Key result
The RED-HART study is a randomized, double-blind, placebo-controlled trial designed to evaluate whether interleukin-1 blockade with anakinra improves aerobic exercise performance in patients with recently decompensated systolic heart failure.
Why the study?
Does anakinra improve aerobic exercise performance in patients with recently decompensated systolic heart failure?
RCT (n=60)
Double-blind
Randomized
Yes
Does anakinra improve aerobic exercise performance in patients with recently decompensated systolic heart failure?
The RED-HART study is designed to evaluate whether IL-1 blockade with anakinra improves aerobic exercise performance in patients with recently decompensated systolic heart failure.
Anakinra's role in exercise capacity after decompensated HF remains untested; RED-HART will deliver the first RCT data.
Heart Failure (HF) is a clinical syndrome characterized by dyspnea, fatigue, and poor exercise capacity due to impaired cardiac function. The incidence of HF is increasing and represents the leading cause of hospitalization in the United States among patients > 65 years of age. Neurohormonal blockade has proven to reduce morbidity and mortality; however the persistent toll of HF demonstrates the urgent need to continue to develop novel drugs that target other pathophysiological paradigms. The presence of inflammation in cardiovascular disease has been well-established and interleukin-1 (IL-1), the prototypical proinflammatory agent, has been shown in preclinical animal models to induce cardiac dysfunction. The current study will investigate the role of IL-1 as an inflammatory mediator of HF progression and investigate whether IL-1 blockade with anakinra, recombinant human IL-1 receptor antagonist, improves aerobic exercise performance in patients with recently decompensated systolic HF. This study will be composed of 3 treatment arms (20 patients each): 1) anakinra 100mg daily for 12 weeks; 2) anakinra 100mg daily for 2 weeks followed by placebo for 10 weeks; or 3) placebo for 12 weeks. All patients will be followed for at least 24 weeks. The co-primary endpoints will be placebo-corrected interval changes in peak oxygen consumption (VO2) and ventilatory efficiency (VE/VCO2 slope) measured by Cardiopulmonary Exercise Testing (CPX) after 2 weeks of anakinra treatment. Secondary endpoints will include interval changes in 1) CPX variables at 4, 12 and 24 weeks; 2) echocardiographic measures of cardiac dimension/function; 3) quality of life assessments; 4) inflammatory biomarkers; and 5) clinical outcome including days alive outside of the hospital and survival free of re-hospitalization for HF. The RED-HART study will be the first study to address the potential benefits of IL-1 blockade on aerobic exercise performance in patients with recently decompensated HF.
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Benjamín W. Van Tassell (2015) conducted an RCT in Recently decompensated systolic heart failure (n=60). Anakinra vs. Placebo was evaluated on Placebo-corrected interval changes in peak oxygen consumption (VO2) and ventilatory efficiency (VE/VCO2 slope) after 2 weeks. The RED-HART study is a randomized, double-blind, placebo-controlled trial designed to evaluate whether interleukin-1 blockade with anakinra improves aerobic exercise performance in patients with recently decompensated systolic heart failure.
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