Intracellular Magnesium and Heart Failure

NCT ID: NCT06353750

Last Updated: 2024-04-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

85 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-04-15

Study Completion Date

2026-04-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Low magnesium levels are surprisingly common in those with a heart condition known as HFpEF, where the heart pumps well but is too rigid to fill properly with blood. While routine blood tests can check magnesium levels, they don't tell us how much magnesium is actually inside the heart and muscle cells, where it's vital for energy and overall function. Our research aims to get a clearer picture by looking directly at the magnesium inside these cells and understanding its role in the body's energy production and usage. We're also interested in how magnesium levels affect symptoms and the body's handling of sugar. We're using advanced medical imaging techniques, like heart magnetic resonance imaging (MRI) and other heart and muscle function tests, at rest and when the heart is working hard to help answer these questions. We'll compare the magnesium levels inside the cells before and after giving a supplement of magnesium to see if this can make a difference in how the heart and muscles work.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Hypomagnesaemia is prevalent among patients suffering from heart failure with preserved ejection fraction (HFpEF), and in those with predisposing risk factors such as obesity and diabetes. The intricate link between hypomagnesaemia and the pathophysiological processes of HFpEF remains to be fully elucidated. However, its notable prevalence suggests a significant role in the onset and advancement of the disease. Serum magnesium (S-Mg) is commonly used to evaluate Mg status, however, it does not accurately reflect true intracellular Mg concentrations (\[Mg2+\]i), where this essential ion exerts its beneficial effects. Thus, previous literature lacks a thorough evaluation of \[Mg2+\]i in HFpEF, and specifically the potential impact of Mg replete physiology.

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

See the medical conditions and disease areas that this research is targeting or investigating.

Heart Failure With Preserved Ejection Fraction Hypomagnesemia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Individuals with heart failure with preserved ejection fraction (HFpEF)

* Clinical diagnosis of HFpEF
* HFA-PEFF score ≥ 5

Magnesium supplement

Intervention Type OTHER

Intravenous magnesium supplement (10mmol).

Healthy controls

* HFA-PEFF \< 3
* No known diagnosis of heart failure

Magnesium supplement

Intervention Type OTHER

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

Intervention Type OTHER

Intravenous magnesium supplement (10mmol).

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Magnesium supplement

Intravenous magnesium supplement (10mmol).

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Participant is willing and able to give informed consent for participation in the study.
* 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

* Participant is unwilling or unable to give informed consent
* 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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

British Heart Foundation

OTHER

Sponsor Role collaborator

Oxford University Hospitals NHS Trust

OTHER

Sponsor Role collaborator

University of Oxford

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Oxford Centre for Magnetic Resonance (OCMR)

Oxford, , United Kingdom

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United Kingdom

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Jennifer L Holland, BMBS

Role: CONTACT

01865 221172

Oliver Rider, BM BCh

Role: CONTACT

01865 221172

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Jennifer L Holland, BMBS

Role: primary

Oliver Rider, BM BCh

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

331039

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Physiological Effects Ketone Ester in Heart
NCT05924802 ACTIVE_NOT_RECRUITING NA
Nutritional Ketosis in Heart Failure
NCT04370600 UNKNOWN PHASE1
Ketones in Heart Failure With Reduced Ejection Fraction
NCT06195982 ENROLLING_BY_INVITATION PHASE2
The Re-Prosper HF Study
NCT04551222 COMPLETED PHASE2/PHASE3
Nicotinamide Riboside in Systolic Heart Failure
NCT03423342 COMPLETED PHASE1/PHASE2