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Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases ( The DIFFUsE Study)

Impact of Diffuse Myocardial Fibrosis on the Ventricular Function in Regurgitant Left-Sided Valve Heart Diseases " The DIFFUsE Study "

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02747485
Acronym
DIFFUsE
Enrollment
316
Registered
2016-04-21
Start date
2016-05-01
Completion date
2026-11-01
Last updated
2026-05-19

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

Conditions

Valve Heart Diseases

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.

Interventions

DEVICECardiac MRI
BIOLOGICALblood samples

Serum levels of biomarkers of myocardial fibrosis (galectine-3 and ST2) will be measured

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
the rate of diffuse myocardial fibrosis6 months

Secondary

MeasureTime frame
Correlations between ECV and the global longitudinal strain and the serum level of Galectin-3 and ST242 months
Correlations between ECV changes and genetic factors42 months
correlations between ECV and the severity of the regurgitation42 months
correlation between ECV and the myocardial deformation quantified by speckle tracking echocardiography (2D Strain)42 months

Countries

France

Contacts

STUDY_DIRECTORCatherine GEINDRE

Assistance Publique Hopitaux De Marseille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026