Essential Hypertension
Conditions
Keywords
essential hypertension, colchicine, vascular function, vascular compliance, blood pressure
Brief summary
In this project the potential beneficial effect of the drug colchicine on vascular reactivity and blood pressure will be assessed. Colchicine is a commonly used anti-inflammatory medication approved for the treatment of gout, Familial Mediterranean Fever and pericarditis in Denmark. The current project idea is based on accumulating evidence in the literature for a beneficial role of colchicine treatment in the prevention of cardiovascular disease in parallel with novel mechanistic insight from our own research. Recently, colchicine was associated with a lower risk of cardiovascular disease, including reduced myocardial infarctions, strokes and acute coronary syndrome . However, none of these trials have investigated the effect of colchicine on arterial tone or stiffness, changes to which may underlie the reduced risk of cardiovascular disease associated with colchicine. In support of the hypothesis that colchicine will improve vascular reactivity, a study in 1985 by Lagrue et al. found that daily, low-dose colchicine improved arterial stiffness in a small cohort of hypertensive patients. More recently, colchicine was shown to improve arterial stiffness in patients with Familial Mediterranean fever supporting a cardiovascular protective role of colchicine. Finally, colchicine is also proposed to have anti-inflammatory effects in the vascular system.
Detailed description
In this project w the potential beneficial effect of the drug colchicine on vascular reactivity and blood pressure is evaluated. Colchicine is a commonly used anti-inflammatory medication approved for the treatment of gout, Familial Mediterranean Fever and pericarditis in Denmark. The current project idea is based on accumulating evidence in the literature for a beneficial role of colchicine treatment in the prevention of cardiovascular disease in parallel with novel mechanistic insight from research of the investigators. Recently, colchicine was associated with a lower risk of cardiovascular disease, including reduced myocardial infarctions, strokes and acute coronary syndrome. However, none of these trials have investigated the effect of colchicine on arterial tone or stiffness, changes to which may underlie the reduced risk of cardiovascular disease associated with colchicine. In support of thehypothesis that colchicine will improve vascular reactivity, a study in 1985 by Lagrue et al. found that daily, low-dose colchicine improved arterial stiffness in a small cohort of hypertensive patients. More recently, colchicine was shown to improve arterial stiffness in patients with Familial Mediterranean fever supporting a cardiovascular protective role of colchicine. Finally, colchicine is also proposed to have anti-inflammatory effects in the vascular system.
Interventions
patients with essential hypertension are randomized to receive either 3 weeks of colchicine
patients with essential hypertension are randomized to receive either 3 weeks of placebo-treatment
Sponsors
Study design
Masking description
Subjects are blinded and randomized to receive either colchicine-treatment or placebo
Intervention model description
Single blinded randomized placebo-controlled intervention
Eligibility
Inclusion criteria
* Diagnosed with essential hypertension * BMI\<30 * blood pressure (sys/dia) ≥120 mmhg and/or ≥80 mmhg while on hypertensive medication OR * blood pressure (sys/dia) ≥130 mmhg and/or ≥85 mmhg without hypertensive medication
Exclusion criteria
* smoking * excessive alcohol use * chronic diseases (beside essential hypertension)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in vascular function with treatment measured as flowchanges with ultrasound doppler in response to infusions of isoprenaline | Change in vascular conductance in response to infusions is assessed after acute treatment and before and within 72 hours after the 3 weeks of colchicine or placebo treatment | Infusions of isoprenalin in the brachial artery, measurement of blood flow with ultrasound doppler and intraarterial blood pressure with an intraarterial transducer for the calculation of leg vascular conductance |
| Changes in vascular function with training measured as flowchanges with ultrasound doppler divided by changes in blood pressure measured with intraarterial canula, in response to infusions of acetylcholine | Change in vascular conductance in response to infusions is assessed after acute treatment before and within 72 hours after the 3 weeks of colchicine or placebo treatment | Infusions of acetylcholine in the brachial artery, measurement of blood flow with ultrasound doppler and intraarterial blood pressure with an intraarterial transducer for the calculation of leg vascular conductance |
| Changes in vascular function with training measured as flowchanges with ultrasound doppler divided by changes in blood pressure measured with intraarterial canula, in response to infusions of sodium nitroprusside | Change in vascular conductance in response to infusions is assessed after acute treatment and before and within 72 hours after the 3 weeks of colchicine or placebo treatment | Infusions of sodium nitroprusside in the brachial artery, measurement of blood flow with ultrasound doppler and intraarterial blood pressure with an intraarterial transducer for the calculation of leg vascular conductance |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Blood pressure | Measurements are made before and after 3 weeks of treatment with colchicine or placebo. | Blood pressure measured at home with an automated blood pressure device |
| Vascular compliance | Measurements are made before and after 3 weeks of treatment with colchicine or placebo. | measured by intraarterial blood pressure and changes in arterial diameter by ultrasound doppler |
Countries
Denmark