Chronic Kidney Disease and Heart Failure With Preserved Ejection Fraction: The Role of Mitochondrial Dysfunction
- Conditions
- Renal Insufficiency, ChronicHeart Failure With Preserved Ejection Fraction
- Interventions
- Dietary Supplement: MitoQDietary Supplement: Placebo
- Registration Number
- NCT03960073
- Lead Sponsor
- Virginia Commonwealth University
- Brief Summary
The purpose of this study is to investigate the role of mitochondrial derived oxidative stress on exercise capacity and arterial hemodynamics in HFpEF patients with and without chronic kidney disease.
- Detailed Description
Heart failure is a public health epidemic affecting 6.5 million Americans. Heart failure with preserved ejection fraction (HFpEF) accounts for a large burden of heart failure with the incidence and cost associated with the disease projected to double in the next 20 years. The pathophysiology of HFpEF has not yet been fully elucidated and no proven therapies for improving outcomes in HFpEF currently exist, posing major diagnostic and therapeutic challenges. The addition of chronic kidney disease (CKD) presents a complicated cardio renal syndrome that manifests a distinctly different phenotype and exacerbates the diagnostic and therapeutic challenges of HFpEF. This study aims to address the urgent need to establish treatment targets and therapies by investigating potential underlying biological contributors to HFpEF and its symptoms.
Mitochondrial dysfunction is consistently reported in CKD and heart failure. Mitochondrial dysfunction has been implicated in cardiac, skeletal muscle and vascular dysfunction and is therefore an attractive target for a 'whole systems' therapeutic approach that would encompass exercise intolerance and abnormal blood vessel hemodynamics. A known contributor to and subsequent cyclical result of mitochondrial dysfunction is an abnormally heightened production of mitochondria derived oxidative stress. This study will address the role of mitochondria derived oxidative stress in mitochondrial dysfunction, exercise intolerance and large blood vessel hemodynamics HFpEF patients with and without CKD.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
- above the age of 18 years
- a clinical diagnosis of stable Stage C Heart Failure with NYHA Class II-III symptoms
- a left ventricular ejection fraction >50%
- current cancer
- current pregnancy
- current antioxidant supplement use and unwilling to have a 7-day antioxidant washout period before the beginning the trial and to continue antioxidant disuse throughout the trial.
- current antiretroviral medication use
- absolute contraindications to exercise testing according to the American College of Sports Medicine guidelines
- fluid overload
- unable to provide informed consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description MitoQ MitoQ 20mg daily oral dose of MitoQ Placebo Placebo Oral TTP placebo
- Primary Outcome Measures
Name Time Method Exercise Capacity Change over 4 weeks Maximal aerobic capacity (VO2peak) obtained from cardiopulmonary exercise testing
- Secondary Outcome Measures
Name Time Method Forward Pulse Wave Amplitude Change over 4 weeks Central hemodynamic assessment of the forward pulse wave amplitude assessed by echocardiography combined with applanation tonometry.
Mitochondrial Respiration Change over 4 weeks High resolution mitochondrial respirometry
Reflected Pulse Wave Amplitude Change over 4 weeks Late systolic pulsatile load on the left ventricle represented by reflected pulse wave amplitude; assessed by echocardiography combined with applanation tonometry.
Trial Locations
- Locations (1)
Virginia Commonwealth University
🇺🇸Richmond, Virginia, United States