R01HL157264

Multidrug Metabolic Approach to Improve Exercise and Skeletal Muscle Oxidative Capacity in HFPEF - Summary:

Heart failure with preserved ejection fraction (HFPEF) is on pace to become the dominant form of heart failure, yet we have no treatments to offer patients, leaving them limited in terms of exercise tolerance and quality of life.

While much attention has been paid to the myocardium, data suggest that abnormalities in skeletal muscle (SKM) oxygen utilization also contribute to exertional intolerance in this condition. Moreover, decreased nitric oxide (NO) bioavailability has been demonstrated in HFPEF patients. NO augments SKM oxygen delivery and plays a key role in enhancing fatty acid oxidation (FAO), both of which are important for submaximal exercise endurance.

Recently, sodium-glucose cotransporter-2 inhibitors such as empagliflozin (EMPA) have demonstrated remarkable benefits in other cardiovascular disease patients, though their use in HFPEF remains unclear. EMPA could be beneficial in HFPEF patients via multiple mechanisms, many of which target abnormalities identified specifically in HFPEF, including: (a) increasing mitochondrial biogenesis, (b) increasing FAO, (c) increasing plasma ketone bodies, providing an additional source of acetyl-CoA for energy production, and (d) increasing blood hemoglobin, augmenting oxygen delivery for any given blood flow.

Moreover, because NO is essential for FAO and a key mediator of exercise SKM blood flow, we propose that combining EMPA with a NO-donor such as potassium nitrate (KNO3) will lead to improvements in exercise capacity in HFPEF patients, as compared to EMPA alone or active control.

Our overarching hypothesis is that impaired SKM oxidative phosphorylation capacity (OXPHOS) limits exercise tolerance in HFPEF. We focus on submaximal exercise endurance in this proposal as submaximal exercise better reflects the level of exertion reached by HFPEF patients during daily activities, is more dependent on FAO than maximal effort exercise, and is less likely to be constrained by cardiac output limitations.

We will test the impact of three interventions in 53 HFPEF participants in a randomized double-blind crossover trial: (1) EMPA; (2) EMPA + KNO3; and (3) potassium chloride (active control).

In Aim 1: Participants will undergo cycle ergometry exercise tests. The primary endpoint will be the change in submaximal exercise endurance.

In Aim 2: We will test the impact of our 3 interventions on SKM OXPHOS using MRI following plantar flexion exercise. Novel MRI sequences will also be employed that quantify intramuscular perfusion.

In Aim 3: We will conduct SKM tissue biopsies to assess mitochondrial respiration, the SKM metabolome, and quantify the SKM proteome, providing in vitro assessments to support our exercise measurements.

Our proposal will target SKM metabolism in HFPEF and comprehensively assess the relationship between SKM OXPHOS and submaximal exercise endurance using complementary techniques. This proposal has the potential to identify SKM metabolism as an important therapeutic target in this disease for which we currently have no approved pharmacologic therapies.

Trustees Of The University Of Pennsylvania

TO FOSTER HEART AND VASCULAR RESEARCH IN THE BASIC, TRANSLATIONAL, CLINICAL AND POPULATION SCIENCES, AND TO FOSTER TRAINING TO BUILD TALENTED YOUNG INVESTIGATORS IN THESE AREAS, FUNDED THROUGH COMPETITIVE RESEARCH TRAINING GRANTS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.

93.837 - Cardiovascular Diseases Research

National Heart Lung and Blood Institute (NHLBI) [HHS - NIH]

Philadelphia, Pennsylvania 191042640 United States

Single Zip Code

Research Project Grant (Parent R01 Clinical Trial Required) (PA-20-183)

Amendment Since initial award the total obligations have increased 394% from $702,347 to $3,467,457.