Prognostic Value of Multiple Circulating Biomarkers for Ventricular Arrhythmias in Left Ventricular
Insights
Big endothelin-1 levels predict ventricular arrhythmias (VA) in patients with left ventricular hypertrabeculation (LVHT). Elevated big endothelin-1 and specific hypertrabeculation locations increase VA risk, aiding in patient risk stratification.
Area of Science:
- Cardiology
- Biomarkers
- Genetics
Background:
- Ventricular arrhythmia (VA) is a significant risk factor for adverse outcomes in patients with left ventricular hypertrabeculation (LVHT).
- Identifying predictive biomarkers for VA in LVHT is crucial for risk stratification and management.
Purpose of the Study:
- To investigate the predictive value of various biomarkers for the occurrence of ventricular arrhythmias in patients diagnosed with left ventricular hypertrabeculation.
- To explore the association between big endothelin-1 concentrations and VA risk in the LVHT cohort.
Main Methods:
- Retrospective cohort study of 265 LVHT patients.
- Analysis of baseline biomarkers including N-terminal pro B-type natriuretic peptide, big endothelin-1, hs-CRP, uric acid, and free fatty acid.
- Multivariable Cox regression and restricted cubic spline analyses to assess VA prediction.
Main Results:
- 82 (30.9%) patients experienced VAs over a median follow-up of 4.34 years.
- Elevated big endothelin-1 concentrations were independently associated with an increased risk of VAs (HR 1.513, P=0.005).
- Higher big endothelin-1 levels, particularly >0.63 pmol/L, especially with cardiomyopathies or specific LV dimensions/function, indicated closer monitoring for VAs.
Conclusions:
- Big endothelin-1 concentrations serve as an independent predictor of VA in LVHT patients.
- The location of hypertrabeculation, in conjunction with big endothelin-1 levels, enhances risk stratification for VAs in this population.
Background:
Ventricular arrhythmia (VA) is an independent risk factor for adverse outcomes in patients with left ventricular hypertrabeculation (LVHT). This study explored the predictive value of biomarkers for VAs in LVHT.
Methods And Results:
This cohort study retrospectively enrolled 265 LVHT patients (mean [±SD] age 44.2±17.0 years, 65.7% male) with data available for N-terminal pro B-type natriuretic peptide, big endothelin-1, high-sensitivity C-reactive protein, uric acid, and free fatty acid. The primary outcome was a composite of non-sustained ventricular tachycardia, sustained ventricular tachycardia, ventricular fibrillation, and appropriate implantable cardioverter defibrillator therapy. Over a median follow-up of 4.34 years, 82 (30.9%) patients experienced VAs. Multivariable Cox regression analysis revealed that baseline concentrations of big endothelin-1 were independently associated with the occurrence of VAs (hazard ratio 1.513; 95% confidence interval 1.136-2.013; P=0.005). Restricted cubic spline analysis showed that susceptibility to VAs increased markedly with increases in big endothelin-1 concentrations. Subgroup analysis revealed that LVHT patients with big endothelin-1 concentrations >0.63 pmol/L should be closely monitored for VAs, particularly when higher concentrations are accompanied by cardiomyopathies, left ventricular (LV) end-diastolic diameters ≥60 mm, or LV ejection fraction <50%. Individuals with elevated big endothelin-1 concentrations and isolated hypertrabeculation in the LV lateral wall had a significantly greater risk of VAs (log-rank P=0.002).
Conclusions:
Big endothelin-1 concentrations and the location of hypertrabeculation can help with risk stratification for VAs in LVHT.
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