Key result
LBBB is linked to ~2.7-fold higher MI rates in adults presenting with chest pain.
Why the study?
The prognostic significance of isolated LBBB in patients presenting with chest pain without prior cardiometabolic or structural heart disease remains unclear.
Does isolated left bundle branch block increase the risk of myocardial infarction, heart failure, and incident heart disease in adults presenting with chest pain without prior cardiometabolic or structural heart disease?
Cohort (n=24,070)
Does isolated left bundle branch block increase the risk of myocardial infarction, heart failure, and incident heart disease in adults presenting with chest pain without prior cardiometabolic or structural heart disease?
Isolated left bundle branch block in patients with chest pain but no prior cardiometabolic disease is a strong prognostic marker for future myocardial infarction, heart failure, and incident heart disease.
Answers are grounded in this paper and cite their sources.
Isolated LBBB signals higher MI risk in chest pain without prior disease; leaves open whether it should guide risk stratification pending prospective validation.
BACKGROUND: Left bundle branch block (LBBB) is a cardiac abnormality frequently associated with structural heart disease and adverse cardiovascular outcomes. However, its prognostic significance in patients without prior cardiometabolic disease remains unclear. OBJECTIVE: To evaluate cardiovascular outcomes in patients presenting with chest pain with versus without LBBB in the absence of prior cardiometabolic or structural heart disease. METHODS: We conducted a retrospective cohort study using TriNetX. Adults presenting with chest pain were divided into two cohorts: patients with LBBB and patients without LBBB. Patients with prior cardiometabolic or structural heart disease were excluded. Propensity score matching was performed, yielding 12,035 patients in each cohort. Outcomes included myocardial infarction, heart failure, and incident heart disease. RESULTS: After matching, patients with LBBB had higher rates of myocardial infarction compared with patients without LBBB (3.8%vs 1.4%, p<0.001). Heart failure was also more common in the LBBB cohort (13.2%vs 4.5%, p<0.001). Incident heart disease occurred in 3.4% of patients with LBBB compared with 0.9% of patients without LBBB (p<0.001). Kaplan-Meier analysis demonstrated significantly worse event-free survival for myocardial infarction, heart failure, and heart disease among patients with LBBB. CONCLUSION: Among patients presenting with chest pain without prior cardiometabolic or structural heart disease, LBBB was associated with increased risks of MI, HF, and heart disease. These findings suggest an association between LBBB and adverse cardiovascular outcomes in this population.
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Abazie et al. (2026) conducted a cohort in Chest pain without prior cardiometabolic or structural heart disease (n=24,070). Left bundle branch block (LBBB) vs. No left bundle branch block was evaluated on Myocardial infarction (p=<0.001). In adults with chest pain and no prior cardiometabolic disease, left bundle branch block was associated with higher rates of myocardial infarction (3.8% vs 1.4%, p<0.001).
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