Dynamic electrocardiogram changes are a novel risk marker for sudden cardiac death

Author:

Pham Hoang Nhat1,Holmstrom Lauri1,Chugh Harpriya1,Uy-Evanado Audrey1,Nakamura Kotoka1,Zhang Zijun2,Salvucci Angelo3,Jui Jonathan4,Reinier Kyndaron1,Chugh Sumeet S12ORCID

Affiliation:

1. Center for Cardiac Arrest Prevention, Department of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center , Advanced Health Sciences Pavilion, Suite A3100, 127 S. San Vicente Blvd., Los Angeles, CA 90048 , USA

2. Division of Artificial Intelligence in Medicine, Department of Medicine, Cedars-Sinai Medical Center , Los Angeles, CA, Advanced Health Sciences Pavilion, Suite A3100, 127 S. San Vicente Blvd., Los Angeles, CA 90048 , USA

3. Ventura County Health Care Agency , Ventura, CA , USA

4. Department of Emergency Medicine, Oregon Health & Science University , Portland, OR , USA

Abstract

Abstract Background and Aims Electrocardiogram (ECG) abnormalities have been evaluated as static risk markers for sudden cardiac death (SCD), but the potential importance of dynamic ECG remodelling has not been investigated. In this study, the nature and prevalence of dynamic ECG remodelling were studied among individuals who eventually suffered SCD. Methods The study population was drawn from two prospective community-based SCD studies in Oregon (2002, discovery cohort) and California, USA (2015, validation cohort). For this present sub-study, 231 discovery cases (2015–17) and 203 validation cases (2015–21) with ≥2 archived pre-SCD ECGs were ascertained and were matched to 234 discovery and 203 validation controls based on age, sex, and duration between the ECGs. Dynamic ECG remodelling was measured as progression of a previously validated cumulative six-variable ECG electrical risk score. Results Oregon SCD cases displayed greater electrical risk score increase over time vs. controls [+1.06 (95% confidence interval +0.89 to +1.24) vs. −0.05 (−0.21 to +0.11); P < .001]. These findings were successfully replicated in California [+0.87 (+0.7 to +1.04) vs. −0.11 (−0.27 to 0.05); P < .001]. In multivariable models, abnormal dynamic ECG remodelling improved SCD prediction over baseline ECG, demographics, and clinical SCD risk factors in both Oregon [area under the receiver operating characteristic curve 0.770 (95% confidence interval 0.727–0.812) increased to area under the receiver operating characteristic curve 0.869 (95% confidence interval 0.837–0.902)] and California cohorts. Conclusions Dynamic ECG remodelling improved SCD risk prediction beyond clinical factors combined with the static ECG, with successful validation in a geographically distinct population. These findings introduce a novel concept of SCD dynamic risk and warrant further detailed investigation.

Funder

National Institutes of Health

National Heart Lung and Blood Institute

Sigrid Juselius Foundation

Finnish Cultural Foundation

Instrumentarium Science Foundation

Orion Research Foundation

Paavo Nurmi Foundation

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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1. Ventricular fibrillation and the proteome problem: can we solve it?;European Heart Journal: Acute Cardiovascular Care;2023-12-01

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