Dilated Cardiomyopathy
Conditions
Keywords
Dilated cardiomyopathy, Left ventricular reverse remodelling, Heart failure
Brief summary
Approximately 30-40% of patients with non-ischaemic dilated cardiomyopathy (DCM) undergo significant left ventricular reverse remodelling in response to guideline-directed therapies. This is characterised by improvement in systolic dysfunction and regression of left ventricular dilatation. In some patients, extensive left ventricular reverse remodelling is accompanied by resolution of symptoms and normalisation of cardiac biomarkers, resulting in a state of clinical remission. The mechanistic drivers behind left ventricular reverse remodelling and clinical remission are poorly understood. Current techniques to predict ventricular remodelling trajectory and clinical remission in patients with recent-onset DCM are limited. The purpose of this study is to characterise predictors and markers of left ventricular reverse remodelling and clinical remission in patients with recent-onset DCM using molecular markers, genetics and advanced CMR imaging.
Detailed description
The REMIT-DCM study is a single-centre pilot observational cohort study. 70 patients with recent-onset DCM (Group A) and up to 40 healthy volunteers (Group B) will be recruited. Patients with DCM will be recruited over a 2-year period and will be followed up for 12 months. Subjects in Group A may be offered an optional further study visit at 24-48 months after enrolment in order to assess whether cardiac remodelling and clinical remission are sustained over the intermediate-term. Patients with DCM (Group A) will attend 3 study visits at The Royal Brompton Hospital (baseline, 2-3 months and 12 months). Each study visit will involve a clinical consultation, blood sample collection (including routine clinical blood tests and sample storage for exploratory biomarkers), urine sample collection, 12-lead ECG, health questionnaire completion and a cardiovascular magnetic resonance scan (CMR). If patients are unable to have a CMR, 3D transthoracic echocardiography will be performed. Healthy volunteers will attend a single study visit at The Royal Brompton Hospital. This will involve a clinical consultation, blood sample collection (including routine clinical blood tests and sample storage for exploratory biomarkers), urine sample collection, 12-lead ECG, health questionnaire completion and a CMR.
Interventions
OTHER12 months of guideline-directed heart failure therapy
Standard guideline-directed heart failure drug +/- device therapy
Sponsors
Royal Brompton & Harefield NHS Foundation Trust
Imperial College London
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
For DCM cohort (Group A): Inclusion Criteria: * Age ≥16. * Able to give informed consent. * Confirmed DCM with symptom-onset within the last 6 months and LVEF ≤ 45%. The diagnosis of DCM will be confirmed using the European Society of Cardiology definition, based on reduced LVEF and elevated LV end-diastolic volume indexed to body surface area, compared to published age- and sex-specific reference values
Exclusion criteria
* Significant coronary artery heart disease, defined as a stenosis of \>50% of an epicardial coronary artery affecting the proximal or mid-portion of the vessel on invasive angiography or computed tomography coronary angiography (CTCA), previous percutaneous coronary intervention, CMR late gadolinium enhancement pattern suggestive of previous myocardial infarction of ≥ 2 segments of ≥ 50% transmural infarction of the LV wall. * High suspicion of concomitant hypertrophic cardiomyopathy, amyloidosis, Fabry disease, sarcoidosis, active myocarditis, Chagas disease or hemochromatosis. * History of primary valvular heart disease or congenital heart disease. * Severe, untreated or untreatable hypertension (systolic blood pressures routinely \>180 mm Hg and/or diastolic blood pressures \>120 mm Hg) * Pregnancy and/or breastfeeding. * Severe renal disease (GFR \<15 mls/min). For healthy volunteer cohort (Group B): Inclusion Criteria: * Age ≥16. * Able to give informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical remission | 12-months | If all 3 of the following criteria are met at 12-month assessment: i. Increase in left ventricular ejection fraction (LVEF) by ≥ 10% to a value ≥ 50% and decrease in indexed left ventricular end diastolic volume (LVEDV) to within normal range according to age-/sex-corrected normograms. ii. NYHA class I. iii. NT-Pro BNP \<250 ng/L. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Major adverse cardiovascular events | 12-months | Composite of cardiovascular death, major heart failure or major arrhythmic events. |
| Change in health status using Kansas City Cardiomyopathy questionnaire | 12-months | Change in Kansas City Cardiomyopathy questionnaire scores from baseline to 12-months |
| Left ventricular reverse remodelling | 12-months | Evaluated by changes in indexed left ventricular end systolic volume (LVESV), indexed LVEDV and LVEF between baseline and 12 months. |
| Change in health status using EQ-5D questionnaire | 12-months | Change in EQ-5D questionnaire scores from baseline to 12-months |
| Sustained clinical remission at 24-48 months after enrolment | 48 months | For those in clinical remission at 12-month timepoint, the proportion that have sustained clinical remission at 24-48 months after enrolment. |
| Change in health status using SF-12 questionnaire | 12-months | Change in SF-12 questionnaire scores from baseline to 12-months |
Countries
United Kingdom
Outcome results
None listed