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Left Ventricular Fibrosis in Chronic Kidney Disease

Onset and Functional Consequences of Left Ventricular (LV) Fibrosis in Chronic Kidney

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03176862
Acronym
FibroCKD
Enrollment
260
Registered
2017-06-06
Start date
2015-09-30
Completion date
2018-08-31
Last updated
2017-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Diseases, Cardio-Renal Syndrome, Myocardial Fibrosis, Uraemic Cardiomyopathy

Brief summary

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.

Detailed 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.

Interventions

DIAGNOSTIC_TESTCardiopulmonary exercise test

An exercise bicycle test. No stress echocardiogram.

An MRI scan of the heart

DIAGNOSTIC_TESTCardiopulmonary exercise test with stress echocardiogram

An exercise bicycle test with echocardiogram done during the exercise.

DIAGNOSTIC_TEST24-hour ECG holter monitor

3 stickers attached to a small monitor are worn for 24 hours.

DIAGNOSTIC_TEST12-lead ECG

Can be done immediately by the bedside.

BIOLOGICALBlood test

20 mls of blood will be taken to measure routine laboratory tests and biomarkers of fibrosis.

Sponsors

British Heart Foundation
CollaboratorOTHER
Dr Manvir Kaur Hayer
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
The effect of eGFR on heart muscle scarring (measured from cardiac MRI using T1 times).One baseline visit onlyeGFR is a measurement of kidney function. Heart muscle scarring levels can be derived from cardiac MRI using a technique called T1 mapping. T1 maps of the heart will be acquired using cardiac MRI. eGFR will be measured from a blood tests, using the MDRD equation. The relationship between the measured T1 times and eGFR will be analysed using statistical tests.

Secondary

MeasureTime frameDescription
The relationship between prolonged myocardial T1 and diastolic function.One baseline visit onlyThe following diastolic function parameters will be measured on echocardiography: E/A, deceleration time and E/e'.
The relationship between prolonged myocardial T1 and effort tolerance.One baseline visit onlyThe percent predicted peak oxygen uptake during exercise testing will be used as a surrogate marker of effort tolerance.
The effect of renal transplantation on myocardial fibrosis.Baseline visit (pre-operation), then follow up at 6 weeks and 1 year.Myocardial T1 times (cardiac MRI) and eGFR (blood testing) will best measured.

Countries

United Kingdom

Contacts

Primary ContactManvir K Hayer, MBChB
manvir.hayer@uhb.nhs.uk07812732857
Backup ContactJonathan N Townend, MD
01213712000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026