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Cornell product is an ECG marker of heart failure with preserved ejection fraction
Eugene Sj Tan1, Siew Pang Chan2,3, Chang Fen Xu4
1Department of Cardiology, National University Heart Centre Singapore, Singapore, Singapore.
Insights
The Cornell product (CP) on ECG effectively identifies heart failure with preserved ejection fraction (HFpEF) and predicts poor prognosis. This easily applicable marker reflects diastolic dysfunction and left ventricular hypertrophy severity.
Area of Science:
- Cardiology
- Electrocardiography
- Heart Failure Research
Background:
- Heart failure with preserved ejection fraction (HFpEF) lacks specific electrocardiogram (ECG) markers.
- Identifying reliable ECG indicators for HFpEF is crucial for risk stratification and prognosis.
Purpose of the Study:
- To investigate the Cornell product (CP) as a potential ECG risk marker for HFpEF.
- To assess the prognostic utility of CP in patients with HFpEF.
Main Methods:
- The Cornell product (CP) was calculated from baseline 12-lead ECG in a prospective study of healthy controls, hypertensive controls, and HFpEF patients (all with ejection fraction ≥50%).
- Participants were followed for 2 years for all-cause mortality and heart failure hospitalizations.
Main Results:
- CP values increased from healthy controls to hypertensive controls to HFpEF, distinguishing HFpEF from hypertension with high specificity.
- A CP cutoff of ≥1800 mm*ms was significantly associated with HFpEF, even after adjusting for clinical and echocardiographic variables.
- Elevated CP independently predicted a composite endpoint of all-cause mortality and HF hospitalizations in HFpEF patients.
Conclusions:
- The Cornell product is a practical ECG marker for identifying HFpEF.
- CP serves as a valuable prognostic tool in HFpEF, reflecting underlying diastolic dysfunction and left ventricular hypertrophy.
Objective:
ECG markers of heart failure (HF) with preserved ejection fraction (HFpEF) are lacking. We hypothesised that the Cornell product (CP) is a risk marker of HFpEF and has prognostic utility in HFpEF.
Methods:
CP =[(amplitude of R wave in aVL+depth of S wave in V3)×QRS] was measured on baseline 12-lead ECG in a prospective Asian population-based study of 606 healthy controls (aged 55±10 years, 45% men), 221 hypertensive controls (62±9 years, 58% men) and 242 HFpEF (68±12 years, 49% men); all with EF ≥50% and followed for 2 years for all-cause mortality and HF hospitalisations.
Results:
CP increased across groups from healthy controls to hypertensive controls to HFpEF, and distinguished between HFpEF and hypertension with an optimal cut-off of ≥1800 mm*ms (sensitivity 40%, specificity 85%). Age, male sex, systolic blood pressure (SBP) and heart rate were independent predictors of CP ≥1800 mm*ms, and CP was associated with echocardiographic E/e' (r=0.27, p<0.01) and left ventricular mass index (r=0.46, p<0.01). Adjusting for clinical and echocardiographic variables and log N-terminal pro B-type natriuretic peptide (NT-proBNP), CP ≥1800 mm*ms was significantly associated with HFpEF (adjusted OR 2.7, 95% CI 1.0 to 7.0). At 2-year follow-up, there were 29 deaths and 61 HF hospitalisations, all within the HFpEF group. Even after adjusting for log NT-proBNP, clinical and echocardiographic variables, CP ≥1800 mm*ms remained strongly associated with a higher composite endpoint of all-cause mortality and HF hospitalisations (adjusted HR 2.1, 95% CI 1.2 to 3.5).
Conclusion:
The Cornell product is an easily applicable ECG marker of HFpEF and predicts poor prognosis by reflecting the severity of diastolic dysfunction and LV hypertrophy.
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