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Left Ventricular Fibrosis in Chronic Kidney Disease (FibroCKD)

D

Dr Manvir Kaur Hayer

Status

Unknown

Conditions

Chronic Kidney Diseases
Myocardial Fibrosis
Cardio-Renal Syndrome
Uraemic Cardiomyopathy

Treatments

Diagnostic Test: Cardiopulmonary exercise test
Biological: Blood test
Diagnostic Test: 12-lead ECG
Diagnostic Test: Cardiopulmonary exercise test with stress echocardiogram
Diagnostic Test: 24-hour ECG holter monitor
Diagnostic Test: cardiac magnetic resonance scan

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to understand the onset an functional consequences of left ventricular interstitial fibrosis in patients with chronic kidney disease (stage 2 to 5), as well as assess whether transplantation results in a regression of cardiac fibrosis.Thus all patients will undergo: 1) a cardiac magnetic resonance imaging (MRI) scan to assess cardiac function and measure left ventricular interstitial fibrosis; 2) a cardiopulmonary stress echocardiogram to understand the functional consequences of fibrosis and rule out any underlying ischaemic heart disease; 3) a 24 hour holter monitor and electrocardiogram (ECG) to assess whether these patients are at higher risk of arrhythmia.

Full description

Aim and objectives:

The primary objective of this study is to test the following hypotheses:

i) Patients with early stage chronic kidney disease (CKD) exhibit diffuse LV fibrosis manifest by prolonged native myocardial T1 times and expansion of the extracellular volume (ECV) measured on MRI with a graded relationship to eGFR (stage of CKD), independent of blood pressure and arterial stiffness.

The secondary research objectives are to test the following hypotheses:

i) Prolonged native myocardial T1 times are associated with impaired diastolic function, altered arterial-ventricular interaction and impaired effort tolerance.

ii) Prolonged T1 times correlate with increases in serum biomarkers of collagen turnover associated with myocardial fibrosis that could be used to risk stratify individuals and enable targeted, personalized clinical care.

iii) Renal transplantation results in a regression of myocardial fibrosis as measured by T1 mapping.

DESIGN:

A cross-sectional analysis of 40 patients in each stage 2-5 CKD will be undertaken. These individuals will only be studied once (at baseline). In addition to this, at least 20 patients will be studied who are about to undergo a kidney transplant. These individuals will be studied at baseline (around the time of surgery), at 6 weeks post-operatively, and then 1 year post-operatively to assess the effect on renal transplantation on myocardial fibrosis.

SUBJECTS:

Patients will be recruited from the clinics run by University Hospitals Birmingham NHS Foundation Trust (UHB) with stages 2, 3, 4 and 5 CKD defined using eGFR calculated with the 4-variable 'Modification of Diet in Renal Disease' (MDRD) equation, with a minimum of two consecutive tests at least 90 days apart. Forty patients will be recruited per group of CKD. All study subjects will undergo a cardiac MRI scan, a cardiopulmonary exercise tests with stress echocardiogram, a 24-hour ECG holter monitor, and blood tests.

CONTROLS:

Forty healthy control subjects and forty hypertensive control subjects will be studied. All patients will undergo the identical research protocol to the CKD subjects, except they will not have a stress echocardiogram or an ECG holter monitor.

Enrollment

260 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • >18 years old
  • CKD stage 2, 3, 4 and 5

Exclusion criteria

  • Pregnancy
  • Ischaemic heart disease (angina, ACS)
  • Cerebral vascular disease
  • Peripheral vascular disease
  • Renovascular disease
  • Diabetes mellitus
  • Valvular heart disease (more than mild)
  • Established diagnosis of heart failure
  • Cannot have an MRI scan

Trial design

260 participants in 3 patient groups

CKD
Description:
40 patients per group of CKD from stage 2 to stage 5.
Treatment:
Diagnostic Test: 12-lead ECG
Biological: Blood test
Diagnostic Test: cardiac magnetic resonance scan
Diagnostic Test: 24-hour ECG holter monitor
Diagnostic Test: Cardiopulmonary exercise test with stress echocardiogram
Kidney transplant recipients
Description:
20 live-donor recipients will be studied pre-operatively and then followed up at 6 weeks and 1 years post-operatively.
Treatment:
Diagnostic Test: 12-lead ECG
Diagnostic Test: Cardiopulmonary exercise test
Biological: Blood test
Diagnostic Test: cardiac magnetic resonance scan
Diagnostic Test: 24-hour ECG holter monitor
Controls
Description:
40 healthy controls and 40 hypertensive controls.
Treatment:
Diagnostic Test: 12-lead ECG
Diagnostic Test: Cardiopulmonary exercise test
Biological: Blood test
Diagnostic Test: cardiac magnetic resonance scan
Diagnostic Test: Cardiopulmonary exercise test with stress echocardiogram

Trial contacts and locations

1

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Central trial contact

Manvir K Hayer, MBChB; Jonathan N Townend, MD

Data sourced from clinicaltrials.gov

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