Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases ( The DIFFUsE Study) (DIFFUsE)
Primary Purpose
Valve Heart Diseases
Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Cardiac MRI
blood samples
myocardial biopsy
blood samples
Sponsored by
About this trial
This is an interventional prevention trial for Valve Heart Diseases
Eligibility Criteria
Inclusion Criteria:
- All consecutive patients referred for organic MR and/or AR at least moderate to severe according to the ESC guidelines criteria⁴ will be eligible. The moderate to severe criteria will defined by echocardiography as followed:
- MR: an effective regurgitant orifice area (EOA) >30mm2 and/or a regurgitant volume (RV) >45mL
- AR: an EOA >20mm2 and/or a RV >45mL
Exclusion Criteria:
- Age < 18 years
- Pregnancy
- Impossibility to maintain a decubitus position
- Arrhythmia that do not allow an ECG synchronization during MRI
- Hemodynamic instability
- Indication of urgent surgery
- Known coronary artery disease
- Severe arterial hypertension
- Cardiomyopathy
- Claustrophobia
- Gadolinium intolerance
- Implantable medical devices that do allow to perform MRI
- Severe renal insufficiency with clearance <35 mL/min
- Vulnerable patients
- Acute infective endocarditis
- Aortic dissection
- Moderate or severe mitral stenosis (mitral area <1.5cm2/m2)
- Moderate or severe aortic stenosis (aortic area <0.8cm2/m2, or Vmax>3m/s, or mean gradient>30mmHg)
- Previous cardiac surgery
Sites / Locations
- Assistance Publique Hopitaux de MarseilleRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
organic left-sided regurgitant valve
Arm Description
Outcomes
Primary Outcome Measures
the rate of diffuse myocardial fibrosis
Secondary Outcome Measures
Correlations between ECV and the global longitudinal strain and the serum level of Galectin-3 and ST2
Correlations between ECV changes and genetic factors
correlations between ECV and the severity of the regurgitation
correlation between ECV and the myocardial deformation quantified by speckle tracking echocardiography (2D Strain)
Full Information
NCT ID
NCT02747485
First Posted
April 19, 2016
Last Updated
March 4, 2019
Sponsor
Assistance Publique Hopitaux De Marseille
1. Study Identification
Unique Protocol Identification Number
NCT02747485
Brief Title
Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases ( The DIFFUsE Study)
Acronym
DIFFUsE
Official Title
Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases " The DIFFUsE Study "
Study Type
Interventional
2. Study Status
Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (Actual)
Primary Completion Date
August 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique Hopitaux De Marseille
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
New strategies are needed to early detect myocardial involvement in these diseases. Histological studies showed that diffuse fibrosis and cardiomyocyte hypertrophy precede the LV remodelling (dilatation) observed by cardiac imaging. Quantification of LV diffuse myocardial fibrosis using magnetic resonance imaging (MRI) could reach this goal. Recently, contrast enhanced cardiac MRI has been used to measure the extracellular volume fraction (ECV) of the myocardium, and it has been able to detect diffuse myocardial fibrosis. In diseases in which increased collagen deposition enlarges the extra-cellular space, the ECV can act as a fibrosis index. ECV is correlated with the amount of fibrosis measured by histology. Left ventricular overloads induced by regurgitant VHD result in cardiomyocyte hypertrophy and diffuse fibrosis. Other methods can be used to estimate the degree of myocardial fibrosis such as the serum level of galectine-3 or ST2. Moreover, although the pathophysiological mechanisms leading to the occurrence of myocardial fibrosis differ in patients with various cardiac diseases, the cellular effectors of fibrotic remodelling are common and involve similar signalling pathways. At the cellular level, key progression of ventricular hypertrophy is associated with increased cardiomyocytes apoptosis and fibrosis, suggesting that these two processes are responsible for the transition.
To our knowledge, no study has analysed the impact of the rate of myocardial diffuse fibrosis, non-invasively estimated by ECV, in the risk of LV dysfunction during MR and AR, especially after surgery. The measurement of ECV could become an important tool for risk stratification in left-sided regurgitant VHD. Thus, it would provide an early marker of LV myocardial involvement before the occurrence of global remodeling, might help physicians in surgical decision, and would improve prognosis. This is an innovative original project because it uses modern imaging modalities to answer to a crucial question. The clinical implications would be important because this work would modify the international surgical indications of MR and AR in order to finally improve the prognosis of patients with this frequent heart disease. Moreover, investigators will analyze the genetic factors that can influence the myocardial reaction resulting from these regurgitations, which will improve the quality of this work and offer new future perspectives.
Investigators hypothesize that the ECV measurement could be used as an early predictor of LV dysfunction in the left-sided valve regurgitations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Valve Heart Diseases
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
316 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
organic left-sided regurgitant valve
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Cardiac MRI
Intervention Type
Biological
Intervention Name(s)
blood samples
Intervention Description
Serum levels of biomarkers of myocardial fibrosis (galectine-3 and ST2) will be measured
Intervention Type
Procedure
Intervention Name(s)
myocardial biopsy
Intervention Type
Genetic
Intervention Name(s)
blood samples
Intervention Description
extract DNA to look for genomic mutations associated with the disease.
Primary Outcome Measure Information:
Title
the rate of diffuse myocardial fibrosis
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Correlations between ECV and the global longitudinal strain and the serum level of Galectin-3 and ST2
Time Frame
42 months
Title
Correlations between ECV changes and genetic factors
Time Frame
42 months
Title
correlations between ECV and the severity of the regurgitation
Time Frame
42 months
Title
correlation between ECV and the myocardial deformation quantified by speckle tracking echocardiography (2D Strain)
Time Frame
42 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All consecutive patients referred for organic MR and/or AR at least moderate to severe according to the ESC guidelines criteria⁴ will be eligible. The moderate to severe criteria will defined by echocardiography as followed:
MR: an effective regurgitant orifice area (EOA) >30mm2 and/or a regurgitant volume (RV) >45mL
AR: an EOA >20mm2 and/or a RV >45mL
Exclusion Criteria:
Age < 18 years
Pregnancy
Impossibility to maintain a decubitus position
Arrhythmia that do not allow an ECG synchronization during MRI
Hemodynamic instability
Indication of urgent surgery
Known coronary artery disease
Severe arterial hypertension
Cardiomyopathy
Claustrophobia
Gadolinium intolerance
Implantable medical devices that do allow to perform MRI
Severe renal insufficiency with clearance <35 mL/min
Vulnerable patients
Acute infective endocarditis
Aortic dissection
Moderate or severe mitral stenosis (mitral area <1.5cm2/m2)
Moderate or severe aortic stenosis (aortic area <0.8cm2/m2, or Vmax>3m/s, or mean gradient>30mmHg)
Previous cardiac surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
THUNY franck, PU PH
Email
franck.thuny@ap-hm.fr
First Name & Middle Initial & Last Name or Official Title & Degree
AVIERINOS Jean-Francois, PU PH
Email
jfavierinos@ap-hm.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine GEINDRE
Organizational Affiliation
Assistance Publique Hopitaux De Marseille
Official's Role
Study Director
Facility Information:
Facility Name
Assistance Publique Hopitaux de Marseille
City
Marseille
State/Province
Bouche DU Rhone
ZIP/Postal Code
13354
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
THUNY FRANCK
Email
franck.thuny@ap-hm.fr
First Name & Middle Initial & Last Name & Degree
AVIERINOS JEAN-FRANCOIS
Email
jfavierinos@ap-hm.fr
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases ( The DIFFUsE Study)
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