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Published on: June 14, 2016
Temporal progression of replacement and interstitial fibrosis in optimally managed dilated cardiomyopathy patients: A
Pawel Rubiś1, Paweł Banyś2, Maciej Krupiński2
1Krakow Specialist Hospital named after St. John Paul II, Pradnicka street 80, 31-202 Krakow, Poland; Department of Cardiac and Vascular Diseases, Jagiellonian University Medical College, Institute of Cardiology, Krakow Specialist Hospital named after St. John Paul II, Poland.
Insights
In dilated cardiomyopathy (DCM) patients, cardiac fibrosis remained stable over one year, but left ventricular (LV) volumes decreased. The LV matrix volume index predicted patient outcomes.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Fibrosis Research
Background:
- Dilated cardiomyopathy (DCM) is characterized by progressive left ventricular (LV) dysfunction.
- Understanding the dynamic evolution of cardiac fibrosis in DCM is crucial for predicting patient outcomes.
- Fibrotic processes, including replacement and interstitial fibrosis, contribute to myocardial stiffening and adverse remodeling.
Purpose of the Study:
- To prospectively evaluate the one-year dynamic changes in replacement and interstitial fibrosis in patients with DCM.
- To assess the relationship between fibrotic changes, left ventricular volumes, and clinical outcomes in DCM patients.
- To identify predictors of adverse events in DCM patients based on cardiac imaging parameters.
Main Methods:
- Prospective observational study involving 102 DCM patients.
- Cardiac magnetic resonance (CMR) imaging including late gadolinium enhancement (LGE) for replacement fibrosis and T1-mapping for interstitial fibrosis (extracellular volume fraction - ECV).
- Assessment of LV matrix and cellular volumes, with follow-up CMR after approximately 14 months and clinical outcome assessment.
Main Results:
- Replacement fibrosis (LGE mass) remained stable, while LGE extent increased significantly (p < 0.01) over one year.
- Interstitial fibrosis (ECV) showed no significant change.
- Left ventricular matrix and cell volumes demonstrated significant regression.
- LV matrix volume index at follow-up was an independent predictor of adverse clinical outcomes (all-cause mortality, heart transplantation, LVAD, or heart failure worsening).
Conclusions:
- In optimally managed DCM patients, cardiac fibrosis (replacement and interstitial) is relatively stable within one year.
- Significant regression of LV matrix and cell volumes occurs over one year in DCM patients.
- The LV matrix volume index derived from CMR is a valuable independent predictor of long-term prognosis in DCM.
Background:
To prospectively examine the dynamic evolution of fibrotic processes within a one-year in patients with dilated cardiomyopathy (DCM).
Methods:
Between May 2019 and September 2020, 102 DCM patients (mean age 45.2 ± 11.8 years, EF 29.9 ± 11.6%) underwent cardiac magnetic resonance (CMR-1). After 13.9 ± 2.9 months, 92 of these patients underwent a follow-up CMR (CMR-2). Replacement fibrosis was assessed via late gadolinium enhancement (LGE), quantified in terms of LGE mass and extent. Interstitial fibrosis was evaluated via T1-mapping and expressed as extracellular volume fraction (ECV). This data, along with left ventricular (LV) mass, facilitated the calculation of LV matrix and cellular volumes.
Results:
At CMR-1, LGE was present in 45 patients (48.9%), whereas at CMR-2 LGE was detected in 46 (50%) (p = 0.88). Although LGE mass remained stable, LGE extent increased from 2.18 ± 4.1% to 2.7 ± 4.6% (p < 0.01). Conversely, ECV remained unchanged [27.7% (25.5-31.3) vs. 26.7% (24.5-29.9); p = 0.19]; however, LV matrix and cell volumes exhibited a noteworthy regression. During a subsequent follow-up of 19.2 ± 9 months (spanning from CMR-2 to April 30th, 2023), the composite primary outcome (all-cause mortality, HTX, LVAD or heart failure worsening) was evident in 18 patients. Only the LV matrix volume index at follow-up was an independent predictor of outcome (OR 1.094; 95%CI 1.004-1.192; p < 0.05).
Conclusions:
In optimally managed DCM patients, both replacement and interstitial fibrosis remained stable over the course of one year. In contrast, LV matrix and cell volumes displayed significant regression. LV matrix volume index at 12-month follow-up was found to be an independent predictor of outcome in DCM.
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