Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
85 participants
OBSERVATIONAL
2024-04-15
2026-04-25
Brief Summary
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Detailed Description
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The research hypothesis is that \[Mg2+\]i is related to myocardial and skeletal muscle (SM) energetics and performance in patients with HFpEF. The study aims to explore the role of \[Mg2+\]i at a functional and cellular level in cardiac and SM, symptomatology, and insulin sensitivity; comparing a HFpEF population with healthy and matched controls.
Using the chemical shift difference in the resonance frequencies of the α- and β- phosphate resonances in magnetic resonance spectroscopy (MRS), \[Mg2+\]i will be measured, comparing it to S-Mg. Blood samples for cardiac biomarkers, electrolytes, and markers of HFpEF risk factors (such as lipid profile, HbA1C and TSH) will be taken and a calf leg raise performed. Advanced imaging techniques at rest and stress including cardiac magnetic resonance imaging (CMR), MRS and echocardiography will be performed. MRS measurements include cellular energetics (Phosphocreatine \[PCr\]/ATP), rate of myocardial ATP delivery (CK flux and KfCK) and skeletal muscle energetics (PCr recovery Tau). At two time points post-Mg augmentation (immediate and delayed \[7-15 days\]), investigations will be repeated.
This study aspires to quantify \[Mg2+\]i in the HFpEF population compared with healthy and matched controls, juxtapose its levels with S-Mg, and examine its significance in the pathophysiology, functional and cellular performance, and symptom presentation of HFpEF. The study aims to recruit 45 individuals with HFpEF, 20 healthy controls and 20 age-and sex-matched individuals over a 2-year period.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Individuals with heart failure with preserved ejection fraction (HFpEF)
* Clinical diagnosis of HFpEF
* HFA-PEFF score ≥ 5
Magnesium supplement
Intravenous magnesium supplement (10mmol).
Healthy controls
* HFA-PEFF \< 3
* No known diagnosis of heart failure
Magnesium supplement
Intravenous magnesium supplement (10mmol).
Matched controls
* HFA-PEFF \< 3
* No known diagnosis of heart failure
* Age and sex-matched individuals to the HFpEF cohort
Magnesium supplement
Intravenous magnesium supplement (10mmol).
Interventions
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Magnesium supplement
Intravenous magnesium supplement (10mmol).
Eligibility Criteria
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Inclusion Criteria
* Participant aged at least 18 years old.
* Clinical diagnosis of HFpEF
* HFA-PEFF score ≥ 5
* HFA-PEFF \< 3
* No known diagnosis of heart failure
Exclusion Criteria
* Any impediment to communication which, in the opinion of the investigator, might prevent the investigator communicating effectively with the patient during the study which could cause a safety or reliability concern.
* Any other condition which, in the opinion of the investigator, might affect the safety of the participant or reduce the reliability of the study results
* Involvement in any other research project where the procedures would affect the outcomes of this study.
* Individuals with NYHA class IV symptoms
* Known ischaemic heart disease, ICD, or CRT in situ.
* Individuals on oral magnesium supplementation
* Insulin dependent diabetes
* Standard contraindications to magnetic resonance imaging (MRI), (Metal clips or metallic foreign body, prior injury to the eye involving fragments of metal, prior shrapnel injuries, any other metallic or electronic implants affected by the magnetic field, history of severe claustrophobia, history of chronic kidneys disease, egg, or soya allergy)
* Heart transplant recipient
* Cardiomyopathy from infiltrative or storage diseases, muscular dystrophies, or with reversible causes, hypertrophic cardiomyopathy
* Moderate or greater valvular heart disease
* Acute HF requiring iv diuretics, inotropes, vasodilators, or hospitalisation within 6 weeks of screening
* BMI\>40kg/m2 (due to MRS sensitivity).
* Pregnancy (due to magnesium infusion).
* Chronic kidney disease stage 4/5 (due to contrast injection)
18 Years
ALL
Yes
Sponsors
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British Heart Foundation
OTHER
Oxford University Hospitals NHS Trust
OTHER
University of Oxford
OTHER
Responsible Party
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Locations
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Oxford Centre for Magnetic Resonance (OCMR)
Oxford, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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331039
Identifier Type: -
Identifier Source: org_study_id
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