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B-type natriuretic peptide and outcome in patients with apical hypertrophic cardiomyopathy
Shota Shirotani1, Yuichiro Minami1, Chihiro Saito1
1Department of Cardiology, Tokyo Women's Medical University, Tokyo, Japan.
Insights
Elevated B-type natriuretic peptide (BNP) levels in apical hypertrophic cardiomyopathy (HCM) patients predict adverse outcomes. High BNP levels independently indicate a greater risk of combined endpoints in this population.
Area of Science:
- Cardiology
- Genetics
- Biomarkers
Background:
- Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease.
- The apical phenotype of HCM presents unique clinical challenges.
- Prognostic value of B-type natriuretic peptide (BNP) in apical HCM is not well-established.
Purpose of the Study:
- To investigate the association between B-type natriuretic peptide (BNP) levels and clinical outcomes in patients with apical hypertrophic cardiomyopathy (HCM).
- To determine if BNP can serve as a prognostic biomarker for adverse events in this specific HCM phenotype.
Main Methods:
- Retrospective analysis of 144 patients with apical HCM phenotype.
- Measurement of plasma BNP levels at initial evaluation.
- Long-term follow-up to assess HCM-related adverse outcomes.
Main Results:
- Median BNP level was 188.5 pg/mL.
- A BNP cutoff of 226.0 pg/mL predicted adverse outcomes (log-rank p<0.001).
- High BNP levels (≥226.0 pg/mL) were an independent determinant of adverse events (aHR: 3.71; p=0.002).
Conclusions:
- B-type natriuretic peptide (BNP) measurement can aid in risk stratification for patients with apical HCM.
- Elevated BNP levels are associated with increased risk of adverse outcomes in apical HCM.
- BNP serves as a valuable prognostic tool for apical HCM management.
Background:
Although elevated B-type natriuretic peptide (BNP) levels predict outcome in patients with hypertrophic cardiomyopathy (HCM), the association between BNP levels and outcome in patients with the apical phenotype of HCM remains unclear. We evaluated the impact of elevated BNP levels on outcome in a cohort of apical HCM patients.
Methods:
Among 432 HCM patients, 144 with an apical phenotype were examined. Plasma BNP levels were measured at the time of the initial evaluation.
Results:
The median (interquartile range) BNP level at initial evaluation in these patients was 188.5 (72.0-334.4) pg/mL. During a median follow-up period of 9.5 years, 34 patients experienced HCM-related adverse outcomes, including 2 patients with sudden death, 5 with appropriate implantable defibrillator shocks, 3 with stroke-related death, 8 with non-fatal stroke, and 16 with heart failure hospitalization. Receiver operating characteristic (ROC) curve analysis of the prognostic value of BNP for the combined endpoint gave an area under the ROC curve of 0.756, and optimal BNP cut-off point of 226.0pg/mL. Patients with high BNP levels (≥226.0pg/mL) were at significantly greater risk of the combined endpoint (log-rank p<0.001) than patients with low BNP levels. Multivariable analysis that included BNP levels and potential confounders showed that high BNP levels were an independent determinant of the combined endpoint (adjusted hazard ratio: 3.71; p=0.002).
Conclusions:
Measuring BNP may help stratify the risk of HCM-related adverse outcome in apical HCM patients.
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