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Chronic kidney disease (CKD) is associated with a high risk of death and morbidity due to cardiovascular disease. Much of this is caused by left ventricular disease characterised by abnormal muscle thickness and scaring. This process appears to start early in the course of CKD and causes heart failure and dangerous abnormal heart rhythms. Previous work suggests that the process may be reversible by kidney transplantation but almost all of the studies are small, retrospective and lack scientific rigour. Furthermore, they almost all use echocardiography, which is inaccurate in patients with CKD. The investigators plan to perform the first large, prospective, controlled, blind-analysed study using cardiac magnetic resonance imaging to determine whether CKD associated cardiomyopathy is reversed by kidney transplantation and if so, whether factors such as blood pressure and mediators of metabolic bone disease/fibrosis are important in effecting this change. Greater understanding of the mechanisms responsible for CKD associated cardiomyopathy could lead to future strategies and treatments to improve the high cardiovascular mortality associated with this condition.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Transplant recipients | Patients undergoing live donor kidney transplant. |
| |
| Non-transplanted | Patients on the deceased donor waiting list without prospect of a live donor transplant. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cardiac MRI | Diagnostic Test | Cardiac Magnetic Resonance Imaging (Siemens Skyra 3T): will be performed using protocols and techniques already in use in our group. All CMR scan derived parameters will be analysed with the investigator blinded to treatment allocation as in previous studies. |
| Measure | Description | Time Frame |
|---|---|---|
| Left Ventricular Mass | Calculated by Cardiac MRI | One year. |
| Measure | Description | Time Frame |
|---|---|---|
| Native Myocardial T1 Times. | Measured using T1 mapping techniques (MOLLI) | One year. |
| Blood Pressure | 24hr Ambulatory Blood pressure monitoring |
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Inclusion Criteria:
Exclusion Criteria
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The study population will comprise of patients with end-stage renal failure currently awaiting either live or deceased donor transplantation.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Luke Pickup, MBBS | Contact | 07828791429 | luke.pickup2@uhb.nhs.uk | |
| Charles Ferro, MD | Contact | 01213715839 | Charles.ferro@uhb.nhs.uk |
| Name | Affiliation | Role |
|---|---|---|
| Charles Ferro, MD | University Hospital Birmingham NHS Foundation Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Queen Elizabeth Hospital | Recruiting | Birmingham | West Midlands | B15 2TH | United Kingdom |
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| ID | Term |
|---|---|
| D009202 | Cardiomyopathies |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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Markers of CKD-MBD: - calcium, phosphate, alkaline phosphatase and PTH will be analyzed in serum by mass spectroscopy and FGF-23 will be analyzed by ELISA at 0 and 12 months.
|
| One year. |
| Pulse Wave Analysis. | To calculate augmentation index as a marker of arterial stiffness. | One Year |