Key result
Left bundle branch block was associated with a significantly increased risk of new-onset heart failure (HR 3.29; 95% CI 1.93-5.63; P<0.001) over 16.5 years of follow-up.
Why the study?
Intraventricular conduction delays are hallmarks of heart failure and structural heart disease, but their prognostic value for these conditions is unclear.
Does the presence of intraventricular conduction delays predict new-onset heart failure and structural heart disease in the general population?
Cohort (n=6,080)
Does the presence of intraventricular conduction delays predict new-onset heart failure and structural heart disease in the general population?
Hazard Ratio: 3.29 (95% CI 1.93–5.63)
p-value: p=< 0.001
LBBB and non-specific IVCD are strong independent predictors of new-onset heart failure and structural heart disease in the general population.
BACKGROUND: Intraventricular conduction delays (IVCDs) are hallmarks of heart failure (HF) and structural heart disease (SHD) but their prognostic value for HF and SHD is unclear. METHODS: Relation of eight IVCDs and the incidence of first-time HF or SHD was studied in a nationally representative random sample of 6080 Finnish subjects aged ≥ 30 years (mean age 52.1, SD 14.5 years) who participated in the health examination including 12-lead ECG. RESULTS: During 16.5 years' follow up, half of the subjects with left bundle branch block (LBBB) and one third of the subjects with non-specific IVCD developed HF. After controlling for known clinical risk factors the hazard ratio (HR) for new-onset HF for LBBB was 3.29 (95% confidence interval 1.93-5.63, P < 0.001) and 3.53 for non-specific IVCD (1.65-7.55, P = 0.001). In corresponding analysis, LBBB predicted SHD with HR 2.60 (1.21-5.62, P = 0.015). Excluding subjects with history of heart disease, including coronary heart disease, did not have impact on results. Right bundle branch block and other IVCDs displayed no relation to endpoints. CONCLUSION: LBBB and non-specific IVCD were associated with more than three-fold risk of new-onset HF. Furthermore, LBBB was associated with novel SHD. Their presence should alert clinician even in subjects free from any known heart disease.
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Rankinen et al. (2020) conducted a cohort in General population (n=6,080). Left bundle branch block (LBBB) and non-specific IVCD vs. Absence of IVCD was evaluated on new-onset heart failure (HR 3.29, 95% CI 1.93-5.63, p=< 0.001). Left bundle branch block was associated with a significantly increased risk of new-onset heart failure (HR 3.29; 95% CI 1.93-5.63; P<0.001) over 16.5 years of follow-up.
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