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Soluble Neprilysin - Cardiac Function and Outcome in Hypertrophic Cardiomyopathy
Akiomi Yoshihisa1,2, Tetsuro Yokokawa1,3, Yasuhiro Ichijo1
1Department of Cardiovascular Medicine, Fukushima Medical University Fukushima Japan.
Insights
Soluble neprilysin (sNEP) correlates with B-type natriuretic peptide and cardiac function in hypertrophic cardiomyopathy (HCM) patients. However, sNEP did not predict cardiac events or mortality in this cohort.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Research
Background:
- Circulating soluble neprilysin (sNEP) is a prognostic marker in heart failure with reduced ejection fraction.
- Its role in hypertrophic cardiomyopathy (HCM) and its prognostic implications remain less understood.
Purpose of the Study:
- To investigate the associations between sNEP and laboratory/echocardiographic parameters in HCM patients.
- To evaluate the predictive value of sNEP for clinical outcomes, including cardiac events and mortality in HCM.
Main Methods:
- Cross-sectional analysis of sNEP levels against laboratory (BNP, troponin I) and echocardiographic (left/right ventricular function, mass) parameters in 93 HCM patients.
- Prospective follow-up for cardiac events (worsening HF, cardiac death) and all-cause mortality.
Main Results:
- sNEP positively correlated with B-type natriuretic peptide (BNP).
- sNEP negatively correlated with left ventricular ejection fraction and right ventricular fractional area change.
- Kaplan-Meier and Cox proportional hazard analyses showed sNEP was not a predictor of cardiac events or all-cause mortality.
Conclusions:
- Soluble neprilysin is associated with established biomarkers and cardiac systolic function in HCM.
- sNEP does not appear to be a significant prognostic marker for clinical outcomes in patients with HCM.
Abstract:
Circulating soluble neprilysin (sNEP) predicts outcome in heart failure (HF) patients with reduced ejection fraction (EF), but not in those with preserved EF. We examined sNEP in patients with hypertrophic cardiomyopathy (HCM), and their correlations with other biomarkers, cardiac function, and clinical outcome. We examined the associations between sNEP and the laboratory and echocardiography parameters in the HCM patients (n=93). Regarding the laboratory data, sNEP had a significant positive correlation with B-type natriuretic peptide (BNP; R=0.326, P=0.003), but not with troponin I. As for the echocardiographic parameters, sNEP negatively correlated with left ventricular EF (R=-0.283, P=0.009) and right ventricular fractional area change (R=-0.277, P=0.012), but not with left ventricular mass. Next, we prospectively followed up on the patients for cardiac events, including worsening HF or cardiac death, and all-cause mortality. On Kaplan-Meier analysis (mean follow-up, 1,021 days), the cardiac event rate and all-cause mortality were similar between the higher sNEP group (sNEP ≥median level of 1.43 ng/mL, n=46) and lower sNEP group (sNEP <1.43 ng/mL, n=47). On Cox proportional hazard analysis, sNEP was not a predictor of cardiac event or all-cause mortality. Soluble neprilysin appears to correlate with BNP and cardiac systolic function, but it is not significantly associated with prognosis in HCM patients.
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