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Manganese-enhanced Magnetic Resonance Imaging (MEMRI) in Heart Failure With Preserved Ejection Fraction

Recruiting
Conditions
Heart Failure With Preserved Ejection Fraction
Type 2 Diabetes
Registration Number
NCT06652763
Lead Sponsor
University of Leicester
Brief Summary

Heart failure with preserved ejection fraction (HFpEF) is a condition in which the heart cannot fill with blood effectively. As a result, people with HFpEF suffer fatigue, breathlessness, and develop swollen limbs. The condition often requires multiple admissions to hospital and is associated with a marked loss of lifespan.

Despite being so common, very little is known about why people develop HFpEF and there are hardly any known treatments. Type 2 diabetes (T2D) is a major risk factor for HFpEF, and people with both HFpEF and diabetes are at a heightened risk of hospitalisation and premature death. It is unclear why the combination of diabetes and HFpEF is particularly harmful. This may be related to the hearts of people with type 2 diabetes being unable to take up the mineral calcium properly, as well as due to their hearts being less energy efficient. Both of these are vital to heart muscle pumping and filling, but until recently it has not been possible to assess these in humans.

New advances in heart MRI scans, with dedicated scanner techniques and dyes (manganese contrast), now allow extremely detailed pictures of heart structure, function, calcium uptake and energy efficiency, all during the same scan. The investigators will enlist 40 volunteers with HFpEF (20 with T2D and 20 without T2D), and up to 20 healthy volunteers, to undergo a heart MRI scan with manganese contrast to assess calcium uptake and energy efficiency. This will allow the comparison of people with HFpEF with and without T2D, to see how their hearts are different to healthy volunteers.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Capacity to provide informed consent
  • Symptoms (e.g. breathlessness, orthopnoea, ankle swelling, fatigue), signs (e.g. elevated jugular venous pressure, peripheral oedema, third heart sound) or established diagnosis of HF with LV ejection fraction ≥ 50%, or
  • Meets HFpEF diagnostic criteria in accordance with the HFA-PEFF diagnostic algorithm form the Heart Failure Association of the European Society of Cardiology, in which a score ≥5 points confirms diagnosis of HFpEF
Exclusion Criteria
  • Known diagnosis of Type 1 Diabetes
  • Pregnancy or breast-feeding or females of child bearing age without a negative pregnancy test
  • Receiving an investigational drug or device within 30 days prior to participating in the study
  • Decompensated heart failure or pulmonary oedema
  • History of prolonged corrected QT interval or torsades de pointes
  • Second- or third-degree atrioventricular block
  • Abnormal liver function tests (> 3x upper limit of normal) or history of liver disease
  • Baseline eGFR < 30mL/min/1.73m2
  • Any contraindications to MRI including implanted devices/pacemakers
  • Severe native valve disease, restrictive cardiomyopathy, constrictive pericarditis or hypertrophic cardiomyopathy, myocarditis or takotsubo cardiomyopathy.
  • Recent myocardial infarction within the previous 3 months
  • Known diagnosis of pheochromocytoma

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
KiBaseline

Manganese influx constant as measured by MEMRI scan

Secondary Outcome Measures
NameTimeMethod
LV mass/volume ratioBaseline

Measured by CMR

Myocardial fibrosisBaseline

CMR assessed markers of LV myocardial fibrosis (extracellular volume)

Myocardial PerfusionBaseline

CMR assessed markers of perfusion (myocardial perfusion reserve)

Associations of Ki with resting PCr/ATPBaseline

Univariate and multivariate models to look for association between Ki and PCr/ATP ratio

LV massBaseline

grams, measured by CMR

T1 valuesBaseline

T1 values measured at 30 minutes post contrast on MEMRI scan

Myocardial PCr/ATP ratioBaseline

Phosphocreatine-to-ATP ratio as measured by 31P-magnetic resonance spectroscopy

Left ventricular ejection fractionBaseline

%, measured by CMR

LV global longitudinal strainBaseline

%, measured by CMR

LV global circumferential strainBaseline

%, measured by CMR

LV PEDSRBaseline

1/s, measured by CMR

Associations of exercise capacity with Ki and PCr/ATP in HFpEFBaseline

Ki values as assessed by MEMRI, myocardial PCr/ATP as measured by 31P-MRS and six minute walk test distance. Associations will be assessed using univariate and multivariate models.

Plasma biomarkers of metabolic dysregulation, fibrosis and inflammationBaseline

This exploratory outcome will assess the differences in a wide range of plasma biomarkers between groups and their association with Ki

10-year outcomesBaseline

10-year outcomes including HF hospitalisation (time to first event and cumulative) and all-cause death.

Trial Locations

Locations (1)

University of Leicester

🇬🇧

Leicester, United Kingdom

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