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.
Abstract