Targeting Sympathetic Overactivity in Heart Failure Patients With Statins

NCT ID: NCT01097785

Last Updated: 2016-11-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-03-31
• Study Completion Date: 2014-07-31

Brief Summary

Heart failure (HF) is a leading cause of morbidity and mortality in the United States with the incidence and prevalence of the disease on a continual rise. An overactive sympathetic nervous system has become a hallmark characteristic of HF. Although sympathetic activation is initially beneficial to maintain cardiac output, blood pressure and perfusion to vital organs, over the long term it becomes deleterious contributing to the worsening of HF and sudden cardiac death. Indeed, recent findings in HF patients suggest that the sympathetic overactivity is not just a marker of poor prognosis but it plays a causative role in the development of the disease. Thus, the sympathetic nervous system constitutes a putative drug target in the treatment of HF. However, despite aggressive medical management, including conventional anti-adrenergic strategies, sympathetic nerve activity (SNA) has been shown to remain abnormally high in HF patients and improvements in survival have been limited. Thus, other treatment strategies that include reducing SNA and its deleterious consequences are warranted. Recent findings from clinical trials indicate that 3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors (statins) improve survival irrespective of cholesterol lowering bringing the pleiotropic (i.e., cholesterol independent) effects of statins to the forefront. An important pleiotropic effect recently reported in experimental HF, that has yet to be directly tested in human HF, is the ability of statins to reduce resting sympathetic outflow. Several studies in pacing-induced HF rabbits have demonstrated that statins normalize the excessive sympathetic activation in the HF state. Thus, the goal of this project is to determine whether these findings in experimental HF can be translated to the clinical setting of human HF. Our central hypothesis is that statins reduce sympathetic overactivity in HF patients. To test this hypothesis we will directly measure muscle SNA and perform a randomized crossover placebo control study. Subjects will come to the research laboratory before and after the administration of Simvastatin at a standard therapeutic dosage of 40 mg. per day or placebo for 1 month

Detailed Description

Heart failure (HF) is a leading cause of morbidity and mortality in the United States with the incidence and prevalence of the disease on a continual rise. An overactive sympathetic nervous system has become a hallmark characteristic of HF. Although sympathetic activation is initially beneficial to maintain cardiac output, blood pressure and perfusion to vital organs, over the long term it becomes deleterious contributing to the worsening of HF and sudden cardiac death. Indeed, recent findings in HF patients suggest that the sympathetic overactivity is not just a marker of poor prognosis but it plays a causative role in the development of the disease. Thus, the sympathetic nervous system constitutes a putative drug target in the treatment of HF. However, despite aggressive medical management, including conventional anti-adrenergic strategies, sympathetic nerve activity (SNA) has been shown to remain abnormally high in HF patients and improvements in survival have been limited. Thus, other treatment strategies that include reducing SNA and its deleterious consequences are warranted. Recent findings from clinical trials indicate that 3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors (statins) improve survival irrespective of cholesterol lowering bringing the pleiotropic (i.e., cholesterol independent) effects of statins to the forefront. An important pleiotropic effect recently reported in experimental HF, that has yet to be directly tested in human HF, is the ability of statins to reduce resting sympathetic outflow. Several studies in pacing-induced HF rabbits have demonstrated that statins normalize the excessive sympathetic activation in the HF state. Thus, the goal of this proposal is to determine whether these findings in experimental HF can be translated to the clinical setting of human HF. Our central hypothesis is that statins reduce sympathetic overactivity in HF patients. To test this hypothesis we will directly measure muscle SNA before and after one month of statin therapy. In addition, to begin to elucidate the potential mechanism(s) involved in statin-induced reductions in SNA we will use the technique of partial autospectral analysis to assess the baroreflex-independent (i.e., central) component of SNA and the application of neck pressure and neck suction to assess the baroreflex-dependent control of SNA. The significance of the proposed experiments is the potential of statin therapy to reduce SNA in HF patients providing a novel therapeutic strategy to target the heightened resting sympathetic drive present in HF.

The study will utilize a randomized crossover placebo-controlled study design. Subjects will come to the research laboratory before, during and after the administration of either a placebo or Simvastatin for one month at a standard therapeutic dosage of 40 mg per day. Subjects will be carefully monitored for any adverse effects by examining blood samples at baseline and 4 weeks for markers of liver, kidney, or muscle damage. If the subject's responses to one month of Simvastatin therapy are minimal, such that the decrease in LDL cholesterol is less than 25%, we will ask them to participate in an additional 2 weeks of Simvastatin administration at a dosage of 80 mg per day. During the baseline, the visit at 4 wks, and during the additional visit (if necessary) subjects will undergo the following experimental measurements and procedures, which will take approximately four hours. All measurements and procedures will be performed by the principal investigator and trained research personnel.

To completely obtain all the data necessary for this project, it would be expected to take 5 years. This is based on the goal of initially collecting additional data to add to the preliminary data of a recent American Heart Association (AHA) grant submission and then submitting the project for an NIH grant. Based on power calculations and previous experience using these experimental measures, it will take approximately 30 heart failure patients to determine the influence of statins on sympathetic nerve activity. This will permit statistical comparisons and takes into account the technical difficulties of obtaining repeat quality sympathetic nerve recordings in the same patient as well as the data collection necessary to determine the potential contribution of baroreflex-dependent and -independent mechanisms. Healthy control subjects matched to each HF patients for age, sex, and body mass index, all of which are known factors that influence resting SNA, will also be studied. These studies are important for comparison to determine whether these statin-induced reductions in SNA specific to HF or a general overall effect of statin therapy. It is anticipated that identifying patients not already on statin therapy may take some time as this therapy is standard in this patients group. We chose Simvastatin for our studies because this was the statin of choice in the pacing-induced HF rabbit studies that have reported a normalization of resting SNA after statin therapy. We anticipate that future studies identifying the efficacy of different statins in reducing SNA, the impact of different dosages, and different durations of treatment will be warranted.

Conditions

Heart Failure

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: DOUBLE

Study Groups

Simvastatin

40 mg Simvastatin 1 pill every day for 30 days

Group Type: ACTIVE_COMPARATOR

Simvastatin

Intervention Type: DRUG

40 mg, P.O.,daily for 30 days

Placebo

Placebo cap 1 pill every day for 30 days

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

1 capsule daily for 30 days

Interventions

Simvastatin

40 mg, P.O.,daily for 30 days

Intervention Type: DRUG

Placebo

1 capsule daily for 30 days

Intervention Type: DRUG

Other Intervention Names

Zocor

Eligibility Criteria

Inclusion Criteria

• Male and females of all ethnic backgrounds ranging aged 18 to 70
• Ages 18-70 yrs
• Patients with congestive heart failure diagnosed on clinical history, a routine exercise test, echocardiography and/or routine cardiac catheterization, in functional class I-III
• Patients with heart failure due to ischemic and non-ischemic etiologies
• Normotensive and not taking blood pressure controlling medications

Exclusion Criteria

• Low blood pressure (<100/60)
• End stage renal disease
• Chronic Obstructive Pulmonary Disease (COPD) with concurrent daily use of inhalers
• Peripheral neuropathy
• Pregnant women

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Nebraska

OTHER

Sponsor Role: collaborator

University of Missouri-Columbia

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Paul J Fadel, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Missouri-Columbia

Anand Chockalingam, M.D.

Role: STUDY_CHAIR

University of Missouri-Columbia

Locations

University of Missouri

Columbia, Missouri, United States

Countries

United States

Other Identifiers

IRB-1135098

Identifier Type: -

Identifier Source: org_study_id