Intracellular Magnesium and Heart Failure
- Conditions
- HypomagnesemiaHeart Failure With Preserved Ejection Fraction
- Interventions
- Other: Magnesium supplement
- Registration Number
- NCT06353750
- Lead Sponsor
- University of Oxford
- Brief Summary
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
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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 85
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Individuals with heart failure with preserved ejection fraction (HFpEF) Magnesium supplement * Clinical diagnosis of HFpEF * HFA-PEFF score ≥ 5 Healthy controls Magnesium supplement * HFA-PEFF \< 3 * No known diagnosis of heart failure Matched controls Magnesium supplement * HFA-PEFF \< 3 * No known diagnosis of heart failure * Age and sex-matched individuals to the HFpEF cohort
- Primary Outcome Measures
Name Time Method Myocardial/ skeletal muscle metabolism and energetics at rest and stress. 7-15 days Measuring myocardial metabolism (PCr/ATP, CK flux and KfCK, PDH flux), and skeletal muscle metabolism (PCr recovery Tau) at rest and stress. Measurements at three time points (pre-Mg infusion, immediately post and delayed (7-15 days) after Mg infusion, comparing HFpEF population with healthy and matched controls.
- Secondary Outcome Measures
Name Time Method Serum versus intracellular magnesium concentration 7-15 days Comparing serum magnesium with intracellular magnesium concentrations using MRS, at all time points (pre-Mg infusion, and post (immediately and 7-15 days after) Mg infusion).
Cardiac function 7-15 days Comparing systolic and diastolic function (echocardiography) at rest and exercise at the three time points (pre-Mg infusion, immediately post and delayed (7-15 days) after Mg infusion), and assessing if \[Mg2+\] has a stronger correlation with cardiac function than serum Mg2+.
Insulin sensitivity 7-15 days To assess if Mg2+ infusion affects a HOMA-IR score (based on fasted serum glucose and insulin levels).
To assess if Mg2+ infusion affects a HOMA-IR score (based on fasted serum glucose and insulin levels).
To assess if Mg2+ infusion affects a HOMA-IR score (based on fasted serum glucose and insulin levels).
To assess if Mg2+ infusion affects a HOMA-IR score (based on fasted serum glucose and insulin levels), comparing 2 time points (pre-Mg infusion, and 7-15 days post-Mg infusion).Skeletal muscle performance 7-15 days Comparing Calf raise test at the three time points (pre-Mg infusion, immediately post and delayed (7-15 days) after Mg infusion), and assessing if \[Mg2+\] has a stronger correlation with test performance than serum Mg2+.
Symptoms 7-15 days To assess if Mg2+ infusion affects perceived exercise tolerance (NYHA class and symptom questionnaire) at 2 time points (pre-Mg infusion, and 7-15 days post-Mg infusion).
Trial Locations
- Locations (1)
Oxford Centre for Magnetic Resonance (OCMR)
🇬🇧Oxford, United Kingdom