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Relationship between myocardial fibrosis and left bundle branch block. Does it exist?
Elena Rimskaya1, Olga Aparina1, Olga Stukalova1
1Chazov National Medical Research Center of Cardiology 121552, Academician Chazov str., 15a, Moscow, Russia.
Insights
Left bundle branch block (LBBB) in dilated cardiomyopathy (DCM) patients is not caused by focal or interstitial fibrosis. Diffuse inflammation may worsen systolic dysfunction, while increased fibrosis in idiopathic LBBB suggests a developing DCM.
Area of Science:
- Cardiology
- Cardiac Imaging
- Pathology
Background:
- Left bundle branch block (LBBB) is a common finding in patients with dilated cardiomyopathy (DCM).
- The underlying substrate and relationship between cardiac fibrosis and LBBB in DCM remain incompletely understood.
- Differentiating LBBB causes is crucial for prognosis and management.
Purpose of the Study:
- To investigate the association between focal and diffuse left ventricular (LV) fibrosis and LBBB in patients with DCM.
- To compare fibrosis patterns in DCM patients with and without LBBB, and in those with idiopathic LBBB.
Main Methods:
- Cardiovascular magnetic resonance (CMR) with late gadolinium enhancement (LGE) was used to assess focal fibrosis (core scar and gray zone) and diffuse fibrosis (diffuse intensity ratio - DIR).
- Endomyocardial biopsy (EMB) quantified collagen volume fraction (CVF) in a subset of patients.
- Study included DCM patients with LBBB (DCM-LBBB), DCM without LBBB (DCM-nonLBBB), idiopathic LBBB, and healthy volunteers (HV).
Main Results:
- No significant difference in focal or diffuse fibrosis was found between DCM-LBBB and DCM-nonLBBB patients.
- CVF correlated with DIR, supporting DIR as a measure of diffuse fibrosis.
- Patients with idiopathic LBBB showed higher DIR values compared to HV, suggesting underlying diffuse myocardial changes.
Conclusions:
- Focal and interstitial fibrosis are not associated with LBBB in DCM.
- Diffuse inflammation in DCM-LBBB may contribute to systolic dysfunction but does not cause LBBB.
- Increased interstitial fibrosis in idiopathic LBBB may indicate a latent process leading to DCM development.
Aim:
to assess the relation of focal and diffuse left ventricular (LV) fibrosis to left bundle branch block (LBBB).
Materials And Methods:
60 patients with dilated cardiomyopathy and LBBB (DCM-LBBB), 50 DCM-nonLBBB patients, 15 patients with LBBB and structurally normal heart (idiopathic LBBB) and 10 healthy volunteers (HV) underwent cardiovascular magnetic resonance (CMR) with late gadolinium enhancement (LGE). LGE LV images were post-proceeded for core scar (CS) and gray zone (GZ) calculation. Diffuse LV fibrosis was estimated on LGE-CMR images with the diffuse intensity ratio (DIR). Endomyocardial biopsy (EMB) was performed in 15(24.6 %) DCM-LBBB and 16 (32 %) non-LBBB DCM patients and allowed the quantification of collagen volume fraction (CVF).
Results:
The percentage of CVF correlated with the DIR value in the same segment (r = 0.66, p < 0.001). The value of CVF in EMB and frequency of LGE in both DCM groups was comparable (p = 0.8). In DCM-nonLBBB patients the percentage of CS was significantly higher (4.0[1.6; 11.7]% versus 1.4[0.1;8.5]% in DCM-LBBB patients, p = 0.047), whereas percentage of GZ and total fibrosis in both DCM groups was comparable. DIR value was higher in patients with idiopathic LBBB than in HV (0.54±0.09 versus 0.34±0.1, р<0,001).
Conclusion:
Neither focal nor interstitial fibrosis is associated with LBBB in DCM patients. Diffuse inflammation in DCM-LBBB patients may contribute to the progression of systolic dysfunction but is not a cause of LBBB. The increased value of interstitial fibrosis in patients with idiopathic LBBB may reflect latent diffuse process in myocardium inexorably leading to DCM development.
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