• Plasma norepinephrine
  

• 1. Seated blood pressure
  
• 2. 24h ambulatory blood pressure
  
• 3. Spectral analysis of heart rate (LF, HF, LF/HF)
  
• 4. Plasma
  
• a. renin
  
• b. aldosterone
  
• c. angiotensin II
  
• d. catecholamines
  
• e. 8-epi-isoprostane
  
• f. Thiobarbituric acid reactive substances (TBARS)
  
• g. nitrotyrosine
  
• h. interleukin 18
  
• i. E selectine
  
• j. C reactive protein
  
• k. Insulin
  
• l. glucose
  
• 5. Urine
  
• a. 8-epi-isoprostane
  

INTRODUCTION.

Three large clinical trials (STOP-2, HOPE, LIFE) {Hansson, Lindholm, et al. 1999}{Dahlof, Devereux, et al. 2002}{Yusuf, Sleight, et al. 2000} have suggested that drugs that specifically inhibit the renin angiotensin system (RAS) such as ACE inhibitors and Angiotensin Receptor Antagonists (ARA) have blood pressure-independant cardiovascular protecting effects. In the most recent of these studies, the LIFE trial, Losartan-based therapy was superior to atenolol-based therapy in hypertensive patients with left ventricular hypertrophy {Dahlof, Devereux, et al. 2002}. Very recently, the ALLHAT mega-trial suggested that diuretics were as good as ACE inhibitors for cardiovascular protection in hypertensive patients {Major outcomes in moderately hypercholesterolemic, hypertensive patients randomized to pravastatin vs usual care: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-LLT)}. These apparently conflicting results underline that the mechanisms of cardiovascular protections are not well understood.

ARAs {Balt, Mathy, et al. 2001}{Moreau, Richer, et al. 1993} have sympathoinhibitory properties while beta-blockers induce a small counterregulatory activation of the sympathetic system {Lijnen, Amery, et al. 1979}{Sundlof, Wallin, et al. 1983}{van den Meiracker, Man in 't Veld AJ, et al. 1988}.We have shown recently that telmisartan prevents the increase in NE normally associated with a reduction in BP while there are reports that diuretics tend to stimulate the sympathetic system {Fernandez, Snedden, et al. 1987}{Lake, Ziegler, et al. 1979}. It has been suggested that the superiority of ARAs could be due to their unique effects on the autonomic nervous system.

Angiotensin II receptor antagonism also decrease the oxidative stress induced by angiotensin II and aldosterone {de Cavanagh, Ferder, et al. 1999}{Hornig, Landmesser, et al. 2001}{Onozato, Tojo, et al. 2002}.We have also shown that telmisartan decreases plasma aldosterone and should therefore decrease the oxidative stress associated with a reduction in aldosterone Hydrochlorothiazide and beta-blockers have not been shown to have antioxidative properties {Welch & Wilcox 2001}{Taddei, Virdis, et al. 2001}. It is possible that oxidative stress partly explains the differences between pharmacological agents.

Patients included in high blood pressure clinical trials are randomized to a therapeutic strategy meaning that a stepped care approach is taken. Hypertensive patients frequently need more than one drug for appropriate blood pressure control. Consequently, about half of study patients in these trials end up taking more than one drug during the study. First step therapy is by definition prescribed to all study subjects but second or third step therapy are not as well defined. In the HOPE trial, ramipril was added on top of usual treatment. Most of the patients included in HOPE, LIFE, STOP-2 and ALLHAT took at least one other antihypertensive drug, most frequently a thiazide diuretic. Though results were reported as being ACE inhibitor or ARA based, they mostly reflect a mix of single drug and multiple drugs therapy. Whether the beneficial effects of ARAs and beta-blockers are modulated by thiazide diuretics is presently unknown.

We designed a parallel study that primarily assesses the differences between ARAs, diuretics and beta-blockers. The simultaneously measured parameters reflect renin-angiotensin system activity, sympathetic activity, oxidative stress and systemic inflammation. Secondarily, this study assesses the effects of ARA-diuretic and B-blocker-diuretic combinations on the same parameters.

Results from this study will help to understand the results from the previously mentioned clinical trials. The forced titration from monotherapy to a combination therapy will allow us to measure the influence of drug addition on clinically significant parameters. The simultaneous assessment of renin-angiotensin system activity , sympathetic activity, oxidative stress and systemic inflammation will allow us to observe baseline and pharmacologically-induced associations.

It is also probable that results from this study will have direct clinical influences on high blood pressure therapeutic strategies. Physicians treating hypertension frequently have to choose between increasing drug doses to their maximum or adding a new drug. It is presently unknown if one strategy offers more benefits than the other. This study should provide physicians with clues about the expected benefits for each approach.

GOALS

To assess and compare the effects of candesartan and atenolol combined with low dose diuretic therapy on the autonomic nervous system, on oxidative stress, on inflammatory markers, and on the renin-angiotensin system.

To assess and compare the effects of candesartan and atenolol and low dose diuretic therapy on the autonomic nervous system, on inflammatory markers, on oxidative stress, on inflammatory markers, and on the renin angiotensin system.

PRIMARY OBJECTIVE:

1. To measure and compare the effects candesartan 16 mg + HCT 12.5 mg, candesartan 16 mg + HCT 25.0 mg, and atenolol 100 + 12.5 mg on noradrenalin release 4h post-dose, at trough, and after a 10 minute stand.

SECONDARY OBJECTIVES:

1. To measure and compare the effects candesartan 16 mg + HCT 12.5 mg, candesartan 16 mg + HCT 25.0 mg, and atenolol 100 + 12.5 mg on :

   1. frequency power spectral analysis 4h post-dose, and after a 10 minute stand.
   2. oxidative stress, inflammatory markers and adhesion molecules 4h post-dose.
   3. renin, aldosterone and angiotensin II release/production 4h post-dose and at trough.
   4. Insulin and glucose plasma concentration

2. To measure and compare the influences of HCT 25 mg, candesartan 16 mg, and atenolol 100 mg monotherapy on:

   1. noradrenalin release 4h post-dose, at trough, and after a 10 minute stand.
   2. frequency power spectral analysis 4h post-dose, and after a 10 minute stand.
   3. oxidative stress, inflammatory markers and adhesion molecules 4h post-dose.
   4. renin, aldosterone and angiotensin II release/production 4h post-dose and at trough.
   5. Insulin and glucose plasma concentration

DESIGN

Prospective, randomized, open label, 3 arm, 2 period parallel study preceded by a placebo run in period in non-diabetic patients with essential hypertension.

Titration period: introduction of hydrochlorothiazide (12.5 mg daily), atenolol (50 mg daily), and candesartan (8 mg daily) in the diuretic, beta-blocker and angiotensin receptor blocker groups respectively. First study period (4 weeks), comparison of hydrochlorothiazide 25 mg, atenolol 100 mg, and candesartan 16mg. Second study period (4 weeks), comparison of hydrochlorothiazide 25 mg + candesartan 16 mg, atenolol 100 mg + HCT 12.5 mg, and candesartan 16mg + HCT 12.5 mg. Measurement of study parameters at trough, 4h post-dose and after a 10 minutes stand after placebo and after each study period.

MEASURED STUDY PARAMETERS

1. Blood pressure
2. 24h blood pressure
3. Spectral analysis of heart rate (LF, HF, LF/HF)

4. Plasma

   1. renin
   2. aldosterone
   3. angiotensin II
   4. catecholamines
   5. 8-epi-isoprostane
   6. Thiobarbituric acid reactive substances (TBARS)
   7. nitrotyrosine
   8. interleukin 18
   9. E selectine
   10. C reactive protein
   11. Insulin
   12. glucose

5. Urine

   1. 8-epi-isoprostane
   2. sodium concentration
   3. creatinine concentration

Protocol Sponsored by Astra Zeneca Canada