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High Fat Diet for Cardiac Metabolic Reprogramming

Cardiac Metabolic Reprogramming by a Nutritional Intervention: the High Fat Diet for Heart Failure (HF4HF) Study, a proof-of Concept Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06747429
Acronym
HF4HF
Enrollment
80
Registered
2024-12-24
Start date
2026-01-15
Completion date
2026-12-01
Last updated
2026-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure With Reduced Ejection Fraction, Non-ischemic Dilated Cardiomyopathy

Keywords

heart failure, high-fat diet, clinical trial, non-ischemic DCM

Brief summary

Heart failure (HF) continues to be a leading cause of morbidity and mortality worldwide, despite advances in treatment. HF is often characterized by an altered metabolism in the heart, where glucose is favored over fatty acids as the primary energy substrate. This metabolic shift has been hypothesized to contribute to disease progression. Previous studies using animal models have demonstrated that restoring fatty acid metabolism through dietary intervention can reverse the adverse metabolic effects and improve heart function. A transgenic murine model with mitochondrial defects, for instance, exhibited improved cardiac function after an HFD intervention. These findings were reinforced by a translational pig model of non-ischemic DCM, where a high-fat diet significantly improved LVEF compared to a standard diet. Building upon these promising preclinical results, a small-scale human study showed that lipid infusion, rather than glucose, improved cardiac function in HF patients. However, the long-term benefits of a HFD in heart failure patients have yet to be thoroughly explored. The HF4HF trial aims to fill this gap by evaluating the effects of an HFD over a two-month period in patients with non-ischemic DCM and reduced LVEF. The "High Fat Diet for Heart Failure" (HF4HF) study is a proof-of-concept randomized controlled trial designed to investigate the efficacy of a high-fat diet (HFD) as a therapeutic intervention in patients with non-ischemic dilated cardiomyopathy (DCM) and reduced left ventricular ejection fraction (LVEF). The study hypothesizes that cardiac metabolic reprogramming, achieved through a controlled nutritional intervention involving an HFD, can enhance systolic function, myocardial energetics, and overall heart function in heart failure (HF) patients. Cofunded by the European Commission and national entities, the trial is spearheaded by a consortium of cardiovascular research centers across four countries: Spain, Italy, France, and Romania.

Detailed description

Despite the notable therapeutic advancements, heart failure (HF) remains a significant cause of morbi-mortality worldwide, that justifies the need of identifying novel treatment strategies targeting non-redundant disease pathways.The heart, being the organ with the highest energy demands, produces over 5 kg of adenosine triphosphate (ATP) per day under normal conditions to support its functions. To meet this substantial energy requirement, the myocardium utilizes various substrates, being the oxidation of fatty acids the primary source, due to their efficiency in ATP production compared to carbohydrates and amino acids.However, HF, regardless of its etiology and across the entire spectrum of left ventricular ejection fraction (LVEF), often involves an altered cardiac metabolism characterized by a preference for glucose over fatty acids as an energy source.While previously considered a protective mechanism, recent findings challenge this notion. Preclinical investigations using a transgenic murine model with mitochondrial alterations in cardiomyocytes revealed a shift in energy substrate utilization from fatty acids to glucose, resulting in progressive dilated cardiomyopathy (DCM) with reduced ejection fraction. Administering a high-fat diet (HFD) to these mice restored normal myocardial metabolism, leading to disease regression.Building upon these findings, a subsequent study was conducted by members of HF4HF Consortium, in a translational pig model of non-ischemic DCM and LVEF \<50%, through the generation of hibernated myocardium. These pigs were randomly assigned to either a standard diet (regular chow) or a HFD (80% regular chow plus 20% lard, rich in palmitic, oleic, stearic and linoleic acids). Following a two-month intervention, pigs receiving the HFD showed a significant increase in LVEF from 41% to 56%, compared to controls whose LVEF only slightly changed from 40% to 38% (p 0.012). At the end of the protocol, the cardiomyocytes from pigs who were on regular diet displayed fragmented mitochondria and presence of abundant lipid droplets, suggestive of poor lipid trafficking and storage. At a molecular level, hibernated myocardium with HF was associated with a significant downregulation of proteins involved in lipid import from cytosol to mitochondria (CRAT and ACOX1), along with a compensatory upregulation of glucose transport proteins (GLUT1), something that was completely restored after 2 months of HFD. Altogether, these data show that HF is associated with an impaired intracellular fatty acid traffic responsible for the metabolic switch. HFD was able to revert the altered lipid handling, allowing a metabolic reprograming having mitochondria use again fatty acids. The metabolic reprograming was further reinforced by the in vivo 18F-FDG PET studies, which showed a significant modification in the glucose uptake in HFD versus control diet pigs. All these outstanding results underscored the potential of high-fat dietary intervention in ameliorating systolic function in non-ischemic DCM. Finally, a recent human study involving 20 patients with non-ischemic HF and reduced LVEF examined the effects of intravenous glucose plus insulin infusion versus lipid infusion of long-chain fatty acids, in terms of cardiac function and energetics, assessed by cardiovascular magnetic resonance (CMR) and MR spectroscopy 1 hour after the infusion. The lipid infusion notably enhanced cardiac function, increasing LVEF from 35% to 40%, whereas glucose plus insulin infusion showed no impact on disease parameters. Moreover, significant improvements in diastolic function, and myocardial energetics, assessed by 13P and the phosphocreatine/ATP ratio, were reported after intralipid infusion; findings that support the hypothesis of remaining metabolic substrate flexibility of the failing heart. However, this study only assessed the acute effects of lipid exposure on cardiac function and energetics, lacking long-term evidence regarding the efficacy of employing a high-fat dietary pattern in HF management. Nonetheless, this novel approach holds promise in the medical-nutritional management of this prevalent disease.

Interventions

Weekly isocaloric dietary profile, with total daily energy intake distributed as follows: 70% from fats, primarily sourced from nuts, extra virgin olive oil, avocados, and animal fats from fish and cheese; protein intake of 0.8-1.2 g per kg body weight (10-20%); and the remaining calories from carbohydrates (10-20%).

OTHERStandard diet

Weekly isocaloric dietary profile, with total daily energy intake distributed as follows: 30% from fats, primarily sourced from nuts, extra virgin olive oil, avocados, and animal fats from fish and cheese; protein intake of 0.8-1.2 g per kg body weight (10-20%); and 50-60% from carbohydrates.

Sponsors

Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
Lead SponsorOTHER
Puerta de Hierro University Hospital
CollaboratorOTHER
European Georges Pompidou Hospital
CollaboratorOTHER
Carol Davila University of Medicine and Pharmacy
CollaboratorOTHER
University of Florence
CollaboratorOTHER
Hospital Universitario Fundación Jiménez Díaz
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Masking description

Masking will be maintained for data analysts.

Intervention model description

The HF4HF trial is a proof-of-concept, independent investigator initiated (non commercial), multicentre, multinational, two-arm parallel randomized controlled trial, designed to evaluate the efficacy and safety of HFD compared to standard diet in patients with non-ischemic DCM and, at least, mildly reduced LVEF on optimal medical therapy. Despite participants and health care providers will not be blinded to the allocation arm, outcome assessors will; hence, it can be classified as a PROBE (prospective randomized open, blinded-endpoint) trial. As regards its duration, the trial will span 4 months in total: an intervention period of 2 months and an additional 2 months follow-up period to assess the sustained effects post-intervention discontinuation.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients of both sexes and ≥18 years old * Patients diagnosed with HF secondary to non-ischemic DCM, according to ESC guidelines definition,1 with or without a known genetic basis. * LVEF ≤49% according to the baseline CMR. * Optimized HF guideline-directed medical therapy for at least 3 months prior to inclusion. * Patients who have provided informed consent.

Exclusion criteria

* Prior diagnosis of ischemic DCM. * Prior diagnosis of established atherosclerotic cardiovascular disease (angina/myocardial infarction, transient ischemic attack/stroke, lower limb ischemia or at any other peripheral level). * Changes in HF therapies within the last 3 months. * HF decompensation within the previous 3 months, including HF hospitalization or the need of ambulatory intravenous diuretic or inotropic treatment such as levosimendan. * Uncontrolled dyslipidemia, defined as LDL-cholesterol \>160 mg/dL and/or triglycerides \>200 mg/dL, despite treatment. * Any contraindication for CMR: Severe claustrophobia. Any device which is known to threaten or pose hazard in all MR environments. //www.mrisafety.com/ Patients with implanted biomedical devices (cardiac artefacts): pacemakers, cardiac defibrillators or cardiac resynchronization therapy. * Liver and biliary diseases, including prior diagnosis of non-alcoholic fatty liver disease and unoperated cholelithiasis. * Prior episodes of acute pancreatitis or chronic pancreatitis. * Prior fish or nut allergy. * Life expectancy less than 12 months. * Pregnancy or planned pregnancy for the next 4 months. * Current lactation. * Patients participating in other randomized clinical trial. * Impossibility to consent or undergo study follow-up

Design outcomes

Primary

MeasureTime frameDescription
Changes in left ventricular ejection fraction (LVEF)At baseline, month 2 and month 4Changes in LVEF assessed using cardiac magnetic resonance imaging (CMR)

Secondary

MeasureTime frameDescription
Left ventricular strainAt baseline, month 2 and month 4Changes in left ventricular strain assessed using cardiac magnetic resonance imaging (CMR)
Diastolic functionAt baseline, month 2 and month 4Changes in diastolic function assessed using cardiac magnetic resonance imaging (CMR)
White blood cellsAt baseline, month 2 and month 4Quantification with standard laboratory procedures
Red blood cellsAt baseline, month 2 and month 4Quantification with standard laboratory procedures
HemoglobinAt baseline, month 2 and month 4Quantification with standard laboratory procedures
PlateletsAt baseline, month 2 and month 4Quantification with standard laboratory procedures
GlucoseAt baseline, month 2 and month 4Quantification with standard laboratory procedures
HDL-cholesterolAt baseline, month 2 and month 4Quantification with standard laboratory procedures
LDL-cholesterolAt baseline, month 2 and month 4Quantification with standard laboratory procedures
TriglyceridesAt baseline, month 2 and month 4Quantification with standard laboratory procedures
Electrolytes (sodium, potassium, calcium, magnesium)At baseline, month 2 and month 4Quantification with standard laboratory procedures
Kidney function (creatinine, urea)At baseline, month 2 and month 4Quantification with standard laboratory procedures
Vitamins (vitamin B12, 25-OH Vitamin D, folate)At baseline, month 2 and month 4Quantification with standard laboratory procedures
AlbuminAt baseline, month 2 and month 4Quantification with standard laboratory procedures
Iron metabolism (iron, ferritin)At baseline, month 2 and month 4Quantification with standard laboratory procedures
Liver function (AST, ALT, γGT)At baseline, month 2 and month 4Quantification with standard laboratory procedures
C-reactive proteinAt baseline, month 2 and month 4Quantification with standard laboratory procedures

Countries

France, Italy, Romania, Spain

Contacts

CONTACTCarlos Nicolás Pérez-García, MD PhD.
carlosnicolas.perez@cnic.es(+34) 914531200
CONTACTClaudia Artiaga, MSc
cartiaga@cnic.es(+34) 914531200
PRINCIPAL_INVESTIGATORFrancesco Sofi, MD PhD

University of Florence, Clinical and Experimental Medicine, Unit of Clinical Nutrition, Florence,

PRINCIPAL_INVESTIGATORPablo García Pavía,, MD PhD

Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro (IIS), Hospital Universitario Puerta de Hierro Majadahonda

PRINCIPAL_INVESTIGATORRuxandra Jurcut, MD PhD

University of Medicine and Pharmacy "Carol Davila", Bucharest,

PRINCIPAL_INVESTIGATORJean-Sébastian Hulot, MD PhD

Hôpital Européen Georges Pompidou, INSERM, Paris,

PRINCIPAL_INVESTIGATORMikel Taibo Urquía, MD

Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain

STUDY_CHAIRBorja Ibánez,, MD PhD

Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 27, 2026