Inflammation and Coronary Artery Disease. Role of AT1-Receptor Antagonism

Condition(s) targeted: Hypertension; Coronary Arteriosclerosis

Intervention: telmisartan 40 mg (Drug); placebo 40 mg (Drug)

Phase: Phase 4

Status: Completed

Sponsored by: Boehringer Ingelheim Pharmaceuticals

Official(s) and/or principal investigator(s):
Boehringer Ingelheim Study Coordinator, Study Chair, Affiliation: B.I. Pharma GmbH & Co. KG

Cardiovascular diseases, especially coronary artery disease, are the most common cause for death in industrialized nations. In coronary artery disease endothelial cell damage and an increased number of monocytes/macrophages and T lymphocytes infiltrating the arterial wall form atherosclerotic lesions. Furthermore, an enhanced migration and proliferation of vascular smooth muscle cells can be demonstrated in the early stages of atherosclerosis. In this process inflammatory events contribute to the progression of atherosclerotic lesions and to the development of unstable plaques. In atherogenesis and especially in unstable rupturing plaques the renin angiotensin system is of considerable significance. In atherosclerotic lesions ACE and AT1 receptor expression is upregulated influencing not only endothelial cells but also macrophages and lymphocytes. ACE inhibition and AT1 receptor antagonism are accompanied by a marked reduction of atherogenesis. The aim of this trial is to assess the efficacy and tolerability of telmisartan (Micardis®, Germany) after one dose daily in patients with hypertension and coronary heart disease. This investigation is intended to test not only the effect on the blood pressure but also whether telmisartan has any effect on inflammatory parameters associated with coronary heart disease.

Official title: Pilot Study: Inflammation and Coronary Artery Disease. Role of AT1 Receptor Antagonism

Study design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study

Primary outcome: Alterations in the inflammatory parameters: hsCRP, IL-6, IL-10, sICAM-1, TNF-alpha, MCP-1, LFA, MAC-1, L- selectin, FcyRIII and PECAM-1

Secondary outcome: Alterations of clinical parameters such as clinical outcome, and changes in blood pressure. Safety and tolerability in terms of incidence and severity of adverse events, changes in physical examination, heart rate, laboratory parameters, and 12-lead-ECG.

Detailed description: Methodology: Randomised, double-blind and placebo-controlled parallel group design Planned/actual number of subjects: Enrolled: 40/50 randomised: 40/42 completed: 40/42 Diagnosis and main criteria for inclusion: Treated esssential hypertension with a mean seated DBP/SBP smaller than 95mmHg/ 160mmHg, coronary artery disease confirmed by catheterization and age equal or greater than 18 years of age Duration of treatment: 12 weeks: telmisartan 40 mg or placebo 40 mg Study Hypothesis: The statistical null hypothesis is that in patients with CAD and mild-to-moderate hypertension a 84 day therapy with 40 mg telmisartan causes changes in inflammatory and leukocyte adhesion parameters. The alternative hypothesis is that this therapy does not influence inflammatory and leukocyte adhesion parameters. This hypothesis is tested by the nonparametric Wilcoxon test for unpaired samples. Comparison(s): Placebo 40 mg

Minimum age: 19 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

INCLUSION CRITERIA Treated essential hypertension with a mean seated DBP < 95 mm Hg and a mean seated SBP < 160 mm Hg at the randomisation visit (baseline) Coronary artery disease confirmed by cardiac catheterization > 18 years of age Ability to stop current antihypertensive therapy with ACE inhibitors, angioten-sin II receptor antagonist or lipid lowering therapy with statines without risk to the patient in the run-in period of two to four weeks and during the study period. Ability to provide written informed consent. EXCLUSION CRITERIA Acute coronary syndromes Acute or chronic heart failure (left ventricular ejection fraction < 45 %) Symptomatic valvular heart disease Inflammatory diseases (e. g. acute infection, rheumatic diseases, collagenosis) Pre-menopausal women (last menstruation < 1 year prior to start of run-in period) who: are not surgically sterile; and/or are nursing are of child-bearing potential and are NOT practicing acceptable means of birth control, do NOT plan to continue using this method throughout the study and do NOT agree to submit to periodic pregnancy testing during participation in studies of > 3-months duration. Acceptable methods of birth control include oral, implantable or injectable contraceptives. Known or suspected secondary hypertension Mean sitting SBP > 160 mm Hg or mean sitting DBP > 95 mm Hg during any visit Hepatic and/or renal dysfunction as defined by the following laboratory parameters: SGPT(ALT) or SGOT(AST) > than 2 times the upper limit of normal range Serum creatinine > 2. 3 mg/dL Bilateral renal artery stenosis, renal artery stenosis in a solitary kidney, patients post-renal transplant or with only one kidney Clinically relevant hypokalaemia or hyperkalaemia Uncorrected volume depletion Uncorrected sodium depletion Primary aldosteronism Hereditary fructose intolerance Biliary obstructive disorders Patients who have previously experienced symptoms characteristic of angioedema during treatment with ACE inhibitors or angiotensin II receptor antagonists History of drug or alcohol dependency within 6 months Chronic administration of any medications known to affect blood pressure, except medication allowed by the protocol (cf. 4. 2.1) Current participation in another trial, or participation in a trial within a period of one month Known hypersensitivity to any component of the formulation Has no contra-indication to a placebo run-in period (e. g. recent stroke or MI) Any other clinical condition which, in the opinion of the principal investigator, would not allow safe completion of the protocol and safe administration of telmisartan

Universitätsklinik des Saarlandes, Homburg/Saar 66421, Germany

Starting date: December 2001
Ending date: May 2004
Last updated: January 12, 2007