CClinicalTrials.gg
CompletedNCT00818779Updated Dec 5, 2017Results posted

Direct Renin Inhibition Effects on Atherosclerotic Biomarkers

A Phase 4 interventional study of Aliskiren and Amlodipine in Coronary Artery Disease and Type 2 Diabetes Mellitus, sponsored by Texas Tech University Health Sciences Center. Completed at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2017-12-05.

Sponsored by Texas Tech University Health Sciences Center · Phase 4, Interventional, and Other

Phase
Phase 4
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The investigators aim to assess if a new blood pressure medication, aliskiren, reduces various biomarkers of heart disease found in the blood in patients with a history of both heart disease and type 2 diabetes. The primary hypothesis is that aliskiren will reduce these biomarkers compared to a calcium channel blocker.

Read the detailed description

Agents that attenuate the renin angiotensin system (RAS), i.e. angiotensin converting enzyme inhibitors (ACE-Is) and angiotensin receptor blockers (ARB), have shown to have therapeutic benefit in a variety of cardiovascular disorders. ACE-Is are considered standard of care for secondary prevention of CAD by the AHA/ACC. Based on the HOPE study, the beneficial effects of ACE-Is in patients at high risk for cardiovascular outcomes may be beyond mere blood pressure control. In addition to their effects on blood pressure, aldosterone, and sodium and water absorption, blockade of the RAS with ACE-Is or ARBs alter key biomarkers of vascular inflammation, vascular endothelial function, and fibrinolytic balance. These surrogate biomarkers are thought to play a role in the progression of atherosclerosis. Biomarkers of vascular inflammation include vascular and intracellular cell adhesion molecule (VCAM and ICAM respectively) and c-reactive protein (CRP). Markers of endothelial function include endothelin-1 (ET-1) and the vasodilator nitric oxide (NO). Plasminogen activator inhibitor-1 (PAI-1) is a prothrombotic marker associated with plaque proliferation and atherosclerosis progression.

ACE-Is block the conversion of angiotensin 1 (Ang 1) to angiotensin 2 (Ang 2). "ACE escape" may attenuate the influence of ACE-Is despite proven benefits in clinical trials.

Aliskiren is the first direct renin inhibitor approved by the FDA for the treatment of hypertension. It is a very specific and potent inhibitor of human renin. As such it may offer an advantage over ACE-I and ARB therapy as it blocks the rate limiting step of the RAS. It does not show a compensatory increase in RAS activity noted with ARBs or non-ACE production of Ang 2 as seen with ACE-Is. Aliskiren appears to have additive blood pressure lowering effects when added to ACE-I or ARB therapy.

A very commonly prescribed antihypertensive, the dihydropyridine calcium channel blocker amlodipine, has a synergistic effect on lowering BP when used with an ACE-I. It has been shown to have mixed effects on atherosclerotic biomarkers in a variety of subjects. Type 2 diabetes affects many of the atherosclerotic markers described above and as such can be a confounding variable in research involving these biomarkers.

With the addition of a new therapeutic agent that affects the RAS, its different pharmacodynamic effects on the RAS compared to ACE-I and ARB therapy, and that Ang 2 levels are not fully blocked by ACE-I therapy, it is critical to better understand how the new class of direct renin inhibitors may influence atherosclerotic biomarkers in patients with a variety of cardiovascular disorders. The objectives of this application are to determine whether the direct renin inhibitor, aliskiren, affects atherosclerotic biomarkers in patients with stable coronary artery disease and diabetes currently receiving standard ACE-I therapy and if aliskiren has a more favorable effect on these markers compared to the calcium antagonist amlodipine.

Large clinical trials have proven the benefit of RAS blockade in reducing cardiovascular morbidity and mortality. The significance of this research is that more information is needed to better understand how antihypertensive agents, particularly those that block the RAS, reduce cardiovascular disease beyond blood pressure reduction alone. Research that elucidates how agents may reduce atherosclerosis is very important to help better target drug therapy to a condition that is the leading cause of death in this country.

02

Conditions studied

  • Coronary Artery Disease
  • Type 2 Diabetes Mellitus

Keywords

  • diabetes
  • heart disease
  • atherosclerosis
03

In context

Coronary Artery Disease

5,596 studies on the registry are indexed under Coronary Artery Disease; 955 are open to participants now.

This study's enrollment of 38 is below the median of 123 across 3,435 interventional studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

Texas Tech University Health Sciences Center is the lead sponsor of 97 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of type 2 diabetes
  • Diagnosis of coronary artery disease
  • Currently receiving therapy with an ACE-Inhibitor or Angiotensin Receptor Blocker
  • Currently receiving antiplatelet therapy and statin therapy
  • Baseline blood pressure > 100/75 mm Hg
  • BMI 25-35 kg/m2

Exclusion criteria

Exclusion Criteria:

  • Concurrent calcium channel blocker therapy
  • Documented peripheral edema
  • Hyperkalemia
  • Serum creatinine > 2.0
  • Diagnosed with proteinuria
  • Diagnosed with liver dysfunction or serious rheumatological disorder
05

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
38 participants (actual)

Study arms

  • Experimental
    Aliskiren

    Aliskiren 150-300 mg once daily

    Drug: Aliskiren

  • Active comparator
    Amlodipine

    5-10 mg amlodipine once daily

    Drug: Amlodipine

Interventions

  • DrugAliskiren

    150 - 300 mg once daily for 6 weeks

    Also known as: Tekturna

  • DrugAmlodipine

    5-10 mg once daily for 6 weeks

    Also known as: Norvasc

06

What researchers measure

Primary outcomes

  1. Plasminogen Activator Inhibitor 1

    Plasminogen Activator Inhibitor 1 is a biomarker found in serum that indirectly assesses blood clotting activity. Lower PAI-1 levels are thought to be better than higher levels. The primary outcome is mean change from baseline and can include negative numbers as a result.

    Time frame: 6 weeks (change from baseline)

Secondary outcomes

  1. Serum Level of Vascular Cell Adhesion Molecule

    Surrogate biomarker cardiovascular risk

    Time frame: 6 week (change from baseline)

  2. Serum Level of Intracellular Cell Adhesion Molecule

    Surrogate biomarker of cardiovascular risk

    Time frame: 6 week (change from baseline)

  3. Serum Level of C-reactive Protein

    Surrogate biomarker of cardiovascular risk

    Time frame: 6 week (change from baseline)

  4. Serum Level of Nitric Oxide

    Surrogate biomarker of cardiovascular risk

    Time frame: 6 week (change from baseline)

07

Results

Posted Nov 19, 2012
Limitations and caveats
Small sample size led to large standard deviation in biomarkers assessed and limited power to detect a diffference

Participant flow

Participant flow — Overall Study
MilestoneAliskirenAmlodipine
Started2216
Completed1615
Not completed61
Withdrew: Protocol violation10
Withdrew: Lost to follow-up10
Withdrew: Adverse event41

Outcome measures

PrimaryPlasminogen Activator Inhibitor 1

Plasminogen Activator Inhibitor 1 is a biomarker found in serum that indirectly assesses blood clotting activity. Lower PAI-1 levels are thought to be better than higher levels. The primary outcome is mean change from baseline and can include negative numbers as a result.

Time frame:
6 weeks (change from baseline)
Reported as:
Mean · ng/ml
Plasminogen Activator Inhibitor 1
ng/mlAliskirenAmlodipine
Plasminogen Activator Inhibitor 10.65 (-7.33 to 8.62)3.82 (-5.16 to 12.81)
SecondarySerum Level of Vascular Cell Adhesion Molecule

Surrogate biomarker cardiovascular risk

Time frame:
6 week (change from baseline)
Reported as:
Mean · ng/ml
Serum Level of Vascular Cell Adhesion Molecule
ng/mlAliskirenAmlodipine
Serum Level of Vascular Cell Adhesion Molecule-2.4 (-41.1 to 36.3)-45.9 (-112.8 to 21.0)
SecondarySerum Level of Intracellular Cell Adhesion Molecule

Surrogate biomarker of cardiovascular risk

Time frame:
6 week (change from baseline)
Reported as:
Mean · ng/ml
Serum Level of Intracellular Cell Adhesion Molecule
ng/mlAliskirenAmlodipine
Serum Level of Intracellular Cell Adhesion Molecule-4.9 (-17.2 to 7.4)-10.3 (-31.2 to 10.6)
SecondarySerum Level of C-reactive Protein

Surrogate biomarker of cardiovascular risk

Time frame:
6 week (change from baseline)
Reported as:
Mean · mg/l
Serum Level of C-reactive Protein
mg/lAliskirenAmlodipine
Serum Level of C-reactive Protein0.0397 (-0.2310 to 0.3104)0.1032 (-0.1974 to 0.4038)
SecondarySerum Level of Nitric Oxide

Surrogate biomarker of cardiovascular risk

Time frame:
6 week (change from baseline)
Reported as:
Mean · mmmol/l
Serum Level of Nitric Oxide
mmmol/lAliskirenAmlodipine
Serum Level of Nitric Oxide2.66 (-7.45 to 12.76)7.49 (-1.43 to 16.41)

Adverse events

Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Aliskiren—0/16 (0%)0/22 (0%)
Amlodipine—0/15 (0%)0/16 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)AliskirenAmlodipineTotal
<=18 years000
Between 18 and 65 years7613
>=65 years151025
Age, Continuous
Age, Continuous(years)AliskirenAmlodipineTotal
Mean68 ± 1063 ± 1665 ± 13
Sex: Female, Male
Sex: Female, Male(Participants)AliskirenAmlodipineTotal
Female8614
Male141024
Region of Enrollment
Region of Enrollment(participants)AliskirenAmlodipineTotal
United States221638
08

Study locations

1 site
  • Texas Tech University Health Sciences Center
    Lubbock, Texas 79430, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 5, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00818779
Lead sponsor
Texas Tech University Health Sciences Center
Responsible party
Sponsor
First posted
Jan 8, 2009
Start date
Jan 2008
Primary completion
Aug 2011
Completion
Aug 2011
Results posted
Nov 19, 2012
Last update
Dec 5, 2017

Study contacts

Gary E Meyerrrose, MD
principal investigator · Texas Tech Health Sciences Center Department of Internal Medicine
Brian K Irons, PharmD
study director · Texas Tech University Health Sciences Center School of Pharmacy

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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