Heart Failure, Congestive Clinical Trial
Official title:
A Double-blind Randomized, Placebo-Controlled, Single-Center Study to Assess the Impact of Statins on the Autonomic Nervous System and Cardiac Structure/Function in Non-Ischemic Heart Failure
The goal of the investigators' study is to further understand the potentially beneficial effects of statin therapy in patients with heart failure. It is hypothesized that statins will 1) increase the heart's pumping ability 2) improve functioning of the sympathetic nervous system and 3) decrease immune activation in heart failure.
Recent evidence suggests that HMG-Coenzyme A (statin) therapy may be associated with improved
survival in both ischemic and non-ischemic heart failure (HF). Large, randomized outcome
studies of statins in HF are currently underway, but these trials will not address underlying
mechanisms. The aim of the study is to investigate statins' potentially beneficial mechanisms
of action in HF, focusing on: 1) sympathetic nervous system activation and 2) myocardial
remodeling, and 3) immune activation in heart failure.
Fifty patients with systolic HF of non-ischemic etiology from a single center will be
randomized in a double-blinded fashion to 3 months of atorvastatin 10mg QD (25 subjects) vs
matching placebo QD (25 subjects). The following exams will be performed at baseline
(pre-treatment) and at end of study (post-treatment): sympathetic microneurography,
echocardiography, and peripheral blood chemokine analysis. Sympathetic microneurography at
the peroneal nerve will directly quantify changes in sympathetic nerve activity
(bursts/minute). Echocardiography (with the addition of MRI in a subset of subjects without
pacemakers or implantable defibrillators) will be used to track changes in cardiac structure
and function; indices of remodeling will include measurement of left ventricular mass index,
left ventricular volume indices, left ventricular ejection fraction, and subendocardial scar
quantification (MRI only). Immune activation will be characterized by circulating cytokines
and chemokines. Additionally, quantification of established cardiac biomarkers (cardiac
troponin, B-type natriuretic peptide, and C-reactive Protein), Holter monitor/heart rate
variability studies, and quality of life and global clinical assessment will be performed
pre- and post- treatment.
Neither sympathetic microneurography nor MRI have been previously utilized to assess statins'
effects in humans with HF. The impact of statin therapy on inflammatory chemokine activation
in HF also has not been studied. The knowledge gained from our proposed investigations may
serve as a basis for understanding how statin therapy has potential to improve clinical
outcomes in HF, and may ultimately lead to new therapeutic strategies for HF.
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