the atherosclerotic plaques [3,4] are found to be elevated in patients with venous thrombosis [5,6]

  • After controlling for factors related to venous thromboembolism (VTE), age and diabetes, the use of renin angiotensin system (RAS) inhibitors was still associated with lower risk of developing VTE

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Summary

Introduction

Venous thromboembolism (VTE) is a serious condition affecting approximately 2 persons per 1000 each year [1,2]. Pathophysiology of venous thromboembolism (VTE) was thought to be different from thrombotic atherosclerosis. Inflammatory cytokines play an important role in both venous and arterial thrombosis. Internleukin-6 (IL-6), IL-8 and tumor necrosis factor alpha (TNF-a) released by the inflammatory cells present in the atherosclerotic plaques [3,4] are found to be elevated in patients with venous thrombosis [5,6]. Platelet activation and adhesion plays a role in arterial thrombosis and in venous thrombosis. Arterial and venous thrombosis may share common pathophysiology involving the activation of platelets and inflammatory mediators. We hypothesized that the use of angiotensin converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) plays a role in protecting against venous thromboembolism (VTE) in patients atherosclerosis

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