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Published on: February 17, 2018
Electrocardiographic left ventricular hypertrophy and sudden cardiac death
Konsta Kivimäki1, Leo-Pekka Lyytikäinen2, Kjell Nikus3
1Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Insights
The Cornell product criterion for electrocardiographic left ventricular hypertrophy (ECG LVH) showed the strongest association with sudden cardiac death (SCD) in high-risk patients. However, the overall predictive performance for SCD events was modest.
Area of Science:
- Cardiology
- Electrophysiology
- Preventive Cardiology
Background:
- Electrocardiographic left ventricular hypertrophy (ECG LVH) is linked to sudden cardiac death (SCD).
- Limited comparative data exist on different ECG LVH criteria in high-risk populations.
- Studies often lack evaluation in diverse coronary syndromes and non-coronary artery disease populations.
Purpose of the Study:
- To compare the association between multiple ECG LVH criteria and SCD events.
- To evaluate these associations in patients with acute and chronic coronary syndromes, including those without significant coronary artery disease.
- To assess the discriminative ability of each criterion for predicting SCD.
Main Methods:
- Retrospective analysis of 19,220 patients from two cohorts.
- Evaluation of seven ECG LVH criteria: Sokolow-Lyon, Cornell voltage, Cornell product, Peguero-Lo Presti, MESA, RaVL, and Romhilt-Estes.
- Fine-Gray subdistribution hazard models and time-varying Cox proportional hazards models were used to assess associations with SCD, accounting for competing risks.
Main Results:
- The Cornell product criterion demonstrated the strongest association with SCD events (SHR 1.29; p=0.003) in multivariable analyses.
- This association remained consistent in time-varying models and after excluding patients with reduced ejection fraction.
- The discriminative ability of ECG LVH criteria for SCD was modest (AUC 0.67).
Conclusions:
- The Cornell product criterion is most strongly associated with SCD events among evaluated ECG LVH criteria, even after risk factor adjustment.
- This association holds true whether LVH is present at baseline or develops during follow-up.
- Despite the strongest association, the overall predictive power of ECG LVH criteria for SCD remains modest.
Background And Objectives:
Electrocardiographic (ECG) left ventricular hypertrophy (LVH) has been associated with sudden cardiac death (SCD), but comparative data on different ECG LVH criteria in high-risk populations are limited. We compared the association between multiple ECG LVH criteria and SCD events in two coronary angiography cohorts spanning acute and chronic coronary syndromes, including patients without angiographic evidence of coronary artery disease.
Methods:
This retrospective study included 19,220 consecutive patients from two cohorts. ECG LVH criteria included Sokolow-Lyon, Cornell voltage, Cornell product, Peguero-Lo Presti, MESA, RaVL, and Romhilt-Estes criteria. Associations with SCD events were assessed using Fine-Gray subdistribution hazard models accounting for the competing risk of non-SCD death. For the most robust criteria, additional time-varying Cox proportional hazards models were conducted to evaluate longitudinal associations based on repeated ECG measurements (>280,000 ECGs). Additionally, the 3-year discriminative ability of each criterion for SCD event was assessed.
Results:
Across the combined cohorts, the median follow-up was 8.4 years, with a total of 858 SCD events. In multivariable Fine-Gray analyses, Cornell product showed the strongest association with SCD events (SHR 1.29, 95% CI 1.09-1.52, p 0.003). This association remained consistent in time-varying Cox models and after excluding patients with left ventricular ejection fraction ≤35%. Discriminative performance was modest (AUC 0.67, 95% CI 0.64-0.70).
Conclusion:
After adjustment for established SCD risk factors, Cornell product showed the strongest association with SCD events, with consistent finding whether ECG LVH criterion was present at baseline or developed during the follow-up. However, both the strength of association and discriminative performance were modest.
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